LIVER-SPECIFIC PROMOTER AND APPLICATION THEREOF

Abstract

Liver-specific promoters and application thereof are provided. A set of small-size recombinant nucleic acid sequences for regulating high specific expression of genes in a liver system are provided. Compared with the currently reported other sequences of similar size, the said recombinant regulatory sequence fragment has the advantage that the ability of driving expression of reporter gene and human coagulation factor FVIII in the liver system is significantly enhanced, thereby being suitable for recombinant adeno-associated virus (rAAV)-mediated gene therapy.

Claims

1. A nucleic acid molecule, comprising: (a) a first polynucleotide having at least 80% nucleic acid sequence identity with a nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2, or a functional fragment of the first polynucleotide; and (b) a second polynucleotide having at least 80% nucleic acid sequence identity with a nucleotide sequence shown in SEQ ID NO: 3, or a functional fragment of the second polynucleotide; wherein the second polynucleotide or the functional fragment of the second polynucleotide and the first polynucleotide or the functional fragment of the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate a transcription of a heterogeneous polynucleotide in a liver tissue of a mammal.

2. The nucleic acid molecule according to claim 1, wherein the nucleic acid molecule comprises: (a) the first polynucleotide having the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2; and (b) the second polynucleotide having the nucleotide sequence shown in SEQ ID NO: 3; wherein the second polynucleotide and the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

3. The nucleic acid molecule according to claim 1, further comprising: (c) a third polynucleotide having at least 80% nucleic acid sequence identity with a nucleotide sequence shown in SEQ ID NO: 4, or a functional fragment of the third polynucleotide; wherein the third polynucleotide or the functional fragment of the third polynucleotide, the second polynucleotide or the functional fragment of the second polynucleotide, and the first polynucleotide or the functional fragment of the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

4. The nucleic acid molecule according to claim 1, wherein the nucleic acid molecule comprises: (a) the first polynucleotide having the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2; and (b) the second polynucleotide having the nucleotide sequence shown in SEQ ID NO: 3; and (c) a third polynucleotide having a nucleotide sequence shown in SEQ ID NO: 4; wherein the third polynucleotide, the second polynucleotide and the first polynucleotide are 5′-3′ linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

5. A method for initiating an expression of a gene or a nucleic acid fragment in a liver, comprising: using a liver-specific promoter, wherein the liver-specific promoter is the nucleic acid molecule according to claim 1.

6. The method according to claim 5, wherein the liver-specific promoter is used for initiating an expression of an FVIII blood coagulation factor gene in the liver.

7. An expression vector, comprising the nucleic acid molecule according to claim 1.

8. The expression vector according to claim 7, wherein the expression vector is a plasmid or a viral vector.

9. A mammal host cell, comprising the expression vector according to claim 7.

10. An mammal, wherein a genome of the mammal comprises the nucleic acid molecule according to claim 1 or an expression vector comprising the nucleic acid molecule.

11. The method according to claim 5, wherein the nucleic acid molecule comprises: (a) the first polynucleotide having the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2; and (b) the second polynucleotide having the nucleotide sequence shown in SEQ ID NO: 3; wherein the second polynucleotide and the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

12. The method according to claim 5, wherein the nucleic acid molecule also comprises: (c) a third polynucleotide having at least 80% nucleic acid sequence identity with a nucleotide sequence shown in SEQ ID NO: 4, or a functional fragment of the third polynucleotide; wherein the third polynucleotide or the functional fragment of the third polynucleotide, the second polynucleotide or the functional fragment of the second polynucleotide, and the first polynucleotide or the functional fragment of the first polynucleotide are 5′-3′ linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

13. The method according to claim 5, wherein the nucleic acid molecule comprises: (a) the first polynucleotide having the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2; and (b) the second polynucleotide having the nucleotide sequence shown in SEQ ID NO: 3; and (c) a third polynucleotide having a nucleotide sequence shown in SEQ ID NO: 4; wherein the third polynucleotide, the second polynucleotide and the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

