COMPOUNDS AND METHODS FOR THE MODULATION OF PROTEINS

Abstract

In certain embodiments, the present disclosure provides compounds and methods of increasing the amount or activity of a target protein in a cell. In certain embodiments, the compounds comprise a translation suppression element inhibitor. In certain embodiments, the translation suppression element inhibitor is a uORF inhibitor. In certain embodiments, the uORF inhibitor is an antisense compound.

Claims

1. A method of increasing translation of a target protein in a cell, comprising contacting the cell with an antisense compound comprising a modified oligonucleotide, wherein the target protein is encoded by a target transcript comprising at least one translation suppression element and wherein the modified oligonucleotide is complementary to a target site within a translation suppression element region of the target transcript; and thereby increasing translation of the target protein in the cell.

2. A method of decreasing suppression of translation of a target protein in a cell, comprising contacting the cell with an antisense compound comprising a modified oligonucleotide, wherein the target protein is encoded by a target transcript comprising at least one translation suppression element and wherein the modified oligonucleotide is complementary to a target site within a translation suppression element region of the target transcript; and thereby decreasing suppression of translation of the target protein in the cell.

3. A method of increasing the amount or activity of a target protein in a cell, comprising contacting the cell with an antisense compound comprising a modified oligonucleotide, wherein the target protein is encoded by a target transcript comprising at least one translation suppression element and wherein the modified oligonucleotide is complementary to a target site within a translation suppression element region of the target transcript; and thereby increasing the amount or activity of the target protein in the cell.

4. A method of increasing the amount a target protein in a cell, comprising contacting the cell with an antisense compound comprising a modified oligonucleotide, wherein the target protein is encoded by a target transcript comprising at least one translation suppression element and wherein the modified oligonucleotide is complementary to a target site within a translation suppression element region of the target transcript; and thereby increasing expression of the target protein in the cell.

5. The method of any of claims 1-4, wherein the translation suppression element region is the 5′ untranslated region.

6. The method of any of claims 1-4, wherein the translation suppression element region is within the 5′ untranslated region.

7. The method of any of claims 1-6, wherein the translation suppression element region comprises one and only one uORF.

8. The method of any of claims 1-7, wherein the translation suppression element region contains at least one uORF.

9. The method of any of claims 1-8, wherein the translation suppression element consists of a uORF.

10. The method of any of claims 1-8, wherein the translation suppression element region contains one or more uORFs, and wherein the one or more uORFs do not suppress translation of the target transcript.

11. The method of any of claims 1-6, wherein the translation suppression element region does not contain a uORF.

12. The method of any of claims 1-11, wherein the translation suppression element region comprises at least one stem-loop structure.

13. The method of claim 12, wherein at least one stem-loop is a translation suppression element.

14. The method of any of claims 1-13, wherein the translation suppression element arises from a mutation.

15. The method of claim 14, wherein the mutation creates a uORF.

16. The method of claim 14 or 15, wherein the mutation creates a disease.

17. The method of any of claims 1-16, wherein the modified oligonucleotide consists of 10 to 40 linked nucleosides.

18. The method of any of claims 1-16, wherein the modified oligonucleotide consists of 12 to 22 linked nucleosides.

19. The method of any of claims 1-16, wherein the modified oligonucleotide consists of 15 to 22 linked nucleosides.

20. The method of any of claims 1-16, wherein the modified oligonucleotide consists of 16 to 20 linked nucleosides.

21. The method of any of claims 1-16, wherein the modified oligonucleotide consists of 18 to 20 linked nucleosides.

22. The method of any of claims 1-16, wherein the modified oligonucleotide consists of 16 to 18 linked nucleosides.

23. The method of any of claims 1-16, wherein the modified oligonucleotide consists of 16 linked nucleosides.

24. The method of any of claims 1-16, wherein the modified oligonucleotide consists of 17 linked nucleosides.

25. The method of any of claims 1-16, wherein the modified oligonucleotide consists of 18 linked nucleosides.

26. The method of any of claims 1-25, wherein at least one nucleoside of the modified oligonucleotide comprises a modified sugar moiety.

27. The method of any of claims 1-26, wherein each nucleoside of the modified oligonucleotide is a modified nucleoside or an unmodified nucleoside.

28. The method of claim 27, wherein each unmodified nucleoside is a 2′-deoxy nucleoside.

29. The method of any of claims 1-26, wherein each nucleoside of the modified oligonucleotide is a modified nucleoside.

30. The method of claim 29, wherein each nucleoside of the modified oligonucleotide is a modified nucleoside, each independently comprising a modified sugar moiety.

31. The method of any of claims 1-30, wherein the modified oligonucleotide comprises at least 15 modified nucleosides, each independently comprising a modified sugar moiety.

32. The method of any of claims 1-30, wherein the modified oligonucleotide comprises at least two modified nucleosides comprising modified sugar moieties that are the same as one another.

33. The method of any of claims 1-30, wherein the modified oligonucleotide comprises at least two modified nucleosides comprising modified sugar moieties that are different from one another.

34. The method of any of claims 1-30, wherein the modified oligonucleotide comprises a modified region of at least 5 contiguous modified nucleosides.

35. The method of any of claims 1-30, wherein the modified oligonucleotide comprises a modified region of at least 10 contiguous modified nucleosides.

36. The method of any of claims 1-30, wherein the modified oligonucleotide comprises a modified region of at least 15 contiguous modified nucleosides.

37. The method of any of claims 1-30, wherein the modified oligonucleotide comprises a modified region of at least 18 contiguous modified nucleosides.

38. The method of any of claims 1-21 and 26-30, wherein the modified oligonucleotide comprises a modified region of at least 20 contiguous modified nucleosides.

39. The method of claim any of claims 26-38, wherein at least one modified sugar moiety is a 2′-substituted sugar moiety.

40. The method of claim 39, wherein the 2′-substitutent of at least one 2′-substituted sugar moiety is selected from among: 2′-OMe, 2′-F, and 2′-MOE.

41. The method of claim 40, wherein the 2′-substitutent of at least one 2′-substituted sugar moiety is 2′-MOE.

42. The method of claim 40, wherein the 2′-substitutent of at least one 2′-substituted sugar moiety is 2′-OMe.

43. The method of claim 40, wherein the 2′-substitutent of at least one 2′-substituted sugar moiety is 2′F.

44. The method of any of claims 26-43, wherein at least one modified sugar moiety is a bicyclic sugar moiety.

45. The method of claim 44, wherein at least one bicyclic sugar moiety is LNA or cEt.

46. The method of claim 44, wherein at least one bicyclic sugar moiety is LNA.

47. The method of claim 44, wherein at least one bicyclic sugar moiety is cEt.

48. The method of any of claims 26-47, wherein at least one sugar moiety is a sugar surrogate.

49. The method of claim 48, wherein at least one sugar surrogate is a morpholino.

50. The method of claim 48, wherein at least one sugar surrogate is a modified morpholino.

51. The method of claim 48, wherein at least one sugar surrogate is a peptide nucleic acid.

52. The method of claim 29 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd and 3.sup.rd 3′-most terminal nucleoside of the modified oligonucleotide are bicyclic sugar moieties.

53. The method of claim 29 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd and 4.sup.th 3′-most terminal nucleoside of the modified oligonucleotide are bicyclic sugar moieties.

54. The method of claim 29 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd, 4.sup.th, and 5.sup.th 3′-most terminal nucleoside are bicyclic sugar moieties.

55. The method of claim 29 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd, 4.sup.th, 5.sup.th, and 6.sup.th 3′-most terminal nucleoside are bicyclic sugar moieties.

56. The method of claims 52-55, wherein each bicyclic sugar moiety of the modified oligonucleotide is independently selected from LNA and cEt.

57. The method of claims 52-55, wherein the bicyclic sugar moiety of the modified oligonucleotide is cEt.

58. The method of any of claims 52-57, wherein each nucleoside in the modified oligonucleotide that does not comprise a bicyclic sugar moiety comprises a modified sugar moiety selected from 2′-F, 2′-OMe, and 2′-MOE.

59. The method of claim 29 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st and 2.sup.nd 3′-most terminal nucleosides of the modified oligonucleotide are 2′-F modified sugar moieties.

60. The method of claim 29 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd and 3.sup.rd 3′-most terminal nucleosides of the modified oligonucleotide are 2′-F modified sugar moieties.

61. The method of claim 29 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd and 4.sup.th 3′-most terminal nucleosides of the modified oligonucleotide are 2′-F modified sugar moieties.

62. The method of claim 29 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd, 4.sup.th, and 5.sup.th 3′-most terminal nucleosides of the modified oligonucleotide are 2′-F modified sugar moieties.

63. The method of claim 29 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd, 4.sup.th, 5.sup.th, and 6.sup.th 3′-most terminal nucleosides of the modified oligonucleotide are 2′-F modified sugar moieties.

64. The method of claim 28, wherein the 1.sup.st, 3.sup.rd and 5.sup.th 3′-most terminal nucleosides of the modified oligonucleotide are cEt nuncleosides, wherein the 2.sup.nd and 4.sup.th 3′-most terminal nucleosides of the modified oligonucleotide are 2′-deoxy nucleosides, and wherein each remaining nucleoside is a 2′-modified nucleoside.

65. The method of claim 64, wherein each remaining nucleoside is a 2′-OMe nucleoside.

66. The method of claim 64, wherein each remaining nucleoside is a 2′-MOE nucleoside.

67. The method of any of claims 1-66, wherein each internucleoside linkage of the modified oligonucleotide is a phosphodiester internucleoside linkage.

68. The method of any of claims 1-66, wherein each internucleoside linkage of the modified oligonucleotide is a phosphorothioate internucleoside linkage.

69. The method of any of claims 1-66, wherein the modified oligonucleotide comprises at least one modified internucleoside linkage.

70. The method of claim 69, wherein the modified internucleoside linkage is a phosphorothioate internucleoside linkage.

71. The method of claim 69 or 70, wherein each internucleoside linkage of the modified oligonucleotide is either a phosphodiester internucleoside linkage or a phosphorothioate internucleoside linkage.

72. The method of claim 71, wherein the modified oligonucleotide has exactly 2 phosphodiester internucleoside linkages.

73. The method of claim 71, wherein the modified oligonucleotide has exactly 3 phosphodiester internucleoside linkages.

74. The method of claim 71, wherein the modified oligonucleotide has exactly 4 phosphodiester internucleoside linkages.

75. The method of any of claims 1-74, wherein the antisense compound comprises at least one conjugate group.

76. The method of claim 75, wherein the conjugate group comprises GalNAc.

77. The method of any of claims 1-75, wherein the antisense compound consists of the modified oligonucleotide.

78. The method of any of claims 1-77, wherein the antisense compound is not a gapmer.

79. The method of any of claims 1-77, wherein the antisense compound does not recruit RNase H.

80. The method of any of claims 1-79, wherein the antisense compound does not alter the amount of the target nucleic acid transcript.

81. The method of any of claims 1-80, wherein the antisense compound is single-stranded.

82. The method of claim 81, wherein the antisense compound has a 5′-terminal group comprising a stabilized phosphate.

83. The method of claim 82, wherein the 5′-terminal stabilized phosphate is a vinyl phosphonate.

84. The method of any of claims 1-83, wherein the cell is contacted by a prodrug of the antisense compound.

85. The method of any of claims 1-84, wherein the expression, translation, or amount or activity of the target protein is increased by at least 10%.

86. The method of any of claims 1-84, wherein the expression, translation, or amount or activity of the target protein is increased by at least 20%.

87. The method of any of claims 1-84, wherein the expression, translation, or amount or activity of the target protein is increased by at least 30%.

88. The method of any of claims 1-84, wherein the expression, translation, or amount or activity of the target protein is increased by at least 50%.

89. The method of any of claims 1-84, wherein the expression, translation, or amount or activity of the target protein is increased by at least 100%.

90. The method of any of claims 1-84, wherein the expression, translation, or amount or activity of the target protein is increased by at least 120%.

91. The method of any of claims 1-84, wherein the expression, translation, or amount or activity of the target protein is increased by at least 150%.

92. The method of any of claims 1-84, wherein the expression, translation, or amount or activity of the target protein is increased by at least 200%.

93. The method of any of claims 1-84, wherein the expression, translation, or amount or activity of the target protein is increased by at least 250%.

94. The method of any of claims 1-93, wherein the cell is in vitro.

95. The method of any of claims 1-93, wherein the cell is in a subject.

96. The method of claim 95, wherein the subject has a disease or condition and wherein at least one symptom of the disease or condition is ameliorated.

97. The method of claim 94 or 95, wherein the cell is in an animal.

98. The method of claim 97, wherein the animal is a human.

99. An antisense compound comprising a modified oligonucleotide consisting of 10-30 linked nucleosides having a nucleobase sequence complementary to a target site within a translation suppression element region of a target transcript and wherein the modified oligonucleotide does not have more than four contiguous unmodified 2′-deoxy nucleosides.

100. The antisense compound of claim 99, wherein the translation suppression element region is the 5′ untranslated region.

101. The antisense compound of claim 99, wherein the translation suppression element region is within the 5′ untranslated region.

102. The antisense compound of any of claims 99-101, wherein the translation suppression element region comprises one and only one uORF.

103. The antisense compound of any of claims 99-101, wherein the translation suppression element region contains at least one uORF.

104. The antisense compound of any of claims 99-103, wherein the translation suppression element consists of a uORF.

105. The antisense compound of any of claims 99-104, wherein the translation suppression element region contains one or more uORFs, and wherein the one or more uORFs do not suppress translation of the target transcript.

106. The antisense compound of any of claims 99-101, wherein the translation suppression element region does not contain a uORF.

107. The antisense compound of any of claims 99-106, wherein the translation suppression element region comprises at least one stem-loop structure.

108. The antisense compound of claim 107, wherein at least one stem-loop is a translation suppression element.

109. The antisense compound of any of claims 99-108, wherein the translation suppression element arises from a mutation.

110. The antisense compound of claim 109, wherein the mutation creates a uORF.

111. The antisense compound of claim 109 or 110, wherein the mutation creates a disease.

112. The antisense compound of any of claims 99-111, wherein the modified oligonucleotide consists of 12 to 22 linked nucleosides.

113. The antisense compound of any of claims 99-111, wherein the modified oligonucleotide consists of 15 to 22 linked nucleosides.

114. The antisense compound of any of claims 99-111, wherein the modified oligonucleotide consists of 16 to 20 linked nucleosides.

115. The antisense compound of any of claims 99-111, wherein the modified oligonucleotide consists of 18 to 20 linked nucleosides.

116. The antisense compound of any of claims 99-111, wherein the modified oligonucleotide consists of 16 to 18 linked nucleosides.

117. The antisense compound of any of claims 99-111, wherein the modified oligonucleotide consists of 16 linked nucleosides.

118. The antisense compound of any of claims 99-111, wherein the modified oligonucleotide consists of 17 linked nucleosides.

119. The antisense compound of any of claims 99-111, wherein the modified oligonucleotide consists of 18 linked nucleosides.

120. The antisense compound of any of claims 99-119, wherein at least one nucleoside of the modified oligonucleotide comprises a modified sugar moiety.

121. The antisense compound of any of claims 99-120, wherein each nucleoside of the modified oligonucleotide is a modified nucleoside or an unmodified nucleoside.

122. The antisense compound of claim 121, wherein each unmodified nucleoside is a 2′-deoxy nucleoside.

123. The antisense compound of any of claims 99-120, wherein each nucleoside of the modified oligonucleotide is a modified nucleoside.

124. The antisense compound of claim 123, wherein each nucleoside of the modified oligonucleotide is a modified nucleoside, each independently comprising a modified sugar moiety.

125. The antisense compound of any of claims 99-124, wherein the modified oligonucleotide comprises at least 15 modified nucleosides, each independently comprising a modified sugar moiety.

126. The antisense compound of any of claims 99-124, wherein the modified oligonucleotide comprises at least two modified nucleosides comprising modified sugar moieties that are the same as one another.

127. The antisense compound of any of claims 99-124, wherein the modified oligonucleotide comprises at least two modified nucleosides comprising modified sugar moieties that are different from one another.

128. The antisense compound of any of claims 99-124, wherein the modified oligonucleotide comprises a modified region of at least 5 contiguous modified nucleosides.

129. The antisense compound of any of claims 99-124, wherein the modified oligonucleotide comprises a modified region of at least 10 contiguous modified nucleosides.

130. The antisense compound of any of claims 99-124, wherein the modified oligonucleotide comprises a modified region of at least 15 contiguous modified nucleosides.

131. The antisense compound of any of claims 99-124, wherein the modified oligonucleotide comprises a modified region of at least 18 contiguous modified nucleosides.

132. The antisense compound of any preceeding claim, wherein the modified oligonucleotide comprises a modified region of at least 20 contiguous modified nucleosides.

133. The antisense compound of any of claims 124-132, wherein at least one modified sugar moiety is a 2′-substituted sugar moiety.

134. The antisense compound of claim 133, wherein the 2′-substitutent of at least one 2′-substituted sugar moiety is selected from among: 2′-OMe, 2′-F, and 2′-MOE.

135. The antisense compound of claim 134, wherein the 2′-substitutent of at least one 2′-substituted sugar moiety is 2′-MOE.

136. The antisense compound of claim 134, wherein the 2′-substitutent of at least one 2′-substituted sugar moiety is 2′-OMe.

137. The antisense compound of claim 134, wherein the 2′-substitutent of at least one 2′-substituted sugar moiety is 2′F.

138. The antisense compound of any of claims 124-138, wherein at least one modified sugar moiety is a bicyclic sugar moiety.

139. The antisense compound of claim 138, wherein at least one bicyclic sugar moiety is LNA or cEt.

140. The antisense compound of claim 138, wherein at least one bicyclic sugar moiety is LNA.

141. The antisense compound of claim 138, wherein at least one bicyclic sugar moiety is cEt.

142. The antisense compound of any of claims 124-141, wherein at least one sugar moiety is a sugar surrogate.

143. The antisense compound of claim 142, wherein at least one sugar surrogate is a morpholino.

144. The antisense compound of claim 142, wherein at least one sugar surrogate is a modified morpholino.

145. The antisense compound of claim 142, wherein at least one sugar surrogate is a peptide nucleic acid.

146. The antisense compound of claim 123 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, and 3.sup.rd 3′-most terminal nucleoside of the modified oligonucleotide are bicyclic sugar moieties.

147. The antisense compound of claim 123 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd, and 4.sup.th 3′-most terminal nucleoside of the modified oligonucleotide are bicyclic sugar moieties.

148. The antisense compound of claim 123 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd, 4.sup.th, and 5.sup.th 3′ most terminal nucleoside are bicyclic sugar moieties.

149. The antisense compound of claim 123 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd, 4.sup.th, 5.sup.th, and 6.sup.th 3′-most terminal nucleoside are bicyclic sugar moieties.

150. The antisense compound of claims 146-149, wherein each bicyclic sugar moiety of the modified oligonucleotide is independently selected from LNA and cEt.

151. The antisense compound of claims 146-149, wherein the bicyclic sugar moiety of the modified oligonucleotide is cEt.

152. The antisense compound of claims 146-151, wherein each nucleoside in the modified oligonucleotide that does not comprise a bicyclic sugar moiety comprises a modified sugar moiety selected from 2′-F, 2′-OMe, and 2′-MOE.

153. The antisense compound of claim 123 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st and 2.sup.nd 3′-most terminal nucleosides of the modified oligonucleotide are 2′-F modified sugar moieties.

154. The antisense compound of claim 123 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, and 3.sup.rd 3′-most terminal nucleosides of the modified oligonucleotide are 2′-F modified sugar moieties.

155. The antisense compound of claim 123 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd, and 4.sup.th 3′-most terminal nucleosides of the modified oligonucleotide are 2′-F modified sugar moieties.

156. The antisense compound of claim 123 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd, 4.sup.th, and 5.sup.th 3′-most terminal nucleosides of the modified oligonucleotide are 2′-F modified sugar moieties.

157. The antisense compound of claim 123 wherein each modified nucleoside comprises a modified sugar moiety, and wherein the 1.sup.st, 2.sup.nd, 3.sup.rd, 4.sup.th, 5.sup.th, and 6.sup.th 3′-most terminal nucleosides of the modified oligonucleotide are 2′-F modified sugar moieties.

158. The antisense compound of claim 122, wherein the 1.sup.st, 3.sup.rd, and 5.sup.th 3′-most terminal nucleosides of the modified oligonucleotide are cEt nuncleosides, wherein the 2.sup.nd and 4.sup.th 3′-most terminal nucleosides of the modified oligonucleotide are 2′-deoxy nucleosides, and wherein each remaining nucleoside is a 2′-modified nucleoside.

159. The antisense compound of claim 158, wherein each remaining nucleoside is a 2′-OMe nucleoside.

160. The antisense compound of claim 158, wherein each remaining nucleoside is a 2′-MOE nucleoside.

161. The antisense compound of any of claims 99-160, wherein each internucleoside linkage of the modified oligonucleotide is a phosphodiester internucleoside linkage.

162. The antisense compound of any of claims 99-160, wherein each internucleoside linkage of the modified oligonucleotide is a phosphorothioate internucleoside linkage.

163. The antisense compound of any of claims 99-160, wherein the modified oligonucleotide comprises at least one modified internucleoside linkage.

164. The antisense compound of claim 163, wherein the modified internucleoside linkage is a phosphorothioate internucleoside linkage.

165. The antisense compound of claim 163 or 164, wherein each internucleoside linkage of the modified oligonucleotide is either a phosphodiester internucleoside linkage or a phosphorothioate internucleoside linkage.

166. The antisense compound of claim 165, wherein the modified oligonucleotide has exactly 2 phosphodiester internucleoside linkages.

167. The antisense compound of claim 165, wherein the modified oligonucleotide has exactly 3 phosphodiester internucleoside linkages.

168. The antisense compound of claim 165, wherein the modified oligonucleotide has exactly 4 phosphodiester internucleoside linkages.

169. The antisense compound of any of claims 99-168, wherein the antisense compound comprises at least one conjugate group.

170. The antisense compound of claim 169, wherein the conjugate group comprises GalNAc.

171. The antisense compound of any of claims 99-170, wherein the antisense compound consists of the modified oligonucleotide.

172. The antisense compound of any of claims 99-170, wherein the antisense compound is not a gapmer.

173. The antisense compound of any of claims 99-170, wherein the antisense compound does not recruit RNase H.

174. The antisense compound of any of claims 99-173, wherein the antisense compound does not alter the amount of the target nucleic acid transcript.

175. The antisense compound of any of claims 99-174, wherein the antisense compound is single-stranded.

176. The antisense compound of claim 175, wherein the antisense compound has a 5′-terminal group comprising a stabilized phosphate.

177. The antisense compound of claim 176, wherein the 5′-terminal stabilized phosphate is a vinyl phosphonate.

178. A pharmaceutical composition comprising a prodrug of the antisense compound of any of claims 99-177.

179. A method comprising contacting a cell with antisense compound of any of claims 99-178.

180. A method of increasing translation of a target protein in a cell, comprising contacting a cell with antisense compound of any of claims 99-178.

181. A method of decreasing suppression of translation of a target protein in a cell, comprising contacting a cell with antisense compound of any of claims 99-178.

182. A method of increasing the amount or activity of a target protein in a cell, comprising contacting a cell with antisense compound of any of claims 99-178.

183. A method of increasing the amount a target protein in a cell, comprising contacting a cell with antisense compound of any of claims 99-178.

184. The method of any of claims 179-183, wherein the expression, translation, or amount or activity of the target protein is increased by at least 10%.

185. The method of any of claims 179-183, wherein the expression, translation, or amount or activity of the target protein is increased by at least 20%.

186. The method of any of claims 179-183, wherein the expression, translation, or amount or activity of the target protein is increased by at least 30%.

187. The method of any of claims 179-183, wherein the expression, translation, or amount or activity of the target protein is increased by at least 50%.

188. The method of any of claims 179-183, wherein the expression, translation, or amount or activity of the target protein is increased by at least 100%.

189. The method of any of claims 179-183, wherein the expression, translation, or amount or activity of the target protein is increased by at least 120%.

190. The method of any of claims 179-183, wherein the expression, translation, or amount or activity of the target protein is increased by at least 150%.

191. The method of any of claims 179-183, wherein the expression, translation, or amount or activity of the target protein is increased by at least 200%.

192. The method of any of claims 179-183, wherein the expression, translation, or amount or activity of the target protein is increased by at least 250%.

193. The method of any of claims 179-192, wherein the cell is in vitro.

194. The method of any of claims 179-192, wherein the cell is in a subject.

195. The method of claim 194, wherein the subject has a disease or condition and wherein at least one symptom of the disease or condition is ameliorated.

196. The method of claim 194 or 195, wherein the cell is in an animal.

197. The method of claim 196, wherein the animal is a human.

Description

DETAILED DESCRIPTION

[0720] It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed. Herein, the use of the singular includes the plural unless specifically stated otherwise. As used herein, the use of “or” means “and/or” unless stated otherwise. Furthermore, the use of the term “including” as well as other forms, such as “includes” and “included”, is not limiting. Also, terms such as “element” or “component” encompass both elements and components comprising one unit and elements and components that comprise more than one subunit, unless specifically stated otherwise.

[0721] The section headings used herein are for organizational purposes only and are not to be construed as limiting the subject matter described. All documents, or portions of documents, cited in this application, including, but not limited to, patents, patent applications, articles, books, and treatises, are hereby expressly incorporated by reference in their entirety for any purpose.

Definitions

[0722] Unless otherwise indicated, the following terms have the following meanings:

[0723] As used herein, “target transcript” means a transcript that encodes a target protein. In certain embodiments, a target transcript contains a primary open reading frame that encodes a primary protein and one or more start sites at which translation of a polypeptide that is not the target protein may be initiated. In certain such embodiments, a target transcript contains a primary open reading frame and a uORF. In certain such embodiments, a target transcript contains a primary open reading frame and more than one uORF. In certain embodiments, a target transcript contains a primary open reading frame and does not contain a uORF. In certain embodiments, a target transcript contains a primary open reading frame and a translation suppression element.

[0724] As used herein, “translation suppression element,” means any sequence and/or secondary structure in the 5′-UTR of a target transcript that reduces, inhibits, and/or suppresses translation of the target transcript. In certain embodiments, a translation suppression element comprises a uORF. In certain embodiments, a translation suppression element does not comprise a uORF. In certain embodiments, a translation suppression element comprises one or more stem-loops. In certain embodiments, a translation suppression element comprises greater than 60%, greater than 70%, or greater than 80% GC content. In certain embodiments, the translation suppression element is a uORF. In certain embodiments, the translation suppression element is a stem-loop.

[0725] As used herein, “translation suppression element inhibitor,” means any means any agent capable of specifically inhibiting the activity of a translation suppression element. In certain embodiments, the activity of a translation suppression element inhibitor is suppression of translation of the pORF polypeptide or protein on the same transcript. For example, translation suppression element inhibitors include nucleic acids (including antisense compounds and siRNA), peptides, antibodies, small molecules, and other agents capable of inhibiting the amount or activity of a translation suppression element.

[0726] As used herein, “translation suppression element region” means a portion of the target transcript that comprises one or more translation suppression elements. In certain embodiments, a translation suppression element region comprises a uORF. In certain embodiments, a translation suppression element region comprises more than one uORF. In certain embodiments, a translation suppression element region comprises a uORF and at least one translation suppression element that is not a uORF. In certain embodiments, a translation suppression element region comprises a translation suppression element that is not a uORF and does not contain a uORF.

[0727] As used herein, “GC content” means the percentage of total nucleosides in a particular portion of a nucleic acid or oligonucleotide that are either G or C or that base pair with G or C.

[0728] As used herein, “consecutive GC nucleosides” or “consecutive GC nucleotides” means a portion of adjacent nucleosides in a nucleic acid or oligonucleotide that are all either G or C or that base pair with G or C.

[0729] As used herein, “target protein” means a protein that one desires to increase in amount, concentration, or activity. In certain embodiments, the target protein is encoded by the primary open reading frame of a target transcript.

[0730] As used herein, “target transcript” means a transcript that encodes a target protein. In certain embodiments, a target transcript contains a primary open reading frame that encodes a primary protein and one or more start sites at which translation of a polypeptide that is not the target protein may be initiated. In certain such embodiments, a target transcript contains a primary open reading frame and a uORF. In certain such embodiments, a target transcript contains a primary open reading frame and more than one uORF.

[0731] As used herein, “primary open reading frame” or “pORF” means the portion of the target transcript that encodes the primary protein associated with the transcript. In certain embodiments, the pORF encodes the target protein.

[0732] As used herein, “primary protein” means a protein encoded by a primary open reading frame.

[0733] As used herein, “target site” means the portion of the target transcript having a nucleobase sequence that is complementary to a portion of the nucleobase sequence of a modified oligonucleotide. In certain embodiments, the modified oligonucleotide is complementary to the target site across the entire length of the modified oligonucleotide.

[0734] As used herein, “start site” means a group of nucleobases on a transcript at which a ribosomal subunit is recruited. In certain embodiments, a start site may result in initiation of translation. In certain embodiments, a start site is an AUG codon. In certain embodiments, a start site is a non-canonical start codon.

[0735] As used herein, “upstream open reading frame start site” or “uORF start site” means a start site that is upstream of the pORF start codon. In certain embodiments, a uORF start site initiates translation of a polypeptide that is not the target protein.

[0736] As used herein, “uORF start site region” means a portion of the target transcript that comprises a uORF start site. In certain embodiments, a uORF start site region comprises a uORF start site and the 100 nucleosides upstream and downstream of the uORF start site. In certain embodiments, a uORF start site region comprises a uORF start site and the 75 nucleosides upstream and downstream of the uORF start site. In certain embodiments, a uORF start site region comprises a uORF start site and the 50 nucleosides upstream and downstream of the uORF start site. In certain embodiments, a uORF start site region comprises a uORF start site and the 30 nucleosides upstream and downstream of the uORF start site. In certain embodiments, a uORF start site region comprises a uORF start site and the 20 nucleosides upstream and downstream of the uORF start site. In certain embodiments, a uORF start site region comprises the 5′ untranslated region. In certain embodiments, a uORF start site region consists of the 5′-UTR.

[0737] As used herein, “uORF” or “upstream open reading frame” means a portion of a target transcript that comprises a start site upstream of (i.e. 5′ of) the pORF and an in frame termination codon. In certain embodiments, a uORF is the portion of the target transcript that is translated when translation is initiated at a uORF start site. In certain embodiments, a uORF does not overlap with a pORF. In certain embodiments, a uORF does overlap with a pORF. In certain embodiments a uORF overlaps with another uORF. In certain embodiments, a uORF is out of frame with a pORF.

[0738] As used herein, “wild-type uORF start site” means a uORF start site that does not arise from a mutation.

[0739] As used herein, “wild-type uORF start site region” means the uORF start site region of a wild-type uORF start site.

[0740] As used herein, “a uORF start site that arises from a mutation” means a uORF start site, where the same portion of the target transcript on the wild-type allele does not contain a uORF start site.

[0741] As used herein, “uORF polypeptide” means a polypeptide encoded by a uORF. In certain embodiments, a uORF polypeptide is a protein.

[0742] As used herein, “uORF inhibitor” means any agent capable of specifically inhibiting the activity of a uORF. In certain embodiments, the activity of a uORF is suppression of translation of the pORF polypeptide or protein on the same transcript. In certain embodiments, the activity of a uORF is suppression of translation of the pORF polypeptide or protein on a different transcript. For example, uORF specific inhibitors include nucleic acids (including antisense compounds and siRNA), peptides, antibodies, small molecules, and other agents capable of inhibiting the amount or activity of a uORF.

[0743] As used herein, “suppression of translation of a target protein in a cell,” means that translation of the target protein is less than the translation of the target protein in the absence of one or more TSEs.

[0744] As used herein, “nucleoside” means a compound comprising a nucleobase moiety and a sugar moiety. Nucleosides include, but are not limited to, naturally occurring nucleosides (as found in DNA and RNA) and modified nucleosides. Nucleosides may be linked to a phosphate moiety.

[0745] As used herein, “chemical modification” means a chemical difference in a compound when compared to a naturally occurring counterpart. Chemical modifications of oligonucleotides include nucleoside modifications (including sugar moiety modifications and nucleobase modifications) and internucleoside linkage modifications. In reference to an oligonucleotide, chemical modification does not include differences only in nucleobase sequence.

[0746] As used herein, “furanosyl” means a structure comprising a 5-membered ring comprising four carbon atoms and one oxygen atom.

[0747] As used herein, “naturally occurring sugar moiety” means a ribofuranosyl as found in naturally occurring RNA or a deoxyribofuranosyl as found in naturally occurring DNA.

[0748] As used herein, “sugar moiety” means a naturally occurring sugar moiety or a modified sugar moiety of a nucleoside.

[0749] As used herein, “modified sugar moiety” means a substituted sugar moiety or a sugar surrogate.

[0750] As used herein, “substituted sugar moiety” means a furanosyl that is not a naturally occurring sugar moiety. Substituted sugar moieties include, but are not limited to furanosyls comprising substituents at the 2′-position, the 3′-position, the 5′-position and/or the 4′-position. Certain substituted sugar moieties are bicyclic sugar moieties.

[0751] As used herein, “2′-substituted sugar moiety” means a furanosyl comprising a substituent at the 2′-position other than H or OH. Unless otherwise indicated, a 2′-substituted sugar moiety is not a bicyclic sugar moiety (i.e., the 2′-substituent of a 2′-substituted sugar moiety does not form a bridge to another atom of the furanosyl ring.

