A kind of plant anther-specific promoter pchf15 and its application
An anther-specific and promoter technology, applied in the fields of genetic engineering and molecular biology, to achieve precise expression levels
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Embodiment 1
[0041] Example 1: Acquisition of rice anther-specific promoter PCHF15
[0042] 1. Extraction of rice genomic DNA
[0043] Rice genomic DNA was extracted according to the method instructions of the Plant DNA Isolation Kit (Chengdu Fuji Biotechnology Co., Ltd.). The genome was derived from fresh leaves of rice Nipponbare variety. The extracted genomic DNA was aliquoted and stored at -20°C for later use.
[0044] 2. Design PCR PCHF15 primers
[0045] Primers were designed using the Gibson Assembly method, and the amplified product was inserted into the NcoI and HindIII restriction sites of the 1300GUSplus vector. Primers for amplifying the PCHF15 gene are shown in the sequences SEQ ID NO.2 and SEQ ID NO.3. Among them, about 15 nucleotide sequences at the 5' ends of the upstream and downstream primers were repeated with the corresponding connection positions of the vector to facilitate Gibson Assembly connection.
[0046] PCR reaction system (100μL):
[0047] DNA template: 3...
Embodiment 2
[0058] Example 2: Construction of the recombinant expression vector 1300gus-PCHF15 of the promoter PCHF15
[0059] See the build process figure 1 , Insert the amplified product of Example 1 into the 1300GUSplus vector NcoI and HindIII restriction sites.
[0060] The primers SEQ ID NO.2 and SEQ ID NO.3 amplify the PCR product and recover the product of about 2000bp by 1% agarose gel electrophoresis. The vector 1300GUSplus was digested with NcoI and HindIII, and the linearized vector was recovered.
[0061] 2X ligation kit ligates promoter PCHF15 to 1300GUSplus, 10μL system is as follows:
[0062] 2.5 μL PCHF15PCR product (50ng)
[0063] 2.5μL enzyme-cut carrier (100ng)
[0064] 5μL Ligation Mix
[0065] Ligation procedure: 50°C 60min.
[0066] Transformation: Take 5 μL of the above ligation product to transform Escherichia coli competent cells by electroporation. Select positive clones for sequencing, the results are as follows image 3 shown. Named 1300gus-PCHF15.
[0...
Embodiment 3
[0068] Example 3: Construction of recombinant expression vector DX2182-PCHF15 containing PCHF15 promoter sequence
[0069] refer to figure 2 The construction process of this method is to construct the recombinant cloning vector pGEM-PCHF15 containing the PCHF15 promoter sequence first, and then construct the recombinant expression vector DX2182-PCHF15 containing the PCHF15 promoter sequence based on it.
[0070] 1. Construction of recombinant cloning vector pGEM-PCHF15 containing PCHF15 promoter sequence
[0071] With reference to the method of Example 1, the primer pair shown in sequence SEQ ID NO.2 and SEQ ID NO.3 is amplified with sequence such as the primer pair shown in SEQ ID NO.5 and SEQ ID NO.6. The obtained amplification product was connected to the pGEM-T vector, and the operation steps were carried out according to the instructions of the pGEM-T vector produced by Promega Company to obtain the recombinant cloning vector pGEM-PCHF15. Transform Escherichia coli com...
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