Plant dwarfing related protein ga2ox and its coding gene and application
A coding gene and gene technology, applied in plant dwarfing-related protein GA2ox and its coding gene and application fields, can solve the problems of high pruning frequency, long improvement cycle, premature aging, etc., and achieve the effect of not being easy to lodging and reducing the frequency of pruning
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Embodiment 1
[0035] Embodiment 1, the discovery of GA2ox protein and its coding gene
[0036] 1. The RNA of tall fescue was extracted by SDS method.
[0037] 2. Using RNA with good integrity and no contamination as a template, use M-MLV enzyme (purchased from Promage) to reverse transcribe the RNA into cDNA.
[0038] 3. Cloning of intermediate fragments
[0039] Primers (F1 and R1; M=A / C, S=G / C, V=A / G / C) were designed according to the homologous conserved sequence of GA2ox, and the cDNA of tall fescue was used as a template for PCR amplification. Recycled and sequenced to obtain a 244bp intermediate fragment.
[0040] F1 (5' primer): 5'-MTS GGG TGG VTC GAG TAC-3';
[0041] R1 (3' primer): 5'-GGT AGT GGT TCA SSC GGA-3'.
[0042] 4. Cloning of 3'-end
[0043] A primer 3'GSP I (gene-specific primer) was designed according to the sequencing results of the intermediate fragment. The primer sequence was 5'-CAC GTC CAC CGC GCT GAG AGA C-3'. In order to improve product specificity, another prim...
Embodiment 2
[0064] Embodiment 2, the acquisition and identification of transgenic plants
[0065] 1. Construction of recombinant plasmid pCAMBIA1302-GA2ox
[0066] See the construction flow chart figure 1 .
[0067] 1. Extract the total RNA of tall fescue and reverse transcribe it into cDNA.
[0068] 2. Using the cDNA in step 1 as a template, carry out PCR amplification with a primer pair consisting of GA2ox_5' and GA2ox_3' to obtain a PCR amplification product (the target sequence is the open reading frame of the GA2ox gene with the stop codon removed).
[0069] GA2ox_5': 5'-ACT AGT ATG GTG GTG CTC GCG AAG-3';
[0070] GA2ox_3': 5'-ACT AGT GGA CCG GTG GTG GTG GCC-3'.
[0071] The 1.0% agarose gel electrophoresis of the PCR amplification product is shown in figure 2 .
[0072] 3. Insert the PCR amplification product in step 2 into the pMD18-T simple vector (purchased from TaKaRa Bioengineering Company) to obtain the recombinant plasmid pMD18-Tsimple-GA2ox.
[0073] 4. The recombin...
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