[0752] As used herein, “MOE” means —OCH.sub.2CH.sub.2OCH.sub.3.

[0753] As used herein, “2′-F nucleoside” refers to a nucleoside comprising a sugar comprising fluoroine at the 2′ position. Unless otherwise indicated, the fluorine in a 2′-F nucleoside is in the ribo position (replacing the OH of a natural ribose).

[0754] As used herein, “2′-(ara)-F” refers to a 2′-F substituted nucleoside, wherein the fluoro group is in the arabino position.

[0755] As used herein the term “sugar surrogate” means a structure that does not comprise a furanosyl and that is capable of replacing the naturally occurring sugar moiety of a nucleoside, such that the resulting nucleoside sub-units are capable of linking together and/or linking to other nucleosides to form an oligonucleotide which is capable of hybridizing to a complementary oligonucleotide. Such structures include rings comprising a different number of atoms than furanosyl (e.g., 4, 6, or 7-membered rings); replacement of the oxygen of a furanosyl with a non-oxygen atom (e.g., carbon, sulfur, or nitrogen); or both a change in the number of atoms and a replacement of the oxygen. Such structures may also comprise substitutions corresponding to those described for substituted sugar moieties (e.g., 6-membered carbocyclic bicyclic sugar surrogates optionally comprising additional substituents). Sugar surrogates also include more complex sugar replacements (e.g., the non-ring systems of peptide nucleic acid). Sugar surrogates include without limitation morpholinos, cyclohexenyls and cyclohexitols.

[0756] As used herein, “bicyclic sugar moiety” means a modified sugar moiety comprising a 4 to 7 membered ring (including but not limited to a furanosyl) comprising a bridge connecting two atoms of the 4 to 7 membered ring to form a second ring, resulting in a bicyclic structure. In certain embodiments, the 4 to 7 membered ring is a sugar ring. In certain embodiments the 4 to 7 membered ring is a furanosyl. In certain such embodiments, the bridge connects the 2′-carbon and the 4′-carbon of the furanosyl.

[0757] As used herein, “nucleotide” means a nucleoside further comprising a phosphate linking group. As used herein, “linked nucleosides” may or may not be linked by phosphate linkages and thus includes, but is not limited to “linked nucleotides.” As used herein, “linked nucleosides” are nucleosides that are connected in a continuous sequence (i.e. no additional nucleosides are present between those that are linked).

[0758] As used herein, “nucleobase” means a group of atoms that can be linked to a sugar moiety to create a nucleoside that is capable of incorporation into an oligonucleotide, and wherein the group of atoms is capable of bonding with a complementary naturally occurring nucleobase of another oligonucleotide or nucleic acid. Nucleobases may be naturally occurring or may be modified.

[0759] As used herein the terms, “unmodified nucleobase” or “naturally occurring nucleobase” means the naturally occurring heterocyclic nucleobases of RNA or DNA: the purine bases adenine (A) and guanine (G), and the pyrimidine bases thymine (T), cytosine (C) (including 5-methyl C), and uracil (U).

[0760] As used herein, “modified nucleobase” means any nucleobase that is not a naturally occurring nucleobase.

[0761] As used herein, “modified nucleoside” means a nucleoside comprising at least one chemical modification compared to naturally occurring RNA or DNA nucleosides. Modified nucleosides comprise a modified sugar moiety and/or a modified nucleobase.

[0762] As used herein, “bicyclic nucleoside” or “BNA” means a nucleoside comprising a bicyclic sugar moiety.

[0763] As used herein, “constrained ethyl nucleoside” or “cEt” means a nucleoside comprising a bicyclic sugar moiety comprising a 4′-CH(CH.sub.3)—O-2′bridge.

[0764] As used herein, “locked nucleic acid nucleoside” or “LNA” means a nucleoside comprising a bicyclic sugar moiety comprising a 4′-CH.sub.2—O-2′bridge.

[0765] As used herein, “2′-substituted nucleoside” means a nucleoside comprising a substituent at the 2′-position other than H or OH. Unless otherwise indicated, a 2′-substituted nucleoside is not a bicyclic nucleoside.

[0766] As used herein, “2′-deoxynucleoside” means a nucleoside comprising 2′-H furanosyl sugar moiety, as found in naturally occurring deoxyribonucleosides (DNA). In certain embodiments, a 2′-deoxynucleoside may comprise a modified nucleobase or may comprise an RNA nucleobase (e.g., uracil).

[0767] As used herein, “oligonucleotide” means a compound comprising a plurality of linked nucleosides. In certain embodiments, an oligonucleotide comprises one or more unmodified ribonucleosides (RNA) and/or unmodified deoxyribonucleosides (DNA) and/or one or more modified nucleosides.

[0768] As used herein “oligonucleoside” means an oligonucleotide in which none of the internucleoside linkages contains a phosphorus atom. As used herein, oligonucleotides include oligonucleosides.

[0769] As used herein, “modified oligonucleotide” means an oligonucleotide comprising at least one modified nucleoside and/or at least one modified internucleoside linkage. Examples of modified oligonucleotides include single-stranded and double-stranded compounds, such as, antisense compounds, siRNAs, shRNAs, ssRNAs, and occupancy-based compounds.

[0770] As used herein “internucleoside linkage” means a covalent linkage between adjacent nucleosides in an oligonucleotide.

[0771] As used herein “naturally occurring internucleoside linkage” means a 3′ to 5′ phosphodiester linkage.

[0772] As used herein, “modified internucleoside linkage” means any internucleoside linkage other than a naturally occurring internucleoside linkage.

[0773] As used herein, “oligomeric compound” means a polymeric structure comprising two or more sub-structures. In certain embodiments, the sub-structures are nucleotides or nucleosides. In certain embodiments, an oligomeric compound comprises an oligonucleotide. In certain embodiments, an oligomeric compound consists of an oligonucleotide. In certain embodiments, an oligomeric compound consists of an antisense compound.

[0774] As used herein, “terminal group” means one or more atom attached to either, or both, the 3′ end or the 5′ end of an oligonucleotide. In certain embodiments a terminal group is a conjugate group. In certain embodiments, a terminal group comprises one or more terminal group nucleosides.

[0775] As used herein, “conjugate group” means an atom or group of atoms bound to an oligonucleotide or oligomeric compound. In general, conjugate groups modify one or more properties of the oligonucleotide or oligomeric compound to which they are attached, including, but not limited to pharmacodynamic, pharmacokinetic, binding, absorption, cellular distribution, cellular uptake, charge and/or clearance properties.

[0776] As used herein, “conjugate linking group” means any atom or group of atoms used to attach a conjugate to an oligonucleotide or oligomeric compound.

[0777] As used herein, “antisense compound” means a compound comprising or consisting of an oligonucleotide at least a portion of which is complementary to a target nucleic acid to which it is capable of hybridizing, resulting in at least one antisense activity.

[0778] As used herein, “antisense activity” means any detectable and/or measurable change attributable to the hybridization of an antisense compound to its target nucleic acid.

[0779] As used herein, “detecting” or “measuring” means that a test or assay for detecting or measuring is performed. Such detection and/or measuring may result in a value of zero. Thus, if a test for detection or measuring results in a finding of no activity (activity of zero), the step of detecting or measuring the activity has nevertheless been performed.

[0780] As used herein, “detectable and/or measureable activity” means a measurable activity that is not zero.

[0781] As used herein, “essentially unchanged” means little or no change in a particular parameter, particularly relative to another parameter which changes much more. In certain embodiments, a parameter is essentially unchanged when it changes less than 5%. In certain embodiments, a parameter is essentially unchanged if it changes less than two-fold while another parameter changes at least ten-fold. For example, in certain embodiments, an antisense activity is a change in the amount of a target nucleic acid. In certain such embodiments, the amount of a non-target nucleic acid is essentially unchanged if it changes much less than the target nucleic acid does, but the change need not be zero.

[0782] As used herein, “expression” means the process by which a gene ultimately results in a protein. Expression includes, but is not limited to, transcription, post-transcriptional modification (e.g., splicing, polyadenlyation, addition of 5′-cap), translation, and post-translational modification.

[0783] As used herein, “translation” means the process in which a polypeptide (e.g. a protein) is translated from an mRNA. In certain embodiments, an increase in translation means an increase in the number of polypeptide (e.g. a protein) molecules that are made per copy of mRNA that encodes said polypeptide.

[0784] As used herein, “target nucleic acid” means a nucleic acid molecule to which an antisense compound is intended to hybridize.

[0785] As used herein, “mRNA” means an RNA molecule that encodes a protein.

[0786] As used herein, “pre-mRNA” means an RNA transcript that has not been fully processed into mRNA. Pre-RNA includes one or more intron.

[0787] As used herein, “targeting” or “targeted to” means the association of an antisense compound to a particular target nucleic acid molecule or a particular region of a target nucleic acid molecule. An antisense compound targets a target nucleic acid if it is sufficiently complementary to the target nucleic acid to allow hybridization under physiological conditions.

[0788] As used herein, “nucleobase complementarity” or “complementarity” when in reference to nucleobases means a nucleobase that is capable of base pairing with another nucleobase. For example, in DNA, adenine (A) is complementary to thymine (T). For example, in RNA, adenine (A) is complementary to uracil (U). In certain embodiments, complementary nucleobase means a nucleobase of an antisense compound that is capable of base pairing with a nucleobase of its target nucleic acid. For example, if a nucleobase at a certain position of an antisense compound is capable of hydrogen bonding with a nucleobase at a certain position of a target nucleic acid, then the position of hydrogen bonding between the oligonucleotide and the target nucleic acid is considered to be complementary at that nucleobase pair. Nucleobases comprising certain modifications may maintain the ability to pair with a counterpart nucleobase and thus, are still capable of nucleobase complementarity.

[0789] As used herein, “non-complementary” in reference to nucleobases means a pair of nucleobases that do not form hydrogen bonds with one another.

[0790] As used herein, “complementary” in reference to oligomeric compounds (e.g., linked nucleosides, oligonucleotides, or nucleic acids) means the capacity of such oligomeric compounds or regions thereof to hybridize to another oligomeric compound or region thereof through nucleobase complementarity under stringent conditions. Complementary oligomeric compounds need not have nucleobase complementarity at each nucleoside. Rather, some mismatches are tolerated. In certain embodiments, complementary oligomeric compounds or regions are complementary at 70% of the nucleobases (70% complementary). In certain embodiments, complementary oligomeric compounds or regions are 80% complementary. In certain embodiments, complementary oligomeric compounds or regions are 90% complementary. In certain embodiments, complementary oligomeric compounds or regions are 95% complementary. In certain embodiments, complementary oligomeric compounds or regions are 100% complementary.

[0791] As used herein, “mismatch” means a nucleobase of a first oligomeric compound that is not capable of pairing with a nucleobase at a corresponding position of a second oligomeric compound, when the first and second oligomeric compound are aligned. Either or both of the first and second oligomeric compounds may be oligonucleotides.

[0792] As used herein, “hybridization” means the pairing of complementary oligomeric compounds (e.g., an antisense compound and its target nucleic acid). While not limited to a particular mechanism, the most common mechanism of pairing involves hydrogen bonding, which may be Watson-Crick, Hoogsteen or reversed Hoogsteen hydrogen bonding, between complementary nucleobases.

[0793] As used herein, “specifically hybridizes” means the ability of an oligomeric compound to hybridize to one nucleic acid site with greater affinity than it hybridizes to another nucleic acid site. In certain embodiments, an antisense compound specifically hybridizes to more than one target site.

[0794] As used herein, “fully complementary” in reference to an oligonucleotide or portion thereof means that each nucleobase of the oligonucleotide or portion thereof is capable of pairing with a nucleobase of a complementary nucleic acid or contiguous portion thereof. Thus, a fully complementary region comprises no mismatches or unhybridized nucleobases in either strand.

[0795] As used herein, “percent complementarity” means the percentage of nucleobases of an oligomeric compound that are complementary to an equal-length portion of a target nucleic acid. Percent complementarity is calculated by dividing the number of nucleobases of the oligomeric compound that are complementary to nucleobases at corresponding positions in the target nucleic acid by the total length of the oligomeric compound.

[0796] As used herein, “percent identity” means the number of nucleobases in a first nucleic acid that are the same type (independent of chemical modification) as nucleobases at corresponding positions in a second nucleic acid, divided by the total number of nucleobases in the first nucleic acid.

[0797] As used herein, “modulation” means a change of amount or quality of a molecule, function, or activity when compared to the amount or quality of a molecule, function, or activity prior to modulation. For example, modulation includes the change, either an increase (stimulation or induction) or a decrease (inhibition or reduction) in gene expression. As a further example, modulation of expression can include a change in splice site selection of pre-mRNA processing, resulting in a change in the absolute or relative amount of a particular splice-variant compared to the amount in the absence of modulation.

[0798] As used herein, “modification motif” means a pattern of chemical modifications in an oligomeric compound or a region thereof. Motifs may be defined by modifications at certain nucleosides and/or at certain linking groups of an oligomeric compound.

[0799] As used herein, “nucleoside motif” means a pattern of nucleoside modifications in an oligomeric compound or a region thereof. The linkages of such an oligomeric compound may be modified or unmodified. Unless otherwise indicated, motifs herein describing only nucleosides are intended to be nucleoside motifs. Thus, in such instances, the linkages are not limited.

[0800] As used herein, “sugar motif” means a pattern of sugar modifications in an oligomeric compound or a region thereof.

[0801] As used herein, “linkage motif” means a pattern of linkage modifications in an oligomeric compound or region thereof. The nucleosides of such an oligomeric compound may be modified or unmodified. Unless otherwise indicated, motifs herein describing only linkages are intended to be linkage motifs. Thus, in such instances, the nucleosides are not limited.

[0802] As used herein, “nucleobase modification motif” means a pattern of modifications to nucleobases along an oligonucleotide. Unless otherwise indicated, a nucleobase modification motif is independent of the nucleobase sequence.

[0803] As used herein, “sequence motif” means a pattern of nucleobases arranged along an oligonucleotide or portion thereof. Unless otherwise indicated, a sequence motif is independent of chemical modifications and thus may have any combination of chemical modifications, including no chemical modifications.

[0804] As used herein, “type of modification” in reference to a nucleoside or a nucleoside of a “type” means the chemical modification of a nucleoside and includes modified and unmodified nucleosides. Accordingly, unless otherwise indicated, a “nucleoside having a modification of a first type” may be an unmodified nucleoside.

[0805] As used herein, “differently modified” mean chemical modifications or chemical substituents that are different from one another, including absence of modifications. Thus, for example, a MOE nucleoside and an unmodified DNA nucleoside are “differently modified,” even though the DNA nucleoside is unmodified. Likewise, DNA and RNA are “differently modified,” even though both are naturally-occurring unmodified nucleosides. Nucleosides that are the same but for comprising different nucleobases are not differently modified. For example, a nucleoside comprising a 2′-OMe modified sugar and an unmodified adenine nucleobase and a nucleoside comprising a 2′-OMe modified sugar and an unmodified thymine nucleobase are not differently modified.

[0806] As used herein, “the same type of modifications” refers to modifications that are the same as one another, including absence of modifications. Thus, for example, two unmodified DNA nucleoside have “the same type of modification,” even though the DNA nucleoside is unmodified. Such nucleosides having the same type modification may comprise different nucleobases.

[0807] As used herein, “pharmaceutically acceptable carrier or diluent” means any substance suitable for use in administering to an animal. In certain embodiments, a pharmaceutically acceptable carrier or diluent is sterile saline. In certain embodiments, such sterile saline is pharmaceutical grade saline.

[0808] As used herein, “substituent” and “substituent group,” means an atom or group that replaces the atom or group of a named parent compound. For example a substituent of a modified nucleoside is any atom or group that differs from the atom or group found in a naturally occurring nucleoside (e.g., a modified 2′-substituent is any atom or group at the 2′-position of a nucleoside other than H or OH). Substituent groups can be protected or unprotected. In certain embodiments, compounds of the present invention have substituents at one or at more than one position of the parent compound. Substituents may also be further substituted with other substituent groups and may be attached directly or via a linking group such as an alkyl or hydrocarbyl group to a parent compound.

[0809] Likewise, as used herein, “substituent” in reference to a chemical functional group means an atom or group of atoms differs from the atom or a group of atoms normally present in the named functional group. In certain embodiments, a substituent replaces a hydrogen atom of the functional group (e.g., in certain embodiments, the substituent of a substituted methyl group is an atom or group other than hydrogen which replaces one of the hydrogen atoms of an unsubstituted methyl group). Unless otherwise indicated, groups amenable for use as substituents include without limitation, halogen, hydroxyl, alkyl, alkenyl, alkynyl, acyl (—C(O)R.sub.aa), carboxyl (—C(O)O—R.sub.aa), aliphatic groups, alicyclic groups, alkoxy, substituted oxy (—O—R.sub.aa), aryl, aralkyl, heterocyclic radical, heteroaryl, heteroarylalkyl, amino (—N(R.sub.bb)(R.sub.cc)), imino (═NR.sub.bb), amido (—C(O)N(R.sub.bb)(R.sub.cc) or —N(R.sub.bb)C(O)R.sub.aa), azido (—N.sub.3), nitro (—NO.sub.2), cyano (—CN), carbamido (—OC(O)N(R.sub.bb)(R.sub.cc) or —N(R.sub.bb)C(O)OR.sub.aa), ureido (—N(R.sub.bb)C(O)N(R.sub.bb)(R.sub.cc)), thioureido (—N(R.sub.bb)C(S)N(R.sub.bb)—(R.sub.cc)), guanidinyl (—N(R.sub.bb)C(═NR.sub.bb)N(R.sub.bb)(R.sub.cc)), amidinyl (—C(═NR.sub.bb)N(R.sub.bb)(R.sub.cc) or —N(R.sub.bb)C(═NR.sub.bb)(R.sub.aa)), thiol (—SR.sub.bb), sulfinyl (—S(O)R.sub.bb), sulfonyl (—S(O).sub.2R.sub.bb) and sulfonamidyl (—S(O).sub.2N(R.sub.bb)(R.sub.cc) or —N(R.sub.bb)S—(O).sub.2R.sub.bb). Wherein each R.sub.aa, R.sub.bb and R.sub.cc is, independently, H, an optionally linked chemical functional group or a further substituent group with a preferred list including without limitation, alkyl, alkenyl, alkynyl, aliphatic, alkoxy, acyl, aryl, aralkyl, heteroaryl, alicyclic, heterocyclic and heteroarylalkyl. Selected substituents within the compounds described herein are present to a recursive degree.

[0810] As used herein, “alkyl,” as used herein, means a saturated straight or branched hydrocarbon radical containing up to twenty four carbon atoms. Examples of alkyl groups include without limitation, methyl, ethyl, propyl, butyl, isopropyl, n-hexyl, octyl, decyl, dodecyl and the like. Alkyl groups typically include from 1 to about 24 carbon atoms, more typically from 1 to about 12 carbon atoms (C.sub.1-C.sub.12 alkyl) with from 1 to about 6 carbon atoms being more preferred.

[0811] As used herein, “alkenyl,” means a straight or branched hydrocarbon chain radical containing up to twenty four carbon atoms and having at least one carbon-carbon double bond. Examples of alkenyl groups include without limitation, ethenyl, propenyl, butenyl, 1-methyl-2-buten-1-yl, dienes such as 1,3-butadiene and the like. Alkenyl groups typically include from 2 to about 24 carbon atoms, more typically from 2 to about 12 carbon atoms with from 2 to about 6 carbon atoms being more preferred. Alkenyl groups as used herein may optionally include one or more further substituent groups.

[0812] As used herein, “alkynyl,” means a straight or branched hydrocarbon radical containing up to twenty four carbon atoms and having at least one carbon-carbon triple bond. Examples of alkynyl groups include, without limitation, ethynyl, 1-propynyl, 1-butynyl, and the like. Alkynyl groups typically include from 2 to about 24 carbon atoms, more typically from 2 to about 12 carbon atoms with from 2 to about 6 carbon atoms being more preferred. Alkynyl groups as used herein may optionally include one or more further substituent groups.

[0813] As used herein, “acyl,” means a radical formed by removal of a hydroxyl group from an organic acid and has the general Formula —C(O)—X where X is typically aliphatic, alicyclic or aromatic. Examples include aliphatic carbonyls, aromatic carbonyls, aliphatic sulfonyls, aromatic sulfinyls, aliphatic sulfinyls, aromatic phosphates, aliphatic phosphates and the like. Acyl groups as used herein may optionally include further substituent groups.

[0814] As used herein, “alicyclic” means a cyclic ring system wherein the ring is aliphatic. The ring system can comprise one or more rings wherein at least one ring is aliphatic. Preferred alicyclics include rings having from about 5 to about 9 carbon atoms in the ring. Alicyclic as used herein may optionally include further substituent groups.

[0815] As used herein, “aliphatic” means a straight or branched hydrocarbon radical containing up to twenty four carbon atoms wherein the saturation between any two carbon atoms is a single, double or triple bond. An aliphatic group preferably contains from 1 to about 24 carbon atoms, more typically from 1 to about 12 carbon atoms with from 1 to about 6 carbon atoms being more preferred. The straight or branched chain of an aliphatic group may be interrupted with one or more heteroatoms that include nitrogen, oxygen, sulfur and phosphorus. Such aliphatic groups interrupted by heteroatoms include without limitation, polyalkoxys, such as polyalkylene glycols, polyamines, and polyimines Aliphatic groups as used herein may optionally include further substituent groups.

[0816] As used herein, “alkoxy” means a radical formed between an alkyl group and an oxygen atom wherein the oxygen atom is used to attach the alkoxy group to a parent molecule. Examples of alkoxy groups include without limitation, methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, sec-butoxy, tert-butoxy, n-pentoxy, neopentoxy, n-hexoxy and the like. Alkoxy groups as used herein may optionally include further substituent groups.

[0817] As used herein, “aminoalkyl” means an amino substituted C.sub.1-C.sub.12 alkyl radical. The alkyl portion of the radical forms a covalent bond with a parent molecule. The amino group can be located at any position and the aminoalkyl group can be substituted with a further substituent group at the alkyl and/or amino portions.

[0818] As used herein, “aralkyl” and “arylalkyl” mean an aromatic group that is covalently linked to a C.sub.1-C.sub.12 alkyl radical. The alkyl radical portion of the resulting aralkyl (or arylalkyl) group forms a covalent bond with a parent molecule. Examples include without limitation, benzyl, phenethyl and the like. Aralkyl groups as used herein may optionally include further substituent groups attached to the alkyl, the aryl or both groups that form the radical group.

[0819] As used herein, “aryl” and “aromatic” mean a mono- or polycyclic carbocyclic ring system radicals having one or more aromatic rings. Examples of aryl groups include without limitation, phenyl, naphthyl, tetrahydronaphthyl, indanyl, idenyl and the like. Preferred aryl ring systems have from about 5 to about 20 carbon atoms in one or more rings. Aryl groups as used herein may optionally include further substituent groups.

[0820] As used herein, “halo” and “halogen,” mean an atom selected from fluorine, chlorine, bromine and iodine.

[0821] As used herein, “heteroaryl,” and “heteroaromatic,” mean a radical comprising a mono- or poly-cyclic aromatic ring, ring system or fused ring system wherein at least one of the rings is aromatic and includes one or more heteroatoms. Heteroaryl is also meant to include fused ring systems including systems where one or more of the fused rings contain no heteroatoms. Heteroaryl groups typically include one ring atom selected from sulfur, nitrogen or oxygen. Examples of heteroaryl groups include without limitation, pyridinyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl, oxadiazolyl, thiophenyl, furanyl, quinolinyl, isoquinolinyl, benzimidazolyl, benzooxazolyl, quinoxalinyl and the like. Heteroaryl radicals can be attached to a parent molecule directly or through a linking moiety such as an aliphatic group or hetero atom. Heteroaryl groups as used herein may optionally include further substituent groups.

[0822] As used herein, “Intracerebroventricular” or “ICV” means administration into the ventricular system of the brain.

[0823] As used herein, “wherein the translation suppression element region comprises one and only one uORF,” means that exactly one uORF is present in the translation suppression element region. In certain embodiments, exactly one uORF is present in the 5′-UTR.

[0824] The compounds described herein include variations in which one or more atoms are replaced with a non-radioactive isotope or radioactive isotope of the indicated element. For example, compounds herein that comprise hydrogen atoms encompass all possible deuterium substitutions for each of the 1H hydrogen atoms.

[0825] Isotopic substitutions encompassed by the compounds herein include but are not limited to: 2H or 3H in place of 1H, 13C or 14C in place of 12C, 15N in place of 14N, 17O or 18O in place of 16O, and 33S, 34S, 35S, or 36S in place of 32S. In certain embodiments, non-radioactive isotopic substitutions may impart new properties on the oligomeric compound that are beneficial for use as a therapeutic or research tool. In certain embodiments, radioactive isotopic substitutions may make the compound suitable for research purposes such as imaging.

[0826] Certain Modified Oligonucleotides

[0827] In certain embodiments, the present invention provides antisense compounds. In certain embodiments, antisense compounds comprise a modified oligonucleotide. In certain embodiments, such antisense compounds comprise modified oligonucleotides and optionally one or more conjugate and/or terminal groups. In certain embodiments, an antisense compound consists of a modified oligonucleotide. In certain embodiments, modified oligonucleotides comprise one or more chemical modifications. Such chemical modifications include modifications of one or more nucleoside (including modifications to the sugar moiety and/or the nucleobase) and/or modifications to one or more internucleoside linkage.

[0828] a. Certain Modified Nucleosides

[0829] In certain embodiments, provided herein are antisense compounds comprising or consisting of oligonuleotides comprising at least one modified nucleoside. Such modified nucleosides comprise a modified sugar moeity, a modified nucleobase, or both a modified sugar moiety and a modified nucleobase.

[0830] i. Certain Sugar Moieties

[0831] In certain embodiments, antisense compounds of the invention comprise one or more modified nucleosides comprising a modified sugar moiety. Such antisense compounds comprising one or more sugar-modified nucleosides may have desirable properties, such as enhanced nuclease stability or increased binding affinity with a target nucleic acid relative to antisense compounds comprising only nucleosides comprising naturally occurring sugar moieties. In certain embodiments, modified sugar moieties are substituted sugar moieties. In certain embodiments, modified sugar moieties are bicyclic or tricyclic sugar moieties. In certain embodiments, modified sugar moieties are sugar surrogates. Such sugar surrogates may comprise one or more substitutions corresponding to those of substituted sugar moieties.

[0832] In certain embodiments, modified sugar moieties are substituted sugar moieties comprising one or more substituent, including but not limited to substituents at the 2′ and/or 5′ positions. Examples of sugar substituents suitable for the 2′-position, include, but are not limited to: 2′-F, 2′-OCH.sub.3 (“OMe” or “O-methyl”), and 2′-O(CH.sub.2).sub.2OCH.sub.3 (“MOE”). In certain embodiments, sugar substituents at the 2′ position is selected from allyl, amino, azido, thio, O-allyl, O—C.sub.1-C.sub.10 alkyl, O—C.sub.1-C.sub.10 substituted alkyl; O—C.sub.1-C.sub.10 alkoxy; O—C.sub.1-C.sub.10 substituted alkoxy, OCF.sub.3, O(CH.sub.2).sub.2SCH.sub.3, O(CH.sub.2).sub.2—O—N(Rm)(Rn), and O—CH.sub.2—C(═O)—N(Rm)(Rn), where each Rm and Rn is, independently, H or substituted or unsubstituted C.sub.1-C.sub.10 alkyl. Examples of sugar substituents at the 5′-position, include, but are not limited to: 5′-methyl (R or S); 5′-vinyl, and 5′-methoxy. In certain embodiments, substituted sugars comprise more than one non-bridging sugar substituent, for example, 2′-F-5′-methyl sugar moieties (see, e.g., PCT International Application WO 2008/101157, for additional 5′,2′-bis substituted sugar moieties and nucleosides).

[0833] Nucleosides comprising 2′-substituted sugar moieties are referred to as 2′-substituted nucleosides. In certain embodiments, a 2′-substituted nucleoside comprises a 2′-substituent group selected from halo, allyl, amino, azido, O—C.sub.1-C.sub.10 alkoxy; O—C.sub.1-C.sub.10 substituted alkoxy, SH, CN, OCN, CF.sub.3, OCF.sub.3, O-alkyl, S-alkyl, N(R.sub.m)-alkyl; O-alkenyl, S-alkenyl, or N(R.sub.m)-alkenyl; O-alkynyl, S-alkynyl, N(R.sub.m)-alkynyl; O-alkylenyl-O-alkyl, alkynyl, alkaryl, aralkyl, O-alkaryl, O-aralkyl, O(CH.sub.2).sub.2SCH.sub.3, O—(CH.sub.2).sub.2—O—N(R.sub.m)(R.sub.n) or O—CH.sub.2—C(═O)—N(R.sub.m)(R.sub.n), where each R.sub.m and R.sub.n is, independently, H, an amino protecting group or substituted or unsubstituted C.sub.1-C.sub.10 alkyl. These 2′-substituent groups can be further substituted with one or more substituent groups independently selected from hydroxyl, amino, alkoxy, carboxy, benzyl, phenyl, nitro (NO.sub.2), thiol, thioalkoxy (S-alkyl), halogen, alkyl, aryl, alkenyl and alkynyl.

[0834] In certain embodiments, a 2′-substituted nucleoside comprises a 2′-substituent group selected from F, NH.sub.2, N.sub.3, OCF.sub.3, O—CH.sub.3, O(CH.sub.2).sub.3NH.sub.2, CH.sub.2—CH═CH.sub.2, O—CH.sub.2—CH═CH.sub.2, OCH.sub.2CH.sub.2OCH.sub.3, O(CH.sub.2).sub.2SCH.sub.3, O—(CH.sub.2).sub.2—O—N(R.sub.m)(R.sub.n), O(CH.sub.2).sub.2O(CH.sub.2).sub.2N(CH.sub.3).sub.2, and N-substituted acetamide (O—CH.sub.2—C(═O)—N(R.sub.m)(R.sub.n) where each R.sub.m and R.sub.n is, independently, H, an amino protecting group or substituted or unsubstituted C.sub.1-C.sub.10 alkyl.

[0835] In certain embodiments, a 2′-substituted nucleoside comprises a sugar moiety comprising a 2′-substituent group selected from F, OCF.sub.3, O—CH.sub.3, OCH.sub.2CH.sub.2OCH.sub.3, O(CH.sub.2).sub.2SCH.sub.3, O—(CH.sub.2).sub.2—O—N(CH.sub.3).sub.2, —O(CH.sub.2).sub.2O(CH.sub.2).sub.2N(CH.sub.3).sub.2, and O—CH.sub.2—C(═O)—N(H)CH.sub.3.

[0836] In certain embodiments, a 2′-substituted nucleoside comprises a sugar moiety comprising a 2′-substituent group selected from F, O—CH.sub.3, and OCH.sub.2CH.sub.2OCH.sub.3.

[0837] Certain modified sugar moieties comprise a bridging sugar substituent that forms a second ring resulting in a bicyclic sugar moiety. In certain such embodiments, the bicyclic sugar moiety comprises a bridge between the 4′ and the 2′ furanose ring atoms. Examples of such 4′ to 2′ sugar substituents, include, but are not limited to: —[C(R.sub.a)(R.sub.b)].sub.n—, —[C(R.sub.a)(R.sub.b)].sub.n—O—, —C(R.sub.aR.sub.b)—N(R)—O— or, —C(R.sub.aR.sub.b)—O—N(R)—; 4′- CH.sub.2-2′, 4′-(CH.sub.2).sub.2-2′, 4′-(CH.sub.2).sub.3-2′, 4′-(CH.sub.2)—O-2′ (LNA); 4′-(CH.sub.2)—S-2; 4′-(CH.sub.2).sub.2—O-2′ (ENA); 4′-CH(CH.sub.3)—O-2′ (cEt) and 4′-CH(CH.sub.2OCH.sub.3)—O-2′, and analogs thereof (see, e.g., U.S. Pat. No. 7,399,845, issued on Jul. 15, 2008); 4′-C(CH.sub.3)(CH.sub.3)—O-2′ and analogs thereof, (see, e.g., WO2009/006478, published Jan. 8, 2009); 4′-CH.sub.2—N(OCH.sub.3)-2′ and analogs thereof (see, e.g., WO2008/150729, published Dec. 11, 2008); 4′-CH.sub.2—O—N(CH.sub.3)-2′ (see, e.g., US2004/0171570, published Sep. 2, 2004); 4′-CH.sub.2—O—N(R)-2′, and 4′-CH.sub.2—N(R)-0-2′-, wherein each R is, independently, H, a protecting group, or C.sub.1-C.sub.12 alkyl; 4′-CH.sub.2—N(R)—O-2′, wherein R is H, C.sub.1-C.sub.12 alkyl, or a protecting group (see, U.S. Pat. No. 7,427,672, issued on Sep. 23, 2008); 4′-CH.sub.2—C(H)(CH.sub.3)-2′ (see, e.g., Chattopadhyaya, et al., J. Org. Chem., 2009, 74, 118-134); and 4′-CH.sub.2—C(═CH.sub.2)-2′ and analogs thereof (see, published PCT International Application WO 2008/154401, published on Dec. 8, 2008).

