GENE OSNIA3 OF RICE NITRATE REDUCTASE NIA3 PROTEIN, AND ITS APPLICATION

Abstract

The present invention discloses a gene OsNia3 of a rice nitrate reductase NIA3 protein. The cDNA sequence of the gene is as set out in SEQ ID NO.1, and the rice NIA3 protein encoded by it has an amino acid sequence as set out in SEQ ID NO.2. A homozygous mutant in which the rice gene OsNia3 is knocked out and a homozygous line in which the OsNia3 is over-expressed are obtained by utilizing a transgenic technology. It has been discovered by analysis that the line in which the OsNia3 gene is knocked out has a shortened plant height and a shorted growth period; while the line in which the OsNia3 is over-expressed has a relatively high plant height and a prolonged growth period.

Claims

1-10. (canceled)

11. A rice gene OsNia3 knockout vector pCas9-OsNia3 obtained by connecting an 18 bp sequence of the gene OsNia3 of a rice nitrate reductase NIA3 protein to a vector pCas9.

12. A rice gene OsNia3 expression vector pCUBi1390-GFP-OsNia3 obtained by cloning a cDNA sequence of a rice gene OsNia3 as set out in SEQ ID NO. 1 into enzyme cleavage sites Hand III and BamH I in a binary expression vector pCUBi1390-GFP.

13. A method of producing a transgenic rice plant, comprising: transferring a rice gene OsNia3 knockout vector pCas9-OsNia3 into Agrobacterium tumefaciens; and transferring the Agrobacterium tumefaciens into a japonica rice variety Kitaake to obtain a homozygous knockout mutant nia3 having mutation of the OsNia3 gene and no backbone of the knockout vector.

14. The method of producing a transgenic rice plant of claim 13, further comprising: producing the rice gene OsNia3 knockout vector, by: designing a primer fragment according to a full-length cDNA sequence of the rice gene OsNia3 as set out in SEQ ID NO. 1 using a CRISPR-P online website, P1 having SEQ ID NO.3 and P2 having SEQ ID NO.4 for two terminals; pasting the sequence of the designed primer fragment and a partial sequence of a sgRNA backbone on a vector pCas9 into an RNA fold Web server for RNA structure prediction, such that a primer fragment P3: SEQ ID NO.5 is obtained; adding a linker sequence onto the primer fragment P3: SEQ ID NO.5 to obtain a primer fragment P4: SEQ ID NO.6 and its reverse complementary sequence P5: SEQ ID NO.7: synthesizing the primer fragment P4 and its reverse complementary sequence P5; annealing the obtained primer fragment P4 and its reverse complementary sequence P5 with a PCR amplifier to obtain an annealed product; and cloning the annealed product into the vector pCas9.

15. The method of producing a transgenic rice plant of claim 14, wherein the primers for two terminals have the sequences TABLE-US-00007 SEQ ID NO. 3: 5-TGAACGCAGAACCGAACAC-3; and SEO ID NO. 4: 5-TCCACGGGCCACCATAC-3.

16. The method of producing a transgenic rice plant of claim 14, wherein the primer fragments have the sequences TABLE-US-00008 SEQ ID NO. 5: 5-GCTCGGGGAACCGCCGCA-3; SEQ ID NO. 6: 5-GCTCGGGGAACCGCCGCAGTTTTAGAGCTATGCTGAAAAGCATAG CAAGTTAAAATAAGGCTAGTCCGTTATCAACTTGAAAAAGTGGCACCG AGTCGGTGC-3; and SEQ ID NO. 7: 5-GCACCGACTCGGTGCCACTTTTTCAAGTTGATAACGGACTAGCCTT ATTTTAACTTGCTATGCTTTTCAGCATAGCTCTAAAACTGCGGCGGTTC CCCGAGC-3.

17. The method of producing a transgenic rice plant of claim 13, further comprising: transferring an expression vector for a rice gene OsNia3 pCUBi1390-GFP-OsNia3 into Agrobacterium tumefaciens; and transferring the Agrobacterium tumefaciens into the homozygous knockout mutant nia3.

