VIGS-based efficient peach leaf gene silencing method
A gene silencing and leaf technology, applied in the field of peach gene silencing, can solve the problems of instability and low efficiency, and achieve good stability, high silencing efficiency and good effect
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Embodiment 1
[0036] In the following, the phytoene dehydrogenase (PDS) gene was used as the target gene to construct the silencing vectors pTRV2-PpPDS and pCaRNA3-PpPDS, using the method mediated by Agrobacterium tumefaciens, and peach leaves were used as the injection material to explore the temperature, inoculation Effects of seedling age and concentration of inoculum on the silencing efficiency of peach TRV-VIGS and PNRSV-VIGS.
[0037] 1. Construction of silencing vectors pTRV2-PpPDS and pCaRNA3-PpPDS
[0038] (1) Using Peach leaves as materials, total RNA was extracted using EASY spin Plus Plant RNA Rapid Extraction Kit (Aidlab, Beijing), and the RNA concentration and quality were tested by Nanodrop one (Thermo, USA) and gel electrophoresis. reverse transcription kit RT Reagent Kit with gDNA Eraser (TaKaRa, Dalian, China) was used for reverse transcription to obtain cDNA;
[0039] (2) Search for the mRNA sequence of PpPDS in the peach genome, and use primer5 to design primers (prim...
Embodiment 2
[0076] In the following, PpERF98 was used as the target gene, and the same method as in Example 1 was used to conduct a silencing effect experiment.
[0077] Such as Figure 9 As shown, the leaves of peach seedlings were infected by leaf injection. After 25 days of infection, the pCaRNA3 empty vector plants and pCaRNA3-PpERF98 plants were analyzed by qRT-PCR with the pCaRNA3 empty vector plants as the control. Five biological replicates were set up in this experiment, named pCaRNA3-PpERF98#1, pCaRNA3-PpERF98#2, pCaRNA3-PpERF98#3, pCaRNA3-PpERF98#4 and pCaRNA3-PpERF98#5. Using PpTEF2 (Translationenlongation factor2) (Tong et al 2009) as an internal reference gene, the expression level of the target gene PpERF98 was analyzed by qRT-PCR. The results showed that, compared with pCaRNA3 control, the expression levels of pCaRNA3-PpERF98 plants were significantly reduced.
[0078] The sequence list of the above-mentioned genes involved is as follows:
[0079] 1. The CDS of PpERF98...
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