Tobacco PDS gene fragment-containing cucumber mosaic virus RNA2 attenuated mutant type plasmid vector and application thereof
A technology of cucumber mosaic virus and plasmid vector, applied in the fields of plant virology and molecular biology, can solve the problems of easy loss of resistance of disease-resistant varieties and long breeding cycle
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Embodiment 1
[0039] Example 1. Intermediate vector pCB301-CMV Fny2 -build of del2b:
[0040] According to CMV Fny Infectious clone RNA2 sequence, design primers Fny2-del2b 3'-BSST-2662-F and Fny2-del2b 3'-B-2661-R, the PCR amplification product of this pair of primers is to construct CMV visible attenuated virus Linearized intermediate vector for mutant plasmid vectors.
[0041] in CMV Fny Infectious cloning plasmid pCB301-Fny2 was used as a template (CMV Fny The construction of the invasive cloning plasmid pCB301-Fny2 refers to "Agrobacterium-mediated CMV invasive cloning and construction of 2b deletion mutants", Yao Min et al., Chinese Agricultural Sciences, 2011, 44(14): 3060-3068) , under the action of PrimeSTAR HS DNA Polymerase (Takara), carry out reverse PCR amplification, the primer pair is Fny2-del2b 3'-BSST-2662-F and Fny2-del2b 3'-B-2661-R; PCR conditions: 98 Denaturation at ℃ for 10s, annealing at 55°C for 5s, extension at 72°C for 8min, 7 cycles; denaturation at 98°C for ...
Embodiment 2
[0045] Cloning of embodiment 2.PDS partial fragments:
[0046] Using TransZol Up (TransGen) to extract the total RNA of Nicotiana benthamiana plant at the 6-leaf stage, under the action of ReverseTranscriptase M-MLV (Takara), carry out reverse transcription reaction, the reverse primer is PDS-BamH1-531-R, the reaction conditions: in Denaturation at 80°C for 3 minutes without adding enzymes; reaction at 42°C for 1.5 hours after adding reverse transcriptase;
[0047] Then use the reverse transcription product cDNA as a template, and carry out PCR reaction under the action of 2×Es Taq MasterMix (Dye) (CWBIO), the primer pair is PDS-Sma1-333-F and PDS-BamH1-531-R; PCR conditions : Pre-denaturation at 94°C for 2min; denaturation at 94°C for 30s, annealing at 53°C for 30s, extension at 72°C for 10s, 30 cycles; extension at 72°C for 2min; storage at 4°C; the PCR product is a 200bp conserved sequence fragment in N. benthamiana PDS. The PCR product was recovered by a DNA recovery kit ...
Embodiment 3
[0049] Example 3. pCB301-CMV Fny2 -PDS-Q build:
[0050] The intermediate vector pCB301-CMV Fny2 -del2b was double digested with BamH I and Sma I, and the digested product was recovered by a DNA recovery kit; the 200bp conserved sequence fragment in Nicotiana benthamiana PDS was double digested with BamH I and Sma I, and the digested product was recovered by a DNA recovery kit . The intermediate vector pCB301-CMV with the same double digestion Fny2 -del2b and PDS fragments at T 4 Under the action of DNA ligase, ligate overnight at 16°C; transform the competent cells of Escherichia coli DH5α with the ligated products, coat LB plates with 100 μg / mL kanamycin, and confirm positive clones by colony PCR screening, enzyme digestion identification and DNA sequencing pCB301-CMV Fny2 -PDS-Q.
[0051] Result analysis: After the ligation product was transformed, the product was first screened by colony PCR, and the plasmid was extracted for enzyme digestion identification. BamH I a...
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