14. The expression vector according to claim 7, wherein the nucleic acid molecule comprises: (a) the first polynucleotide having the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2; and (b) the second polynucleotide having the nucleotide sequence shown in SEQ ID NO: 3; wherein the second polynucleotide and the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

15. The expression vector according to claim 7, wherein the nucleic acid molecule also comprises: (c) a third polynucleotide having at least 80% nucleic acid sequence identity with a nucleotide sequence shown in SEQ ID NO: 4, or a functional fragment of the third polynucleotide; wherein the third polynucleotide or the functional fragment of the third polynucleotide, the second polynucleotide or the functional fragment of the second polynucleotide, and the first polynucleotide or the functional fragment of the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

16. The expression vector according to claim 7, wherein the nucleic acid molecule comprises: (a) the first polynucleotide having the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2; and (b) the second polynucleotide having the nucleotide sequence shown in SEQ ID NO: 3; and (c) a third polynucleotide having a nucleotide sequence shown in SEQ ID NO: 4; wherein the third polynucleotide, the second polynucleotide and the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

17. The mammal host cell according to claim 9, wherein the expression vector is a plasmid or a viral vector.

18. The mammal according to claim 10, wherein the nucleic acid molecule comprises: (a) the first polynucleotide having the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2; and (b) the second polynucleotide having the nucleotide sequence shown in SEQ ID NO: 3; wherein the second polynucleotide and the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

19. The mammal according to claim 10, wherein the nucleic acid molecule also comprises: (c) a third polynucleotide having at least 80% nucleic acid sequence identity with a nucleotide sequence shown in SEQ ID NO: 4, or a functional fragment of the third polynucleotide; wherein the third polynucleotide or the functional fragment of the third polynucleotide, the second polynucleotide or the functional fragment of the second polynucleotide, and the first polynucleotide or the functional fragment of the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

20. The mammal according to claim 10, wherein the nucleic acid molecule comprises: (a) the first polynucleotide having the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2; and (b) the second polynucleotide having the nucleotide sequence shown in SEQ ID NO: 3; and (c) a third polynucleotide having a nucleotide sequence shown in SEQ ID NO: 4; wherein the third polynucleotide, the second polynucleotide and the first polynucleotide are 5′-3′linked, and the nucleic acid molecule is configured to facilitate the transcription of the heterogeneous polynucleotide in the liver tissue of the mammal.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0038] FIG. 1 shows a structural schematic diagram of PFD-rAAV-CMV-mCHERRY-bGHpA vector.

[0039] FIG. 2 shows a structural schematic diagram of PFD-rAAV-HLP-BDD-FVIIIopt(WJ)-spolyA vector.

[0040] FIG. 3 shows a comparison of effects of different promoters for initiating mCHERRY fluorescence in mouse liver tissue.

[0041] FIG. 4 shows a comparison of effects of different promoters for initiating mCHERRY fluorescence in mouse liver tissue.

[0042] FIG. 5 shows a gray scale scan diagram of effects of different promoters for initiating mCHERRY fluorescence in mouse liver tissue.

[0043] FIG. 6 shows SDS-PAGE protein gel silver staining diagrams of different rAAV viruses.

[0044] FIG. 7 shows different AAV virus titers determined by an RT-PCR method.

[0045] FIG. 8 shows a comparison of effects of different promoters for expressing FVIII in C57 mice.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0046] In order to make the purpose, the technical solution and the advantage of the present disclosure more clear and distinct, the present disclosure will be described in more detail below in conjunction with the accompanying drawings and the examples. It should be understood that, the specific examples described herein are merely intended to explain the present disclosure, and not to limit the present disclosure. In addition, the technical features involved in the various embodiments of the present disclosure described below can be combined with one another, as long as they do not conflict with one another.

