BGIos116 gene and application thereof
A technology for use and transgenic plants, applied in the field of genes, can solve the problems of gene research related to rice differentiation and emergence that have not been seen
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Embodiment 1
[0056] Example 1: PCR amplification of BGIos116 gene and construction of pMD18-T+BGIos116 recombinant vector
[0057] PCR amplification
[0058]Genomic DNA (gDNA) of common wild rice Yuanjiang (Oryza. , respectively design a pair of PCR-specific amplification primers at the beginning and end (upstream primer F1, plus restriction site BamHI and protection base, downstream primer R1, plus restriction site XbaI and protection base). Using the gDNA extracted from Yuanjiang as a template, high-fidelity Ex Taq (TaKaRa, DRR100B) polymerase was used for PCR amplification. As shown in Table 1.
[0059] Table 1 PCR system for target gene amplification
[0060]
[0061] Composition Volume (μl)
[0062]
[0063] Genomic DNA 0.2
[0064] dNTPs (2.5mM) 2
[0065] 10×Ex Buffer (with magnesium ions) 2.5
[0066] Primer F1 (50μM) 1
[0067] Primer R1 (50μM) 1 ...
Embodiment 2
[0085] Embodiment 2: Construction of p6 recombinant vector
[0086] 1) PCR amplification of maize Ubiquitin promoter fragment and construction of pMD18-T+Ubi recombinant vector
[0087] Ubi promoter PCR amplification
[0088] Genomic DNA of maize variety B73 (Zea mays mays cv.B73) was extracted using a plant genomic DNA extraction kit (TIANGEN New Plant Genomic DNA Extraction Kit, catalog number: DP320-02) (http: / / www.maizegdb.org / ), according to the sequence of the promoter in maize B73gDNA, a pair of PCR-specific amplification primers were designed at the beginning and the end respectively (upstream primer F2: GG CTGCAG TGCAGCGTGACCCGGTCGT (SEQ ID NO: 4), plus restriction site Pst I and protection base, downstream primer R2: GG CTGCAG AAGTAACACCAAAC (SEQ ID NO: 5), plus restriction site Pst I and protection bases). Using the above extracted gDNA of corn B73 as a template, high-fidelity Ex Taq (TaKaRa, DRR100B) polymerase was used for PCR amplification. As shown in t...
Embodiment 3
[0155] Embodiment 3: Construction of p6+BGIos116 recombinant vector
[0156] Extract the pMD18-T+BGIos116 plasmid, and recover the BGIos116 gene fragment after digestion with the restriction endonuclease BamHI / XbaI, and extract the p6 plasmid at the same time, and recover the large fragment after digestion with the corresponding restriction endonuclease BamHI / XbaI. The product was ligated, and then the competent cell DH5α was transformed to obtain the recombinant vector p6+BGIos116. Positive clones were screened for PCR detection and then sequenced for confirmation.
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