Verticillium dahliae ADP-ATP carrier protein pathogenesis key target gene as well as interference vector and application thereof
A technology of Verticillium dahliae and carrier protein, which is applied in the key target gene of ADP-ATP carrier protein disease course of Verticillium dahliae and its interference carrier and application field, which can solve the problems of less research and improve disease resistance Effect
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Embodiment 1
[0048] Example 1 Screening of ADP-ATP carrier protein disease course key target genes of Verticillium dahliae
[0049] 1. Experimental method
[0050] 1.1 Construction of VIGS interference vector
[0051] In order to obtain the fragment with the best interference effect on the target gene, according to the cDNA sequence of Verticillium dahliae ADP, ATPcarrierprotein (VDAG_07535.1), design specific primers (Table 1), with BamHI and EcoRI restriction sites at both ends of the primers , PCR amplification was performed on the target gene, and the PCR product was detected by 1% agarose gel electrophoresis. Then, the recovered fragments were ligated into TRV2 vectors, verified by enzyme digestion and sequencing, and the verified plasmids were transformed into Agrobacterium GV3101.
[0052] Table 1 Primer information for different segments of AACP
[0053]
[0054] Note: The bolded part is the restriction site.
[0055] 1.2 VIGS transformation method
[0056] Agrobacterium si...
Embodiment 2
[0072] Construction and plant transformation of embodiment 2Gateway interference vector
[0073] 1. Experimental method
[0074] 1.1 Construction of stable genetic vector
[0075] In order to obtain stably inherited Nicotiana benthamiana containing the target gene dsRNA, according to the change of the tobacco disease index of transient transformation in Example 1, three DNA segments were selected (the nucleotide sequences are respectively SEQIDNo.1, SEQIDNo.3, SEQIDNo. 5), redesign the primers containing part of the BP sites at both ends, and then use attb primers to amplify (Table 3) for the construction of Gateway interference vectors. According to the BP reaction, the target sequence was ligated into pDONR207; then it was constructed into pK7GWIWG2(I),0 by the LR reaction. Finally, the constructed vector was transformed into Agrobacterium LBA4404.
[0076] Table 3 Gateway interference primer information
[0077]
[0078] 1.2 Plant Transformation
[0079] Cut the ste...
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