[0047] The present disclosure provides a nucleic acid molecule, including:

[0048] (a) a first polynucleotide having at least 80% nucleic acid sequence identity with a nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2, or a functional fragment of the first polynucleotide; and

[0049] (b) a second polynucleotide having at least 80% nucleic acid sequence identity with a nucleotide sequence shown in SEQ ID NO: 3, or a functional fragment of the second polynucleotide;

[0050] wherein (b) and (a) are 5′-3′ linked, and the nucleic acid molecule is able to facilitate efficient transcription of a heterogeneous polynucleotide in liver tissue of mammal.

[0051] In some examples, the nucleic acid molecule includes:

[0052] (a) a first polynucleotide having the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2; and

[0053] (b) a second polynucleotide having the nucleotide sequence shown in SEQ ID NO: 3.

[0054] wherein (b) and (a) are 5′-3′linked, and said nucleic acid molecule is able to facilitate efficient transcription of the heterogeneous polynucleotide in liver tissue of mammal.

[0055] In some examples, the nucleic acid molecule also includes:

[0056] (c) a third polynucleotide having at least 80% nucleic acid sequence identity with a nucleotide sequence shown in SEQ ID NO: 4, or a functional fragment of the third polynucleotide;

[0057] wherein (c), (b) and (a) are 5′-3′ linked, and the nucleic acid molecule is able to facilitate efficient transcription of the heterogeneous polynucleotide in liver tissue of mammal.

[0058] In some other examples, the nucleic acid molecule includes:

[0059] (a) a first polynucleotide having the nucleotide sequence shown in SEQ ID NO: 1 or SEQ ID NO: 2; and

[0060] (b) a second polynucleotide having the nucleotide sequence shown in SEQ ID NO: 3; and

[0061] (c) a third polynucleotide having the nucleotide sequence shown in SEQ ID NO: 4;

[0062] wherein (c), (b) and (a) are 5′-3′ linked, and the nucleic acid molecule is able to facilitate efficient transcription of the heterogeneous polynucleotide in liver tissue of mammal.

[0063] The present disclosure also provides an application of the nucleic acid molecule, and the nucleic acid molecule is used as a liver-specific promoter.

[0064] In some examples, the promoter can be used in but not limited to initiation of the expression of FVIII blood coagulation factor gene in liver.

[0065] The present disclosure also provides an expression vector including the nucleic acid molecule of the present disclosure, wherein the nucleic acid molecule is operably linked to the heterogeneous polynucleotide.

[0066] In preferred examples, the expression vector is a plasmid or a viral vector. Examples of the mammal expression vector include an adenovirus vector, plasmid vectors of pSV and pCMV series, a vaccinia vector and a retrovirus vector, as well as a baculovirus vector. In some embodiments, the expression vector is an adeno-associated virus vector rAAV.

[0067] The expression vector also includes one or more of the following elements: a replication origin, a selectable marker and a multiple cloning site.

[0068] The present disclosure also provides a mammal host cell including the expression vector of the present disclosure. The expression vector can be transfected into the host cell by any suitable method. Preferably, the host cell is a mammal cell (such as a human cell), for example those mentioned above. These host cells may be isolated cells.

[0069] The nucleic acid molecule is able to facilitate the transcription of the heterogeneous polynucleotides operably linked in the mammal cell. Preferred mammal cells include a mouse cell, a rat cell, a hamster cell, a monkey cell and a human cell. Examples of such cells include an FMK cell and a derivative (such as HEK293, HEK293T, HEK293A), a PerC6 cell, 911 cell, a CHO cell, an HCT116 cell, an HeLa cell, a COS cell and a VERO cell; cancer cells such as HepG2, A549 and MCF7; primary cells isolated from human or animal in biopsy; and stem cells (including pluripotent cells, such as embryonic stem cells and induced pluripotent stem cells (iPS); as well as pluripotent stem cells, such as hemopoietic stem cells, mesenchymal stem cells, and so forth).