[0838] In certain embodiments, such 4′ to 2′ bridges independently comprise from 1 to 4 linked groups independently selected from —[C(R.sub.a)(R.sub.b)].sub.n—, —C(R.sub.a)═C(R.sub.b)—, —C(R.sub.a)═N—, —C(═NR.sub.a)—, —C(═O)—, —C(═S)—, —O—, —Si(R.sub.a).sub.2—, —S(═O).sub.x—, and —N(R.sub.a)—;

[0839] wherein:

[0840] x is 0, 1, or 2;

[0841] n is 1, 2, 3, or 4;

[0842] each R.sub.a and R.sub.b is, independently, H, a protecting group, hydroxyl, C.sub.1-C.sub.12 alkyl, substituted C.sub.1-C.sub.12 alkyl, C.sub.2-C.sub.12 alkenyl, substituted C.sub.2-C.sub.12 alkenyl, C.sub.2-C.sub.12 alkynyl, substituted C.sub.2-C.sub.12 alkynyl, C.sub.5-C.sub.20 aryl, substituted C.sub.5-C.sub.20 aryl, heterocycle radical, substituted heterocycle radical, heteroaryl, substituted heteroaryl, C.sub.5-C.sub.7 alicyclic radical, substituted C.sub.5-C.sub.7 alicyclic radical, halogen, OJ.sub.1, NJ.sub.1J.sub.2, SJ.sub.1, N.sub.3, COOJ.sub.1, acyl (C(═O)—H), substituted acyl, CN, sulfonyl (S(═O).sub.2-J.sub.1), or sulfoxyl (S(═O)-J.sub.1); and

[0843] each J.sub.1 and J.sub.2 is, independently, H, C.sub.1-C.sub.12 alkyl, substituted C.sub.1-C.sub.12 alkyl, C.sub.2-C.sub.12 alkenyl, substituted C.sub.2-C.sub.12 alkenyl, C.sub.2-C.sub.12 alkynyl, substituted C.sub.2-C.sub.12 alkynyl, C.sub.5-C.sub.20 aryl, substituted C.sub.5-C.sub.20 aryl, acyl (C(═O)—H), substituted acyl, a heterocycle radical, a substituted heterocycle radical, C.sub.1-C.sub.12 aminoalkyl, substituted C.sub.1-C.sub.12 aminoalkyl, or a protecting group.

[0844] Nucleosides comprising bicyclic sugar moieties are referred to as bicyclic nucleosides or BNAs. Bicyclic nucleosides include, but are not limited to, (A) α-L-Methyleneoxy (4′-CH.sub.2—O-2′) BNA, (B) β-D-Methyleneoxy (4′-CH.sub.2—O-2′) BNA (also referred to as locked nucleic acid or LNA), (C) Ethyleneoxy (4′-(CH.sub.2).sub.2—O-2′) BNA, (D) Aminooxy (4′-CH.sub.2—O—N(R)-2′) BNA, (E) Oxyamino (4′-CH.sub.2—N(R)—O-2′) BNA, (F) Methyl(methyleneoxy) (4′-CH(CH.sub.3)—O-2′) BNA (also referred to as constrained ethyl or cEt), (G) methylene-thio(4′-CH.sub.2—S-2′) BNA, (H) methylene-amino (4′-CH2-N(R)-2′) BNA, (I) methyl carbocyclic (4′-CH.sub.2—CH(CH.sub.3)-2′) BNA, (J) propylene carbocyclic (4′-(CH.sub.2).sub.3-2′) BNA, and (M) 4′-CH.sub.2—O—CH.sub.2-2′ as depicted below.

##STR00001## ##STR00002##

wherein Bx is a nucleobase moiety and R is, independently, H, a protecting group, or C.sub.1-C.sub.12 alkyl.

[0845] Additional bicyclic sugar moieties are known in the art, for example: Singh et al., Chem. Commun., 1998, 4, 455-456; Koshkin et al., Tetrahedron, 1998, 54, 3607-3630; Wahlestedt et al., Proc. Natl. Acad. Sci. U.S.A, 2000, 97, 5633-5638; Kumar et al., Bioorg. Med. Chem. Lett., 1998, 8, 2219-2222; Singh et al., J. Org. Chem., 1998, 63, 10035-10039; Srivastava et al., J. Am. Chem. Soc., 129(26) 8362-8379 (Jul. 4, 2007); Elayadi et al., Curr. Opinion Invens. Drugs, 2001, 2, 558-561; Braasch et al., Chem. Biol., 2001, 8, 1-7; Orum et al., Curr. Opinion Mol. Ther., 2001, 3, 239-243; U.S. Pat. Nos. 7,053,207, 6,268,490, 6,770,748, 6,794,499, 7,034,133, 6,525,191, 6,670,461, and 7,399,845; WO 2004/106356, WO 1994/14226, WO 2005/021570, and WO 2007/134181; U.S. Patent Publication Nos. US2004/0171570, US2007/0287831, and US2008/0039618; U.S. patent Ser. Nos. 12/129,154, 60/989,574, 61/026,995, 61/026,998, 61/056,564, 61/086,231, 61/097,787, and 61/099,844; and PCT International Applications Nos. PCT/US2008/064591, PCT/US2008/066154, and PCT/US2008/068922.

[0846] In certain embodiments, bicyclic sugar moieties and nucleosides incorporating such bicyclic sugar moieties are further defined by isomeric configuration. For example, a nucleoside comprising a 4′-2′ methylene-oxy bridge, may be in the α-L configuration or in the β-D configuration. Previously, α-L-methyleneoxy (4′-CH.sub.2—O-2′) bicyclic nucleosides have been incorporated into antisense oligonucleotides that showed antisense activity (Frieden et al., Nucleic Acids Research, 2003, 21, 6365-6372).

[0847] In certain embodiments, substituted sugar moieties comprise one or more non-bridging sugar substituent and one or more bridging sugar substituent (e.g., 5′-substituted and 4′-2′ bridged sugars). (see, PCT International Application WO 2007/134181, published on Nov. 22, 2007, wherein LNA is substituted with, for example, a 5′-methyl or a 5′-vinyl group).

[0848] In certain embodiments, modified sugar moieties are sugar surrogates. In certain such embodiments, the oxygen atom of the naturally occurring sugar is substituted, e.g., with a sulfer, carbon or nitrogen atom. In certain such embodiments, such modified sugar moiety also comprises bridging and/or non-bridging substituents as described above. For example, certain sugar surrogates comprise a 4′-sulfer atom and a substitution at the 2′-position (see, e.g., published U.S. Patent Application US2005/0130923, published on Jun. 16, 2005) and/or the 5′ position. By way of additional example, carbocyclic bicyclic nucleosides having a 4′-2′ bridge have been described (see, e.g., Freier et al., Nucleic Acids Research, 1997, 25(22), 4429-4443 and Albaek et al., J. Org. Chem., 2006, 71, 7731-7740).

[0849] In certain embodiments, sugar surrogates comprise rings having other than 5-atoms. For example, in certain embodiments, a sugar surrogate comprises a six-membered tetrahydropyran. Such tetrahydropyrans may be further modified or substituted. Nucleosides comprising such modified tetrahydropyrans include, but are not limited to, hexitol nucleic acid (HNA), anitol nucleic acid (ANA), manitol nucleic acid (MNA) (see Leumann, C J. Bioorg. & Med. Chem. (2002) 10:841-854), fluoro HNA (F-HNA), and those compounds having Formula VII:

##STR00003##

wherein independently for each of said at least one tetrahydropyran nucleoside analog of Formula VII:

[0850] Bx is a nucleobase moiety;

[0851] T.sub.3 and T.sub.4 are each, independently, an internucleoside linking group linking the tetrahydropyran nucleoside analog to the antisense compound or one of T.sub.3 and T.sub.4 is an internucleoside linking group linking the tetrahydropyran nucleoside analog to the antisense compound and the other of T.sub.3 and T.sub.4 is H, a hydroxyl protecting group, a linked conjugate group, or a 5′ or 3′-terminal group;

q.sub.1, q.sub.2, q.sub.3, q.sub.4, q.sub.5, q.sub.6 and q.sub.7 are each, independently, H, C.sub.1-C.sub.6 alkyl, substituted C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, substituted C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, or substituted C.sub.2-C.sub.6 alkynyl; and

[0852] each of R.sub.1 and R.sub.2 is independently selected from among: hydrogen, halogen, substituted or unsubstituted alkoxy, NJ.sub.1J.sub.2, SJ.sub.1, N.sub.3, OC(═X)J.sub.1, OC(═X)NJ.sub.1J.sub.2, NJ.sub.3C(═X)NJ.sub.1J.sub.2, and CN, wherein X is O, S or NJ.sub.1, and each J.sub.1, J.sub.2, and J.sub.3 is, independently, H or C.sub.1-C.sub.6 alkyl.

[0853] In certain embodiments, the modified THP nucleosides of Formula VII are provided wherein q.sub.1, q.sub.2, q.sub.3, q.sub.4, q.sub.5, q.sub.6 and q.sub.7 are each H. In certain embodiments, at least one of q.sub.1, q.sub.2, q.sub.3, q.sub.4, q.sub.5, q.sub.6 and q.sub.7 is other than H. In certain embodiments, at least one of q.sub.1, q.sub.2, q.sub.3, q.sub.4, q.sub.5, q.sub.6 and q.sub.7 is methyl. In certain embodiments, THP nucleosides of Formula VII are provided wherein one of R.sub.1 and R.sub.2 is F. In certain embodiments, R.sub.1 is fluoro and R.sub.2 is H, R.sub.1 is methoxy and R.sub.2 is H, and R.sub.1 is methoxyethoxy and R.sub.2 is H.

[0854] Many other bicyclic and tricyclic sugar and sugar surrogate ring systems are known in the art that can be used to modify nucleosides (see, e.g., review article: Leumann, J C, Bioorganic & Medicinal Chemistry, 2002, 10, 841-854).

[0855] In certain embodiments, sugar surrogates comprise rings having more than 5 atoms and more than one heteroatom. For example nucleosides comprising morpholino sugar moieties and their use in oligomeric compounds has been reported (see for example: Braasch et al., Biochemistry, 2002, 41, 4503-4510; and U.S. Pat. Nos. 5,698,685; 5,166,315; 5,185,444; and 5,034,506). As used here, the term “morpholino” means a sugar surrogate having the following structure:

##STR00004##

In certain embodiments, morpholinos may be modified, for example by adding or altering various substituent groups from the above morpholino structure. Such sugar surrogates are referred to herein as “modified morpholinos.”

[0856] Combinations of modifications are also provided without limitation, such as 2′-F-5′-methyl substituted nucleosides (see PCT International Application WO 2008/101157 Published on Aug. 21, 2008 for other disclosed 5′,2′-bis substituted nucleosides) and replacement of the ribosyl ring oxygen atom with S and further substitution at the 2′-position (see published U.S. Patent Application US2005-0130923, published on Jun. 16, 2005) or alternatively 5′-substitution of a bicyclic nucleic acid (see PCT International Application WO 2007/134181, published on Nov. 22, 2007 wherein a 4′-CH.sub.2—O-2′ bicyclic nucleoside is further substituted at the 5′ position with a 5′-methyl or a 5′-vinyl group). The synthesis and preparation of carbocyclic bicyclic nucleosides along with their oligomerization and biochemical studies have also been described (see, e.g., Srivastava et al., J. Am. Chem. Soc. 2007, 129(26), 8362-8379).

[0857] ii. Certain Modified Nucleobases

[0858] In certain embodiments, nucleosides of the present invention comprise one or more unmodified nucleobases. In certain embodiments, nucleosides of the present invention comprise one or more modified nucleobases.

[0859] In certain embodiments, modified nucleobases are selected from: universal bases, hydrophobic bases, promiscuous bases, size-expanded bases, and fluorinated bases as defined herein. 5-substituted pyrimidines, 6-azapyrimidines and N-2, N-6 and O-6 substituted purines, including 2-aminopropyladenine, 5-propynyluracil; 5-propynylcytosine; 5-hydroxymethyl cytosine, xanthine, hypoxanthine, 2-aminoadenine, 6-methyl and other alkyl derivatives of adenine and guanine, 2-propyl and other alkyl derivatives of adenine and guanine, 2-thiouracil, 2-thiothymine and 2-thiocytosine, 5-halouracil and cytosine, 5-propynyl (—C≡C—CH.sub.3) uracil and cytosine and other alkynyl derivatives of pyrimidine bases, 6-azo uracil, cytosine and thymine, 5-uracil (pseudouracil), 4-thiouracil, 8-halo, 8-amino, 8-thiol, 8-thioalkyl, 8-hydroxyl and other 8-substituted adenines and guanines, 5-halo particularly 5-bromo, 5-trifluoromethyl and other 5-substituted uracils and cytosines, 7-methylguanine and 7-methyladenine, 2-F-adenine, 2-amino-adenine, 8-azaguanine and 8-azaadenine, 7-deazaguanine and 7-deazaadenine, 3-deazaguanine and 3-deazaadenine, universal bases, hydrophobic bases, promiscuous bases, size-expanded bases, and fluorinated bases as defined herein. Further modified nucleobases include tricyclic pyrimidines such as phenoxazine cytidine([5,4-b][1,4]benzoxazin-2(3H)-one), phenothiazine cytidine (1H-pyrimido[5,4-b][1,4]benzothiazin-2(3H)-one), G-clamps such as a substituted phenoxazine cytidine (e.g. 9-(2-aminoethoxy)-H-pyrimido[5,4-b][1,4]benzoxazin-2(3H)-one), carbazole cytidine (2H-pyrimido[4,5-b]indol-2-one), pyridoindole cytidine (H-pyrido[3′,2′:4,5]pyrrolo[2,3-d]pyrimidin-2-one). Modified nucleobases may also include those in which the purine or pyrimidine base is replaced with other heterocycles, for example 7-deaza-adenine, 7-deazaguanosine, 2-aminopyridine and 2-pyridone. Further nucleobases include those disclosed in U.S. Pat. No. 3,687,808, those disclosed in The Concise Encyclopedia Of Polymer Science And Engineering, Kroschwitz, J. I., Ed., John Wiley & Sons, 1990, 858-859; those disclosed by Englisch et al., Angewandte Chemie, International Edition, 1991, 30, 613; and those disclosed by Sanghvi, Y. S., Chapter 15, Antisense Research and Applications, Crooke, S. T. and Lebleu, B., Eds., CRC Press, 1993, 273-288.

[0860] Representative United States patents that teach the preparation of certain of the above noted modified nucleobases as well as other modified nucleobases include without limitation, U.S. Pat. Nos. 3,687,808; 4,845,205; 5,130,302; 5,134,066; 5,175,273; 5,367,066; 5,432,272; 5,457,187; 5,459,255; 5,484,908; 5,502,177; 5,525,711; 5,552,540; 5,587,469; 5,594,121; 5,596,091; 5,614,617; 5,645,985; 5,681,941; 5,750,692; 5,763,588; 5,830,653 and 6,005,096, certain of which are commonly owned with the instant application, and each of which is herein incorporated by reference in its entirety.

[0861] b. Certain Internucleoside Linkages

[0862] In certain embodiments, nucleosides may be linked together using any internucleoside linkage to form oligonucleotides. The two main classes of internucleoside linking groups are defined by the presence or absence of a phosphorus atom. Representative phosphorus containing internucleoside linkages include, but are not limited to, phosphodiesters (P═O), phosphotriesters, methylphosphonates, phosphoramidate, and phosphorothioates (P═S). Representative non-phosphorus containing internucleoside linking groups include, but are not limited to, methylenemethylimino (—CH.sub.2—N(CH.sub.3)—O—CH.sub.2—), thiodiester (—O—C(O)—S—), thionocarbamate (—O—C(O)(NH)—S—); siloxane (—O—Si(H).sub.2—O—); and N,N′-dimethylhydrazine (—CH.sub.2—N(CH.sub.3)—N(CH.sub.3)—). Modified linkages, compared to natural phosphodiester linkages, can be used to alter, typically increase, nuclease resistance of the oligonucleotide. In certain embodiments, internucleoside linkages having a chiral atom can be prepared as a racemic mixture, or as separate enantiomers. Representative chiral linkages include, but are not limited to, alkylphosphonates and phosphorothioates. Methods of preparation of phosphorous-containing and non-phosphorous-containing internucleoside linkages are well known to those skilled in the art.

[0863] The oligonucleotides described herein contain one or more asymmetric centers and thus give rise to enantiomers, diastereomers, and other stereoisomeric configurations that may be defined, in terms of absolute stereochemistry, as (R) or (S), α or β such as for sugar anomers, or as (D) or (L) such as for amino acids etc. Included in the antisense compounds provided herein are all such possible isomers, as well as their racemic and optically pure forms.

[0864] Neutral internucleoside linkages include without limitation, phosphotriesters, methylphosphonates, MMI (3′-CH.sub.2—N(CH.sub.3)—O-5′), amide-3 (3′-CH.sub.2—C(═O)—N(H)-5′), amide-4 (3′-CH.sub.2—N(H)—C(═O)-5′), formacetal (3′-O—CH.sub.2—O-5′), and thioformacetal (3′-S—CH.sub.2—O-5′). Further neutral internucleoside linkages include nonionic linkages comprising siloxane (dialkylsiloxane), carboxylate ester, carboxamide, sulfide, sulfonate ester and amides (See for example: Carbohydrate Modifications in Antisense Research; Y. S. Sanghvi and P. D. Cook, Eds., ACS Symposium Series 580; Chapters 3 and 4, 40-65). Further neutral internucleoside linkages include nonionic linkages comprising mixed N, O, S and CH.sub.2 component parts.

[0865] c. Certain Motifs

[0866] In certain embodiments, the invention provides modified oligonucleotides. In certain embodiments, modified oligonucleotides comprise one or more modified sugars. In certain embodiments, modified oligonucleotides comprise one or more modified nucleobases. In certain embodiments, modified oligonucleotides comprise one or more modified internucleoside linkages. In certain embodiments, the modifications (sugar modifications, nucleobase modifications, and/or linkage modifications) define a pattern or motif. In certain embodiments, the patterns of chemical modifications of sugar moieties, internucleoside linkages, and nucleobases are each independent of one another. Thus, a modified oligonucleotide may be described by its sugar modification motif, internucleoside linkage motif and/or nucleobase modification motif (as used herein, nucleobase modification motif describes the chemical modifications to the nucleobases independent of the sequence of nucleobases).

[0867] In certain embodiments, every sugar moiety of the modified oligonucleotides of the present invention is modified. In certain embodiments, modified oligonucleotides include one or more unmodified sugar moiety.

[0868] d. Certain Overall Lengths

[0869] In certain embodiments, the present invention provides modified oligonucleotides of any of a variety of ranges of lengths. In certain embodiments, the invention provides oligomeric compounds or oligonucleotides consisting of X to Y linked nucleosides, where X represents the fewest number of nucleosides in the range and Y represents the largest number of nucleosides in the range. In certain such embodiments, X and Y are each independently selected from 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, and 50; provided that X≦Y. For example, in certain embodiments, the invention provides modified oligonucleotides which comprise oligonucleotides consisting of 8 to 9, 8 to 10, 8 to 11, 8 to 12, 8 to 13, 8 to 14, 8 to 15, 8 to 16, 8 to 17, 8 to 18, 8 to 19, 8 to 20, 8 to 21, 8 to 22, 8 to 23, 8 to 24, 8 to 25, 8 to 26, 8 to 27, 8 to 28, 8 to 29, 8 to 30, 9 to 10, 9 to 11, 9 to 12, 9 to 13, 9 to 14, 9 to 15, 9 to 16, 9 to 17, 9 to 18, 9 to 19, 9 to 20, 9 to 21, 9 to 22, 9 to 23, 9 to 24, 9 to 25, 9 to 26, 9 to 27, 9 to 28, 9 to 29, 9 to 30, 10 to 11, 10 to 12, 10 to 13, 10 to 14, 10 to 15, 10 to 16, 10 to 17, 10 to 18, 10 to 19, 10 to 20, 10 to 21, 10 to 22, 10 to 23, 10 to 24, 10 to 25, 10 to 26, 10 to 27, 10 to 28, 10 to 29, 10 to 30, 11 to 12, 11 to 13, 11 to 14, 11 to 15, 11 to 16, 11 to 17, 11 to 18, 11 to 19, 11 to 20, 11 to 21, 11 to 22, 11 to 23, 11 to 24, 11 to 25, 11 to 26, 11 to 27, 11 to 28, 11 to 29, 11 to 30, 12 to 13, 12 to 14, 12 to 15, 12 to 16, 12 to 17, 12 to 18, 12 to 19, 12 to 20, 12 to 21, 12 to 22, 12 to 23, 12 to 24, 12 to 25, 12 to 26, 12 to 27, 12 to 28, 12 to 29, 12 to 30, 13 to 14, 13 to 15, 13 to 16, 13 to 17, 13 to 18, 13 to 19, 13 to 20, 13 to 21, 13 to 22, 13 to 23, 13 to 24, 13 to 25, 13 to 26, 13 to 27, 13 to 28, 13 to 29, 13 to 30, 14 to 15, 14 to 16, 14 to 17, 14 to 18, 14 to 19, 14 to 20, 14 to 21, 14 to 22, 14 to 23, 14 to 24, 14 to 25, 14 to 26, 14 to 27, 14 to 28, 14 to 29, 14 to 30, 15 to 16, 15 to 17, 15 to 18, 15 to 19, 15 to 20, 15 to 21, 15 to 22, 15 to 23, 15 to 24, 15 to 25, 15 to 26, 15 to 27, 15 to 28, 15 to 29, 15 to 30, 16 to 17, 16 to 18, 16 to 19, 16 to 20, 16 to 21, 16 to 22, 16 to 23, 16 to 24, 16 to 25, 16 to 26, 16 to 27, 16 to 28, 16 to 29, 16 to 30, 17 to 18, 17 to 19, 17 to 20, 17 to 21, 17 to 22, 17 to 23, 17 to 24, 17 to 25, 17 to 26, 17 to 27, 17 to 28, 17 to 29, 17 to 30, 18 to 19, 18 to 20, 18 to 21, 18 to 22, 18 to 23, 18 to 24, 18 to 25, 18 to 26, 18 to 27, 18 to 28, 18 to 29, 18 to 30, 19 to 20, 19 to 21, 19 to 22, 19 to 23, 19 to 24, 19 to 25, 19 to 26, 19 to 29, 19 to 28, 19 to 29, 19 to 30, 20 to 21, 20 to 22, 20 to 23, 20 to 24, 20 to 25, 20 to 26, 20 to 27, 20 to 28, 20 to 29, 20 to 30, 21 to 22, 21 to 23, 21 to 24, 21 to 25, 21 to 26, 21 to 27, 21 to 28, 21 to 29, 21 to 30, 22 to 23, 22 to 24, 22 to 25, 22 to 26, 22 to 27, 22 to 28, 22 to 29, 22 to 30, 23 to 24, 23 to 25, 23 to 26, 23 to 27, 23 to 28, 23 to 29, 23 to 30, 24 to 25, 24 to 26, 24 to 27, 24 to 28, 24 to 29, 24 to 30, 25 to 26, 25 to 27, 25 to 28, 25 to 29, 25 to 30, 26 to 27, 26 to 28, 26 to 29, 26 to 30, 27 to 28, 27 to 29, 27 to 30, 28 to 29, 28 to 30, or 29 to 30 linked nucleosides. In embodiments where the number of nucleosides of an oligomeric compound or oligonucleotide is limited, whether to a range or to a specific number, the oligomeric compound or oligonucleotide may, nonetheless further comprise additional other substituents. For example, an oligonucleotide comprising 8-30 nucleosides excludes oligonucleotides having 31 nucleosides, but, unless otherwise indicated, such an oligonucleotide may further comprise, for example one or more conjugates, terminal groups, or other substituents. In certain embodiments, a modified oligonucleotides has any of the above lengths.

[0870] Further, where an oligonucleotide is described by an overall length range and by regions having specified lengths, and where the sum of specified lengths of the regions is less than the upper limit of the overall length range, the oligonucleotide may have additional nucleosides, beyond those of the specified regions, provided that the total number of nucleosides does not exceed the upper limit of the overall length range.

[0871] e. Certain Oligonucleotides

[0872] In certain embodiments, oligonucleotides of the present invention are characterized by their modification motif and overall length. In certain embodiments, such parameters are each independent of one another.

[0873] I. Certain Oligomeric Compounds

[0874] In certain embodiments, the invention provides oligomeric compounds, which consist of an oligonucleotide (modified or unmodified) and optionally one or more conjugate groups and/or terminal groups. Conjugate groups consist of one or more conjugate moiety and a conjugate linker which links the conjugate moiety to the oligonucleotide. Conjugate groups may be attached to either or both ends of an oligonucleotide and/or at any internal position. In certain embodiments, conjugate groups are attached to the 2′-position of a nucleoside of a modified oligonucleotide. In certain embodiments, conjugate groups that are attached to either or both ends of an oligonucleotide are terminal groups. In certain such embodiments, conjugate groups or terminal groups are attached at the 3′ and/or 5′-end of oligonucleotides. In certain such embodiments, conjugate groups (or terminal groups) are attached at the 3′-end of oligonucleotides. In certain embodiments, conjugate groups are attached near the 3′-end of oligonucleotides. In certain embodiments, conjugate groups (or terminal groups) are attached at the 5′-end of oligonucleotides. In certain embodiments, conjugate groups are attached near the 5′-end of oligonucleotides.

[0875] Examples of terminal groups include but are not limited to conjugate groups, capping groups, phosphate moieties, protecting groups, abasic nucleosides, modified or unmodified nucleosides, and two or more nucleosides that are independently modified or unmodified.

[0876] In certain embodiments, antisense compounds are provided wherein the 5′-terminal group comprises a 5 ‘-terminal stabilized phosphate. A “5’-terminal stabilized phosphate” is a 5 ‘-terminal phosphate group having one or more modifications that increase nuclease stability relative to a 5’-phosphate.

[0877] In certain embodiments, antisense compounds are provided wherein the 5′-terminal group has Formula IIe:

##STR00005##

wherein:

[0878] Bx is uracil, thymine, cytosine, 5-methyl cytosine, adenine or guanine;

[0879] T2 is a phosphorothioate internucleoside linking group linking the compound of Formula IIe to the oligomeric compound; and

[0880] G is halogen, OCH3, OCF3, OCH2CH3, OCH2CF3, OCH2-CH═CH2, O(CH2)2-OCH3, O(CH2)2-O(CH2)2-N(CH3)2, OCH2C(═O)—N(H)CH3, OCH2C(═O)—N(H)—(CH2)2-N(CH3)2 or OCH2-N(H)—C(═NH)NH2.

[0881] In certain embodiments, antisense compounds are provided wherein said 5′-terminal compound has Formula IIe wherein G is F, OCH3 or O(CH2)2-OCH3.

[0882] In certain embodiments, the 5′-terminal group is a 5′-terminal stabilized phosphate comprising a vinyl phosphonate represented by Formula IIe above.

[0883] f. Certain Conjugate Groups

[0884] In certain embodiments, the oligonucleotides or oligomeric compounds as provided herein are modified by covalent attachment of one or more conjugate groups. In general, conjugate groups modify one or more properties of the attached oligonucleotide or oligomeric compound including but not limited to pharmacodynamics, pharmacokinetics, stability, binding, absorption, cellular distribution, cellular uptake, charge and clearance. As used herein, “conjugate group” means a radical group comprising a group of atoms that are attached to an oligonucleotide or oligomeric compound. In general, conjugate groups modify one or more properties of the compound to which they are attached, including, but not limited to pharmacodynamic, pharmacokinetic, binding, absorption, cellular distribution, cellular uptake, charge and/or clearance properties. Conjugate groups are routinely used in the chemical arts and can include a conjugate linker that covalently links the conjugate group to an oligonucleotide or oligomeric compound. In certain embodiments, conjugate groups include a cleavable moiety that covalently links the conjugate group to an oligonucleotide or oligomeric compound. In certain embodiments, conjugate groups include a conjugate linker and a cleavable moiety to covalently link the conjugate group to an oligonucleotide or oligomeric compound. In certain embodiments, a conjugate group has the general formula:

##STR00006##

[0885] wherein n is from 1 to about 3, m is 0 when n is 1 or m is 1 when n is 2 or 3, j is 1 or 0, k is 1 or 0 and the sum of j and k is at least one.

[0886] In certain embodiments, n is 1, j is 1 and k is 0. In certain embodiments, n is 1, j is 0 and k is 1. In certain embodiments, n is 1, j is 1 and k is 1. In certain embodiments, n is 2, j is 1 and k is 0. In certain embodiments, n is 2, j is 0 and k is 1. In certain embodiments, n is 2, j is 1 and k is 1. In certain embodiments, n is 3, j is 1 and k is 0. In certain embodiments, n is 3, j is 0 and k is 1. In certain embodiments, n is 3, j is 1 and k is 1.

[0887] Conjugate groups are shown herein as radicals, providing a bond for forming covalent attachment to an oligomeric compound such as an oligonucleotide. In certain embodiments, the point of attachment on the oligomeric compound is at the 3′-terminal nucleoside or modified nucleoside. In certain embodiments, the point of attachment on the oligomeric compound is the 3′-oxygen atom of the 3′-hydroxyl group of the 3′ terminal nucleoside or modified nucleoside. In certain embodiments, the point of attachment on the oligomeric compound is at the 5′-terminal nucleoside or modified nucleoside. In certain embodiments the point of attachment on the oligomeric compound is the 5′-oxygen atom of the 5′-hydroxyl group of the 5′-terminal nucleoside or modified nucleoside. In certain embodiments, the point of attachment on the oligomeric compound is at any reactive site on a nucleoside, a modified nucleoside or an internucleoside linkage.

[0888] As used herein, “cleavable moiety” and “cleavable bond” mean a cleavable bond or group of atoms that is capable of being split or cleaved under certain physiological conditions. In certain embodiments, a cleavable moiety is a cleavable bond. In certain embodiments, a cleavable moiety comprises a cleavable bond. In certain embodiments, a cleavable moiety is a group of atoms. In certain embodiments, a cleavable moiety is selectively cleaved inside a cell or sub-cellular compartment, such as a lysosome. In certain embodiments, a cleavable moiety is selectively cleaved by endogenous enzymes, such as nucleases. In certain embodiments, a cleavable moiety comprises a group of atoms having one, two, three, four, or more than four cleavable bonds.

[0889] In certain embodiments, conjugate groups comprise a cleavable moiety. In certain such embodiments, the cleavable moiety covalently attaches the oligomeric compound to the conjugate linker. In certain such embodiments, the cleavable moiety covalently attaches the oligomeric compound to the cell-targeting moiety.

[0890] In certain embodiments, a cleavable bond is selected from among: an amide, a polyamide, an ester, an ether, one or both esters of a phosphodiester, a phosphate ester, a carbamate, a di-sulfide, or a peptide. In certain embodiments, a cleavable bond is one of the esters of a phosphodiester. In certain embodiments, a cleavable bond is one or both esters of a phosphodiester. In certain embodiments, the cleavable moiety is a phosphodiester linkage between an oligomeric compound and the remainder of the conjugate group. In certain embodiments, the cleavable moiety comprises a phosphodiester linkage that is located between an oligomeric compound and the remainder of the conjugate group. In certain embodiments, the cleavable moiety comprises a phosphate or phosphodiester. In certain embodiments, the cleavable moiety is attached to the conjugate linker by either a phosphodiester or a phosphorothioate linkage. In certain embodiments, the cleavable moiety is attached to the conjugate linker by a phosphodiester linkage. In certain embodiments, the conjugate group does not include a cleavable moiety.

[0891] In certain embodiments, the cleavable moiety is a cleavable nucleoside or a modified nucleoside. In certain embodiments, the nucleoside or modified nucleoside comprises an optionally protected heterocyclic base selected from a purine, substituted purine, pyrimidine or substituted pyrimidine. In certain embodiments, the cleavable moiety is a nucleoside selected from uracil, thymine, cytosine, 4-N-benzoylcytosine, 5-methylcytosine, 4-N-benzoyl-5-methylcytosine, adenine, 6-N-benzoyladenine, guanine and 2-N-isobutyrylguanine.

[0892] In certain embodiments, the cleavable moiety is 2′-deoxy nucleoside that is attached to either the 3′ or 5′-terminal nucleoside of an oligomeric compound by a phosphodiester linkage and covalently attached to the remainder of the conjugate group by a phosphodiester or phosphorothioate linkage. In certain embodiments, the cleavable moiety is 2′-deoxy adenosine that is attached to either the 3′ or 5′-terminal nucleoside of an oligomeric compound by a phosphodiester linkage and covalently attached to the remainder of the conjugate group by a phosphodiester or phosphorothioate linkage. In certain embodiments, the cleavable moiety is 2′-deoxy adenosine that is attached to the 3′-oxygen atom of the 3′-hydroxyl group of the 3′-terminal nucleoside or modified nucleoside by a phosphodiester linkage. In certain embodiments, the cleavable moiety is 2′-deoxy adenosine that is attached to the 5′-oxygen atom of the 5′-hydroxyl group of the 5′-terminal nucleoside or modified nucleoside by a phosphodiester linkage. In certain embodiments, the cleavable moiety is attached to a 2′-position of a nucleoside or modified nucleoside of an oligomeric compound.