18. The method of producing a transgenic rice plant of claim 17, further comprising: producing the expression vector for the rice gene OsNia3 pCUBi1390-GFP-OsNia3, by: designing an upstream primer P6: SEQ ID NO.8 and a downstream primer P7: SEQ ID NO.9 which carry restriction enzyme cleavage sites Hand III and BamH I that are completely encoded at the amplification position; amplifying an over-expression vector pCUbi1390-GFP-Nia3 by PCR; and cloning cDNA of the rice gene OsNia3 to the enzyme cleavage sites Hand III and BamH I in a binary expression vector pCUBi1390-GFP.

19. The method of producing a transgenic rice plant of claim 18, further comprising: producing the over-expression vector pCUbi1390-GFP-Nia3, by: extracting total RNA of rice leaves; designing primers P1 having SEQ ID NO.3 and P2 having SEQ ID NO.4 for two terminals according to a full-length sequence of the rice gene OsNia3; transcribing the total RNA of rice leaves to synthesize a first chain of cDNA; amplifying the first chain of the cDNA by PCR; extracting the cDNA using a TaKaRa MiniBEST Agarose Gel DNA Extraction Kit; and ligating the cDNA with an over-expression vector pCUbi1390-GFP.

20. The method of producing a transgenic rice plant of claim 19, wherein the primers for two terminals have the sequences TABLE-US-00009 SEQ ID NO. 3: 5-TGAACGCAGAACCGAACAC-3; and SEQ ID NO. 4: 5-TCCACGGGCCACCATAC-3.

21. The method of producing a transgenic rice plant of claim 18, wherein the upstream and downstream primers have the sequences TABLE-US-00010 SEQ ID NO. 8: 5-TCTGCACTAGGTACCTGCAGATGGCTGCTTCCGTGC-3; and SEQ ID NO. 9: 5-ATGGATCCGTCGACCTGCAGGAACACGATGAAAGAATTGGCC-3.

Description

DESCRIPTION OF THE EMBODIMENTS

[0031] In order to make the technical means, creative features, goals and effects achieved by the present invention easy to understand, the present invention will be further explained with specific embodiments.

[0032] The gene OsNia3 of the rice nitrate reductase NIA3 protein is applied to a rice transgenic plant, and the specific steps are as follows.

[0033] 1) Extraction of Total RNA

[0034] The rice variety Kitaake is selected as an extracting material of RNA, rice seedlings are allowed to grow to about 20 d, then the leaves are taken and cryopreserved with liquid nitrogen, thereafter some of the leaves cryopreserved with liquid nitrogen are taken and crushed with a mortar, the total RNA of the rice leaves is extracted according to the instructions of a RNAprep pure Plant Kit, then the concentration and mass of the total RNA are detected by using a NanoDrop microvolume spectrophotometers and fluorometer, and the integrity of the total RNA is detected with 1% agarose gel electrophoresis.

[0035] 2) Clone of Rice Gene OsNia3

[0036] The mRNA sequence of the Nia1 gene is searched from NCBI (http://www.ncbi.nlm.nih.gov/), then it is found that the mRNA of the Nia1 gene is highly homologous with the mRNA of the [NADH]1-like (LOC4345798) (with the homology of 99%), the [NADH]1-like (LOC4345798) is named OsNia3 in subsequent experiments, and primers P1: SEQ ID NO.3 and P2: SEQ ID NO.4 for two terminals are designed according to the full-length sequence of the rice OsNia3;

TABLE-US-00004 SEQ ID NO. 3: 5-TGAACGCAGAACCGAACAC-3; SEQ ID NO. 4: 5-TCCACGGGCCACCATAC-3;

[0037] the total RNA of rice leaves obtained in the step 1) is transcribed to synthesize a first chain of the cDNA, PCR amplification is conducted by taking the first chain of the cDNA as a template, extraction is conducted by using a TaKaRa MiniBEST Agarose Gel DNA Extraction Kit, the gene of interest is ligated with an over-expression vector pCUbi1390-GFP to obtain an over-expression vector pCUbi1390-GFP-Nia3, and then sequencing is conducted to obtain the cDNA sequence SEQ ID NO.1 of the rice gene OsNia3 and the amino acid sequence SEQ ID NO.2 of the rice protein NIA3 encoded by the rice gene OsNia3.