[0070] The present disclosure also provides a mammal, its genome includes the nucleic acid molecule of the present disclosure or the expression vector of the present disclosure. Preferably, the nucleic acid molecule of the present disclosure or the expression vector of the present disclosure is inserted into the genome of the mammal, such that the heterogeneous polynucleotides operably linked to the nucleic acid molecule of the present disclosure or operably inserted into the expression vector of the present disclosure are expressed in one or more cells of the mammal. Preferably, the mammal is mouse or rat. In some embodiments, the mammal is a non-human mammal.

[0071] A person skilled in the art will easily understand that, the promoter provided by the present disclosure can be used to not only initiate the expression of FVIII blood coagulation factor gene in liver, but also initiate the expression of non-encoded RNA, such as initiate the expression of siRNA.

[0072] The following are examples:

Example 1

[0073] Recombinant Promoter Fragment

[0074] Production of the recombinant promoter fragment consisting of the sequence identified in Table 1.

TABLE-US-00001 TABLE 1 Sequence of the recombinant promoter fragment Name of Third Second First promoters polynucleotide polynucleotide polynucleotide ATh1 promoter None SEQ ID NO: 3 SEQ ID NO: 2 ATh2 promoter None SEQ ID NO: 3 SEQ ID NO: 1 ATh3 promoter SEQ ID NO: 4 SEQ ID NO: 3 SEQ ID NO: 2 ATh4 promoter SEQ ID NO: 4 SEQ ID NO: 3 SEQ ID NO: 1 ATh5 promoter SEQ ID NO: 5 SEQ ID NO: 3 SEQ ID NO: 2

[0075] The first polynucleotide, the second polynucleotide and the third polynucleotide (if present) are consecutively linked in the above-mentioned promoter fragment.

Example 2

[0076] Construction of the rAAV expression vector including different promoters Human al-antitrypsin (hAAT) is a serine protease inhibitor encoded and synthesized by SERPINA1 gene, it is primarily synthesized by liver and secreted into blood; an hAAT promoter, as a liver-specific promoter, has a stronger initiation capacity, its expression regulatory elements are dispersed within a range of 1.3 Kb (−1200 bp-+46 bp) (Perlino et al., 1987; Rong-Fong Shen et al., 1989), the larger size restricts its application in the AAV vector. Literature reviews indicate that, an hAAT core promoter region is located in the −142/+44 bp region of a transcription start site (TSS), in which transcription factor binding sites such as HNF1, HNF4, CEBP are distributed. In a remote enhancer region (Distal region, DRI), −261/−181 bp upstream of the transcription start site (TSS), there also exists binding sites for transcription factors CEBP and HNF3, they regulate high level expression of the hAAT in liver tissue.

[0077] The present disclosure chose a −142/+44 bp region of the hAAT promoter (186 bp, NCBI Reference Sequence: NG_008290.1: 6948nt-7133nt), named as a mini-hAAT promoter; and chose a −261/+44 bp region of the hAAT promoter (305 bp, NCBI Reference Sequence: NG_008290.1: 6829nt-7133nt), named as an hAAT promoter; and chose a −142/—62 bp region of the hAAT promoter (81 bp, NCBI Reference Sequence: NG_008290.1: 6948nt-7029nt, SEQ ID NO: 3), named as a truncated-hAAT hAAT promoter; and chose a −261/—208 bp region of the hAAT promoter (54 bp, NCBI Reference Sequence: NG_008290.1: 6829nt-6882nt, SEQ ID NO: 4), named as hAAT enhancer/hAATe.

[0078] Transthyretin (TTR) is a thyroxine transporter, it is secreted into blood after being primarily synthesized in liver tissue, and it is secreted into cerebrospinal fluid after being synthesized in choroid plexus epidermic cells. Expression of mouse TTR is regulated by two liver-specific regions: a proximal regulatory region of −200/+1 (a promoter region) and a distal regulatory region of −1.86/−1.96 kbp (an enhancer region). A TTR promoter, as a liver-specific promoter, due to its smaller size and stronger initiation effects, is also widely used in gene therapy. Multiple transcription factor binding sites such as AP1, CEBP, HNF4, HNF1, HNF3 are distributed in mouse TTR enhancer and promoter regions, they regulate the efficient and specific expression of TTR protein.