[0893] As used herein, “conjugate linker” in the context of a conjugate group means a portion of a conjugate group comprising any atom or group of atoms that covalently link the cell-targeting moiety to the oligomeric compound either directly or through the cleavable moiety. In certain embodiments, the conjugate linker comprises groups selected from alkyl, amino, oxo, amide, disulfide, polyethylene glycol, ether, thioether (—S—) and hydroxylamino (—O—N(H)—). In certain embodiments, the conjugate linker comprises groups selected from alkyl, amino, oxo, amide and ether groups. In certain embodiments, the conjugate linker comprises groups selected from alkyl and amide groups. In certain embodiments, the conjugate linker comprises groups selected from alkyl and ether groups. In certain embodiments, the conjugate linker comprises at least one phosphorus linking group. In certain embodiments, the conjugate linker comprises at least one phosphodiester group. In certain embodiments, the conjugate linker includes at least one neutral linking group.

[0894] In certain embodiments, the conjugate linker is covalently attached to the oligomeric compound. In certain embodiments, the conjugate linker is covalently attached to the oligomeric compound and the branching group. In certain embodiments, the conjugate linker is covalently attached to the oligomeric compound and a tethered ligand. In certain embodiments, the conjugate linker is covalently attached to the cleavable moiety. In certain embodiments, the conjugate linker is covalently attached to the cleavable moiety and the branching group. In certain embodiments, the conjugate linker is covalently attached to the cleavable moiety and a tethered ligand. In certain embodiments, the conjugate linker includes one or more cleavable bonds. In certain embodiments, the conjugate group does not include a conjugate linker.

[0895] As used herein, “branching group” means a group of atoms having at least 3 positions that are capable of forming covalent linkages to two or more tether-ligands and the remainder of the conjugate group. In general a branching group provides a plurality of reactive sites for connecting tethered ligands to the oligomeric compound through the conjugate linker and/or the cleavable moiety. In certain embodiments, the branching group comprises groups selected from alkyl, amino, oxo, amide, disulfide, polyethylene glycol, ether, thioether and hydroxylamino groups. In certain embodiments, the branching group comprises a branched aliphatic group comprising groups selected from alkyl, amino, oxo, amide, disulfide, polyethylene glycol, ether, thioether and hydroxylamino groups. In certain such embodiments, the branched aliphatic group comprises groups selected from alkyl, amino, oxo, amide and ether groups. In certain such embodiments, the branched aliphatic group comprises groups selected from alkyl, amino and ether groups. In certain such embodiments, the branched aliphatic group comprises groups selected from alkyl and ether groups. In certain embodiments, the branching group comprises a mono or polycyclic ring system.

[0896] In certain embodiments, the branching group is covalently attached to the conjugate linker. In certain embodiments, the branching group is covalently attached to the cleavable moiety. In certain embodiments, the branching group is covalently attached to the conjugate linker and each of the tethered ligands. In certain embodiments, the branching group comprises one or more cleavable bond. In certain embodiments, the conjugate group does not include a branching group.

[0897] In certain embodiments, conjugate groups as provided herein include a cell-targeting moiety that has at least one tethered ligand. In certain embodiments, the cell-targeting moiety comprises two tethered ligands covalently attached to a branching group. In certain embodiments, the cell-targeting moiety comprises three tethered ligands covalently attached to a branching group.

[0898] As used herein, “tether” means a group of atoms that connect a ligand to the remainder of the conjugate group. In certain embodiments, each tether is a linear aliphatic group comprising one or more groups selected from alkyl, substituted alkyl, ether, thioether, disulfide, amino, oxo, amide, phosphodiester and polyethylene glycol groups in any combination. In certain embodiments, each tether is a linear aliphatic group comprising one or more groups selected from alkyl, ether, thioether, disulfide, amino, oxo, amide and polyethylene glycol groups in any combination. In certain embodiments, each tether is a linear aliphatic group comprising one or more groups selected from alkyl, substituted alkyl, phosphodiester, ether and amino, oxo, amide groups in any combination. In certain embodiments, each tether is a linear aliphatic group comprising one or more groups selected from alkyl, ether and amino, oxo, amide groups in any combination. In certain embodiments, each tether is a linear aliphatic group comprising one or more groups selected from alkyl, amino and oxo groups in any combination. In certain embodiments, each tether is a linear aliphatic group comprising one or more groups selected from alkyl and oxo groups in any combination. In certain embodiments, each tether is a linear aliphatic group comprising one or more groups selected from alkyl and phosphodiester in any combination. In certain embodiments, each tether comprises at least one phosphorus linking group or neutral linking group.

[0899] In certain embodiments, tethers include one or more cleavable bond. In certain embodiments, each tethered ligand is attached to a branching group. In certain embodiments, each tethered ligand is attached to a branching group through an amide group. In certain embodiments, each tethered ligand is attached to a branching group through an ether group. In certain embodiments, each tethered ligand is attached to a branching group through a phosphorus linking group or neutral linking group. In certain embodiments, each tethered ligand is attached to a branching group through a phosphodiester group. In certain embodiments, each tether is attached to a ligand through either an amide or an ether group. In certain embodiments, each tether is attached to a ligand through an ether group.

[0900] In certain embodiments, each tether comprises from about 8 to about 20 atoms in chain length between the ligand and the branching group. In certain embodiments, each tether comprises from about 10 to about 18 atoms in chain length between the ligand and the branching group. In certain embodiments, each tether comprises about 13 atoms in chain length.

[0901] In certain embodiments, the present disclosure provides ligands wherein each ligand is covalently attached to the remainder of the conjugate group through a tether. In certain embodiments, each ligand is selected to have an affinity for at least one type of receptor on a target cell. In certain embodiments, ligands are selected that have an affinity for at least one type of receptor on the surface of a mammalian liver cell. In certain embodiments, ligands are selected that have an affinity for the hepatic asialoglycoprotein receptor (ASGP-R). In certain embodiments, each ligand is a carbohydrate. In certain embodiments, each ligand is, independently selected from galactose, N-acetyl galactoseamine, mannose, glucose, glucosamone and fucose. In certain embodiments, each ligand is N-acetyl galactoseamine (GalNAc). In certain embodiments, the targeting moiety comprises 1 to 3 ligands. In certain embodiments, the targeting moiety comprises 3 ligands. In certain embodiments, the targeting moiety comprises 2 ligands. In certain embodiments, the targeting moiety comprises 1 ligand. In certain embodiments, the targeting moiety comprises 3 N-acetyl galactoseamine ligands. In certain embodiments, the targeting moiety comprises 2 N-acetyl galactoseamine ligands. In certain embodiments, the targeting moiety comprises 1 N-acetyl galactoseamine ligand.

[0902] In certain embodiments, each ligand is a carbohydrate, carbohydrate derivative, modified carbohydrate, multivalent carbohydrate cluster, polysaccharide, modified polysaccharide, or polysaccharide derivative. In certain embodiments, each ligand is an amino sugar or a thio sugar. For example, amino sugars may be selected from any number of compounds known in the art, for example glucosamine, sialic acid, α-D-galactosamine, N-Acetylgalactosamine, 2-acetamido-2-deoxy-D-galactopyranose (GalNAc), 2-Amino-3-O—[(R)-1-carboxyethyl]-2-deoxy-β-D-glucopyranose (β-muramic acid), 2-Deoxy-2-methylamino-L-glucopyranose, 4,6-Dideoxy-4-formamido-2,3-di-O-methyl-D-mannopyranose, 2-Deoxy-2-sulfoamino-D-glucopyranose and N-sulfo-D-glucosamine, and N-Glycoloyl-α-neuraminic acid. For example, thio sugars may be selected from the group consisting of 5-Thio-β-D-glucopyranose, Methyl 2,3,4-tri-O-acetyl-1-thio-6-O-trityl-α-D-glucopyranoside, 4-Thio-β-D-galactopyranose, and ethyl 3,4,6,7-tetra-O-acetyl-2-deoxy-1,5-dithio-α-D-gluco-heptopyranoside.

[0903] In certain embodiments, conjugate groups as provided herein comprise a carbohydrate cluster. As used herein, “carbohydrate cluster” means a portion of a conjugate group wherein two or more carbohydrate residues are attached to a branching group through tether groups. (see, e.g., Maier et al., “Synthesis of Antisense Oligonucleotides Conjugated to a Multivalent Carbohydrate Cluster for Cellular Targeting,” Bioconjugate Chemistry, 2003, (14): 18-29, which is incorporated herein by reference in its entirety, or Rensen et al., “Design and Synthesis of Novel N-Acetylgalactosamine-Terminated Glycolipids for Targeting of Lipoproteins to the Hepatic Asiaglycoprotein Receptor,” J. Med. Chem. 2004, (47): 5798-5808, for examples of carbohydrate conjugate clusters).

[0904] As used herein, “modified carbohydrate” means any carbohydrate having one or more chemical modifications relative to naturally occurring carbohydrates.

[0905] As used herein, “carbohydrate derivative” means any compound which may be synthesized using a carbohydrate as a starting material or intermediate.

[0906] As used herein, “carbohydrate” means a naturally occurring carbohydrate, a modified carbohydrate, or a carbohydrate derivative.

[0907] In certain embodiments, conjugate groups are provided wherein the cell-targeting moiety has the formula:

##STR00007##

[0908] In certain embodiments, conjugate groups are provided wherein the cell-targeting moiety has the formula:

##STR00008##

[0909] In certain embodiments, conjugate groups are provided wherein the cell-targeting moiety has the formula:

##STR00009##

[0910] In certain embodiments, conjugate groups have the formula:

##STR00010##

[0911] Representative United States patents, United States patent application publications, and international patent application publications that teach the preparation of certain of the above noted conjugate groups, conjugated oligomeric compounds such as antisense compounds comprising a conjugate group, tethers, conjugate linkers, branching groups, ligands, cleavable moieties as well as other modifications include without limitation, U.S. Pat. No. 5,994,517, U.S. Pat. No. 6,300,319, U.S. Pat. No. 6,660,720, U.S. Pat. No. 6,906,182, U.S. Pat. No. 7,262,177, U.S. Pat. No. 7,491,805, U.S. Pat. No. 8,106,022, U.S. Pat. No. 7,723,509, US 2006/0148740, US 2011/0123520, WO 2013/033230 and WO 2012/037254, each of which is incorporated by reference herein in its entirety.

[0912] Representative publications that teach the preparation of certain of the above noted conjugate groups, conjugated oligomeric compounds such as antisense compounds comprising a conjugate group, tethers, conjugate linkers, branching groups, ligands, cleavable moieties as well as other modifications include without limitation, BIESSEN et al., “The Cholesterol Derivative of a Triantennary Galactoside with High Affinity for the Hepatic Asialoglycoprotein Receptor: a Potent Cholesterol Lowering Agent” J. Med. Chem. (1995) 38:1846-1852, BIESSEN et al., “Synthesis of Cluster Galactosides with High Affinity for the Hepatic Asialoglycoprotein Receptor” J. Med. Chem. (1995) 38:1538-1546, LEE et al., “New and more efficient multivalent glyco-ligands for asialoglycoprotein receptor of mammalian hepatocytes” Bioorganic & Medicinal Chemistry (2011) 19:2494-2500, RENSEN et al., “Determination of the Upper Size Limit for Uptake and Processing of Ligands by the Asialoglycoprotein Receptor on Hepatocytes in Vitro and in Vivo” J. Biol. Chem. (2001) 276(40):37577-37584, RENSEN et al., “Design and Synthesis of Novel N-Acetylgalactosamine-Terminated Glycolipids for Targeting of Lipoproteins to the Hepatic Asialoglycoprotein Receptor” J. Med. Chem. (2004) 47:5798-5808, SLIEDREGT et al., “Design and Synthesis of Novel Amphiphilic Dendritic Galactosides for Selective Targeting of Liposomes to the Hepatic Asialoglycoprotein Receptor” J. Med. Chem. (1999) 42:609-618, and Valentijn et al., “Solid-phase synthesis of lysine-based cluster galactosides with high affinity for the Asialoglycoprotein Receptor” Tetrahedron, 1997, 53(2), 759-770, each of which is incorporated by reference herein in its entirety.

[0913] In certain embodiments, conjugate groups include without limitation, intercalators, reporter molecules, polyamines, polyamides, polyethylene glycols, thioethers, polyethers, cholesterols, thiocholesterols, cholic acid moieties, folate, lipids, phospholipids, biotin, phenazine, phenanthridine, anthraquinone, adamantane, acridine, fluoresceins, rhodamines, coumarins and dyes. Certain conjugate groups have been described previously, for example: cholesterol moiety (Letsinger et al., Proc. Natl. Acad. Sci. USA, 1989, 86, 6553-6556), cholic acid (Manoharan et al., Bioorg. Med. Chem. Let., 1994, 4, 1053-1060), a thioether, e.g., hexyl-S-tritylthiol (Manoharan et al., Ann. N.Y. Acad. Sci., 1992, 660, 306-309; Manoharan et al., Bioorg. Med. Chem. Let., 1993, 3, 2765-2770), a thiocholesterol (Oberhauser et al., Nucl. Acids Res., 1992, 20, 533-538), an aliphatic chain, e.g., do-decan-diol or undecyl residues (Saison-Behmoaras et al., EMBO J., 1991, 10, 1111-1118; Kabanov et al., FEBS Lett., 1990, 259, 327-330; Svinarchuk et al., Biochimie, 1993, 75, 49-54), a phospholipid, e.g., di-hexadecyl-rac-glycerol or triethyl-ammonium 1,2-di-O-hexadecyl-rac-glycero-3-H-phosphonate (Manoharan et al., Tetrahedron Lett., 1995, 36, 3651-3654; Shea et al., Nucl. Acids Res., 1990, 18, 3777-3783), a polyamine or a polyethylene glycol chain (Manoharan et al., Nucleosides & Nucleotides, 1995, 14, 969-973), or adamantane acetic acid (Manoharan et al., Tetrahedron Lett., 1995, 36, 3651-3654), a palmityl moiety (Mishra et al., Biochim. Biophys. Acta, 1995, 1264, 229-237), or an octadecylamine or hexylamino-carbonyl-oxycholesterol moiety (Crooke et al., J. Pharmacol. Exp. Ther., 1996, 277, 923-937).

[0914] In certain embodiments, a conjugate group comprises an active drug substance, for example, aspirin, warfarin, phenylbutazone, ibuprofen, suprofen, fen-bufen, ketoprofen, (S)-(+)-pranoprofen, carprofen, dansylsarcosine, 2,3,5-triiodobenzoic acid, flufenamic acid, folinic acid, a benzothiadiazide, chlorothiazide, a diazepine, indo-methicin, a barbiturate, a cephalosporin, a sulfa drug, an antidiabetic, an antibacterial or an antibiotic.

[0915] Some nonlimiting examples of conjugate linkers include pyrrolidine, 8-amino-3,6-dioxaoctanoic acid (ADO), succinimidyl 4-(N-maleimidomethyl) cyclohexane-1-carboxylate (SMCC) and 6-aminohexanoic acid (AHEX or AHA). Other connugate linkers include, but are not limited to, substituted C.sub.1-C.sub.10 alkyl, substituted or unsubstituted C.sub.2-C.sub.10 alkenyl or substituted or unsubstituted C.sub.2-C.sub.10 alkynyl, wherein a nonlimiting list of preferred substituent groups includes hydroxyl, amino, alkoxy, carboxy, benzyl, phenyl, nitro, thiol, thioalkoxy, halogen, alkyl, aryl, alkenyl and alkynyl.

[0916] Conjugate groups may be attached to either or both ends of an oligonucleotide (terminal conjugate groups) and/or at any internal position.

[0917] In certain embodiments, conjugate groups are at the 3′-end of an oligonucleotide of an oligomeric compound. In certain embodiments, conjugate groups are near the 3′-end. In certain embodiments, conjugates are attached at the 3′ end of an oligomeric compound, but before one or more terminal group nucleosides. In certain embodiments, conjugate groups are placed within a terminal group.

B. Antisense Compounds

[0918] In certain embodiments, modified oligonucleotides provided herein are antisense compounds. Such antisense compounds are capable of hybridizing to a target nucleic acid, resulting in at least one antisense activity. In certain embodiments, antisense compounds specifically hybridize to one or more target nucleic acid. In certain embodiments, a specifically hybridizing antisense compound has a nucleobase sequence comprising a region having sufficient complementarity to a target nucleic acid to allow hybridization and result in antisense activity and insufficient complementarity to any non-target so as to avoid non-specific hybridization to any non-target nucleic acid sequences under conditions in which specific hybridization is desired (e.g., under physiological conditions for in vivo or therapeutic uses, and under conditions in which assays are performed in the case of in vitro assays).

[0919] In certain embodiments, the present invention provides antisense compounds comprising oligonucleotides that are fully complementary to the target nucleic acid over the entire length of the oligonucleotide. In certain embodiments, oligonucleotides are 99% complementary to the target nucleic acid. In certain embodiments, oligonucleotides are 95% complementary to the target nucleic acid. In certain embodiments, such oligonucleotides are 90% complementary to the target nucleic acid.

[0920] In certain embodiments, such oligonucleotides are 85% complementary to the target nucleic acid. In certain embodiments, such oligonucleotides are 80% complementary to the target nucleic acid. In certain embodiments, an antisense compound comprises a region that is fully complementary to a target nucleic acid and is at least 80% complementary to the target nucleic acid over the entire length of the oligonucleotide. In certain such embodiments, the region of full complementarity is from 6 to 14 nucleobases in length.

[0921] a. Certain Antisense Compounds

[0922] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 45, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, or 77.

[0923] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 17, 18, 19, 41, or 32.

[0924] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NO: 21.

[0925] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 25 or 44.

[0926] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NO: 23.

[0927] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 79, 80, 84, 85, 86, 87, 88, 89, 90, 92, or 93.

[0928] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 82 or 83.

[0929] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NO: 95.

[0930] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NO: 97.

[0931] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 99, 101, 102, 103, or 104.

[0932] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence consisting of the nucleobase sequence of any of SEQ ID NOs: 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 45, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, or 77.

[0933] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence consisting of the nucleobase sequence of any of SEQ ID NOs: 17, 18, 19, 41, or 32.

[0934] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence consisting of the nucleobase sequence of SEQ ID NO: 21.

[0935] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence consisting of the nucleobase sequence of any of SEQ ID NOs: 25 or 44.

[0936] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence consisting of the nucleobase sequence of SEQ ID NO: 23.

[0937] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence consisting of the nucleobase sequence of any of SEQ ID NOs: 79, 80, 84, 85, 86, 87, 88, 89, 90, 92, or 93.

[0938] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence consisting of the nucleobase sequence of any of SEQ ID NOs: 82 or 83.

[0939] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence consisting of the nucleobase sequence of SEQ ID NO: 95.

[0940] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence consisting of the nucleobase sequence of SEQ ID NO: 97.

[0941] In certain embodiments, a modified oligonucleotide described herein has a nucleobase sequence consisting of the nucleobase sequence of any of SEQ ID NOs: 99, 101, 102, 103, or 104.

[0942] In certain embodiments, the present disclosure provides methods for increasing the expression of RNAse H1 by contacting a cell with a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 45, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, or 77.

[0943] In certain embodiments, the present disclosure provides methods for increasing the expression of LRPPRC by contacting a cell with a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 17, 18, 19, 41, or 32.

[0944] In certain embodiments, the present disclosure provides methods for increasing the expression of SFXN3 by contacting a cell with a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of the nucleobase sequences of SEQ ID NO: 21.

[0945] In certain embodiments, the present disclosure provides methods for increasing the expression of THPO by contacting a cell with a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 25 or 44.

[0946] In certain embodiments, the present disclosure provides methods for increasing the expression of MRPL11 by contacting a cell with a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of the nucleobase sequences of SEQ ID NO: 23.

[0947] In certain embodiments, the present disclosure provides methods for increasing the expression of ACP1 by contacting a cell with a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 79, 80, 84, 85, 86, 87, 88, 89, 90, 92, or 93.

[0948] In certain embodiments, the present disclosure provides methods for increasing the expression of CFTR by contacting a cell with a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 82 or 83.

[0949] In certain embodiments, the present disclosure provides methods for increasing the expression of ARF1 by contacting a cell with a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of the nucleobase sequences of SEQ ID NO: 95.

[0950] In certain embodiments, the present disclosure provides methods for increasing the expression of USP16 by contacting a cell with a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of the nucleobase sequences of SEQ ID NO: 97.

[0951] In certain embodiments, the present disclosure provides methods for increasing the expression of LDLr by contacting a cell with a modified oligonucleotide described herein has a nucleobase sequence comprising at least 14 contiguous nucleobases of any of the nucleobase sequences of SEQ ID NOs: 99, 101, 102, 103, or 104.

[0952] b. Certain Antisense Activities and Mechanisms

[0953] The 5′-UTR has emerged as playing an important role in the regulation of translation of many transcripts. In certain embodiments, the 5′-UTR contains translation suppression elements (TSEs), which serve to suppress translation of a target protein. In certain embodiments, translation suppression elements are uORFs. In certain embodiments, translation suppression elements are G-quartets. In certain embodiments, translation suppression elements are stem-loops. Disruption of a TSE will decrease the TSE's suppression of translation of a given transcript and will therefore result in an increase in translation of a target protein. In certain embodiments, antisense compounds are used to disrupt a TSE and to increase translation of a target protein.

[0954] Upstream open reading frames have emerged as an important mechanism by which translation is regulated. Approximately 50% of human transcripts have uORFs and most appear to be functional. When functional, uORFs typically reduce the translation of a polypeptide or protein from the downstream pORF. Characteristics of uORFs such as the strength of Kozak sequence and\or the distance from the 5′cap, affect the effectiveness of each uORF in reducing the translation of the downstream protein. Other factors, such as the secondary structure of the uORF or the number of uORFs per transcript also affect the effectiveness of each uORF in reducing the translation of the downstream protein. Certain embodiments of the present disclosure provide uORF inhibitors (e.g. antisense compounds) that serve to block the initiation of translation from a uORF. In certain embodiments, the uORF inhibitors do not activate RNase H. In certain such embodiments, translation of the protein encoded by a downstream ORF (e.g., the pORF) is enhanced. Certain embodiments of the present invention block the initiation of translation from a uORF with a uORF inhibitor. In certain such embodiments, translation of the protein encoded by the downstream ORF (e.g., the pORF) is enhanced. Certain embodiments of the present disclosure provide TSE inhibitors and/or uORF inhibitors (e.g. antisense compounds) that when bound to a complementary target transcript, do not activate RNase H. Certain embodiments of the present disclosure provide TSE inhibitors and/or uORF inhibitors (e.g. antisense compounds), wherein the antisense compounds are modified oligonucleotides that are not gapmers.

[0955] Upstream open reading frames can regulate translation of polypeptides or proteins encoded by pORFs by a variety of mechanisms. The polypeptide or protein encoded by the uORF may be translated, and the resulting uORF polypeptide may block translation of the polypeptide or protein encoded by the pORF on the same mRNA molecule (cis regulation) or on a separate mRNA molecule (trans regulation). In another example of cis regulation, the ribosomal subunits may dissociate from the mRNA following translation of the uORF polypeptide, thus failing to recognize and translate the pORF polypeptide or protein. Alternatively, the uORF stop codon may be recognized as a premature stop codon and initiate nonsense mediated decay. The extent to which a uORF suppresses translation of a pORF polypeptide or protein depends on how often it is recognized by the translational machinery, which is in turn affected by many factors, including the strength of the associated Kozak sequence, the number of uORFs in the 5′-UTR, the position of the stop codon, and the secondary structure of the uORF. uORF inhibitors may be employed to disrupt, alter, or exploit any of these mechanisms. In certain embodiments, uORF inhibitors are antisense compounds, and antisense compounds may be employed to disrupt, alter, or exploit any of these mechanisms. In certain embodiments, uORF inhibitors are antisense compounds, and antisense compounds may be employed to disrupt, alter, or exploit any of these mechanisms to increase expression of a target protein in a cell.

[0956] In certain embodiments, a uORF inhibitor (e.g. an antisense compound) disrupts one or more of the factors that contribute to the recognition of a uORF start site by a ribosomal subunit. In certain embodiments, a uORF inhibitor (e.g. an antisense compound) may prevent or decrease one or more of the uORF mediated translational suppressors of pORF polypeptide or protein translation discussed above. For example, in certain embodiments, a uORF inhibitor (e.g. an antisense compound) will disrupt one or more elements of a Kozak sequence, and thereby inhibit recognition of a uORF start site by a ribosomal subunit. For example, in certain embodiments, an antisense compound complementary to a portion of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence. In certain embodiments, an antisense compound complementary to a portion of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence and would therefore cause the ribosome to pass by the uORF start site and initiate translation at a downstream start site (e.g. the pORF start site). A uORF inhibitor (e.g. an antisense compound) would thereby increase the amount or activity of the target protein encoded by the pORF.

[0957] In certain embodiments, an antisense compound complementary to a portion of a target transcript upstream of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence. In certain embodiments, an antisense compound complementary to a portion of a target transcript upstream of a uORF start site may prevent one or more ribosomal subunits from recognizing the uORF start site. In certain embodiments, an antisense compound complementary to a portion of a target transcript 10 nucleobases upstream of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence. In certain embodiments, an antisense compound complementary to a portion of a target transcript 20 nucleobases upstream of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence. In certain embodiments, an antisense compound complementary to a portion of a target transcript 30 nucleobases upstream of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence. In certain embodiments, an antisense compound complementary to a portion of a target transcript 40 nucleobases upstream of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence. In certain embodiments, an antisense compound complementary to a portion of a target transcript 50 nucleobases upstream of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence. In certain embodiments, an antisense compound complementary to a portion of a target transcript 60 nucleobases upstream of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence. In certain embodiments, an antisense compound complementary to a portion of a target transcript at least 60 nucleobases upstream of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence. Therefore, in certain embodiments, an antisense compound complementary to a portion of a target transcript upstream of a uORF start site would increase the amount or activity the target protein encoded by the pORF.

[0958] In certain embodiments, an antisense compound complementary to a portion of a target transcript downstream of a uORF start site may prevent one or more ribosomal subunits from recognizing a Kozak consensus sequence. In certain embodiments, an antisense compound complementary to a portion of a target transcript downstream of a uORF start site may prevent one or more ribosomal subunits from recognizing the uORF start site. Therefore, in certain embodiments, an antisense compound complementary to a portion of a target transcript downstream of a uORF start site would increase the amount or activity the target protein encoded by the pORF.

[0959] In certain embodiments, disruption one or more of the factors that contribute to the recognition of a uORF start site by a ribosomal subunit by a uORF inhibitor (e.g. an antisense compound) increases expression of a downstream pORF. For example, a uORF inhibitor (e.g. an antisense compound) may prevent the dissociation of ribosomal submits after uORF polypeptide translation and thereby increase expression of a downstream pORF. For example, a uORF inhibitor (e.g. an antisense compound) may prevent the recognition of the uORF termination codon as premature and prevent nonsense-mediated decay of the transcript comprising the pORF.

[0960] In certain embodiments the ribosomal subunits recognize a uORF start site and after translation of all or part of the uORF polypeptide, the ribosomal subunits dissociate from the transcript before recognition of the pORF start site. In certain embodiments, the ribosomal subunits are the 60 s ribosomal subunit and/or the 40 s ribosomal subunit. In certain embodiments, a uORF inhibitor (e.g. an antisense compound) may increase the amount of translation reinitiation at the pORF after uORF polypeptide translation. For example, in certain embodiments, a uORF inhibitor (e.g. an antisense compound) prevents the amount of the 60 s ribosomal subunit and/or the 40 s ribosomal subunit that dissociate from the transcript after translation of all or part of the uORF polypeptide and thereby increases translation of the pORF polypeptide or protein.

[0961] In certain embodiments, a uORF inhibitor is a small molecule. In certain embodiments, a uORF inhibitor is an antibody. In certain embodiments, a uORF inhibitor is a polypeptide. In certain embodiments, a uORF inhibitor (e.g. a small molecule, antibody, polypeptide, and/or siRNA) increases the amount or activity a target protein encoded by a pORF via any of the mechanisms described herein.

[0962] Upstream open reading frames are one type of translation suppression element. In addition to uORFs, translation can be regulated by other types of translation suppression elements (TSEs) in the 5′-UTR. Translation may be suppressed by structural elements in the 5′-UTR, such as stem-loops and hairpins. In certain embodiments, the extent to which a structural element suppresses translation may be correlated with the sequence and/or stability of the structural element. For example, the extent to which a structural element suppresses translation may increase as the distance between the 5′-cap of the target transcript and the structural element decreases. For another example, in certain embodiments, GC content and/or the number of consecutive GC nucleosides in the structural element may positively correlate with the extent to which translation is suppressed, due to increased stability of the structural element. Thus, in certain embodiments, transcripts with a 5′-UTR containing multiple stretches of at least 3 consecutive GC nucleosides may comprise at least one TSE. In certain embodiments, transcripts with a 5′-UTR containing at least one stretch of at least 7 GC nucleosides may comprise at least one TSE.

[0963] TSEs that are structural elements may sterically block one or more ribosomal subunits from accessing the coding region. Without wishing to be bound by mechanism, TSE inhibitors may increase translation of a target protein by relieving such steric blockage. In certain embodiments, antisense compounds that are complementary to at least a portion of a TSE structural element alter the structure of the structural element, resulting in increased translation of the target protein. In certain embodiments, such antisense compounds unfold the structural element. In certain embodiments, antisense compounds that are TSE inhibitors have at least 60% GC content. In certain embodiments, antisense compounds that are TSE inhibitors have at least 70% GC content. In certain embodiments, antisense compounds that are TSE inhibitors have at least 80% GC content. In certain embodiments, antisense compounds that are TSE inhibitors have at least 90% GC content. In certain embodiments, antisense compounds that are TSE inhibitors have 100% GC content. In certain embodiments, antisense compounds that are TSE inhibitors have 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or at least 20 consecutive GC nucleosides. In certain embodiments, antisense compounds that are TSE inhibitors are complementary to the stem portion of a stem-loop in the 5′-UTR of the target transcript. In certain embodiments, antisense compounds that are TSE inhibitors are complementary to a hairpin in the 5′-UTR of the target transcript.

[0964] A third type of TSE is a G quartet. In certain embodiments, the extent to which a G quartet suppresses translation may increase as the distance between the 5′-cap of the target transcript and the G quartet decreases.

[0965] A fourth type of TSE is a stem-loop structure. In certain embodiments, transcripts having a stem-loop structure within the 5′-UTR suppress translation of the target protein. In certain embodiments, the extent to which a stem-loop suppresses translation may increase as the distance between the 5′-cap of the target transcript and the stem-loop decreases.

[0966] c. Certain Compositions and Methods for Increasing Antisense Activity

[0967] In certain embodiments the present disclosure provides methods for increase the activity of an antisense compound in a cell, comprising contact the cell with a translation suppression element inhibitor and thereby increasing the activity of an antisense compound.

[0968] In certain embodiments, a translation suppression element inhibitor (e.g. an antisense compound) as described herein increases the amount or activity of a target protein in a cell. In certain embodiments, a uORF inhibitor (e.g. an antisense compound) as described herein increases the amount or activity of a target protein in a cell. In certain embodiments, the target protein plays a role in antisense activity. Therefore, in certain embodiments, increasing the amount or activity of a target protein may also increase the amount or activity of an antisense compound. For example, in certain embodiments, the target protein may play a role in subcellular localization of antisense compounds. In certain embodiments, the target protein may play a role in RNA binding. In certain embodiments, the target protein may play a role in nuclear transport. In certain embodiments, the target protein may play a role in membrane binding. In certain embodiments, the target protein may play a role in DNA binding. In certain embodiments, the target protein may play a role in nuclear import. In certain embodiments, the target protein is a heat shock protein.

[0969] In certain embodiments, a translation suppression element inhibitor is used to increase the amount or activity of a target protein that plays a role in antisense activity, thereby increasing the amount or activity of an antisense compound. In this manner, a translation suppression element inhibitor may be used to increase the activity of an antisense compound by contacting a cell with the translation suppression element inhibitor and then contacting the cell with an antisense compound. In certain embodiments, a uORF inhibitor is used to increase the amount or activity of a target protein that plays a role in antisense activity, thereby increasing the amount or activity of an antisense compound. In this manner, a uORF inhibitor may be used to increase the activity of an antisense compound by contacting a cell with the uORF inhibitor and then contacting the cell with an antisense compound.

[0970] For example, in certain embodiments, the target protein is RNase H. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of RNase H increases the amount or activity of RNase H protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is La/SSB. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of La/SSB increases the amount or activity of La/SSB protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is NPM1. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of NPM1 increases the amount or activity of NPM1 protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is TCP1-alpha. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of TCP1-alpha increases the amount or activity of TCP1-alpha protein in a cell, thereby increasing antisense activity in the cell.

[0971] In certain embodiments, the target protein is TCP1-epsilon. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of TCP1-epsilon increases the amount or activity of TCP1-epsilon protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is TCP1-beta. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of TCP1-beta increases the amount or activity of TCP1-beta protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is HSP90-AA1. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of HSP90-AA1 increases the amount or activity of HSP90-AA1 protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is HSP90-AB. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of HSP90-AB increases the amount or activity of HSP90-AB protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is HSPA1L. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of HSPA1L increases the amount or activity of HSPA1L protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is RAN. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of RAN increases the amount or activity of RAN protein in a cell, thereby increasing antisense activity in the cell.

[0972] In certain embodiments, the target protein is IMP9. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of IMP9 increases the amount or activity of IMP9 protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is Annexin A2. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of Annexin A2 increases the amount or activity of Annexin A2 protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is FTCD/58 k. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of FTCD/58 k increases the amount or activity of FTCD/58 k protein in a cell, thereby increasing antisense activity in the cell.

