Soybean Salt-Inducible Artificial Synthetic Promoter ap2 and Its Application
A technology of artificial synthesis and promoter, applied in the field of promoters, which can solve the problems of low expression activity and low specificity
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Embodiment 1
[0015] The design of embodiment 1 soybean salt-inducible artificial synthetic promoter
[0016] The applicant's previous research found that the 300bp (P4) promoter region of the GmST1 gene of Shengdou No. 9 was the basic promoter, and the genomic DNA of Shengdou No. 9 was extracted by CTAB method, and the extracted genomic DNA was diluted to 100ug / ul for amplification Promoter template. Using the high-fidelity enzyme HIFI (Takara) to amplify the target fragment and sequence it, and simultaneously synthesize six tandem repeats of GT1GMSCAM4 cis-element nucleic acid sequences that respond to salt stress, and connect the two sequences to construct a synthetic promoter, named It is a soybean salt-inducible artificially synthesized promoter AP2, and the nucleotide sequence of the promoter is shown in SEQ ID No.1.
Embodiment 2
[0017] Example 2 Using Arabidopsis protoplast transient transformation technology to verify that the salt-inducible artificial promoter AP2 in soybean is induced by salt.
[0018] 2.1 Construction of pGmST1::BM2::P4::pGreenII-0800LUC vector
[0019] 2.1.1 Cloning of the AP2 promoter fragment containing restriction sites
[0020] The dual fluorescent reporter vector pGmST1::BM2::P4::pGreenII-0800LUC of the soybean salt-inducible artificial promoter AP2 was constructed by double enzyme digestion-ligation method. Using the restriction site analysis on Primer5 AP2 and comparing it with the multiple cloning site on pGreen II-0800LUC, the available restriction sites were kpnI and SpeI.
[0021] PCR amplification was carried out using primers containing enzyme cleavage sites in AP2.
[0022] The reaction system for high-fidelity enzyme HIFI amplification is as follows (20 μl system):
[0023]
[0024]
[0025] The amplification conditions are as follows:
[0026]
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