[0079] The present disclosure obtains multiple chimeric promoters by chimerism of important regulatory regions of the hAAT promoter and the mouse TTR promoter; five promoters with stronger initiation effects being screened out in subsequent tests are respectively named as an ATh1 promoter, an ATh2 promoter, an ATh3 promoter, an ATh4 promoter and an ATh5 promoter.

[0080] To compare the initiation intensities of different promoters, the present disclosure constructs the above-mentioned chimeric promoters and the above-mentioned stronger liver-specific promoter that has been reported together onto PFD-rAAV-CMV-mCHERRY-bGHpA of the AAV vector, as shown in FIG. 1. Based on the initiation of mCHERRY fluorescent protein expression, initiation levels of different promoters are compared. In FIG. 1, ITR (inverted terminal repeat) is an inverted terminal repeat with a length of 145 bp; CMV enhancer/promoter is human cytomegalovirus early promoter; mCHERRY is red luciferase gene reading frame; BGH polyA is bovine growth hormone polyadenylation signal; Amp is ampicillin resistant gene reading frame; GmR is hygromycin resistant gene reading frame; Tn7F/R is Tn7 transposon; ori is replication origin site; XhoI, AgeI, Sad are restriction endonuclease sites. The detailed construction strategy is:

[0081] 1) PFD-rAAV-CMV-mCHERRY-bGHpA is double digested with restriction enzymes XhoI and AgeI, and linearized;

[0082] 2) a primer is designed for synthesis of a promoter fragment required for template amplification, when the primer is designed, a restriction enzyme site and a homologous recombinant arm of approximately 18 bp are reserved for recombination with the vector after the linearization;

[0083] 3) ClonExpress II One Step Cloning Kit (Vazyme, C112) and ClonExpress MultiS One Step Cloning Kit (Vazyme, C113) are chosen on the basis of the number of the needed recombinant fragments to perform a homologous recombination on the target fragment and the vector backbone; and

[0084] 4) the homologous recombination product is transformed into STBL3 competence, coated onto a LB plate and cultivated at 37° C. overnight and the monoclone is picked for identification, the clone identified correctly is shaken and plasmid is extracted.

[0085] The detailed sequence information is as follow:

[0086] hAAT promoter (−261/+44 bp): (NCBI Reference Sequence: NG_008290.1: 6829nt-7133nt)

[0087] mini-hAAT promoter (−142/+44 bp): (NCBI Reference Sequence: NG_008290.1: 6948nt-7133nt)

[0088] mTTR promoter (NCBI Reference Sequence: NC 000084.6, 1961nt-2164nt, −203/+1bp), SEQ ID NO: 1

[0089] mini-mTTR promoter (NCBI Reference Sequence: NC 000084.6, 2014nt-2164nt, −150/+1bp), SEQ ID NO: 2

[0090] truncated-hAAT hAAT promoter (−142/—62 bp): (NCBI Reference Sequence: NG_008290.1: 6948nt-7029nt), SEQ ID NO: 3

[0091] AAT enhancer (NCBI Reference Sequence: NG_008290.1: 6829nt-6882nt), SEQ ID NO: 4

[0092] mTTR enhancer (NCBI Reference Sequence: NC_000084.6, 286nt-405nt, −1878/−1758 bp), SEQ ID NO: 5

[0093] ATh1 Promoter, SEQ ID NO: 6

[0094] ATh2 Promoter, SEQ ID NO: 7

[0095] ATh3 Promoter, SEQ ID NO: 8

[0096] ATh4 Promoter, SEQ ID NO: 9

[0097] ATh5 Promoter, SEQ ID NO: 10

[0098] Biomarin-HLP promoter, promoter in BMN270 project in BIOMARIN Company, ClinicalTrials.gov number, NCT02576795