[0973] In certain embodiments, the target protein is PC4/SUB1. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of PC4/SUB1 increases the amount or activity of PC4/SUB1 protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is VARS. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of VARS increases the amount or activity of VARS protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is DHX36. In certain embodiments, a translation suppression element inhibitor targeted to the 5′-UTR of DHX36 increases the amount or activity of DHX36 protein in a cell, thereby increasing antisense activity in the cell.

[0974] For example, in certain embodiments, the target protein is RNase H. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of RNase H increases the amount or activity of RNase H protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is La/SSB. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of La/SSB increases the amount or activity of La/SSB protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is NPM1. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of NPM1 increases the amount or activity of NPM1 protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is TCP1-alpha. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of TCP1-alpha increases the amount or activity of TCP1-alpha protein in a cell, thereby increasing antisense activity in the cell.

[0975] In certain embodiments, the target protein is TCP1-epsilon. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of TCP1-epsilon increases the amount or activity of TCP1-epsilon protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is TCP1-beta. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of TCP1-beta increases the amount or activity of TCP1-beta protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is HSP90-AA1. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of HSP90-AA1 increases the amount or activity of HSP90-AA1 protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is HSP90-AB. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of HSP90-AB increases the amount or activity of HSP90-AB protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is HSPA1L. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of HSPA1L increases the amount or activity of HSPA1L protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is RAN. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of RAN increases the amount or activity of RAN protein in a cell, thereby increasing antisense activity in the cell.

[0976] In certain embodiments, the target protein is IMP9. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of IMP9 increases the amount or activity of IMP9 protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is Annexin A2. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of Annexin A2 increases the amount or activity of Annexin A2 protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is FTCD/58 k. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of FTCD/58 k increases the amount or activity of FTCD/58 k protein in a cell, thereby increasing antisense activity in the cell.

[0977] In certain embodiments, the target protein is PC4/SUB1. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of PC4/SUB1 increases the amount or activity of PC4/SUB1 protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is VARS. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of VARS increases the amount or activity of VARS protein in a cell, thereby increasing antisense activity in the cell. In certain embodiments, the target protein is DHX36. In certain embodiments, a uORF inhibitor targeted to the 5′-UTR of DHX36 increases the amount or activity of DHX36 protein in a cell, thereby increasing antisense activity in the cell.

[0978] In certain embodiments, the target protein is LDLr. Increasing expression of the LDLr protein decreases cholesteral levels.

[0979] In certain embodiments, the target protein is CFTR. Mutations in the CFTR gene lead to cystic fibrosis. In certain embodiments, increasing expression of the CFTR protein may ameliorate one or more symptoms of cystic fibrosis.

[0980] d. Certain Compositions and Methods for Decreasing Antisense Activity

[0981] In certain embodiments, antisense compounds disclosed herein may target microRNAs or other naturally occurring non-coding transcripts that are complementary to a uORF region or a translation suppression element. Certain such antisense compounds would therefore inhibit expression of a target transcript by increasing the effect of a translation suppression element or uORF. For example, in certain embodiments, a non-coding transcript, such as a microRNA may be complementary to a uORF or uORF region and serve to increase expression of a target protein. An antisense compound complementary to the microRNA would sequester the microRNA and the uORF would then suppress translation of the target protein. In such a manner, an antisense compound would inhibit expression of a target protein.

C. Certain Target Genes

[0982] The present disclosure provides compounds and methods that may be used to increase expression of any target protein, provided there is at least one uORF on a transcript encoding the target protein. The present disclosure also provides compounds and methods that may be used to increase expression of any target protein, provided there is at least one TSE on a transcript encoding the target protein. In certain embodiments, the at least one TSE comprises a uORF. In certain embodiments, there are at least two TSEs on a transcript encoding a target protein. In certain embodiments neither of the at least two TSEs comprise a uORF. In certain embodiments, one of the at least two TSEs comprises a uORF. In certain embodiments, both of the at least two TSEs comprise a uORF. In certain embodiments, a deficiency of the target protein is associated with disease and so increasing the amount or activity of the protein is expected to ameliorate one or more symptoms of the disease or delay the onset of one or more symptoms of the disease. Table 1 and Table 2, below, list certain genes and associated diseases. In certain embodiments, a target transcript is encoded by a gene listed in Table 1 or Table 2. In certain embodiments, the associated disease or disorder in Table 1 or Table 2 is treated by use of an antisense compound of the present invention targeting such transcript. The diseases associated with each gene in Table 1 include diseases that arise due to or are correlated with an insufficiency of the corresponding uORF-containing gene as well as diseases that could be ameliorated by up-regulation of the corresponding uORF-containing gene. The diseases associated with each gene in Table 2 include diseases that correlate with a mutation or SNP that introduces a uORF in the corresponding gene.

[0983] In certain embodiments, antisense compounds are targeted to one or more TSEs in the 5′UTR of a gene in Table 1 or Table 2. In certain embodiments, antisense compounds are not targeted to one or more TSEs in the 5′UTR of a gene in Table 1 or Table 2.

TABLE-US-00001 TABLE 1 uORF-containing genes and associated diseases NCBI Gene Gene ID Associated disease(s) ABCA1 19 Cardiovascular, Dry AMD, dyslipidemia, and atherosclerosis ABCB11 8647 Cholestasis, primary sclerosing cholangitis and biliary cirrhosis ABCC2 1244 Dubin-Johnson syndrome-but overexpressed in cancer ABCG5 64240 Cholestasis, primary sclerosing cholangitis and biliary cirrhosis ADAM10 102 Alzheimer's Disease ALB 213 liver disease, nephrotic syndrome, renal disease, and analbuminemia ANK1 286 Hereditary spherocytosis APOE 348 Cancer, melanoma, pulmonary hypertension, dyslipidemia, atherosclerosis, Alzheimer disease, Lipoprotein glomerulopathy, and Sea-blue histiocyte disease ATP2A2 488 cardiac diseases, congenital heart disease, aortic aneurysms, aortic dissections, arrhythmia, cardiomyopathy, congestive heart failure, Darier- White disease, muscular dystrophy, and Acrokeratosis verruciformis ATP7B 540 wilson disease, and menkes disease. ATRX 546 alpha-thalassemia myelodysplasia syndrome, somatic, and mental retardation-hypotonic facies syndrome, x-linked. ATXN1 6310 Spinocerebellar ataxia-1 ATXN1L 342371 Spinocerebellar ataxia-1 BAX 581 Cancer BCL2L11 10018 Cancer, e.g. human T-cell acute lymphoblastic leukemia and lymphoma BDNF 627 neurodegeneration diseases, amyotrophic lateral sclerosis, Alzheimer's Disease, Huntington's disease (HD), or Parkinson's Disease (PD) BLM 641 bloom syndrome, and rothmund-thomson syndrome. BRCA1 672 Cancer, e.g. breast cancer, pancreatic cancer C/EBPa 1050 B-cell maligancy (B-ALL, DLBCL), AML CA2 760 autoimmune retinopathy, and multifocal fibrosclerosis. CASP8 841 CASP8 deficiency, breast cancer, HCC, lung cancer CCBE1 147372 hennekam syndrome, and immune hydrops fetalis. CD36 948 platelet glycoprotein IV deficiency, coronary heart disease, CHDS7 CD3D 915 severe combined immune deficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive, cd3d-related, and immunodeficiency 19. CDKN1B 1027 cancer, multiple endocrine neoplasia CDKN2A 1029 cancer, melanoma CEP290 80184 Leber's congenital amaurosis (LCA), Bardet-Biedl syndrome (BBS), Joubert syndrome, Meckel syndrome, Sior-Loken syndrome CFH 3075 C3 glomerulopathy, AMD, PNH, RA etc CFTR 1080 Cystic fibrosis, Disseminated bronchiectasis, congenital bilateral absence of vas deferens (CBAVD) CHRNA4 1137 nicotine addiction CHRNA5 1138 nicotine addiction CNTF 1270 Multiple Sclerosis CNTFR 1271 Multiple Sclerosis COL1A1 1277 Osteogenesis Imperfecta Type I CR1 1378 Alzherimer's Disease CSPP1 79848 joubert syndrome 21, and joubert syndrome with jeune asphyxiating thoracic dystrophy. CTNND2 1501 Cri-du-chat syndrome CTNS 1497 intermediate cystinosis, and cystinosis, atypical nephropathic CYP1B1 1545 Glaucoma, Peters anomaly DBT 1629 maple syrup urine disease type 2, and maple syrup urine disease type 1a DCAF17 80067 sakati syndrome, and hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome DNASE1 1773 cystic fibrosis, acute bronchitis DDIT3 1649 Myxoid liposarcoma DICER1 23405 DICER1 symdrome, pleuropulmonary blastoma, cystic nephroma, Sertoli- Leydig tumors, multinodular goiter, cancer DRD3 1814 mood disorders EED 8726 HIV-1 EFNB1 1947 CFNS EPO 2056 erythropoiesis and anemia ESR1 2099 inhibits ERBB1, breast cancer ETHE1 23474 ethylmalonic encephalopathy EZH2 2146 weaver syndrome, ezh2-related overgrowth, lymphomas and leukemias F8 (and F2, 2147, Hemophilia, bleeding 3, 5, 7, 11, ′52, 13) ′53, ′55, ′57, ′60, FAP 2191 glomuvenous malformations FMR1 2332 Fragile X syndrome and premature ovarian failure FNDC5 252995 Obesity, Type 2 Diabetes FXN 2395 Friedreich's ataxia GALNS 2588 mucopolysaccharidosis iv, and kniest dysplasia GATA3 2625 Cancer GBA 2629 Synucleinopathies, Gaucher's disease GCH1 2643 gtp cyclohydrolase I deficiency, Parkinson's disease, movement disorders, CNS disease, doparesponsive dystonia, hyperpehnylalaninemia, and atypical severe phenylketonuria GCK 2645 Obesity, Type 2 Diabetes, and Hyperinsulinemic hypoglycemia GH2 2689 idiopathic short stature, growth delay GRN 2896 autoimmune, inflammatory, dementia, FTD, cancer, e.g. hepatic cancer HBB 3043 thallasemia, sickle cell disease, and anemia HBD 3045 thallasemia, sickle cell disease, and anemia HBE1 3046 thallasemia, sickle cell disease, and anemia HBG1 3047 Anemia (e.g., Fanconi's anemia), thalassemia (e.g., beta-thalassemia etc.), sickle cell disease, leukemia, cellular dyscrasia, dyserythropoiesis, anisocytosis and poikilocytosis. HBG2 3048 thallasemia, sickle cell disease, and anemia HCRT 3060 Narcolepsy/Excessive Daytime Sleepiness HGF 3082 Ischemic disease, restenosis after percutaneous transluminal coronary angioplasty (PTCA), arteriosclerosis, insufficiency of peripheral circulation, myocardial infarction, myocardia, peripheral angiostenosis, cardiac insufficiency, nerve degeneration, neuropathy, neurotoxin induced lesions, injury of nerve cell, lesions of nerve cell by infection, epilepsy, head trauma, dementia, cerebral stroke, cerebral infarction, amyotrophic lateral sclerosis, Parkinson's disease, Alzheimer's disease, cancer, tumor, liver cirrhosis, Nonalcoholic fatty liver disease, renal fibrosis, rhabdomyolysis, pulmonary fibrosis, blood coagulopathy, adenosine deaminase deficiency, Chronic Ulcerative Colitis, Crohn's Disease, necrotizing enterocolitis, severe acute gastroenteritis, chronic gastroenteritis, cholera, chronic infections of the bowel, AIDS, pustulous fibrosis, fibrosis, osteoporosis, Arterial sclerosis, chronic glomerulonephritis, cutis keloid formation, progressive systemic sclerosis (PSS), liver fibrosis, pulmonary fibrosis, cystic fibrosis, chronic graft versus host disease, scleroderma (local and systemic), Peyronie's disease, penis fibrosis, inner accretion after surgery, myelofibrosis, idiopathic retroperitoneal fibrosis, hemophilia, decubitus ulcer, scar, atopic dermatitis, or skin damage following a skin graft HNF4a 3172 HCC, fibrosis HR 55806 atrichia with papular lesions, and hypotrichosis 4 HSD17B4 3295 D-bifunctional protein deficiency IDO1 3620 autoimmune and inflammatory diseases IFNE and 338376, Cancer, HBV, and other virus infection other others interferon genes IFRD1 3475 Cystic fibrosis, Chronic obstructive pulmonary disease (COPD), inflammation, lung cancer, sensory/motor neuropathy, a neuronal injury IGF1 3479 CNS diseases, metabolic disease, delayed growth, cancer IGF1R 3480 Insulin-like growth factor I resistance IGF2 3481 Russell-Silver syndrome IGF2BP2 10644 Type 2 diabetes, insulin resistance susceptibility IGFBP3 3486 growth delay IGHMBP2 3508 progressive multifocal leukoencephalopathy, and spinal muscular atrophy with respiratory distress 1 IL6 3569 infectious disease, vaccination, and cancer INS 3630 Diabetes or related disorders thereof, an insulin resistant non diabetic state, obesity, impaired glucose tolerance (IGT), Metabolic Syndrome, MODY syndrome, Polycystic Ovary Syndrome, cancer, inflammation, hirsuitism, and hypertension. IQGAP1 8826 Cancer, obesity, diabetes, multiple sclerosis, neoplastic transformation, inflammation, Nonsmall cell lung carcinoma (NSCLCs), hypercholesterolemia, liposarcoma, gastric cancer, immunodeficiency, glomerulonephritis, venous thrombosis, glioma IQGAP2 10788 Obesity, diabetes, multiple sclerosis, neoplastic transformation, inflammation, Nonsmall cell lung carcinoma (NSCLCs), hypercholesterolemia, liposarcoma, gastric cancer, immunodeficiency, glomerulonephritis, venous thrombosis, glioma IRF6 3664 van der Woude syndrome IRS2 8660 Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, insulin resistance, diabetes, Polycystic Ovary Syndrome, atherosclerosis, cancer ITGA7 3679 muscular dystrophy, congenital, due to itga7 deficiency, and congenital muscular dystrophy due to integrin alpha-7 deficiency JAG1 182 Alagille syndrome KCNJ11 3767 Congenital hyperinsulinism, hyperinsulinemic hypoglycemia, 2 KCNMA1 3778 vascular disease, kidney disease, Obesity, Type 2 Diabetes, inflammatory disease, autoimmune disease, and cancer, e.g. kidney, lung, or ovarian cancer KCNMB1 3779 vascular disease, kidney disease, Obesity, Type 2 Diabetes, inflammatory disease, autoimmune disease, and cancer, e.g. kidney, lung, or ovarian cancer KCNMB2 10242 vascular disease, kidney disease, Obesity, Type 2 Diabetes, inflammatory disease, autoimmune disease, and cancer, e.g. kidney, lung, or ovarian cancer KCNMB3 27094 vascular disease, kidney disease, Obesity, Type 2 Diabetes, inflammatory disease, autoimmune disease, and cancer, e.g. kidney, lung, or ovarian cancer KCNQ3 3786 kcnq3-related benign familial neonatal epilepsy, and seizures, benign neonatal, type 2 KLF4 9314 thallasemia, sickle cell disease, and anemia KMT2D 8085 Kabuki Syndrome LDLR 3949 dyslipidemias, atherosclerosis, and hypercholesterolemia, cardiovascular disease LRP1 4035 Cancer, melanoma LRP5, 4041, exudative vitreoretinopathy 4, and hyperostosis, endosteal LRP8 7804 Cancer, melanoma LRPPRC 10128 Leigh syndrome Frencn-Canadian type, Cytochrome c oxidase deficiency MBTPS1 8720 Colitis, obesity, diabetes, hypercholesterolemia, dyslipidemia, Crimean- Congo hemorrhagic fever, chondrodysplasia MECP2 4204 Rett Syndrome, MECP2-related severe neonatal encephalopathy, Angelman syndrome, and PPM-X syndrome MSRA 4482 cancer, macular degeneration, eye aging, cataract MSX2 4488 tooth agenesis (dentin dysplasia), developmental disorders e.g. Craniosynostosis and Parietal foramina MTR 4548 Homocystinuria MUTYH 4595 Familial adenomatous polyposis MYCN 4613 Feingold syndrome MYF6 4618 Centronuclear Myopathy 3 NAMPT 10135 cancer, cytopenia of the myeloid or lymphoid lineage, neutropenia, leukaemia, acute myeloid leukaemia (AML), atherosclerosis, inflammatory bowel disease, Crohn's disease, ulcerative colitis, psoriasis, arthritis, chronic ulcer, ischemic stroke, myocardial infarction, angina and vascular dementia, inflammation, nonalcoholic fatty liver disease NANOG 79923 diabetes, osteoarthritis, rheumatoid arthritis, cancer, Duchenne muscular dystrophy, Parkinson's, Alzheimer's, Gaucher disease, type I diabetes, spinal cord injury, burns (tissue regeneration) NEU4 129807 cancer, diabetes, Tay Sachs disease, inflammatory bowel disease, Crohn's disease, ulcerative colitis, psoriasis, arthritis, inflammation, insulin resistance syndrome, hyperlipidemia, fatty liver disease, cachexia, obesity, atherosclerosis, artcriosccrlosis, elevated blood pressure, viral infection NF1 4763 neurofibromatosis and cancer, e.g., neurofibrosarcoma, malignant peripheral nerve sheath tumors, and myelomonocytic leukemia NKX2-3, -5, 159296, cancer, e.g., lung cancer -8 1482, 26257 NOD2 64127 Crohn disease NR5A1 2516 nr5a1-related 46,xy dsd and 46,xy cgd, and adrenocortical insufficiency, without ovarian defect NRF1 4899 Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, insulin resistance, diabetes, hepatic tumor, non-small cell bronchopulmonary cancer, mitochondrial disease NSD1 64324 Sotos syndrome (cerebral gigantism)autosomal dominant disorder. The cause is haploinsufficiency of the NSD1 gene PAH 5053 Phenylketonuria (PKU) PARK2 5071 Parkinson's PKD1 5310 Polycystic kidney disease PLAT 5327 ischemic stroke PON1, 2 5444, diabetes, obesity, hypercholesterolemia, high blood pressure, atherosclerosis, 5445 coronary heart disease, autism/autism spectrum disorder, epilepsy, cancer, inflammation, stroke, trauma, a renal disease, rheumatoid arthritis, Fish-Eye disease, purpura, Polycystic Ovary Syndrome, hyperthyroidism, a hepatic diseases, vascular dementia, an infectious disease PPARD 5467 Metabolic disease PRKAR1A 5573 Carney complex PRPF31 26121 adRP PTEN 5728 cancer PYCR1 5831 cystic fibrosis, myocardial fibrosis, myelofibrosis, hepatic fibrosis, interstitial lung fibrosis, neoplastic fibrosis, pancreatic fibrosis, pulmonary fibrosis, subepidermal fibrosis, panmural fibrosis of the bladder, proliferative fibrosis, replacement fibrosis, retroperitoneal fibrosis and root sleeve fibrosis, osteogenesis imperfecta, Ehlers-Danlos syndrome, chondrodysplasias, Marfan syndrome, Alport syndrome, familial aortic aneurysm, achondroplasia, mucopolysaccharidoses, osteoporosis, osteopetrosis, Paget's disease, rickets, osteomalacia, hyperparathyroidism, renal osteodystrophy, osteonecrosis, osteomyelitis, osteoma, osteoid osteoma, osteoblastoma, osteosarcoma, osteochondroma, chondroma, chondroblastoma, chondromyxoid fibroma, chondrosarcoma, fibrous cortical defect, nonossifying fibroma, fibrous dysplasia, fibrosarcoma, malignant fibrous histiocytoma, Ewing's sarcoma RB1, RBL1, 5925, cancer, e.g. bladder cancer, osteosarcoma, retinoblastoma, small cell lung RBL2 5933, cancer 5934 RBBP4 5928 intermediate charcot-marie-tooth neuropathy, retinoblastoma, Alzheimer's RNASEH1 246243 leishmaniasis, a disease or disorder associated with mitochondrial dysfunction, cancer, Aicardi-Goutieres syndrome, AIDS ROR2 4920 brachydactyly, type b1, and brachydactyly type b RPS14 6208 5q syndrome (myelodysplastic syndrome) RPS19 6223 Diamond-Blackfan Anemia SCN1A 6323 convulsion, pain, paralysis, hyperkalemic periodic paralysis, paramyotonia congenita, potassium-aggravated myotonia, long Q-T syndrome 3, motor endplate disease, ataxia, colitis, ileitis, inflammatory bowel syndrome, hypertension, congestive heart failure, benign prostrate hyperplasia, impotence, muscular dystrophy, multiple sclerosis, epilepsy, autism, migraine, severe myoclonic epilepsy of infancy (SMEI or Dravet's syndrome) SCN2A 6326 epileptic encephalopathy, early infantile, 11, and benign familial neonatal- infantile seizures SERPINF1 5176 cancer, choroidal neovascularization, cardiovascular disease, diabetes, and osteogenesis imperfecta SERPING1 710 Hereditary Angioedema SHBG 6462 disorders of mood and affect, a memory dysfunction disease or disorder, an amnestic disease or disorder, a motor and tic disorder, substance abuse disease or disorder, a psychotic disease or disorder, an anxiety disease or disorder, schizophrenia, schizofreniform disorder, schizoaffective disorder, and delusional disorder, panic disorder, phobias, an obsessive-compulsive disorder, posttraumatic stress disorder, infertility, hirsutism, Tourette's disorder, Asperger syndrome, hypothyroidism, fibromyalgia, chronic fatigue syndrome, hypothalamic-pituitary axis dysregulation, chronic sleep deprivation, alopecia, prostate cancer, breast cancer, polycystic ovary syndrome, osteoporosis, hyperinsulinemia, glucose intolerance, insulin resistance, diabetes SIRT1 23411 cancer, Alzheimer's Disease (AD), Huntington's disease, Parkinson's disease, Amyotrophic Lateral Sclerosis (ALS), Multiple Sclerosis, Duchene muscular dystrophy, skeletal muscle atrophy, Becker's dystrophy, myotonic dystrophy, insulin resistance, diabetes, obesity, Hypercholesterolemia, dyslipidemia hyperlipidemia, sensory neuropathy, autonomic neuropathy, motor neuropathy, retinopathy, hepatitis, fatty liver disease, age-related macular degeneration, osteoporosis, leukemia, bone resorption, dementia, Bell's Palsy, atherosclerosis, cardiac dysrhymias, chronic congestive heart failure, ischemic stroke, coronary artery disease, cardiac muscle disease, chronic renal failure, ulceration, cataract, presbiopia, glomerulonephritis, Guillan- Barre syndrome, hemorrhagic stroke, rheumatoid arthritis, inflammatory bowel disease, SLE, Crohn's disease, osteoarthritis, Chronic Obstructive Pulmonary Disease (COPD), pneumonia, urinary incontinence, mitochondrial myopathy, encephalopathy, Leber's disease, Leigh encephalopathia, Pearson's disease, lactic acidosis, mitochondrial encephalopathy, lactic acidosis and stroke like symptoms (MELAS), inflammation SLC1A2 6506 ALS SMAD7 4092 Acute kidney injury (anti-TGFb), colorectal cancer SMCHD1 23347 FSHD SMN1, 6606, Spinal muscular atrophy SMN2 6607 5NX27 81609 Downs' Syndrome SPINK1 6690 Pancreatits SRB1 949 Cardiovascular disease SRY 6736 Gonadal dysgenesis ST7, ST7L 7982, cancer, e.g. myeloid cancer, head and neck squamous cell carcinomas, breast 54879 cancer, colon carcinoma, and prostate cancer STAT3 6774 tissue regeneration and Hyper-IgE recurrent infection syndrome TFE3 7030 diabetes, obesity, impaired glucose tolerance (IGT) and Metabolic Syndrome, Polycystic Ovary Syndrome, atherosclerosis, cancer, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, diabetic retinopathy, diabetic neuropathy, diabetic amyotrophy, diabetic nephropathy, diabetic cardiomyopathy, angina, myocardial infarction, stroke, a peripheral vascular disease TFEB 7942 Lysosomal storage diseases TGFB3 7043 Rienhoff syndrome THPO 7066 Myelosuppressive chemo, Bleeding disorders TP63 8626 cancer, tumor, Corneal dystrophy, premature menopause, alopecia, cctrodaclyly-ectodermal dysplasia-cleft syndrome, Hay-Wells syndrome, limb mammary syndrome, acro-dermato-ungual-lacrimal-tooth syndrome, nonsyndromic split-hand/foot malformation, isolated cleft lip/palate, Rapp- Hodgkin syndrome TP73 7161 Cancer UCP2 7351 cancer, obesity, cachexia, anorexia nervosa, bulimia nery osa, diabetes, hyperinsulincmia, glucose intolerance, atherosclerosis, inflammation USP9Y/SP3 8287 Y chromosome infertility UTRN 7402 muscular dystrophies, Duchenne muscular dystrophy (DMD), Becker Muscular Dystrophy (BMD), and myotonic dystrophy VEGFA 7422 diabetes, coronary artery disease, congestive heart failure, and peripheral vascular disease, cancer, infectious diseases, rheumatoid arthritis, DiGeorge syndrome, HHT, cavernous hemangioma, atherosclerosis, transplant ateriopathy, obesity, psoriasis, warts, allergic dermatitis, scar keloids, pyogenic granulomas, blistering disease, Kaposi sarcoma, persistent hyperplastic vitreous syndrome, Autosomal dominant polycystic kidney disease (ADPKD), diabetic retinopathy, retinopathy of prematurity, macular degeneration, choroidal neovascularization, primary pulmonary hypertension, asthma, nasal polyps, inflammatory bowel disease, Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, periodontal disease, ascites, peritoneal adhesions, endometriosis, uterine bleeding, ovarian cysts, ovarian hyperstimulation, arthritis, synovitis, osteomyelitis, and/or osteophyte formation, ulceration, verruca vulgaris, angiofibroma of tuberous sclerosis, pot-wine stains, Sturge Weber syndrome, Kippel-Trenaunay-Weber syndrome, Osler-Weber-Rendu syndrome

TABLE-US-00002 TABLE 2 Genes with mutations or SNPs that create uORFs and associated diseases NCBI Gene Gene ID Associated disease(s) ATP7B 540 wilson disease, and menkes disease. ATRX 546 alpha-thalassemia myelodysplasia syndrome, somatic, and mental retardation-hypotonic facies syndrome, x-linked. BLM 641 bloom syndrome, and rothmund-thomson syndrome. BRCA1 672 primary peritoneal carcinoma, and hereditary site-specific ovarian cancer syndrome. CA2 760 autoimmune retinopathy, and multifocal fibrosclerosis. CCBE1 147372 hennekam syndrome, and immune hydrops fetalis. CD3D 915 severe combined immune deficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive, cd3d-related, and immunodeficiency 19. CD4 920 okt4 epitope deficiency, and lymphatic system disease. CDKN2A 1029 Melanoma predisposition, Melanoma CFL2 1073 cfl2-related nemaline myopathy, and nemaline myopathy 7, autosomal recessive. CFTR 1080 Cystic fibrosis, Disseminated bronchiectasis CSPP1 79848 joubert syndrome 21, and joubert syndrome with jeune asphyxiating thoracic dystrophy. CTNS 1497 intermediate cystinosis, and cystinosis, atypical nephropathic DBT 1629 maple syrup urine disease type 2, and maple syrup urine disease type 1a DCAF17 80067 sakati syndrome, and hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome DCLRE1C 64421 severe combined immunodeficiency, athabascan type, and artemis deficiency. DFNB31 25861 deafness, autosomal recessive 31, and dfnb31 nonsyndromic hearing loss and deafness. DLG4 1742 schizophrenia. DMD 1756 duchenne muscular dystrophy, and becker muscular dystrophy. DNASE1 1773 cystic fibrosis, acute bronchitis ETHE1 23474 ethylmalonic encephalopathy GALNS 2588 mucopolysaccharidosis iv, and kniest dysplasia GCH1 2643 Levodopa responsive dystonia HAMP 57817 Juvenile hemochromatosis, thalassemia HBB 3043 Beta-Thalassemia HMBS 3145 histrionic personality disorder, and acute porphyria. HR 55806 atrichia with papular lesions, and hypotrichosis 4 IGHMBP2 3508 progressive multifocal leukoencephalopathy, and spinal muscular atrophy with respiratory distress 1 IRF6 3664 Van der Woude syndrome ITGA7 3679 muscular dystrophy, congenital, due to itga7 deficiency, and congenital muscular dystrophy due to integrin alpha-7 deficiency ITGB2 3689 leukocyte adhesion deficiency type 1, and leukocyte adhesion deficiency. KCNJ11 3767 Congenital hyperinsulinism, hyperinsulinemic hypoglycemia, 2 KCNQ3 3786 kcnq3-related benign familial neonatal epilepsy, and seizures, benign neonatal, type 2 LDLR 3949 Cardiovascular disease, Familial hypercholesterolemia LRP5, 4041, exudative vitreoretinopathy 4, and hyperostosis, endosteal LRP5L 91355 MECP2 4204 autism susceptibility, x-linked 3, and bruxism. MLH1 4292 mlh1-related lynch syndrome, and solitary rectal ulcer syndrome. MSH6 2956 msh6-related lynch syndrome, colorectal cancer, hereditary nonpolyposis, type 5 MUTYH 4595 adenomas, multiple colorectal, stomach cancer. NR5A1 2516 nr5a1-related 46,xy dsd and 46,xy cgd, and adrenocortical insufficiency, without ovarian defect PALB2 79728 fanconi anemia, complementation group n, and pancreatic cancer susceptibility 3. PANK2 80025 classic pantothenate kinase-associated neurodegeneration, and harp syndrome. PEX7 5191 peroxisome biogenesis disorder 9b, and rhizomelic chondrodysplasia punctata. PHYH 5264 phyh-related refsum disease, and refsum disease. PIK3R5 23533 ataxia-oculomotor apraxia 3, and spinocerebellar ataxia autosomal recessive 1 POMC 5443 Proopiomelanocortin deficiency POMT1 10585 pomt1-related muscle diseases, and walker-warburg syndrome. ROR2 4920 brachydactyly, type b1, and brachydactyly type b SCN2A 6326 epileptic encephalopathy, early infantile, 11, and benign familial neonatal- infantile seizures SGCA 6442 sarcoglycanopathies, and limb-girdle muscular dystrophy, type 2d. SGCD 6444 limb-girdle muscular dystrophy type 2f, and delta-sarcoglycanopathy. SLC16A1 6566 erythrocyte lactate transporter defect, and exercise-induced hyperinsulinemic hypoglycemia. SLC19A3 80704 basal ganglia disease, and biotin-responsive basal ganglia disease. SLC2A2 6514 fanconi bickel syndrome, fanconi syndrome SLC7A9 11136 stinuria, and aminoaciduria. SPINK1 6690 Hereditary pancreatitis SRY 6736 Gonadal dysgenesis STIL 6491 primary autosomal recessive microcephaly type 7, and ideomotor apraxia. TK2 7084 mitochondrial dna depletion syndrome, myopathic form, and tk2-related mitochondrial dna depletion syndrome, myopathic form. TMPRSS3 64699 deafness, autosomal recessive 8/10, and dfnb 8/10 nonsyndromic hearing loss and deafness. TP53 7157 hepatocellular carcinoma, and osteosarcoma TPI1 7167 hemolytic anemia due to triosephosphate isomerase deficiency, and triose phosphate-isomerase deficiency. TPM3 7170 nemaline myopathy, and nemaline myopathy 1 TRMU 55687 liver failure acute infantile, and melas, mt-th-related. TSEN54 283989 tsen54-related pontocerebellar hypoplasia, and pontocerebellar hypoplasia type 4. ZEB1 6935 corneal dystrophy, posterior polymorphous, 3, and corneal dystrophy, fuchs endothelial, 6.

[0984] In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the CDKN2A transcript and thereby increases expression of CDKN2A. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the CFTR transcript and thereby increases expression of CFTR. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the FXII transcript and thereby increases expression of FXII. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the GCH1 transcript and thereby increases expression of GCH1. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the HAMP transcript and thereby increases expression of HAMP.

[0985] In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the HBB transcript and thereby increases expression of HBB. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the IRF6 transcript and thereby increases expression of IRF6. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the KCNJ11 transcript and thereby increases expression of KCNJ11. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the LDLR transcript and thereby increases expression of LDLR. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the PEX7 transcript and thereby increases expression of PEX7.

[0986] In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the POMC transcript and thereby increases expression of POMC. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the PRKAR1A transcript and thereby increases expression of PRKAR1A. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the SPINK1 transcript and thereby increases expression of SPINK1. In certain embodiments, a uORF inhibitor (e.g. an antisense compound), inhibits ribosomal recognition or uORF activity of a uORF start site on the SRY transcript and thereby increases expression of SRY.

[0987] In certain embodiments, a TSE inhibitor (e.g. an antisense compound) may be used to upregulate a expression of ATM, lipoprotein lipase (LPL), DMD, sphingomyelinase, Factor VIII, insulin, growth hormone, thyroid stimulating hormone, follicle stimulating hormone, or hepcidin.

