Turnip yellow mosaic virus (TYMV)-induced cruciferous endogenous gene silencing method and application thereof
A technology of cruciferous and endogenous genes, which is applied in the field of plant bioengineering, can solve the problems of low infection efficiency and difficulty in constructing TYMV vectors, and achieve the effects of improving infection efficiency, improving silencing efficiency, and reducing plant damage
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Embodiment 1
[0060] Embodiment 1 A kind of TYMV virus-induced cruciferous endogenous gene silencing method
[0061] (1) Cloning and sequencing verification of PDS gene
[0062] The PDS gene sequences of two cabbage crops, non-heading cabbage and Chinese cabbage, were searched through the NCBI database. The cDNA was used as the template for PCR amplification, and the target band was cut under UV light to recover the target fragment, connected to the blunt-zero vector (purchased from TransGenBiotech), and chemically transformed into Trans-T1 Escherichia coli, LB plate containing ampicillin 37 Cultivate overnight at ℃, pick a single colony for PCR identification, extract and sequence the positive plasmid, and obtain the full-length sequence of the PDS gene.
[0063] (2) Vector construction and mass extraction of plasmids
[0064] Select the appropriate 40bp sequence and its reverse complement, and the selection principle is as follows image 3 and Figure 4 Shown: the 2-4 bases are TGA, T...
Embodiment 2
[0069] Example 2 Phenotype and PCR detection after silencing
[0070] 15-17 days after the bombardment of the gene gun, the seedlings appeared photobleaching, such as Image 6 (A. Infection with non-heading Cruciferae pTY-s; B. Infection with non-heading Brassicaceae pTY-PDS; C. Infection with non-heading Cruciferae pTY-s; D. Infection with Brassicaceae pTY-s -PDS infestation) and Figure 7 (Nonheading Cruciferae causes silent phenotypes in different organs, 1, Aheading Cruciferae uninfected 2 Aheading Cruciferae pTY-PDS infection 3 Aheading Cruciferae pTY-s infection ), the results showed that the PDS gene was effectively silenced in multiple organs of leaves, stems, roots, pedicels, and fruit pods. To further verify the effect of gene silencing at the molecular level, PCR detection was performed. The total RNA of the seedlings was extracted and reverse transcribed to obtain cDNA, which was first identified by PCR with CP-F / R, and detected by 2% agarose gel electrophoresis...
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