[0099] SPARK-TTRm (NCBI Reference Sequence: NC_000084.6, 1961nt-2183nt, −203 bp/+20 bp), wherein −136 bp/−133 bp TGTG mutation is GACT

[0100] ApoE enhancer (GenBank: U32510.1, 78nt-231nt)

[0101] HS-CRM8 enhancer (NCBI Reference Sequence: NM 000295.4, 163 nt-93nt)

[0102] MVM intron (GenBank: NC_001510.1, 2312nt-2403nt)

Example 3

[0103] Comparison of Effects of Different Promoters for Initiating mCHERRY Fluorescent Gene

[0104] The promoter, fluorescent protein mCHERRY and bGHpolyA AAV expression vector constructed in Example 2 were packaged into the AAV2/8 serotype virus through a 293 three-plasmid system, and the viruses were precipitated with PEG8000, then AAV virus was purified by iodixanol density gradient ultracentrifugation. Virus titer was quantified by RT-PCR and silver staining.

[0105] Different AAV viruses were injected into bodies of C57 mice (n=3) at the same dose of 3E+13 vg/kg by tail vein injection, 5 weeks after injection of the viruses, heart perfusion was conducted with physiological saline and 4% paraformaldehyde, and the heart, liver, spleen, lung, kidney, brain etc. were taken and immersed in 4% paraformaldehyde overnight, and then immersed in a 30% sucrose solution for 72 hours. Liver tissue was taken and low temperature freezing microtomy was conducted, and fluorescence was observed under a fluorescence microscope.

[0106] A comparison of mCHERRY fluorescence was conducted between the ATh1 Promoter (SEQ ID NO: 6) and ATh2 Promoter (SEQ ID NO: 7) after the recombination of the present disclosure and the mini-hAAT promoter, mTTR promoter (SEQ ID NO: 1, a mouse TTR promoter region), TBG promoter, hAAT promoter, TTRm promoter (TTR promoter after mutation in spark-8011 project in SPARK Company, ClinicalTrials.gov number, NCT03003533), HLP promoter (promoter in BMN270 project in BIOMARIN Company, ClinicalTrials.gov number, NCT02576795), TTRe/TTRp promoter (a mouse TTR enhancer region and a promoter region), TTRe/TTRp/MVM (MVM intron that was added behind the mouse TTR enhancer region and promoter region) and CRM8/TTRp/MVM (MVM intron that was added behind the mouse TTR promoter region, CRM8 enhancer sequence that was added in front of the promoter region, promoter in SB525 project in sangoma Company, ClinicalTrials.gov number, NCT03061201), to compare their initiation levels in liver tissue, the results are as shown in FIG. 3 and FIG. 4.

[0107] FIG. 3 shows a comparison of effects of different promoters for initiating mCHERRY fluorescence in mouse liver tissue. AAV viruses of different promoters were injected into C57 mice (n=3) at the same dose of 3E+13 vg/kg by tail vein injection, 5 weeks after injection of the viruses, liver tissue mCHERRY fluorescence intensities were compared. Exposure time was 10 ms left 20 and right 500.

[0108] FIG. 4 shows a comparison of effects of different promoters for initiating mCHERRY fluorescence in mouse liver tissue. AAV viruses of different promoters were injected into C57 mice (n=3) at the same dose of 3E+13 vg/kg by tail vein injection, 5 weeks after injection of the viruses, liver tissue mCHERRY fluorescence intensities were compared. Exposure time was 10 ms left 20 and right 4000.

[0109] FIG. 5 shows a grayscale scan diagram of effects of different promoters for initiating mCHERRY fluorescence in mouse liver tissue. A grayscale scan was conducted for the mCHERRY fluorescence expressed by different promoters in mouse liver tissue in FIG. 4 by using graphpad software, the gray scale value was a relative intensity with respect to the HLP promoter.