D. Certain Pharmaceutical Compositions

[0988] In certain embodiments, the present invention provides pharmaceutical compositions comprising one or more antisense compound. In certain embodiments, such pharmaceutical composition comprises a suitable pharmaceutically acceptable diluent or carrier. In certain embodiments, a pharmaceutical composition comprises a sterile saline solution and one or more antisense compound. In certain embodiments, such pharmaceutical composition consists of a sterile saline solution and one or more antisense compound. In certain embodiments, the sterile saline is pharmaceutical grade saline. In certain embodiments, a pharmaceutical composition comprises one or more antisense compound and sterile water. In certain embodiments, a pharmaceutical composition consists of one or more antisense compound and sterile water. In certain embodiments, the sterile saline is pharmaceutical grade water. In certain embodiments, a pharmaceutical composition comprises one or more antisense compound and phosphate-buffered saline (PBS). In certain embodiments, a pharmaceutical composition consists of one or more antisense compound and sterile phosphate-buffered saline (PBS). In certain embodiments, the sterile saline is pharmaceutical grade PBS.

[0989] In certain embodiments, antisense compounds may be admixed with pharmaceutically acceptable active and/or inert substances for the preparation of pharmaceutical compositions or formulations. Compositions and methods for the formulation of pharmaceutical compositions depend on a number of criteria, including, but not limited to, route of administration, extent of disease, or dose to be administered.

[0990] Pharmaceutical compositions comprising antisense compounds encompass any pharmaceutically acceptable salts, esters, or salts of such esters. In certain embodiments, pharmaceutical compositions comprising antisense compounds comprise one or more oligonucleotide which, upon administration to an animal, including a human, is capable of providing (directly or indirectly) the biologically active metabolite or residue thereof. Accordingly, for example, the disclosure is also drawn to pharmaceutically acceptable salts of antisense compounds, prodrugs, pharmaceutically acceptable salts of such prodrugs, and other bioequivalents. Suitable pharmaceutically acceptable salts include, but are not limited to, sodium and potassium salts.

[0991] A prodrug can include the incorporation of additional nucleosides at one or both ends of an oligomeric compound which are cleaved by endogenous nucleases within the body, to form the active compound.

[0992] Lipid moieties have been used in nucleic acid therapies in a variety of methods. In certain such methods, the nucleic acid is introduced into preformed liposomes or lipoplexes made of mixtures of cationic lipids and neutral lipids. In certain methods, DNA complexes with mono- or poly-cationic lipids are formed without the presence of a neutral lipid. In certain embodiments, a lipid moiety is selected to increase distribution of a pharmaceutical agent to a particular cell or tissue. In certain embodiments, a lipid moiety is selected to increase distribution of a pharmaceutical agent to fat tissue. In certain embodiments, a lipid moiety is selected to increase distribution of a pharmaceutical agent to muscle tissue.

[0993] In certain embodiments, pharmaceutical compositions provided herein comprise one or more modified oligonucleotides and one or more excipients. In certain such embodiments, excipients are selected from water, salt solutions, alcohol, polyethylene glycols, gelatin, lactose, amylase, magnesium stearate, talc, silicic acid, viscous paraffin, hydroxymethylcellulose and polyvinylpyrrolidone.

[0994] In certain embodiments, a pharmaceutical composition provided herein comprises a delivery system. Examples of delivery systems include, but are not limited to, liposomes and emulsions. Certain delivery systems are useful for preparing certain pharmaceutical compositions including those comprising hydrophobic compounds. In certain embodiments, certain organic solvents such as dimethylsulfoxide are used.

[0995] In certain embodiments, a pharmaceutical composition provided herein comprises one or more tissue-specific delivery molecules designed to deliver the one or more pharmaceutical agents of the present invention to specific tissues or cell types. For example, in certain embodiments, pharmaceutical compositions include liposomes coated with a tissue-specific antibody.

[0996] In certain embodiments, a pharmaceutical composition provided herein comprises a co-solvent system. Certain of such co-solvent systems comprise, for example, benzyl alcohol, a nonpolar surfactant, a water-miscible organic polymer, and an aqueous phase. In certain embodiments, such co-solvent systems are used for hydrophobic compounds. A non-limiting example of such a co-solvent system is the VPD co-solvent system, which is a solution of absolute ethanol comprising 3% w/v benzyl alcohol, 8% w/v of the nonpolar surfactant Polysorbate 80™ and 65% w/v polyethylene glycol 300. The proportions of such co-solvent systems may be varied considerably without significantly altering their solubility and toxicity characteristics. Furthermore, the identity of co-solvent components may be varied: for example, other surfactants may be used instead of Polysorbate 80™; the fraction size of polyethylene glycol may be varied; other biocompatible polymers may replace polyethylene glycol, e.g., polyvinyl pyrrolidone; and other sugars or polysaccharides may substitute for dextrose.

[0997] In certain embodiments, a pharmaceutical composition provided herein is prepared for oral administration. In certain embodiments, pharmaceutical compositions are prepared for buccal administration.

[0998] In certain embodiments, a pharmaceutical composition is prepared for administration by injection (e.g., intravenous, subcutaneous, intramuscular, etc.). In certain of such embodiments, a pharmaceutical composition comprises a carrier and is formulated in aqueous solution, such as water or physiologically compatible buffers such as Hanks's solution, Ringer's solution, or physiological saline buffer. In certain embodiments, other ingredients are included (e.g., ingredients that aid in solubility or serve as preservatives). In certain embodiments, injectable suspensions are prepared using appropriate liquid carriers, suspending agents and the like. Certain pharmaceutical compositions for injection are presented in unit dosage form, e.g., in ampoules or in multi-dose containers. Certain pharmaceutical compositions for injection are suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents. Certain solvents suitable for use in pharmaceutical compositions for injection include, but are not limited to, lipophilic solvents and fatty oils, such as sesame oil, synthetic fatty acid esters, such as ethyl oleate or triglycerides, and liposomes. Aqueous injection suspensions may contain.

E. Administration

[0999] In certain embodiments, the compounds and compositions as described herein are administered parenterally.

[1000] In certain embodiments, parenteral administration is by infusion. Infusion can be chronic or continuous or short or intermittent. In certain embodiments, infused pharmaceutical agents are delivered with a pump. In certain embodiments, parenteral administration is by injection.

[1001] In certain embodiments, compounds and compositions are delivered to the CNS. In certain embodiments, compounds and compositions are delivered to the cerebrospinal fluid. In certain embodiments, compounds and compositions are administered to the brain parenchyma. In certain embodiments, compounds and compositions are delivered to an animal by intrathecal administration, or intracerebroventricular administration. Broad distribution of compounds and compositions, described herein, within the central nervous system may be achieved with intraparenchymal administration, intrathecal administration, or intracerebroventricular administration.

[1002] In certain embodiments, parenteral administration is by injection. The injection may be delivered with a syringe or a pump. In certain embodiments, the injection is a bolus injection. In certain embodiments, the injection is administered directly to a tissue, such as striatum, caudate, cortex, hippocampus and cerebellum.

[1003] Therefore, in certain embodiments, delivery of a compound or composition described herein can affect the pharmacokinetic profile of the compound or composition. In certain embodiments, injection of a compound or composition described herein, to a targeted tissue improves the pharmacokinetic profile of the compound or composition as compared to infusion of the compound or composition. In a certain embodiment, the injection of a compound or composition improves potency compared to broad diffusion, requiring less of the compound or composition to achieve similar pharmacology. In certain embodiments, similar pharmacology refers to the amount of time that a target mRNA and/or target protein is down-regulated (e.g. duration of action). In certain embodiments, methods of specifically localizing a pharmaceutical agent, such as by bolus injection, decreases median effective concentration (EC50) by a factor of about 50 (e.g. 50 fold less concentration in tissue is required to achieve the same or similar pharmacodynamic effect). In certain embodiments, methods of specifically localizing a pharmaceutical agent, such as by bolus injection, decreases median effective concentration (EC50) by a factor of 20, 25, 30, 35, 40, 45 or 50. In certain embodiments the pharmaceutical agent in an antisense compound as further described herein. In certain embodiments, the targeted tissue is brain tissue. In certain embodiments the targeted tissue is striatal tissue. In certain embodiments, decreasing EC50 is desirable because it reduces the dose required to achieve a pharmacological result in a patient in need thereof.

[1004] In certain embodiments, an antisense compound is delivered by injection or infusion once every month, every two months, every 90 days, every 3 months, every 6 months, twice a year or once a year.

F. Certain Combination Therapies

[1005] In certain embodiments, one or more pharmaceutical compositions are co-administered with one or more other pharmaceutical agents. In certain embodiments, such one or more other pharmaceutical agents are designed to treat the same disease, disorder, or condition as the one or more pharmaceutical compositions described herein. In certain embodiments, such one or more other pharmaceutical agents are designed to treat a different disease, disorder, or condition as the one or more pharmaceutical compositions described herein. In certain embodiments, such one or more other pharmaceutical agents are designed to treat an undesired side effect of one or more pharmaceutical compositions as described herein. In certain embodiments, one or more pharmaceutical compositions are co-administered with another pharmaceutical agent to treat an undesired effect of that other pharmaceutical agent. In certain embodiments, one or more pharmaceutical compositions are co-administered with another pharmaceutical agent to produce a combinational effect. In certain embodiments, one or more pharmaceutical compositions are co-administered with another pharmaceutical agent to produce a synergistic effect.

[1006] In certain embodiments, one or more pharmaceutical compositions and one or more other pharmaceutical agents are administered at the same time. In certain embodiments, one or more pharmaceutical compositions and one or more other pharmaceutical agents are administered at different times. In certain embodiments, one or more pharmaceutical compositions and one or more other pharmaceutical agents are prepared together in a single formulation. In certain embodiments, one or more pharmaceutical compositions and one or more other pharmaceutical agents are prepared separately.

[1007] In certain embodiments, pharmaceutical agents that may be co-administered with a pharmaceutical composition of include antipsychotic agents, such as, e.g., haloperidol, chlorpromazine, clozapine, quetapine, and olanzapine; antidepressant agents, such as, e.g., fluoxetine, sertraline hydrochloride, venlafaxine and nortriptyline; tranquilizing agents such as, e.g., benzodiazepines, clonazepam, paroxetine, venlafaxin, and beta-blockers; mood-stabilizing agents such as, e.g., lithium, valproate, lamotrigine, and carbamazepine; paralytic agents such as, e.g., Botulinum toxin; and/or other experimental agents including, but not limited to, tetrabenazine (Xenazine), creatine, conezyme Q10, trehalose, docosahexanoic acids, ACR16, ethyl-EPA, atomoxetine, citalopram, dimebon, memantine, sodium phenylbutyrate, ramelteon, ursodiol, zyprexa, xenasine, tiapride, riluzole, amantadine, [123I]MNI-420, atomoxetine, tetrabenazine, digoxin, detromethorphan, warfarin, alprozam, ketoconazole, omeprazole, and minocycline.

[1008] In certain embodiments, the present invention may be used to increase expression of a protein, which sensitizes the cell to other treatment. For example, in certain embodiments, the invention may be used to increase expression of RNase H. Cells with increased RNase H may be more sensitive to subsequent treatment with RNase H-dependent antisense compounds.

NONLIMITING DISCLOSURE AND INCORPORATION BY REFERENCE

[1009] While certain compounds, compositions and methods described herein have been described with specificity in accordance with certain embodiments, the following examples serve only to illustrate the compounds described herein and are not intended to limit the same. Each of the references, GenBank accession numbers, and the like recited in the present application is incorporated herein by reference in its entirety.

[1010] Although the sequence listing accompanying this filing identifies each sequence as either “RNA” or “DNA” as required, in reality, those sequences may be modified with any combination of chemical modifications. One of skill in the art will readily appreciate that such designation as “RNA” or “DNA” to describe modified oligonucleotides is, in certain instances, arbitrary. For example, an oligonucleotide comprising a nucleoside comprising a 2′-OH sugar moiety and a thymine base could be described as a DNA having a modified sugar (2′-OH for the natural 2′-H of DNA) or as an RNA having a modified base (thymine (methylated uracil) for natural uracil of RNA).

[1011] Accordingly, nucleic acid sequences provided herein, including, but not limited to those in the sequence listing, are intended to encompass nucleic acids containing any combination of natural or modified RNA and/or DNA, including, but not limited to such nucleic acids having modified nucleobases. By way of further example and without limitation, an oligomeric compound having the nucleobase sequence “ATCGATCG” encompasses any oligomeric compounds having such nucleobase sequence, whether modified or unmodified, including, but not limited to, such compounds comprising RNA bases, such as those having sequence “AUCGAUCG” and those having some DNA bases and some RNA bases such as “AUCGATCG” and oligomeric compounds having other modified or naturally occurring bases, such as “AT.sup.mCGAUCG,” wherein .sup.mC indicates a cytosine base comprising a methyl group at the 5-position.

EXAMPLES

[1012] The following examples illustrate certain embodiments of the present invention and are not limiting. Moreover, where specific embodiments are provided, the inventors have contemplated generic application of those specific embodiments. For example, disclosure of an oligonucleotide having a particular motif provides reasonable support for additional oligonucleotides having the same or similar motif And, for example, where a particular high-affinity modification appears at a particular position, other high-affinity modifications at the same position are considered suitable, unless otherwise indicated.

Example 1: Effects of Antisense Oligonucleotides Targeting the uORF of RNase H1 on RNase H1 Protein Expression

[1013] Human RNase H1 mRNA (GENBANK accession number NM_001286834.1, designated herein as SEQ ID NO: 1) comprises an upstream open reading frame (uORF). Antisense oligonucleotides designed to target the start codon of the uORF of human RNase H1 were tested for their effects on RNase H1 expression in vitro. These antisense oligonucleotides, described in Table 3, were uniformly modified in order to avoid inducing cleavage of the target RNA. The start and stop sites listed in Table 3 indicate the positions on SEQ ID NO: 1 that the antisense oligonucleotides target. The targeted uORF begins at position 86. HeLa cells were transfected with Lipofectamine RNAiMAX (Life Technologies) and one of the antisense oligonucleotides at a final concentration of 25 nM or were mock transfected as a control. Thirty hours after transfection, the cells were lysed, and expression of RNase H1 was analyzed by western blot and RT-PCR. The primary antibody used for the western blot was made as described in Wu et al. Determination of the Role of the Human RNase H1 in the Pharmacology of DNA-like Antisense Drugs. J. Biol. Chem. 279, 17181 (2004), and the secondary antibody was purchased from Biorad (catalog #170-6515). The western blot was quantified using Image J, and the results are shown in Table 3 as percent protein levels relative to mock transfected cells following normalization to the Annexin A2 loading control. The RT-PCR results are shown in Table 3 as percent mRNA levels relative to mock transfected cells following normalization to Ribogreen. The results show that antisense oligonucleotides targeting a portion of the RNase H1 uORF that includes the uORF start codon increased RNase H1 expression. Furthermore, certain antisense oligonucleotides did not significantly affect RNase H1 mRNA levels, indicating that the increased RNase H1 expression exhibited by those oligonucleotides occurred mainly via increased translation.

TABLE-US-00003 TABLE 3 RNase H1 expression Start Stop RNase H1 protein RNase H1 mRNA SEQ ID Isis No. Sequence Site Site (% mock) (% mock) NO. 761909 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.mo 73 88 166 106 3 U.sub.moC.sub.moC.sub.moC.sub.moG.sub.moG.sub.moC.sub.m 761910 A.sub.moG.sub.moC.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.mo 75 90 146 113 4 A.sub.moC.sub.moU.sub.moC.sub.moC.sub.moC.sub.moG.sub.m 761911 G.sub.moA.sub.moA.sub.moG.sub.moC.sub.moA.sub.moU.sub.moU.sub.moU.sub.mo 77 92 139 114 5 C.sub.moG.sub.moA.sub.moC.sub.moU.sub.moC.sub.moC.sub.m 761912 G.sub.moG.sub.moG.sub.moA.sub.moA.sub.moG.sub.moC.sub.moA.sub.moU.sub.mo 79 94 106 109 6 U.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.m 761913 C.sub.moC.sub.moG.sub.moG.sub.moG.sub.moA.sub.moA.sub.moG.sub.moC.sub.mo 81 96 104 113 7 A.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.m Subscripts: “m” indicates a 2′-O-methyl modification, and “o” indicates a phosphodiester internucleoside linkage.

Example 2: Time Course of RNase H1 Protein Expression Following Treatment with an Antisense Oligonucleotide Targeting the uORF In Vitro

[1014] HeLa cells were transfected with 25 nM Isis No. 761909 (see Table 3). At various time points following transfection, the cells were harvested and RNase H1 expression was analyzed by western blot as described in Example 1. The results are shown in Table 4 as the percent RNase H1 protein expression relative to cells that did not receive antisense oligonucleotide treatment (harvested at the 0 hour time point) following normalization to the Annexin A2 loading control. The results show that the induction of RNase H1 expression was observed within 4 hours following transfection, and maximal expression was observed at approximately 12 hours following transfection.

TABLE-US-00004 TABLE 4 RNase H1 expression RNase H1 (% 0 h) following transfection with 25 nM 761909 4 h 8 h 12 h 15 h 143 145 214 176

Example 3: Dose Response Effect of an Antisense Oligonucleotide Targeting the uORF of RNase H1 on RNase H1 Protein Expression In Vitro

[1015] Isis No. 761909 (see Table 3) was tested at five different doses for its effect on RNase H1 expression in vitro. HeLa cells were transfected with 761909 at a concentration listed in Table 5 or were not treated as a control. Fifteen hours after transfection, RNase H1 expression was analyzed as described in Example 1. The results are shown in Table 5 as the percent protein levels relative to untreated control cells following normalization to the Annexin A2 loading control and as mRNA levels relative to untreated control cells following normalization to Ribogreen. The results show that an antisense oligonucleotide targeting a portion of the RNase H1 uORF increased RNase H1 protein levels in a dose dependent manner; and mRNA levels did not increase, indicating that the antisense oligonucleotide increased RNase H1 expression via increased translation.

TABLE-US-00005 TABLE 5 RNase H1 expression following transfection with 761909 761909 mRNA concentration (nM) Protein (% untreated cells) (% untreated cells) 10 108 100 15 93 100 20 183 96 25 169 92 30 182 96

Example 4: Effects of Antisense Oligonucleotides Targeting the 5′-Untranslated Region Upstream of the RNase H1 uORF on RNase H1 Protein Expression

[1016] Antisense oligonucleotides designed to target the 5′-untranslated region upstream of the uORF of human RNase H1 were tested for their effects on RNase H1 protein expression in vitro. These antisense oligonucleotides, described in Table 6, were uniformly modified in order to avoid inducing cleavage of the target RNA. The start and stop sites listed in Table 6 indicate the positions on SEQ ID NO: 1 that the antisense oligonucleotides target. Isis 761909 was included for reference. HeLa cells were transfected with 20 nM antisense oligonucleotide or were mock transfected as a control. Fifteen hours after transfection, RNase H1 expression was analyzed as described in Example 1. The results are shown in Table 6 below as percent protein expression relative to mock transfected cells following normalization to the γ-tubulin loading control and percent mRNA levels relative to mock transfected cells following normalization to Ribogreen. The results show that antisense oligonucleotides do not necessarily need to target the start codon of an uORF in order to induce increased translation of the target. Antisense oligonucleotides that target the 5′-untranslated region upstream of an uORF and antisense oligonucleotides that target at least a portion of the uORF itself can induce translation of the target. Furthermore, the antisense oligonucleotides targeting the 5′-untranslated region upstream of the uORF did not increase mRNA levels, indicating that they increased RNase H1 expression via increased translation.

TABLE-US-00006 TABLE 6 RNase H1 expression Start Stop Protein (% mRNA SEQ ID Isis No. Sequence Site Site mock) (% mock) NO. 761918 U.sub.moC.sub.moA.sub.moC.sub.moC.sub.moG.sub.moG.sub.moC.sub.moG.sub.moC.sub.mo 14 29 155 96 8 G.sub.moG.sub.moG.sub.moA.sub.moA.sub.moG.sub.m 761919 C.sub.moU.sub.moC.sub.moA.sub.moA.sub.moC.sub.moA.sub.moC.sub.moC.sub.moG.sub.mo 32 47 214 100 9 C.sub.moA.sub.moC.sub.moU.sub.moU.sub.moC.sub.m 761917 A.sub.moC.sub.moU.sub.moC.sub.moC.sub.moC.sub.moG.sub.moG.sub.moC.sub.moC.sub.mo 66 81 116 98 10 C.sub.moA.sub.moG.sub.moC.sub.moG.sub.moU.sub.m 761916 C.sub.moG.sub.moA.sub.moC.sub.moU.sub.moC.sub.moC.sub.moC.sub.moG.sub.moG.sub.mo 68 83 142 96 11 C.sub.moC.sub.moC.sub.moA.sub.moG.sub.moC.sub.m 761915 U.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.moC.sub.moC.sub.moC.sub.mo 70 85 218 96 12 G.sub.moG.sub.moC.sub.moC.sub.moC.sub.moA.sub.m 761909 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.mo 73 88 151 94 3 C.sub.moC.sub.moC.sub.moG.sub.moG.sub.moC.sub.m Subscripts: “m” indicates a 2′-O-methyl modification, and “o” indicates a phosphodiester internucleoside linkage.

Example 5: Effects of Antisense Oligonucleotides of Varying Lengths on RNase H1 Protein Expression

[1017] Antisense oligonucleotides of varying lengths designed to target at least a portion of the uORF of human RNase H1 were tested for their effects on RNase H1 expression in vitro. These antisense oligonucleotides, described in Table 7, were uniformly modified in order to avoid inducing cleavage of the target RNA. The start and stop sites listed in Table 7 indicate the positions on SEQ ID NO: 1 that the antisense oligonucleotides target. HeLa cells were transfected with 20 nM antisense oligonucleotide or were mock transfected as a control. Fifteen hours after transfection, RNase H1 expression was analyzed as described in Example 1. The results are shown in Table 7 below as the percent protein expression relative to mock transfected cells following normalization to the γ-tubulin loading control and percent mRNA levels relative to mock transfected cells following normalization to Ribogreen. The results show that antisense oligonucleotides of various lengths increased RNase H1 expression mainly via increased translation of the target.

TABLE-US-00007 TABLE 7 RNase H1 expression following transfection with 5′-UTR targeting antisense oligonucleotides mRNA SEQ Start Stop Protein (% (% ID Isis No. Sequence Site Site Length mock) mock) NO. 761928 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.moC.sub.mo 77 88 12 143 104 13 C.sub.m 761927 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.moC.sub.mo 75 88 14 142 101 14 C.sub.moC.sub.moG.sub.m 761909 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.moC.sub.mo 73 88 16 244 94 3 C.sub.moC.sub.moG.sub.moG.sub.moC.sub.m 761926 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.moC.sub.mo 71 88 18 187 110 15 C.sub.moC.sub.moG.sub.moG.sub.moC.sub.moC.sub.moC.sub.m 761925 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.moC.sub.mo 69 88 20 126 100 16 C.sub.moC.sub.moG.sub.moG.sub.moC.sub.moC.sub.moC.sub.moA.sub.moG.sub.m Subscripts: “m” indicates a 2′-O-methyl modification, and “o” indicates a phosphodiester internucleoside linkage.

Example 6: Effects of Antisense Oligonucleotides Targeting the uORF of Mouse LRPPRC on LRPPRC Protein Expression

[1018] Mouse Leucine-Rich PPR-Motif Containing (LRPPRC) mRNA (GENBANK accession number NM_028233.2, designated herein as SEQ ID NO: 2) comprises an upstream open reading frame. Antisense oligonucleotides with various lengths and internucleoside linkages designed to target the start codon of the uORF of mouse LRPPRC were tested for their effects on LRPPRC protein expression in vitro. These antisense oligonucleotides, described in Table 8, were uniformly modified in order to avoid inducing cleavage of the target RNA. The start and stop sites listed in Table 8 indicate the positions on SEQ ID NO: 2 that the antisense oligonucleotides target. The targeted uORF begins at position 70. MHT cells were transfected with Lipofectamine RNAiMAX (Life Technologies) and an antisense oligonucleotide at a concentration listed in Table 8 or were untreated as a control. Fifteen hours after transfection, the cells were lysed, and a western blot was performed with an LRPPRC antibody purchased from Abcam (catalog # ab97505) to analyze expression of LRPPRC. The western blot was quantified using Image J, and the results are shown in Table 8 below as the percent expression relative to untreated control cells following normalization to the loading control (Annexin A2 for 761932 and 761933, and hnRNP K for 759704 and 761930). The results show that antisense oligonucleotides of various lengths targeting the start codon of the uORF of mouse LRPPRC increased LRPPRC expression, including oligonucleotides comprising phosphodiester internucleoside linkages and an oligonucleotide comprising phosphorothioate internucleoside linkages. Thus, the results in Table 8 along with the results in the Examples above show that various antisense oligonucleotides targeting at least a portion of an uORF can increase expression of multiple targets in multiple species.

TABLE-US-00008 TABLE 8 LRPPRC expression Start Stop Concentration LRPPRC SEQ ID Isis No. Sequence Site Site (nM) (% UTC) NO. 761932 C.sub.moA.sub.moU.sub.moU.sub.moG.sub.moU.sub.moU.sub.moU.sub.moU.sub.moU.sub.moU.sub.mo 55 72 10 127 17 G.sub.moU.sub.moC.sub.moU.sub.moU.sub.moC.sub.moC.sub.m 20 184 30 214 40 173 50 178 60 228 761933 C.sub.msA.sub.msU.sub.msU.sub.msG.sub.msU.sub.msU.sub.msU.sub.msU.sub.msU.sub.msU.sub.ms 55 72 10 123 17 G.sub.msU.sub.msC.sub.msU.sub.msU.sub.msC.sub.msC.sub.m 20 141 30 126 40 131 50 105 759704 C.sub.moA.sub.moU.sub.moU.sub.moG.sub.moU.sub.moU.sub.moU.sub.moU.sub.mo 57 72 10 187 18 U.sub.moU.sub.moG.sub.moU.sub.moC.sub.moU.sub.moU.sub.m 20 182 30 189 40 170 50 243 60 203 761930 C.sub.moA.sub.moU.sub.moU.sub.moG.sub.moU.sub.moU.sub.moU.sub.moU.sub.mo 53 72 10 164 19 U.sub.moU.sub.moG.sub.moU.sub.moC.sub.moU.sub.moU.sub.moC.sub.moC.sub.mo 20 149 G.sub.moU.sub.m 30 218 40 142 50 219 60 255 Subscripts: “m” indicates a 2′-O-methyl modification, “o” indicates a phosphodiester internucleoside linkage, and “s” indicates a phosphorothioate internucleoside linkage.

Example 7: Effect of Antisense Oligonucleotide Targeting the uORF of Human SFXN3 on SFXN3 Protein Expression

[1019] Human Sideroflexin 3 (SFXN3) mRNA (GENBANK accession number NM_030971.3, designated herein as SEQ ID NO: 20) comprises an upstream open reading frame. An antisense oligonucleotide designed to target the start codon of the uORF of human SFXN3 was tested for its effect on SFXN3 protein expression in vitro. The antisense oligonucleotide, described in Table 9, was uniformly modified in order to avoid inducing cleavage of the target RNA. The start and stop sites listed in Table 9 indicate the positions on SEQ ID NO: 20 that the antisense oligonucleotide targets. The targeted uORF begins at position 388. HeLa cells were transfected with Lipofectamine RNAiMAX (Life Technologies) and an antisense oligonucleotide at a concentration listed in Table 9 or were untreated as a control. Ten hours after transfection, the cells were lysed, and SFXN3 mRNA and protein expression were analyzed by RT-PCR and western blot, respectively. The western blot was performed with an SFXN3 antibody purchased from Abcam (catalog # ab181163) and quantified using Image J. The results are shown in Table 9 below as the percent protein expression relative to untreated control cells (“UTC”) following normalization to the loading control (Ku70, detected with Abcam antibody, catalog # ab3114). SFXN3 mRNA levels normalized to Ribogreen are also shown. The results show that an antisense oligonucleotide targeting the start codon of the uORF of human SFXN3 increased SFXN3 protein expression. SFXN3 mRNA levels did not increase, indicating that the antisense oligonucleotide increased SFXN3 expression via increased translation.

TABLE-US-00009 TABLE 9 SFXN3 expression Start Stop Concentration Protein mRNA SEQ ID Isis No. Sequence Site Site (nM) (% UTC) (% UTC) NO. 759677 C.sub.moA.sub.moU.sub.moC.sub.moA.sub.moC.sub.moG.sub.mo 375 390 10 100 106 21 C.sub.moG.sub.moG.sub.moG.sub.mo 20 120 102 A.sub.moC.sub.moG.sub.moU.sub.moC.sub.m 30 124 97 40 126 94 60 134 109 80 133 103 100 125 107 Subscripts: “m” indicates a 2′-O-methyl modification, “o” indicates a phosphodiester internucleoside linkage.

Example 8: Effect of Antisense Oligonucleotide Targeting the uORF of Mouse MRPL11 on MRPL11 Protein Expression

[1020] Mouse Mitochondrial Ribosomal protein L11 (MRPL11) mRNA (GENBANK accession number NM_025553.4, designated herein as SEQ ID NO: 22) comprises an upstream open reading frame. An antisense oligonucleotide designed to target the start codon of the uORF of mouse MRPL11 was tested for its effect on MRPL11 protein expression in vitro. The antisense oligonucleotide, described in Table 10, was uniformly modified in order to avoid inducing cleavage of the target RNA. The start and stop sites listed in Table 10 indicate the positions on SEQ ID NO: 22 that the antisense oligonucleotide targets. The targeted uORF begins at position 24. bEND cells were transfected with Lipofectamine RNAiMAX (Life Technologies) and an antisense oligonucleotide at a concentration listed in Table 10 or were untreated as a control. Ten hours after transfection, the cells were lysed, and MRPL11 mRNA and protein expression were analyzed by RT-PCR and western blot, respectively. The western blot was performed with an MRPL11 antibody purchased from Abcam (catalog # ab2066s) and quantified using Image J. The results are shown in Table 10 below as the percent protein expression relative to untreated control cells (“UTC”) following normalization to the loading control (GAPDH, detected with Santa Cruz Biotechnology antibody, catalog # sc-32233). MRPL11 mRNA levels normalized to Ribogreen are also shown. The results show that an antisense oligonucleotide targeting the start codon of the uORF of mouse MRPL11 increased MRPL11 protein expression. MRPL11 mRNA levels did not increase, indicating that the antisense oligonucleotide increased MRPL11 expression via increased translation.

TABLE-US-00010 TABLE 10 MRPL11 expression Start Stop Concentration Protein mRNA SEQ ID Isis No. Sequence Site Site (nM) (% UTC) (% UTC) NO. 773534 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moU.sub.moG.sub.mo 9 26 5 95 93 23 G.sub.moG.sub.moU.sub.moC.sub.mo 10 146 95 A.sub.moG.sub.moA.sub.moG.sub.moG.sub.moU.sub.moG.sub.m 20 137 96 40 134 109 80 125 104 Subscripts: “m” indicates a 2′-O-methyl modification, “o” indicates a phosphodiester internucleoside linkage.

Example 9: Effects of Antisense Oligonucleotides Targeting the uORF of Human THPO on THPO Protein Expression

[1021] Human Thrombopoietin (THPO) mRNA (GENBANK accession number NM_000460.3, designated herein as SEQ ID NO: 24) comprises seven upstream open reading frames. An antisense oligonucleotide designed to target the start codon of the last uORF of human THPO was tested for its effect on THPO protein expression in vitro. The antisense oligonucleotide, described in Table 11, was uniformly modified in order to avoid inducing cleavage of the target RNA. The start and stop sites listed in Table 11 indicate the positions on SEQ ID NO: 24 that the antisense oligonucleotide targets. The targeted uORF begins at position 210. Hep3B cells were transfected with Lipofectamine RNAiMAX (Life Technologies) and an antisense oligonucleotide at a concentration listed in Table 11 or cells were untreated as a control. Ten hours after transfection, medium was changed to serum-free medium and cells were incubated for an additional 12 hr. Proteins from the medium were precipitated using trichloroacetic acid, and THPO protein expression was analyzed by western blot using a THPO antibody purchased from Abcam (catalog # ab196026) and quantified using Image J. The results are shown in Table 11 below as the percent protein expression relative to untreated control cells (“UTC”) following normalization to the loading control (Transferrin). The results show that an antisense oligonucleotide targeting the start codon of the uORF of human THPO increased THPO protein expression.

TABLE-US-00011 TABLE 11 THPO expression Start Stop Concentration Protein SEQ ID Isis No. Sequence Site Site (nM) (% UTC) NO. 806734 C.sub.moA.sub.moU.sub.moG.sub.moG.sub.moA.sub.moG.sub.mo 195 212 5 155 25 G.sub.moC.sub.moG.sub.moG.sub.mo 10 176 C.sub.moU.sub.moU.sub.moA.sub.moG.sub.moG.sub.moC.sub.m 20 167 40 172 60 130 Subscripts: “m” indicates a 2′-O-methyl modification, “o” indicates a phosphodiester internucleoside linkage.