[0038] 3) Construction of Rice Gene OsNia3 Knockout Vector pCas9-OsNia3

[0039] A primer fragment is designed according to the full-length cDNA sequence of the rice gene OsNia3 obtained in the step 2) by using a CRISPR-P online website (http://cbi.hzau.edu.cn/cgi-bin/CRISPR), then the sequence of the designed primer fragment and the partial sequence of a sgRNA backbone on a vector pCas9 are together pasted into a RNA fold Web server for RNA structure prediction, such that a suitable primer fragment P3: SEQ ID NO.5 is obtained, then a linker sequence is added onto the primer fragment P3: SEQ ID NO.5 to obtain a primer fragment P4: SEQ ID NO.6 and its reverse complementary sequence P5: SEQ ID NO.7, the primer fragment P4 and its reverse complementary sequence P5 are sent to a company for synthesis, then the obtained primer fragment P4 and the reverse complementary sequence P5 are bound by annealing with a PCR amplifier to obtain an annealed product, finally the annealed product (i.e., the 18 bp sequence of the rice gene OsNia3) is cloned into the vector pCas9, and sequencing is conducted for identification to ensure that the sequence of the gene of interest is correct, thereby obtaining the rice gene OsNia3 knockout vector pCas9-OsNia3;

TABLE-US-00005 SEQ ID NO. 5: 5-GCTCGGGGAACCGCCGCA-3; SEQ ID NO. 6: 5-GCTCGGGGAACCGCCGCAGTTTTAGAGCTATGCTGAAAAGCATAG CAAGTTAAAATAAGGCTAGTCCGTTATCAACTTGAAAAAGTGGCACCGAG TCGGTGC-3; SEQ ID NO. 7: 5-GCACCGACTCGGTGCCACTTTTTCAAGTTGATAACGGACTAGCCTT ATTTTAACTTGCTATGCTTTTCAGCATAGCTCTAAAACTGCGGCGGTTCC CCCGAGC-3.

[0040] 4) Construction of Expression Vector pCUBi1390-GFP-OsNia3 for Rice Gene OsNia3

[0041] According to the cDNA sequence SEQ ID NO.1 of the rice gene OsNia3, an upstream primer P6: SEQ ID NO.8 and a downstream primer P7: SEQ ID NO.9 which carry restriction enzyme cleavage sites Hand III and BamH I that are completely encoded at the amplification position, are designed;

TABLE-US-00006 SEQ ID NO. 8: 5-TCTGCACTAGGTACCTGCAGATGGCTGCTTCCGTGC-3; SEQ ID NO. 9: 5-ATGGATCCGTCGACCTGCAGGAACACGATGAAAGAATTGGCC-3;

[0042] after PCR amplification is conducted by taking the over-expression vector pCUbi1390-GFP-Nia3 obtained in the step 2) as a template, the cDNA of the rice gene OsNia3 is cloned to the enzyme cleavage sites Hand III and BamH I in the binary expression vector pCUBi1390-GFP, and sequencing is conducted for identification to ensure that the reading frame of a coding region in the expression vector is correct, thereby obtaining the rice gene OsNia3 expression vector pCUBi1390-GFP-OsNia3.

[0043] 5) Genetic Transformation of Rice

[0044] The rice gene OsNia3 knockout vector pCas9-OsNia3 obtained in the step 3) is transferred into Agrobacterium tumefaciens and further transferred into the japonica rice variety Kitaake, and the transgenic plant is identified by PCR and sequencing to obtain a homozygous knockout mutant nia3 having mutation of the OsNia3 gene and no backbone of the vector, wherein the rice mutant nia3 shows a reduced plant height and a shortened growth period;

[0045] the expression vector pCUBi1390-GFP-OsNia3 of the rice gene OsNia3, as obtained in the step 4), is transferred into Agrobacterium tumefaciens and further transferred into the homozygous knockout mutant nia3, and the transgenic plant is verified by PCR and RT-PCR to obtain a homozygous OsNia3 over-expression line which shows an increased plant height and a prolonged growth period.