[0110] By comparison of the mCHERRY fluorescences, the present disclosure finds that, in liver tissue, after the recombination, the initiation levels of promoters ATh1 Promoter (SEQ ID NO: 1) and ATh2 Promoter (SEQ ID NO: 2) were significantly superior to mini-hAAT promoter and mTTR promoter before recombination, and also superior to the TBG promoter, hAAT promoter, TTRm promoter, HLP promoter, TTRe/TTRp promoter, TTRe/TTRp/MVM and CRM8/TTRp/MVM.

Example 4

[0111] Construction of Different Promoters that Initiate BDD-FVIII Vector

[0112] To further discuss whether the strong liver-specific initiation levels of ATh1 and ATh2 promoters were influenced by the gene linked at downstream, as well as whether addition of expression regulatory enhancer elements (ATh3, ATh4) in front of ATh1 and ATh2 was able to further increase expression of the target gene; meanwhile to study whether ATh1-4 initiate expression of a large exogenous gene, and whether AAV was able to be normally packaged, this example constructed different promoters, BDD-FVIII (B domain deleted FVIII) and an sPolyA expression cassette according to the molecular cloning method in the above-mentioned Example 2, and they were constructed onto the AAV vector PFD-rAAV-HLP-BDD-FVIII-spolyA (FIG. 2), wherein the PFD-rAAV-HLP-BDD-FVIII-spolyA vector was double enzyme digested by using restriction enzymes XhoI and AscI, and linearized.

[0113] FIG. 2 shows a structural schematic diagram of PFD-rAAV-HLP-BDD-FVIIIopt (WJ)-spolyA vector. Wherein ITR (inverted terminal repeat) is a inverted terminal repeat with a length of 145 bp; HLP promoter is a promoter (SEQ ID NO: 8) adopted for the project BMN270 of Biomarin Company for therapy of hemophilia A, BDD-FVIIIopt (WJ) is BDD-FVIII in which codon has been optimized; polyA is polyadenylation signal; Amp is ampicillin resistant gene reading frame; GmR is hygromycin resistant gene reading frame; Tn7F/R is Tn7 transposon; ori is replication origin site; XhoI and AscI are restriction enzyme sites.

[0114] FIG. 6 shows SDS-PAGE protein gel silver staining diagrams for different AAV viruses. The AAV viruses loaded with different promoters and FVIII gene expression cassettes were subjected to polyacrylamide gel electrophoresis, then a silver staining was conducted, to determine the purity and titer of the viruses. FIG. 7 shows different AAV virus titers determined by an RT-PCR method. Absolute quantitative PCR was conducted on AAV viruses in which different promoters express FVIII by using primers on the ITR, to determine the virus titer. From the silver staining result and the RT-PCR quantitative result, the above-mentioned vectors were able to be normally packaged.

Example 5

[0115] Comparison of Levels of Expressing FVIII by Different Promoters

[0116] The plasmid constructed in the above-mentioned Example 4 was packaged as the AAV2/8 serotype virus by the sf9 One-bac system. Different AAV viruses were injected into bodies of C57 mice (n=6) at the same dose of 5E+12 vg/kg via tail veins, 2, 5, 8, 10 weeks after the virus injection, blood was sampled from orbital venous plexuses and the FVIII expression level was detected by ELISA. The ELISA antibody pair used was F8C-EIA (enzyme research laboratories), a standard curve was drawn by using human coagulation factor VIII (green cross), and the concentration of blood coagulation factor VIII was determined by using BiYunTian Enhanced BCA Protein Assay Kit (product number: P0010S).

[0117] FIG. 8 shows a comparison of the effects of different promoters for expressing FVIII in C57 mice. AAV viruses of different promoters were injected into C57 mice (n=6) at the same dose of 5E+12 vg/kg by tail vein injection, 2 weeks, 5 weeks, 8 weeks, 10 weeks after injection of the viruses, mouse blood plasma were collected respectively, and the FVIII content in blood plasma was determined by an ELISA method.

[0118] From the overall trend of the detection results, due to timeliness of the AAV expression, from week 2 to week 5, the levels of promoters for expressing FVIII all increased, at week 5 the expression level reached the highest level, at the subsequent two time-points, the expression levels all decreased by different degrees.