Example 10: Effects of Mismatched Antisense Oligonucleotides Targeting the uORF of RNase H1 on RNase H1 Protein Expression

[1022] Antisense oligonucleotides designed to target the start codon of the uORF of human RNase H1 with two mismatches between the antisense oligonucleotide and the target sequence were tested for their effects on RNase H1 expression in vitro. These antisense oligonucleotides, described in Table 12, were uniformly modified in order to avoid inducing cleavage of the target RNA. The start and stop sites listed in Table 12 indicate the positions on SEQ ID NO: 1 that the antisense oligonucleotides target, and the mismatched nucleotides are bolded. The targeted uORF begins at position 86. HeLa cells were transfected with Lipofectamine RNAiMAX (Life Technologies) and an antisense oligonucleotide at a final concentration of 25 nM or were mock transfected as a control. Twenty-four hours after transfection, the cells were lysed, and expression of RNase H1 was analyzed by western blot as described in Example 1. The results are shown in Table 12 as percent protein levels relative to mock transfected cells following normalization to the Ku70 loading control. The results show that antisense oligonucleotides with mismatches to the uORF start codon or near to the uORF start codon had little to no effect on RNase H1 protein expression, whereas antisense oligonucleotides with mismatches further away from the uORF start codon increased RNase H1 protein expression.

TABLE-US-00012 TABLE 12 RNase H1 expression Start Stop RNase H1 protein SEQ ID Isis No. Sequence Site Site (% mock) NO. 773519 G.sub.moU.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.mo 73 88 96 26 C.sub.moC.sub.moC.sub.moG.sub.moG.sub.moC.sub.m 773520 C.sub.moA.sub.moA.sub.moA.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.mo 73 88 82 27 C.sub.moC.sub.moC.sub.moG.sub.moG.sub.moC.sub.m 773521 C.sub.moA.sub.moU.sub.moU.sub.moA.sub.moG.sub.moG.sub.moA.sub.moC.sub.moU.sub.mo 73 88 103 28 C.sub.moC.sub.moC.sub.moG.sub.moG.sub.moC.sub.m 773522 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moC.sub.moU.sub.moC.sub.moU.sub.mo 73 88 89 29 C.sub.moC.sub.moC.sub.moG.sub.moG.sub.moC.sub.m 773523 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moG.sub.moA.sub.mo 73 88 121 30 C.sub.moC.sub.moC.sub.moG.sub.moG.sub.moC.sub.m 773524 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.mo 73 88 158 31 G.sub.moG.sub.moC.sub.moG.sub.moG.sub.moC.sub.m 773525 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.mo 73 88 150 32 C.sub.moC.sub.moG.sub.moC.sub.moG.sub.moC.sub.m 773526 C.sub.moA.sub.moU.sub.moU.sub.moU.sub.moC.sub.moG.sub.moA.sub.moC.sub.moU.sub.mo 73 88 153 33 C.sub.moC.sub.moC.sub.moG.sub.moC.sub.moG.sub.m Subscripts: “m” indicates a 2′-O-methyl modification, and “o” indicates a phosphodiester internucleoside linkage.

Example 11: Effects of Antisense Oligonucleotides Comprising Various Modifications

[1023] Antisense oligonucleotides targeting the start codon of the uORF in human RNase H1 (SEQ ID NO: 1) or mouse LRPPRC (SEQ ID NO: 2) were designed with various lengths and with various modifications to the internucleoside linkages and to the sugars. These antisense oligonucleotides were tested for their effects on target protein expression in vitro. HEK293 cells (RNase H1 targeting oligonucleotides) or MHT cells (LRPPRC targeting oligonucleotides) were transfected with Lipofectamine RNAiMAX (Life Technologies) and an antisense oligonucleotide at a concentration listed in the tables below. Ten hours after transfection, the cells were lysed, and target protein expression was analyzed by western blot as described in Example 1 (for RNase H1) or Example 6 (for LRPPRC). The results are shown in the tables below as the percent protein expression relative to untreated control cells (“UTC”) following normalization to the loading control (Ku70, γ-tubulin, Annexin A2, or a non-specific band detected by the primary antibody). The results show that antisense oligonucleotides of various lengths and with modified internucleoside linkages and various 2′-modifications and bicyclic nucleosides increased target protein expression.

TABLE-US-00013 TABLE 13 RNase H1 expression Protein SEQ Start Stop Concentration (% ID Isis No. Sequence Site Site Length (nM) mock) NO. 783683 C.sub.msA.sub.msU.sub.msU.sub.msU.sub.msC.sub.msG.sub.msA.sub.msC.sub.msU.sub.ms 77 88 12 20 191 34 C.sub.msC.sub.m 783681 C.sub.msA.sub.msU.sub.msU.sub.msU.sub.msC.sub.msG.sub.msA.sub.msC.sub.msU.sub.ms 75 88 14 20 178 35 C.sub.msC.sub.msC.sub.msG.sub.m 783682 C.sub.msA.sub.msU.sub.msU.sub.msU.sub.msC.sub.msG.sub.msA.sub.msC.sub.msU.sub.ms 73 88 16 20 186 3 C.sub.msC.sub.msC.sub.msG.sub.msG.sub.msC.sub.m 783679 C.sub.msA.sub.msU.sub.msU.sub.msU.sub.msC.sub.msG.sub.msA.sub.msC.sub.msU.sub.ms 71 88 18 20 149 15 C.sub.msC.sub.msC.sub.msG.sub.msG.sub.msC.sub.msC.sub.msC.sub.m 783680 C.sub.msA.sub.msU.sub.msU.sub.msU.sub.msC.sub.msG.sub.msA.sub.msC.sub.msU.sub.ms 69 88 20 20 83 16 C.sub.msC.sub.msC.sub.msG.sub.msG.sub.msC.sub.msC.sub.msC.sub.msA.sub.msG.sub.m Subscripts: “m” indicates a 2′-O-methyl modification, and “s” indicates a phosphorothioate internucleoside linkage.

TABLE-US-00014 TABLE 14 RNase H1 expression Isis No. 783679 concentration (nM) Protein (% UTC) 5 140 10 179 20 186 40 174 60 195

TABLE-US-00015 TABLE 15 RNase H1 expression Protein SEQ Start Stop Concentration (% ID Isis No. Sequence Site Site Length (nM) mock) NO. 783674 .sup.mC.sub.esA.sub.esT.sub.esT.sub.esT.sub.es.sup.mC.sub.esG.sub.esA.sub.es.sup.mC.sub.esT.sub.es.sup.mC.sub.es.sup.mC.sub.e 77 88 12 20 70 36 783673 .sup.mC.sub.esA.sub.esT.sub.esT.sub.esT.sub.es.sup.mC.sub.esG.sub.esA.sub.es.sup.mC.sub.esT.sub.es.sup.mC.sub.es 75 88 14 20 104 37 .sup.mC.sub.es.sup.mC.sub.esG.sub.e 759304 .sup.mC.sub.esA.sub.esT.sub.esT.sub.esT.sub.es.sup.mC.sub.esG.sub.esA.sub.es.sup.mC.sub.esT.sub.es.sup.mC.sub.es 73 88 16 20 136 38 .sup.mC.sub.es.sup.mC.sub.esG.sub.esG.sub.es.sup.mC.sub.e 773517 .sup.mC.sub.esA.sub.esT.sub.esT.sub.esT.sub.es.sup.mC.sub.esG.sub.esA.sub.es.sup.mC.sub.esT.sub.es.sup.mC.sub.es 71 88 18 20 178 39 .sup.mC.sub.es.sup.mC.sub.esG.sub.esG.sub.es.sup.mC.sub.es.sup.mC.sub.es.sup.mC.sub.e 773516 .sup.mC.sub.esA.sub.esT.sub.esT.sub.esT.sub.es.sup.mC.sub.esG.sub.esA.sub.es.sup.mC.sub.esT.sub.es.sup.mC.sub.es 69 88 20 20 122 40 .sup.mC.sub.es.sup.mC.sub.esG.sub.esG.sub.es.sup.mC.sub.es.sup.mC.sub.es.sup.mC.sub.esA.sub.esG.sub.e Subscripts: “e” indicates a 2′-O-methoxyethyl modification, and “s” indicates a phosphorothioate internucleoside linkage. Superscript “m” in front of a “C” indicates a 5′-methylcytosine.

TABLE-US-00016 TABLE 16 RNase H1 expression Isis No. 759304 concentration (nM) Protein (% UTC) 5 137 10 211 20 218 40 208 60 193

TABLE-US-00017 TABLE 17 RNase H1 expression Protein SEQ Start Stop Concentration (% ID Isis No. Sequence Site Site Length (nM) mock) NO. 783678 .sup.mC.sub.eoA.sub.eoT.sub.eoT.sub.eoT.sub.eo.sup.mC.sub.eoG.sub.eoA.sub.eo.sup.mC.sub.eoT.sub.eo.sup.mC.sub.eo 77 88 12 5 187 36 .sup.mC.sub.e 783677 .sup.mC.sub.eoA.sub.eoT.sub.eoT.sub.eoT.sub.eo.sup.mC.sub.eoG.sub.eoA.sub.eo.sup.mC.sub.eoT.sub.eo.sup.mC.sub.eo 75 88 14 5 144 37 .sup.mC.sub.eo.sup.mC.sub.eoG.sub.e 759388 .sup.mC.sub.eoA.sub.eoT.sub.eoT.sub.eoT.sub.eo.sup.mC.sub.eoG.sub.eoA.sub.eo.sup.mC.sub.eoT.sub.eo.sup.mC.sub.eo 73 88 16 5 148 38 .sup.mC.sub.eo.sup.mC.sub.eoG.sub.eoG.sub.eo.sup.mC.sub.e 783676 .sup.mC.sub.eoA.sub.eoT.sub.eoT.sub.eoT.sub.eo.sup.mC.sub.eoG.sub.eoA.sub.eo.sup.mC.sub.eoT.sub.eo.sup.mC.sub.eo 71 88 18 5 101 39 .sup.mC.sub.eo.sup.mC.sub.eoG.sub.eoG.sub.eo.sup.mC.sub.eo.sup.mC.sub.eo.sup.mC.sub.e 783675 .sup.mC.sub.eoA.sub.eoT.sub.eoT.sub.eoT.sub.eo.sup.mC.sub.eoG.sub.eoA.sub.eo.sup.mC.sub.eoT.sub.eo.sup.mC.sub.eo 69 88 20 5 84 40 .sup.mC.sub.eo.sup.mC.sub.eoG.sub.eoG.sub.eo.sup.mC.sub.eo.sup.mC.sub.eo.sup.mC.sub.eoA.sub.eoG.sub.e Subscripts: “e” indicates a 2′-O-methoxyethyl modification, and “s” indicates a phosphorothioate internucleoside linkage. Superscript “m” in front of a “C” indicates a 5′-methylcytosine.

TABLE-US-00018 TABLE 18 RNase H1 expression Start Stop Concentration Protein SEQ ID Isis No. Sequence Site Site (nM) (% UTC) NO. 766733 C.sub.foA.sub.foU.sub.foU.sub.foU.sub.foC.sub.foG.sub.foA.sub.foC.sub.fo 73 88 5 115 3 U.sub.foC.sub.foC.sub.foC.sub.foG.sub.foG.sub.foC.sub.f 10 126 20 137 40 134 60 127 Subscripts: “f” indicates a 2′-fluoro modification, “o” indicates a phosphodiester internucleoside linkage.

TABLE-US-00019 TABLE 19 RNase H1 expression Start Stop Concentration Protein SEQ ID Isis No. Sequence Site Site (nM) (% UTC) NO. 768080 .sup.mC.sub.esA.sub.esT.sub.esT.sub.esT.sub.es.sup.mC.sub.esG.sub.esA.sub.es 73 88 5 150 38 .sup.mC.sub.esT.sub.es.sup.mC.sub.es.sup.mC.sub.esC.sub.fsG.sub.fsG.sub.fsC.sub.f 10 125 20 100 40 81 60 78 Subscripts: “e” indicates a 2′-O-methoxyethyl modification, “f” indicates a 2′-fluoro modification, “s” indicates a phosphorothioate internucleoside linkage. Superscript “m” in front of a “C” indicates a 5′-methylcytosine.

TABLE-US-00020 TABLE 20 RNase H1 expression Start Stop Concentration Protein SEQ ID Isis No. Sequence Site Site (nM) (% UTC) NO. 766741 .sup.mC.sub.esA.sub.esT.sub.esT.sub.esT.sub.es.sup.mC.sub.esG.sub.esA.sub.es 73 88 5 126 38 .sup.mC.sub.esT.sub.es.sup.mC.sub.es.sup.mC.sub.es.sup.mC.sub.es 10 151 G.sub.ksG.sub.ks.sup.mC.sub.k 20 122 40 121 80 62 Subscripts: “e” indicates a 2′-O-methoxyethyl modification, “k” indicates a cEt bicyclic nucleoside, “s” indicates a phosphorothioate internucleoside linkage. Superscript “m” in front of a “C” indicates a 5′-methylcytosine.

TABLE-US-00021 TABLE 21 RNase H1 expression Protein SEQ Start Stop Concentration (% ID Isis No. Sequence Site Site (nM) mock) NO. 806735 C.sub.msA.sub.msU.sub.msU.sub.msU.sub.msC.sub.msG.sub.msA.sub.msC.sub.msU.sub.msC.sub.ms 73 88 20 152 3 C.sub.msC.sub.msG.sub.msG.sub.ks.sup.mC.sub.k 806736 C.sub.msA.sub.msU.sub.msU.sub.msU.sub.msC.sub.msG.sub.msA.sub.msC.sub.msU.sub.msC.sub.ms 73 88 20 165 3 C.sub.msC.sub.msG.sub.ksG.sub.ks.sup.mC.sub.k 806737 C.sub.msA.sub.msU.sub.msU.sub.msU.sub.msC.sub.msG.sub.msA.sub.msC.sub.msU.sub.msC.sub.ms 73 88 20 183 3 C.sub.ms.sup.mC.sub.ksG.sub.ksG.sub.ks.sup.mC.sub.k 806738 C.sub.msA.sub.msU.sub.msU.sub.msU.sub.msC.sub.msG.sub.msA.sub.msC.sub.msU.sub.msC.sub.ms 73 88 20 145 3 .sup.mC.sub.ks.sup.mC.sub.ksG.sub.ksG.sub.ks.sup.mC.sub.k Subscripts: “m” indicates a 2′-O-methyl modification, “k” indicates a cEt bicyclic nucleoside, and “s” indicates a phosphorothioate internucleoside linkage. Superscript “m” in front of a “C” indicates a 5′-methylcytosine.

TABLE-US-00022 TABLE 22 LRPPRC expression Protein SEQ Start Stop Concentration (% ID Isis No. Sequence Site Site (nM) mock) NO. 806739 C.sub.msA.sub.msU.sub.msU.sub.msG.sub.msU.sub.msU.sub.msU.sub.msU.sub.msU.sub.msU.sub.ms 55 72 20 149 17 G.sub.msU.sub.msC.sub.msU.sub.msU.sub.ms.sup.mC.sub.ks.sup.mC.sub.k 806740 C.sub.msA.sub.msU.sub.msU.sub.msG.sub.msU.sub.msU.sub.msU.sub.msU.sub.msU.sub.msU.sub.ms 55 72 20 191 41 G.sub.msU.sub.msC.sub.msU.sub.msT.sub.ks.sup.mC.sub.ks.sup.mC.sub.k 806741 C.sub.msA.sub.msU.sub.msU.sub.msG.sub.msU.sub.msU.sub.msU.sub.msU.sub.msU.sub.msU.sub.ms 55 72 20 212 42 G.sub.msU.sub.msC.sub.msT.sub.ksT.sub.ks.sup.mC.sub.ks.sup.mC.sub.k 806742 C.sub.msA.sub.msU.sub.msU.sub.msG.sub.msU.sub.msU.sub.msU.sub.msU.sub.msU.sub.msU.sub.ms 55 72 20 213 42 G.sub.msU.sub.ms.sup.mC.sub.ksT.sub.ksT.sub.ks.sup.mC.sub.ks.sup.mC.sub.k Subscripts: “m” indicates a 2′-O-methyl modification, “k” indicates a cEt bicyclic nucleoside, and “s” indicates a phosphorothioate internucleoside linkage. Superscript “m” in front of a “C” indicates a 5′-methylcytosine.

Example 12: Effects of Antisense Oligonucleotides Targeting the uORF of Mouse LRPPRC In Vivo

[1024] Isis No. 761933 (see Example 6) was tested for its effect on LRPPRC protein expression in vivo. Groups of three or four male, seven week old BALB/c mice were systemically administered Isis No. 761933, at a dose listed in the tables below, or saline by subcutaneous injection. Animals were sacrificed (Table 23) or received a second dose (Table 24) 48 hours later Animals that received a second dose were sacrificed 48 hours after the second dose. Liver homogenates were prepared, and LRPPRC protein expression was analyzed by western blot, as described in Example 6. The results are shown in the tables below as the percent expression relative to saline treated animals following normalization to the loading control (GAPDH or hnRNP K). The results show that LRPPRC protein expression was increased in vivo following treatment with an antisense oligonucleotide targeting the LRPPRC uORF.

TABLE-US-00023 TABLE 23 LRPPRC expression following single dose in vivo Isis No. 761933 dose (mg/kg) Protein (% UTC) 75 137

TABLE-US-00024 TABLE 24 LRPPRC expression following two doses in vivo Isis No. 761933 dose (mg/kg) Protein (% UTC) 3.125 109 6.25 124 12.5 136 25 183 50 169 100 109 200 98

Example 13: Effects of Antisense Oligonucleotides Targeting the uORF of Mouse THPO In Vivo

[1025] Mouse Thrombopoietin (THPO) mRNA (GENBANK accession number NM_009379.2, designated herein as SEQ ID NO: 43) comprises an upstream open reading frame. Isis No. 809793 (see the table below) was designed to target the start codon of the uORF of mouse THPO and tested for its effect on THPO protein expression in vivo. The start and stop sites listed in Table 25 indicate the positions on SEQ ID NO: 43 that the antisense oligonucleotide targets. Groups of three mice were systemically administered Isis No. 809793, at a dose listed in the table below, or saline by subcutaneous injection. The animals were sacrificed 48 hours later, and serum and bone marrow was collected. Serum THPO protein expression was analyzed by western blot, as described in Example 9, and bone marrow THPO mRNA expression was analyzed by RT-PCR. Bone marrow THPO mRNA levels were unaffected by the antisense oligonucleotide treatment (data not shown). The results shown in the table below are the average of two independent experiments and are shown as the percent expression relative to saline treated animals following normalization to the loading control (Transferrin). The results show that THPO protein expression was increased in vivo following treatment with an antisense oligonucleotide targeting the THPO uORF.

TABLE-US-00025 TABLE 25 Mouse THPO expression Start Stop Dose THPO protein (% SEQ ID Isis No. Sequence Site Site (mg/kg) mock) NO. 809793 C.sub.msA.sub.msU.sub.msG.sub.msG.sub.msA.sub.msG.sub.msG.sub.msC.sub.msG.sub.ms 309 325 12.5 146 44 G.sub.msC.sub.msU.sub.msU.sub.msG.sub.msA.sub.msG.sub.m 25 457 50 240 75 244 Subscripts: “m” indicates a 2′-O-methyl modification, and “s” indicates a phosphorothioate internucleoside linkage.

Example 14: Inhibition of a uORF Targeting Oligonucleotide with a Complementary Oligonucleotide

[1026] In order to test whether increased translation that is mediated by an oligonucleotide targeting a uORF could be reversed, the effect of an oligonucleotide complementary to the uORF targeting oligonucleotide was tested in vitro. HeLa cells were transfected with 20 nM of Isis No. 761909, as described in Example 1. Five hours later, the cells were transfected with a concentration of Isis No. 761929, which is complementary to Isis No. 761909, listed in the table below. Five hours after the second transfection, cells were lysed and RNase H1 protein expression was analyzed as described in Example 1, with γ-tubulin used as the loading control. The results are shown in the table below as the percent expression relative to mock transfected cells following normalization to the γ-tubulin loading control. The results show that an oligonucleotide targeted to a uORF targeting oligonucleotide blocked the uORF targeting oligonucleotide's ability to increase translation in a dose dependent manner

TABLE-US-00026 TABLE 26 RNase H1 expression Concentration Concentration RNase H1 protein SEQ ID Isis No. Sequence 761909 (nM) 761929 (nM) (% mock) NO. 761929 G.sub.moC.sub.moC.sub.moG.sub.moG.sub.moG.sub.moA.sub.mo 20 0 185 45 G.sub.moU.sub.moC.sub.moG.sub.moA.sub.moA.sub.moA.sub.mo 20 10 161 U.sub.moG.sub.m 20 20 120 20 30 103 20 40 97 Subscripts: “m” indicates a 2′-O-methyl modification and “o” indicates a phosphodiester internucleoside linkage.

Example 15: Inhibition of a uORF Targeting Oligonucleotide by Globally Blocking Translation

[1027] In order to test whether increases in protein expression mediated by antisense oligonucleotides targeting a uORF are due to increased protein stability, translation was blocked following transfection of the oligonucleotide. HeLa cells were transfected with Isis No. 761909 (see Example 1) or mock transfected. Twelve hours later, cells were treated with DMSO or 15 μg/ml cycloheximide at 37° C. Cells were then collected at various time points and cell lysates were prepared and subjected to western analysis, as described in Example 1. A duplicate SDS-PAGE gel was silver-stained and served as loading control. RNase H1 protein levels were calculated relative to mock transfected cells following normalization to the loading control. The results (data not shown) showed that the rates of reduction of RNase H1 protein levels following cycloheximide treatment were similar for mock and Isis No. 761909 transfected cells. Thus, these results, along with the lack of increase in mRNA shown in several above examples, show that increases in protein expression mediated by antisense oligonucleotides targeting a uORF are due to increased protein translation.

Example 16: Effect of a uORF Targeting Antisense Oligonucleotide on Nascent Protein Translation

[1028] In order to further confirm that antisense oligonucleotides targeting a uORF mediate an increase in translation of new protein, pulse-chase labeling and immunoprecipitation of LRPPRC was performed. MHT cells were transfected with Isis No. 761930 for 7 hours, and incubated with pre-warmed medium lacking methionine (Invitrogen, RPMI 1640) at 37° C. for 30 minutes. Cells were then pulse-labeled with 35 μCi/ml S.sup.35-methionine in RPMI1640 medium for 20 minutes and chased with 1 mM methionine for 40 minutes. Cells were washed with cold PBS containing 10 μg/ml cycloheximide and cell lysate were prepared using IP buffer (Life Technologies). Immunoprecipitation was conducted using anti-LRPPRC antibody (Proteintech) at 4° C. for 3 hours. After 4 washes, the precipitated proteins were analyzed on a 4-12% SDS-PAGE gel, transferred to a membrane, and visualized by autoradiography. The LRPPRC band in the immunoprecipitate from the mock treated cells was significantly lighter than in the immunoprecipitate from the Isis No. 761930 treated cells (data not shown), further confirming that antisense oligonucleotides targeting a uORF increase protein expression via increasing target protein translation. Furthermore, the lysate inputs for both the mock and Isis No. 761930 transfected cells were also analyzed via autoradioagraphy and were very similar, indicating that the increased translation was target specific.

Example 17: Effect of an Antisense Oligonucleotide Targeting the uORF of RNase H1 on RNase H1 Activity

[1029] In order to test whether the increase in RNase H1 protein levels mediated by antisense oligonucleotides targeting a RNase H1 uORF results in an increase in RNase H1 activity, cells were first transfected with Isis No. 761909 (see Example 1) or a control oligonucleotide that does not target RNase H1, Isis No. 759704, then transfected with an antisense oligonucleotide targeting U16 snoRNA or NCL1 mRNA. Ten hours after the first transfection, the cells were reseeded at approximately 50% confluency. Cells were transfected a second time 14 hours later with Isis No. 462026 (U16) or Isis No. 110074 (NCL1) for an additional 4 hours. Cells were then collected, lysed, and U16 snoRNA or NCL1 mRNA levels were analyzed by RT-qPCR using TaqMan primer probe sets. The primer probe set sequences used were: Forward: 5′-CTTGCAATGATGTCGTAATTTGC-3′, SEQ ID NO: 46, Reverse: 5′-TCGTCAACCTTCTGTACCAGCTT-3′, SEQ ID NO: 47, and Probe: 5″-TTACTCTGTTCTCAGCGACAGTTGCCTGC-3′, SEQ ID NO: 48 for U16; and Forward: 5′-GCTTGGCTTCTTCTGGACTCA-3′, SEQ ID NO: 49, Reverse: 5′-TCGCGAGCTTCACCATGA-3′, SEQ ID NO: 50, and Probe: 5′-CGCCACTTGTCCGCTTCACACTCC-3′, SEQ ID NO: 51 for NCL1. The results are shown in the tables below as the percent RNA levels relative to untreated control cells that were not transfected with any oligonucleotide, normalized to total RNA as measured using Ribogreen. The results show that Isis No. 761909 targeting a RNase H1 uORF increased the antisense activity of U16 and NCl1 antisense oligonucleotides.

TABLE-US-00027 TABLE 27 U16 snoRNA expression 1.sup.st ASO SEQ 2.sup.nd ASO SEQ Isis Concentration ID Concentration mRNA ID No. Sequence (nM) No. Isis No. Sequence (nM) (%) No. Control C.sub.mo A.sub.mo U.sub.mo U.sub.mo 20 18 462026 .sup.mC.sub.esA.sub.esG.sub.es.sup.mC.sub.esA.sub.es.sup.G.sub.ds 1.25 97 52 759704 G.sub.mo U.sub.mo U.sub.mo U.sub.mo 20 G.sub.ds.sup.mC.sub.dsA.sub.dsA.sub.ds.sup.mC.sub.ds 2.5 98 U.sub.mo U.sub.mo U.sub.mo G.sub.mo 20 T.sub.dsG.sub.dsT.sub.ds.sup.mC.sub.dsG.sub.es.sup.mC.sub.es 5 97 U.sub.mo C.sub.mo U.sub.mo U.sub.m 20 T.sub.esG.sub.esA.sub.e 10 83 20 20 75 uORF C.sub.moA.sub.moU.sub.moU.sub.moU.sub.mo 20 3 462026 .sup.mC.sub.esG.sub.es.sup.mC.sub.esA.sub.esG.sub.ds 1.25 90 52 761909 C.sub.moG.sub.moA.sub.moC.sub.mo 20 G.sub.ds.sup.mC.sub.dsA.sub.dsA.sub.ds.sup.mC.sub.ds 2.5 76 U.sub.moC.sub.moC.sub.moG.sub.mo 20 T.sub.dsG.sub.dsT.sub.ds.sup.mC.sub.dsG.sub.es.sup.mC.sub.es 5 70 G.sub.moC.sub.m 20 T.sub.esG.sub.esA.sub.e 10 61 20 20 49 Subscripts: “e” indicates a 2′-O-methoxyethyl modification, “d” indicates a 2′-deoxynucleoside, and “s” indicates a phosphorothioate internucleoside linkage. Superscript “m” in front of a “C” indicates a 5′-methylcytosine.

TABLE-US-00028 TABLE 28 NCL1 mRNA expression 1.sup.st ASO SEQ 2.sup.nd ASO SEQ Isis Concentration ID Concentration mRNA ID No. Sequence (nM) No. Isis No. Sequence (nM) (%) No. Control C.sub.mo A.sub.mo U.sub.mo U.sub.mo 20 18 110074 G.sub.esT.sub.es.sup.mC.sub.esA.sub.esT.sub.es.sup.mC.sub.ds 1.25 96 53 759704 G.sub.mo U.sub.mo U.sub.mo U.sub.mo 20 G.sub.dsT.sub.ds.sup.mC.sub.dsA.sub.dsT.sub.ds 2.5 95 U.sub.mo U.sub.mo U.sub.mo G.sub.mo 20 .sup.mC.sub.ds.sup.mC.sub.dsT.sub.ds.sup.mC.sub.dsA.sub.es 5 96 U.sub.mo C.sub.mo U.sub.mo U.sub.m 20 T.sub.es.sup.mC.sub.esA.sub.esT.sub.e 10 79 20 20 45 uORF C.sub.moA.sub.moU.sub.moU.sub.moU.sub.mo 20 3 110074 G.sub.esT.sub.es.sup.mC.sub.esA.sub.esT.sub.es.sup.mC.sub.ds 1.25 93 53 761909 C.sub.moG.sub.moA.sub.moC.sub.mo 20 G.sub.dsT.sub.ds.sup.mC.sub.dsA.sub.dsT.sub.ds 2.5 91 U.sub.moC.sub.moC.sub.moC.sub.moG.sub.mo 20 .sup.mC.sub.ds.sup.mC.sub.dsT.sub.ds.sup.mC.sub.dsA.sub.es 5 87 G.sub.moC.sub.m 20 T.sub.es.sup.mC.sub.esA.sub.esT.sub.e 10 62 20 20 32 Subscripts: “e” indicates a 2′-O-methoxyethyl modification, “d” indicates a 2′-deoxynucleoside, and “s” indicates a phosphorothioate internucleoside linkage. Superscript “m” in front of a “C” indicates a 5′-methylcytosine.

Example 18: Effects of Antisense Oligonucleotides Targeting the 5′-Untranslated Region of RNase H1

[1030] Antisense oligonucleotides designed to target the 5′-untranslated region upstream of the uORF of human RNase H1 were tested for their effects on RNase H1 protein expression in vitro. The start and stop sites listed in the tables below indicate the positions on SEQ ID NO: 1 that the antisense oligonucleotides target. HEK 293 cells were transfected with 20 nM antisense oligonucleotide or were mock transfected as a control. Ten hours after transfection, RNase H1 protein expression was analyzed as described in Example 1. The results are shown in the tables below as percent protein expression relative to mock transfected cells following normalization to the GAPDH loading control. The results show that many antisense oligonucleotides targeting the 5′-untranslated region upstream of the RNase H1 uORF induced translation of the target.

TABLE-US-00029 TABLE 29 RNase H1 expression Start Stop Protein (% SEQ ID Isis No. Sequence Site Site mock) NO. 761772 A.sub.mo A.sub.mo G.sub.mo A.sub.mo U.sub.mo G.sub.mo A.sub.mo C.sub.mo G.sub.mo 1 16 142 54 C.sub.mo A.sub.mo C.sub.mo G.sub.mo U.sub.mo C.sub.mo U.sub.m 761773 G.sub.mo G.sub.mo A.sub.mo A.sub.mo G.sub.mo A.sub.mo U.sub.mo G.sub.mo A.sub.mo 3 18 155 55 C.sub.mo G.sub.mo C.sub.mo A.sub.mo C.sub.mo G.sub.mo U.sub.m 761774 C.sub.mo G.sub.mo G.sub.mo G.sub.mo A.sub.mo A.sub.mo G.sub.mo A.sub.mo U.sub.mo 5 20 179 56 G.sub.mo A.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo C.sub.m 761775 C.sub.mo G.sub.mo C.sub.mo G.sub.mo G.sub.mo G.sub.mo A.sub.mo A.sub.mo G.sub.mo 7 22 259 57 A.sub.mo U.sub.mo G.sub.mo A.sub.mo C.sub.mo G.sub.mo C.sub.m

TABLE-US-00030 TABLE 30 RNase H1 expression Start Stop Protein (% SEQ ID Isis No. Sequence Site Site mock) NO. 761778 C.sub.mo A.sub.mo C.sub.mo C.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo 13 28 132 58 G.sub.mo G.sub.mo G.sub.mo A.sub.mo A.sub.mo G.sub.mo A.sub.m 761779 G.sub.mo U.sub.mo C.sub.mo A.sub.mo C.sub.mo C.sub.mo G.sub.mo G.sub.mo C.sub.mo 15 30 164 59 G.sub.mo C.sub.mo G.sub.mo G.sub.mo G.sub.mo A.sub.mo A.sub.m 761780 C.sub.mo C.sub.mo G.sub.mo U.sub.mo C.sub.mo A.sub.mo C.sub.mo C.sub.mo G.sub.mo 17 32 182 60 G.sub.mo C.sub.mo G.sub.mo C.sub.mo G.sub.mo G.sub.mo G.sub.m 761781 U.sub.mo U.sub.mo C.sub.mo C.sub.mo G.sub.mo U.sub.mo C.sub.mo A.sub.mo C.sub.mo 19 34 226 61 C.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo G.sub.m 761782 A.sub.mo C.sub.mo U.sub.mo U.sub.mo C.sub.mo C.sub.mo G.sub.mo U.sub.mo C.sub.mo 21 36 229 62 A.sub.mo C.sub.mo C.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.m 761783 G.sub.mo C.sub.mo A.sub.mo C.sub.mo U.sub.mo U.sub.mo C.sub.mo C.sub.mo G.sub.mo 23 38 259 63 U.sub.mo C.sub.mo A.sub.mo C.sub.mo C.sub.mo G.sub.mo G.sub.m 761784 C.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo C.sub.mo U.sub.mo U.sub.mo C.sub.mo 25 40 237 64 C.sub.mo G.sub.mo U.sub.mo C.sub.mo A.sub.mo C.sub.mo C.sub.m

TABLE-US-00031 TABLE 31 RNase H1 expression Start Stop Protein (% SEQ ID Isis No. Sequence Site Site mock) NO. 761785 C.sub.mo A.sub.mo C.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo C.sub.mo U.sub.mo 27 42 170 65 U.sub.mo C.sub.mo C.sub.mo G.sub.mo U.sub.mo C.sub.mo A.sub.m 761786 A.sub.mo A.sub.mo C.sub.mo A.sub.mo C.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo 29 44 186 66 C.sub.mo U.sub.mo U.sub.mo C.sub.mo C.sub.mo G.sub.mo U.sub.m 761787 U.sub.mo C.sub.mo A.sub.mo A.sub.mo C.sub.mo A.sub.mo C.sub.mo C.sub.mo G.sub.mo 31 46 197 67 C.sub.mo A.sub.mo C.sub.mo U.sub.mo U.sub.mo C.sub.mo C.sub.m 761788 G.sub.mo C.sub.mo U.sub.mo C.sub.mo A.sub.mo A.sub.mo C.sub.mo A.sub.mo C.sub.mo 33 48 210 68 C.sub.mo G.sub.mo C.sub.mo A.sub.mo C.sub.mo U.sub.mo U.sub.m 761789 G.sub.mo C.sub.mo G.sub.mo C.sub.mo U.sub.mo C.sub.mo A.sub.mo A.sub.mo C.sub.mo 35 50 211 69 A.sub.mo C.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo C.sub.m 761790 C.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo U.sub.mo C.sub.mo A.sub.mo 37 52 202 70 A.sub.mo C.sub.mo A.sub.mo C.sub.mo C.sub.mo G.sub.mo C.sub.m 761791 G.sub.mo C.sub.mo C.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo U.sub.mo 39 54 173 71 C.sub.mo A.sub.mo A.sub.mo C.sub.mo A.sub.mo C.sub.mo C.sub.m 761792 C.sub.mo C.sub.mo G.sub.mo C.sub.mo C.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo 41 56 120 72 C.sub.mo U.sub.mo C.sub.mo A.sub.mo A.sub.mo C.sub.mo A.sub.m

TABLE-US-00032 TABLE 32 RNase H1 expression Start Stop Protein (% SEQ ID Isis No. Sequence Site Site mock) NO. 761776 G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo G.sub.mo G.sub.mo G.sub.mo A.sub.mo 9 24 130 73 A.sub.mo G.sub.mo A.sub.mo U.sub.mo G.sub.mo A.sub.mo C.sub.m 761794 C.sub.mo G.sub.mo A.sub.mo G.sub.mo C.sub.mo C.sub.mo G.sub.mo C.sub.mo C.sub.mo 45 60 92 74 G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo U.sub.mo C.sub.m 761796 G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo G.sub.mo A.sub.mo G.sub.mo C.sub.mo 49 64 94 75 C.sub.mo G.sub.mo C.sub.mo C.sub.mo G.sub.mo G.sub.mo C.sub.m 761798 C.sub.mo G.sub.mo U.sub.mo G.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo 53 68 84 76 G.sub.mo A.sub.mo G.sub.mo C.sub.mo C.sub.mo G.sub.mo C.sub.m 761800 C.sub.mo C.sub.mo A.sub.mo G.sub.mo C.sub.mo G.sub.mo U.sub.mo G.sub.mo G.sub.mo 57 72 71 77 G.sub.mo C.sub.mo G.sub.mo C.sub.mo G.sub.mo A.sub.mo G.sub.m Subscripts: “m” indicates a 2′-O-methyl modification, and “o” indicates a phosphodiester internucleoside linkage.