[0119] As a whole, at each time-point, the capacity of initiating FVIII by ATh1, ATh2, ATh3, ATh4 are significantly superior to TTRm of Spark Company and HLP promoter of Biomarin Company, at week 2, the levels of expressing FVIII by these four promoters were 2-3 times of that of T Wm, and 10 times or above of that of HLP, at week 5, the levels of expressing FVIII by these four promoters were 1.5-2 times of that of TTRm, and 3-4 times of that of HLP, at week 8, the levels of expressing FVIII by these four promoters were 1.3-1.9 times of that of TTRm, and 1.9-2.6 times of that of HLP, and at week 10, the levels of expressing FVIII by these for promoters were 1.2-2.1 times of that of TTRm, and 1.7-3 times of that of HLP; compared to ApoE/TTRp/MVM and CRM8/TTRp/MVM promoters, at each time-point, levels of expressing FVIII by these four promoters also increased by 1-2 times, although the increasing effect was not evident compared to those of mTTR and HLP, sizes of ATh1 and ATh2 reduced by 83-211 bp, this is important for AAV with limited packaging capacity to load macromolecules such as FVIII. Compared with ATh1 and ATh2, the expression levels of ATh3 and ATh4 increased by 1.4-1.8 times at week 10, although the effect on expression did not significantly increase in the early by adding some expression enhancer elements, being more superior in respect of expression persistence.

[0120] However, for the recombinant promoter ATh5 using the same strategic component, its effect of expressing FVIII is significantly less than those of the other four recombinant promoters proposed by the present disclosure, indicating that there is not necessarily a synergistic effect on the chimerism between the different expression regulatory elements, and there might also be a situation of competing for transcription factors; based on analysis, on one hand, there may be a steric effect within a small space range, binding of one transcription factor prevents other transcription factor from entering an adjacent site, on the other hand, there is certain interaction between different transcription regulatory factors, not just a sequential arrangement, and the additionally bonded regulatory factors may disrupt the original interaction.

[0121] The base numbers of the constructed recombinant promoters and other expression regulatory elements for comparison of the present disclosure are listed in Table 2.

TABLE-US-00002 TABLE 2 Base number of different expression regulatory elements Name Base number (bp) hAAT promoter (−261/+44 bp) 305 mini-hAAT promoter (−142/+44 bp) 186 hAAT enhancer (−261/−208 bp) 54 Truncted-hAAT promoter (−142/−62 bp) 81 mTTR enhancer 99 mTTR promoter 203 mini-mTTR promoter 151 TBG promoter 460 ATh1 promoter 232 ATh2 promoter 284 ATh3 promoter 286 ATh4 promoter 338 ATh5 promoter 331 Biomarin-HLP promoter 252 SPARK-TTRm 223 ApoE enhancer 154 HS-CRM8 enhancer 78 MVM intron 92 CRM8/TTRp/MVM 366 ApoE/TTRp/MVM 449 TTRe/TTRp/MVM 394

[0122] As known from the above table, the recombinant promoters of the ATh1 promoter and ATh2 promote provided by the present disclosure achieve an effect of increasing the FVIII expression level by 1.2-10 times at a size similar to HLP and TTRm (ATh1, 232 bp; ATh2, 284 bp; HLP, 232 bp; T 223 bp), compared with ApoE/TTRp/MVM and CRM8/TTRp/MVM promoter, the level of expressing FVIII also increases by 1-2 times, whereas the size reduces by 83-211 bp. For ATh3 and ATh4 (ATh3, 286 bp; ATh4, 338 bp), compared with ATh1 and ATh2, their lengths slightly increase, but time duration for efficiently expressing FVIII is longer.

[0123] A person skilled in the art will easily understand that, the above mentioned are merely the preferred examples of the present disclosure and not intended to restrict the present disclosure. Any modifications, equivalent substitutions and improvements and so forth within the sprit and the principle of the present disclosure are all included in the protection scope of the present disclosure