Example 19: Effects of Antisense Oligonucleotides Targeting the 5′-Untranslated Region of ACP1

[1031] Antisense oligonucleotides designed to target the 5′-untranslated region of cytoplasmic phosphotyrosine protein phosphatase (ACP1), which does not comprise a uORF, were tested for their effects on ACP1 protein expression in vitro. The antisense oligonucleotides target the human ACP1 mRNA (GENBANK accession number NM_004300.3, designated herein as SEQ ID NO: 78) and were designed to target at least one stem loop structure in the 5′-untranslated region. The start and stop sites listed in the table below indicate the positions on SEQ ID NO: 78 that the antisense oligonucleotides target. HEK 293 cells were transfected with a concentration of antisense oligonucleotide shown in the table below or were not transfected as a control. Ten hours after transfection, ACP1 protein expression was analyzed by western blot using an Abcam antibody to ACP1 (catalog # ab166896). The results are shown in the tables below as percent protein expression relative to untreated control cells following normalization to the p32 loading control. The results show that the antisense oligonucleotides targeting the 5′-untranslated region of human ACP1 induced translation of the target.

TABLE-US-00033 TABLE 33 ACP1 expression Start Stop Concentration Protein SEQ ID Isis No. Sequence Site Site (nM) (% mock) NO. 812652 C.sub.mo G.sub.mo A.sub.mo C.sub.mo G.sub.mo C.sub.mo G.sub.mo G.sub.mo C.sub.mo 36 51 5 112 79 G.sub.mo C.sub.mo A.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.m 10 130 20 116 40 165 80 172 812658 G.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo 27 44 5 121 80 C.sub.mo A.sub.mo C.sub.mo U.sub.mo G.sub.mo C.sub.mo C.sub.mo A.sub.mo C.sub.m 10 161 20 164 40 119 80 129 Subscripts: “m” indicates a 2′-O-methyl modification and “o” indicates a phosphodiester internucleoside linkage.

Example 20: Effects of Antisense Oligonucleotides Targeting the 5′-Untranslated Region Downstream of the CFTR uORF Start Codon on CFTR Protein Expression

[1032] Antisense oligonucleotides designed to target the 5′-untranslated region downstream of the uORF start codon of human cystic fibrosis transmembrane conductance regulator (CFTR) were tested for their effects on CFTR protein expression in vitro. These antisense oligonucleotides, described in the table below, were designed to target the CFTR mRNA (GENBANK accession number NM_000492.3, designated herein as SEQ ID NO: 81) and were uniformly modified in order to avoid inducing cleavage of the target RNA. The start and stop sites listed in the table below indicate the positions on SEQ ID NO: 81 that the antisense oligonucleotides target. One uORF begins at position 13 of SEQ ID NO: 81. Isis No. 786455 targets a portion of the uORF that is just downstream of the uORF start codon. Isis No. 786456 targets a stem loop structure further downstream.

[1033] HT-29 cells were transfected with a concentration of antisense oligonucleotide listed in the table below or were mock transfected as a control. Twelve or twenty-two hours after transfection, CFTR expression was analyzed by western blot using Anti-CFTR purchased from EMD Millipore (catalog #05-583, clone M3A7). The results are shown in the table below as percent protein expression relative to mock transfected cells following normalization to the HSP90 loading control. The results show that the antisense oligonucleotides increased CFTR protein expression.

TABLE-US-00034 TABLE 34 CFTR expression Time SEQ Start Stop point Concentration Protein ID Isis No. Sequence Site Site (h) (nM) (% mock) NO. 786455 U.sub.ms U.sub.ms C.sub.ms U.sub.ms C.sub.ms U.sub.ms G.sub.ms A.sub.ms 19 36 12 12.5 142 82 C.sub.ms C.sub.ms U.sub.ms G.sub.ms C.sub.ms U.sub.ms G.sub.ms U.sub.ms 25 151 G.sub.ms A.sub.m 50 150 100 86 22 12.5 59 25 93 50 146 100 192 786456 C.sub.ms C.sub.ms A.sub.ms A.sub.ms A.sub.ms G.sub.ms A.sub.ms C.sub.ms 60 77 22 12.5 105 83 C.sub.ms U.sub.ms A.sub.ms C.sub.ms U.sub.ms A.sub.ms C.sub.ms U.sub.ms 25 140 C.sub.ms U.sub.m 50 186 75 186 100 390 150 181 200 262 Subscripts: “m” indicates a 2′-O-methyl modification, and “s” indicates a phosphorothioate internucleoside linkage.

Example 21: Identification of a Translation Suppression Element that does not Comprise a uORF

[1034] In order to test the effect of portions of the RNase H1 5′-UTR sequence on RNase H1 expression, the wild type and mutant 5′-UTR sequences were cloned into a plasmid and fused to firefly luciferase. Renila luciferase was cloned into the same plasmids for normalization. The plasmids were transfected into HeLa cells and firefly and Renila luciferase activities were detected using standard methods. The mutants and their firefly luciferase activity relative to the wild type 5′-UTR reporters, normalized to Renila luciferase activity, are shown in the table below. The nucleotide positions reported in the table below refer to the positions of the 5′-UTR of SEQ ID NO: 1 that were mutated or deleted. The results are the averages of multiple experiments and show that the mutation and/or deletion of portions of the 5′-UTR sequence of RNase H1, including portions that do not comprise a uORF, resulted in increased expression in a reporter system, indicating that the mutated portions are part of a translation suppression element.

TABLE-US-00035 TABLE 35 Firefly luciferase activity Firefly luciferase Mutation Deletion activity (%) AUG -> UUG (uORF start codon) n/a 770 AUG -> UUG (uORF start codon) Nucleotides 30-60 980 GACGGAAGT-> CAGCCTTCA, n/a 1380 nucleotides 28-36 CGGTG->GCCAC n/a 680 nucleotides 38-42 CGGTG->GCCAC & CGCCG->GCGGC, n/a 600 nucleotides 38-42 & 48-52

Example 22: Effects of Antisense Oligonucleotides Targeting the uORF of Mouse LRPPRC In Vivo

[1035] Isis No. 806740 (see Example 11) was tested for its effect on LRPPRC protein expression in vivo. Groups of three, male, seven week old BALB/c mice were systemically administered Isis No. 806740, at a dose listed in the table below, or saline by subcutaneous injection. 48 hours later, the mice received a second dose listed in the table below. Animals were sacrificed 48 hours after the second dose. Liver homogenates were prepared, and LRPPRC protein expression was analyzed by western blot, as described in Example 6. The results are shown in the tables below as the percent expression relative to saline treated animals following normalization to the loading control (PSF). The results show that LRPPRC protein expression was increased in vivo following treatment with an antisense oligonucleotide targeting the LRPPRC uORF and comprising bicyclic nucleic acids.

TABLE-US-00036 TABLE 36 LRPPRC expression in vivo Isis No. 806740 dose (mg/kg) Protein (% UTC) 12.5 126 25 171 50 113 100 120

Example 23: Effects of Antisense Oligonucleotides Targeting the 5′-Untranslated Region of ACP1

[1036] Effects of antisense oligonucleotides designed to target the 5′-untranslated region of ACP1, which does not comprise a uORF, are shown above (see Example 19). Additional antisense oligonucleotides designed to target the 5′-untranslation region of ACP1 were tested for their effects on ACP1 protein expression in vitro. The antisense oligonucleotides target the human ACP1 mRNA (GENBANK accession number NM_004300.3, designated herein as SEQ ID NO: 78). The start and stop sites listed in the table below indicate the positions on SEQ ID NO: 78 that the antisense oligonucleotides target. HeLa cells were transfected with 25 nM of an antisense oligonucleotide shown in the table below or were not transfected as a control. Ten hours after transfection, ACP1 protein expression was analyzed by western blot using an Abcam antibody to ACP1 (catalog # ab166896). The results are shown in the tables below as percent protein expression relative to untreated control cells following normalization to the Annexin A2 loading control.

TABLE-US-00037 TABLE 37 ACP1 expression Start Stop Protein SEQ ID Isis No. Sequence Site Site (% mock) NO. 812658 G.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo 27 44 127 80 A.sub.mo C.sub.mo U.sub.mo G.sub.mo C.sub.mo C.sub.mo A.sub.mo C.sub.m 812650 A.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo C.sub.mo U.sub.mo G.sub.mo 27 40 142 84 C.sub.mo C.sub.mo A.sub.mo C.sub.m (XL500) G.sub.mo C.sub.mo A.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo C.sub.mo 29 42 147 85 U.sub.mo G.sub.mo C.sub.mo C.sub.m 812651 G.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo 31 44 107 86 A.sub.mo C.sub.mo U.sub.mo G.sub.m (XL502) C.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo G.sub.mo G.sub.mo C.sub.mo 33 46 100 87 G.sub.mo C.sub.mo A.sub.mo C.sub.m (XL503) C.sub.mo G.sub.mo C.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo G.sub.mo 35 48 58 88 G.sub.mo C.sub.mo G.sub.mo C.sub.m (XL504) G.sub.mo A.sub.mo C.sub.mo G.sub.mo C.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo 37 50 107 89 A.sub.mo G.sub.mo G.sub.mo C.sub.m Subscripts: “m” indicates a 2′-O-methyl modification, and “o” indicates a phosphodiester internucleoside linkage.

Example 24: Effects of Antisense Oligonucleotides Targeting ACP1 Comprising Various Modifications

[1037] Antisense oligonucleotides designed to target the same or similar site of the 5′-untranslated region of ACP1 as Isis No. 812658 (see Examples 19 and 23) were designed with various modifications and tested for their effects on ACP1 protein expression in vitro. The start and stop sites listed in the table below indicate the positions on SEQ ID NO: 78 that the antisense oligonucleotides target. HeLa cells were transfected with a concentration of an antisense oligonucleotide shown in the tables below or were not transfected as a control. Ten hours after transfection, ACP1 protein expression was analyzed by western blot using an Abcam antibody to ACP1 (catalog # ab166896). The results are shown in the tables below as percent protein expression relative to untreated control cells following normalization to the Annexin A2 or TMED9 loading control.

TABLE-US-00038 TABLE 38 ACP1 expression Start Stop Concentration Protein SEQ ID Isis No. Sequence Site Site (nM) (% mock) NO. 812675 G.sub.ms C.sub.ms A.sub.ms G.sub.ms G.sub.ms C.sub.ms G.sub.ms C.sub.ms A.sub.ms 27 42 5 161 90 C.sub.ms U.sub.ms G.sub.ms C.sub.ms C.sub.ms A.sub.ms C.sub.m 10 147 20 227 40 193 80 98 812653 G.sub.mo C.sub.mo A.sub.mo G.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo 27 42 5 87 90 A.sub.mo C.sub.mo U.sub.mo G.sub.mo C.sub.mo C.sub.mo A.sub.mo C.sub.m 10 167 20 182 40 139 80 124

TABLE-US-00039 TABLE 39 ACP1 expression Start Stop Concentration Protein SEQ ID Isis No. Sequence Site Site (nM) (% mock) NO. 813860 G.sub.ms C.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms G.sub.ms C.sub.ms G.sub.ms 27 44 25 87 80 C.sub.ms A.sub.ms C.sub.ms U.sub.ms G.sub.ms C.sub.ms .sup.mC.sub.ks A.sub.ks .sup.mC.sub.k 826061 G.sub.ms C.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms G.sub.ms C.sub.ms G.sub.ms 27 44 25 109 80 C.sub.ms A.sub.ms C.sub.ms U.sub.ms G.sub.ms C.sub.ms .sup.mC.sub.ko A.sub.ks .sup.mC.sub.k 826062 G.sub.ms C.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms G.sub.ms C.sub.ms G.sub.ms 27 44 25 111 80 C.sub.ms A.sub.ms C.sub.mo U.sub.ms G.sub.mo C.sub.ms .sup.mC.sub.ko A.sub.ks .sup.mC.sub.k 826063 G.sub.ms C.sub.mo G.sub.ms C.sub.mo A.sub.ms G.sub.ms G.sub.ms C.sub.ms G.sub.ms 27 44 25 111 80 C.sub.ms A.sub.ms C.sub.ms U.sub.ms G.sub.ms C.sub.ms .sup.mC.sub.ks A.sub.ks .sup.mC.sub.k 826064 G.sub.ms C.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms G.sub.mo C.sub.ms G.sub.mo 27 44 25 151 80 C.sub.ms A.sub.ms C.sub.ms U.sub.ms G.sub.ms C.sub.ms .sup.mC.sub.ks A.sub.ks .sup.mC.sub.k 826065 G.sub.ms C.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms G.sub.mo C.sub.ms G.sub.mo 27 44 25 158 80 C.sub.ms A.sub.ms C.sub.ms U.sub.ms G.sub.ms C.sub.ms .sup.mC.sub.ks A.sub.ks .sup.mC.sub.k 826066 G.sub.ms C.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms G.sub.ms C.sub.mo G.sub.ms 27 44 25 140 80 C.sub.mo A.sub.ms C.sub.ms U.sub.ms G.sub.ms C.sub.ms .sup.mC.sub.ks A.sub.ks .sup.mC.sub.k 826069 G.sub.ms C.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms G.sub.ms C.sub.ms G.sub.ms 27 44 25 196 80 C.sub.ms A.sub.ms C.sub.ms U.sub.ms G.sub.ks C.sub.ds .sup.mC.sub.ks A.sub.ds .sup.mC.sub.k Subscripts: “m” indicates a 2′-O-methyl modification, “o” indicates a phosphodiester internucleoside linkage, “s” indicates a phosphorothioate internucleoside linkage, “k” indicates a cEt bicyclic nucleoside, “d” indicates a 2′-deoxynucleoside. Superscript “m” preceding a “C” indicates a 5-methylcytosine.

TABLE-US-00040 TABLE 40 ACP1 expression Concentration Protein SEQ Isis No. Start Site Stop Site (nM) (% mock) ID NO. 813860 27 44 5 130 80 10 104 20 47 40 95 80 89 826065 27 44 5 143 80 10 137 20 182 40 153 80 127 826069 27 44 5 127 80 20 139 40 184 80 133

Example 25: Effects of Antisense Oligonucleotides Targeting the 5′-UTR of Mouse ACP1

[1038] Antisense oligonucleotides designed to target the 5′-untranslated region of mouse ACP1 were tested for their effects on ACP1 protein expression in vitro. The antisense oligonucleotides target the mouse ACP1 mRNA (GENBANK accession number NM_021330.4, designated herein as SEQ ID NO: 91) and were designed to target at least one stem loop structure in the 5′-UTR. The start and stop sites listed in the table below indicate the positions on SEQ ID NO: 91 that the antisense oligonucleotides target. MHT cells were transfected with a concentration of antisense oligonucleotide shown in the table below or were not transfected as a control. Ten hours after transfection, ACP1 protein expression was analyzed by western blot. The results are shown in the table below as percent protein expression relative to untreated control cells following normalization to the TCP-1β loading control. The results show that the antisense oligonucleotides targeting the 5′-untranslated region of mouse ACP1 induced translation of the target.

TABLE-US-00041 TABLE 41 ACP1 expression Start Stop Concentration Protein SEQ ID Isis No. Sequence Site Site (nM) (% mock) NO. (XL546) G.sub.mo C.sub.mo A.sub.mo U.sub.mo G.sub.mo C.sub.mo G.sub.mo C.sub.mo A.sub.mo 20 34 5 88 92 C.sub.mo U.sub.mo G.sub.mo C.sub.mo C.sub.mo A.sub.m 10 133 20 153 40 125 80 126 (XL547) G.sub.ms C.sub.ms A.sub.ms U.sub.ms G.sub.ms C.sub.ms G.sub.ms C.sub.ms A.sub.ms 20 34 5 161 92 C.sub.ms U.sub.ms G.sub.ms C.sub.ms C.sub.ms A.sub.m 10 198 20 219 40 227 80 194 See above Tables for subscripts legend.

Example 26: Effect of an Antisense Oligonucleotide Targeting the 5′-UTR Mouse ACP1 In Vivo

[1039] Isis No. 827815 (see the table below) was tested for its effect on mouse ACP1 protein expression in vivo. Groups of three, male, seven week old BALB/c mice were systemically administered Isis No. 827815, at a dose listed in the table below, or saline by subcutaneous injection. Animals were sacrificed 72 hours later. Liver homogenates were prepared, and ACP1 protein expression was analyzed by western blot. The results are shown in the table below as the percent expression relative to saline treated animals following normalization to the TMED9 loading control. The results show that ACP1 protein expression was increased in vivo following treatment with an antisense oligonucleotide targeting the ACP1 5′-UTR.

TABLE-US-00042 TABLE 42 ACP1 expression in vivo Start Stop Dose Protein SEQ ID Isis No. Sequence site site (mg/kg) (% UTC) NO. 827815 G.sub.ms C.sub.ms A.sub.ms U.sub.ms G.sub.ms C.sub.ms G.sub.ms C.sub.ms A.sub.ms 19 34 12.5 145 93 C.sub.ms U.sub.ms G.sub.ms C.sub.ms C.sub.ms A.sub.ms G.sub.m 25 114 50 116 100 94 See above Tables for subscripts legend.

Example 27: Effect of Antisense Oligonucleotide Targeting the 5′-UTR of Mouse ARF1

[1040] An antisense oligonucleotide designed to target the 5′-untranslated region of mouse ADP-ribosylation factor 1 (ARF1) was tested for its effects on ARF1 protein expression in vitro. The antisense oligonucleotide targets the mouse ARF1 mRNA (GENBANK accession number NM_007476.3, designated herein as SEQ ID NO: 94), which does not comprise a uORF, and was designed to target at least one stem loop structure in the 5′-UTR. The start and stop sites listed in the table below indicate the positions on SEQ ID NO: 94 that the antisense oligonucleotide targets. MHT cells were transfected with a concentration of antisense oligonucleotide shown in the table below or were not transfected as a control. Ten hours after transfection, ARF1 protein expression was analyzed by western blot. The results are shown in the table below as percent protein expression relative to untreated control cells following normalization to the TCP-1β loading control. The results show that the antisense oligonucleotide targeting the 5′-untranslated region of mouse ARF1 induced translation of the target.

TABLE-US-00043 TABLE 43 ARF1 expression Start Stop Concentration Protein SEQ ID Isis No. Sequence Site Site (nM) (% mock) NO. 814929 C.sub.mo G.sub.mo C.sub.mo T.sub.mo C.sub.mo C.sub.mo C.sub.mo A.sub.mo C.sub.mo 44 60 5 112 95 A.sub.mo A.sub.mo G.sub.mo A.sub.mo T.sub.mo G.sub.mo G.sub.mo C.sub.m 10 179 20 215 40 181 80 122 See above Tables for subscripts legend.

Example 28: Effect of antisense oligonucleotide targeting the 5′-UTR of mouse USP16

[1041] An antisense oligonucleotide designed to target the 5′-untranslated region of mouse ubiquitin processing protease (USP16) was tested for its effects on USP16 protein expression in vitro. The antisense oligonucleotide targets the mouse USP16 mRNA (GENBANK accession number NM_024258.2, designated herein as SEQ ID NO: 96), and was designed to target at least one stem loop structure in the 5′-UTR. The start and stop sites listed in the table below indicate the positions on SEQ ID NO: 96 that the antisense oligonucleotide targets. MHT cells were transfected with a concentration of antisense oligonucleotide shown in the table below or were not transfected as a control. Ten hours after transfection, USP16 protein expression was analyzed by western blot. The results are shown in the table below as percent protein expression relative to untreated control cells following normalization to the β-actin (ACTB) loading control. The results show that the antisense oligonucleotide targeting the 5′-untranslated region of mouse USP16 induced translation of the target.

TABLE-US-00044 TABLE 44 USP16 expression Start Stop Concentration Protein SEQ ID Isis No. Sequence Site Site (nM) (% mock) NO. 814928 G.sub.mo A.sub.mo G.sub.mo A.sub.mo G.sub.mo C.sub.mo G.sub.mo A.sub.mo C.sub.mo 21 37 5 124 97 G.sub.mo C.sub.mo G.sub.mo G.sub.mo T.sub.mo G.sub.mo G.sub.mo A.sub.m 10 133 20 133 40 116 80 116 See above Tables for subscripts legend.

Example 29: Effects of Antisense Oligonucleotides Targeting the 5′-UTR of Human LDLr

[1042] Antisense oligonucleotides designed to target the 5′-untranslated region of human low density lipoprotein receptor (LDLr) were tested for their effects on LDLr protein expression and LDL uptake in vitro. The antisense oligonucleotides target the human LDLr mRNA (GENBANK accession number NM_000527.4, designated herein as SEQ ID NO: 98) and were designed to target at least one stem loop structure in the 5′-UTR. The start and stop sites listed in the table below indicate the positions on SEQ ID NO: 98 that the antisense oligonucleotides target. HEK293 or HeLa cells were transfected with a concentration of antisense oligonucleotide shown in the table below or were not transfected as a control. Ten hours after transfection, LDLr protein expression was analyzed by ELISA (R & D Systems, cat. # DLDLR0). The results are shown in the table below as percent protein expression relative to untreated control cells. The results show that the antisense oligonucleotides targeting the 5′-untranslated region of human LDLr induced translation of the target.

[1043] In order to test the effects of the antisense oligonucleotides in the tables below on LDL uptake, HEK 293 or HeLa cells were transfected with an antisense oligonucleotide at a concentration shown in the table below or were not transfected as a control. Approximately fourteen hours after transfection, the medium was changed to lipid-free medium, incubated at 37° C. for one hour, then 5 to 10 μg/mL of Bodipy labeled LDL was added at 4° C. for 30 to 60 minutes to all cells, including untransfected control cells. The cells were then washed with cold PBS, harvested, and lysed with RIPA buffer. The Bodipy fluorescence was measured, and the results in the table below show the percent Bodipy fluorescence relative to untransfected control cells.

TABLE-US-00045 TABLE 45 LDLr expression SEQ Start Stop Concentration Protein ID Isis No. Sequence Site Site Cell type (nM) (% UTC) NO. 814923 U.sub.mo G.sub.mo C.sub.mo A.sub.mo G.sub.mo U.sub.mo G.sub.mo G.sub.mo 28 43 HEK293 5 131 99 G.sub.mo G.sub.mo U.sub.mo G.sub.mo A.sub.mo U.sub.mo U.sub.mo U.sub.m 10 146 20 169 40 188 80 238 814923 U.sub.mo G.sub.mo C.sub.mo A.sub.mo G.sub.mo U.sub.mo G.sub.mo G.sub.mo 28 43 HeLa 5 124 99 G.sub.mo G.sub.mo U.sub.mo G.sub.mo A.sub.mo U.sub.mo U.sub.mo U.sub.m 10 154 20 113 40 128 80 106 842196? U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms U.sub.ms G.sub.ms G.sub.ms 28 43 HeLa 5 112 99 (XL512) G.sub.ms G.sub.ms U.sub.ms G.sub.ms A.sub.ms U.sub.ms U.sub.ms U.sub.m 10 111 20 128 40 121 80 137 See above Tables for subscripts legend.

TABLE-US-00046 TABLE 46 LDL uptake Bodipy-LDL LDL incubation Concentration uptake (% SEQ Isis No. Cell type time (min) (nM) UTC) ID NO. 814923 HEK293 60 40 152 99 842196 HEK293 30 40 115 99 60 40 130 842196 HeLa 30 12.5 108 99 25 108 50 127 100 132

Example 30: Effects of Antisense Oligonucleotides Targeting the 5′-Untranslated Region Downstream of the CFTR uORF Start Codon on CFTR Protein Expression

[1044] Antisense oligonucleotides designed to target a uORF start codon of human CFTR were tested for their effects on CFTR protein expression in vitro. These antisense oligonucleotides, described in the table below, were designed to target the CFTR mRNA (GENBANK accession number NM_000492.3, designated herein as SEQ ID NO: 81) and were uniformly modified in order to avoid inducing cleavage of the target RNA. The start and stop sites listed in the table below indicate the positions on SEQ ID NO: 81 that the antisense oligonucleotides target.

[1045] HT-29 cells were transfected with a concentration of antisense oligonucleotide listed in the table below or were mock transfected as a control. Twenty-four hours after transfection, CFTR expression was analyzed by western blot, as described in Example 20. The results are shown in the table below as percent protein expression relative to mock transfected cells following normalization to a loading control. The results show that the antisense oligonucleotides increased CFTR protein expression.

TABLE-US-00047 TABLE 47 CFTR expression SEQ Start Stop Concentration Protein ID Isis No. Sequence Site Site (nM) (% mock) NO. 812022 U.sub.mo G.sub.mo C.sub.mo U.sub.mo G.sub.mo U.sub.mo G.sub.mo A.sub.mo U.sub.mo 9 26 50 132 100 G.sub.mo U.sub.mo C.sub.mo A.sub.mo U.sub.mo U.sub.mo U.sub.mo G.sub.mo C.sub.m 75 117 100 125 150 112 812023 U.sub.ms G.sub.ms C.sub.ms U.sub.ms G.sub.ms U.sub.ms G.sub.ms A.sub.ms U.sub.ms 9 26 50 130 100 G.sub.ms U.sub.ms C.sub.ms A.sub.ms U.sub.ms U.sub.ms U.sub.ms G.sub.ms C.sub.m 75 126 100 124 150 128 See above Tables for subscripts legend.

Example 31: Effects of Antisense Oligonucleotides Targeting the 5′-UTR of Human LDLr

[1046] Antisense oligonucleotides designed to target the 5′-untranslated region of human low density lipoprotein receptor (LDLr) were tested for their effects on LDLr protein expression in vitro. The antisense oligonucleotides target the human LDLr mRNA (SEQ ID NO: 98) and were designed to target at least one stem loop structure in the 5′-UTR. The start and stop sites listed in the table below indicate the positions on SEQ ID NO: 98 that the antisense oligonucleotides target. HEK293 cells were transfected with a concentration of antisense oligonucleotide shown in the table below or were not transfected as a control. Sixteen hours after transfection, LDLr protein expression was analyzed by ELISA (R & D Systems, cat. # DLDLR0). The results are shown in the table below as percent protein expression relative to untreated control cells. The results show that the antisense oligonucleotides targeting the 5′-untranslated region of human LDLr induced translation of the target.

TABLE-US-00048 TABLE 48 LDLr expression SEQ Start Stop Concentration Protein ID Isis No. Sequence Site Site (nM) (% UTC) NO. 842196 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms U.sub.ms G.sub.ms G.sub.ms 28 43 20 125 99 G.sub.ms G.sub.ms U.sub.ms G.sub.ms A.sub.ms U.sub.ms U.sub.ms U.sub.m 40 195 80 222 842197 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms U.sub.ms G.sub.ms G.sub.ms 28 43 20 176 101 G.sub.ms G.sub.ms U.sub.ms G.sub.ms A.sub.ms T.sub.ks T.sub.ks T.sub.k 40 266 80 214 842198 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.mo U.sub.ms G.sub.mo G.sub.ms 28 43 20 160 101 G.sub.mo G.sub.ms U.sub.ms G.sub.ms A.sub.ms T.sub.ks T.sub.ks T.sub.k 40 157 80 194 842200 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.mo U.sub.ms G.sub.mo G.sub.ms 28 43 20 131 99 G.sub.mo G.sub.ms U.sub.mo G.sub.ms A.sub.ms U.sub.ms U.sub.ms U.sub.m 40 175 80 170 842202 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.mo U.sub.ms G.sub.mo G.sub.ms 28 43 20 125 99 G.sub.ms G.sub.ms U.sub.ms G.sub.ms A.sub.ms U.sub.ms U.sub.ms U.sub.m 40 132 80 145 842205 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms U.sub.ms G.sub.ms G.sub.ms 26 43 20 123 102 G.sub.ms G.sub.ms U.sub.ms G.sub.ms A.sub.ms U.sub.ms U.sub.ms U.sub.ms 40 136 U.sub.ms C.sub.m 80 107 842206 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms U.sub.ms G.sub.ms G.sub.ms 26 43 20 155 103 G.sub.ms G.sub.ms U.sub.ms G.sub.ms A.sub.ms U.sub.ms U.sub.ms T.sub.ks T.sub.ks 40 173 .sup.mC.sub.k 80 134 842207 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.mo U.sub.ms G.sub.mo G.sub.ms 26 43 20 125 103 G.sub.mo G.sub.ms U.sub.ms G.sub.ms A.sub.ms U.sub.ms U.sub.ms T.sub.ks T.sub.ks 40 147 .sup.mC.sub.k 80 129 842211 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.mo U.sub.ms G.sub.mo G.sub.ms 26 43 20 136 102 G.sub.ms G.sub.ms U.sub.ms G.sub.ms A.sub.ms U.sub.ms U.sub.ms U.sub.ms 40 143 U.sub.ms C.sub.m 80 142 842212 U.sub.ms G.sub.ms C.sub.mo A.sub.ms G.sub.mo U.sub.ms G.sub.mo G.sub.ms 26 43 20 103 102 G.sub.mo G.sub.ms U.sub.mo G.sub.ms A.sub.mo U.sub.ms U.sub.mo U.sub.ms 40 101 U.sub.ms C.sub.m 80 120 842213 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms U.sub.ms G.sub.ms G.sub.ms 26 43 20 128 104 G.sub.ms G.sub.ms U.sub.ms G.sub.ms A.sub.ms T.sub.ks T.sub.ds T.sub.ks T.sub.ds 40 135 .sup.mC.sub.k 80 139 842214 U.sub.ms G.sub.ms C.sub.ms A.sub.ms G.sub.ms U.sub.ms G.sub.ms G.sub.ms 28 43 20 134 101 G.sub.ms G.sub.ms U.sub.ms G.sub.ks A.sub.ds T.sub.ks T.sub.ds T.sub.k 40 152 80 139 See above Tables for subscripts legend.

Example 32: Time Course of LDLr Protein Expression Following Treatment with an Antisense Oligonucleotide Targeting the 5′-UTR

[1047] Hep3B cells were transfected with 30 nM Isis No. 842196 (see Table 45) and Lipofectamine 2000 (Life Technologies). At various time points following transfection, the cells were harvested and LDLr protein expression was analyzed by ELISA as described in Examples 30 and 31. The results are shown in Table 49 as the percent LDLr protein expression relative to cells that did not receive antisense oligonucleotide treatment (harvested at the 0 hour time point). The results show that LDLr expression was increased over 4-fold relative to baseline expression by Isis No. 842196, at the 48 hour time point.

TABLE-US-00049 TABLE 49 LDLr expression LDLr (% 0 h) following transfection with 30 nM Isis No. 842196 24 h 36 h 48 h 212 230 457