Tobacco mosaic virus gene fragment, attenuated vaccine, preparation method and application thereof for efficient production of siRNA
A technology of tobacco mosaic virus and gene fragment, applied in the field of plant antiviral genetic engineering, can solve the problems of inconvenient popularization and use of inoculation and propagation, limited transgenic tobacco, and inability to promote planting, etc. Injury, delay plant disease effects
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Embodiment 1
[0049] Construction of embodiment one multi-site TVBMV attenuated mutant
[0050] 1. Construction of an infectious clone of tobacco vein mosaic virus
[0051] Tobacco vein mosaic virus RNA was used as a template for reverse transcription with random primers. According to the existing restriction enzyme map of the whole genome of tobacco vein mosaic virus, it can be amplified in three parts, and assembled into a TVBMV full-length cDNA clone after enzyme digestion. First, the 35S promoter was fused to the upstream of the fragment from the 5' untranslated region of TVBMV to the Nru I restriction site of the HC-pro gene by Overlap-PCR, and the inventor named the fragment p35S-HC; PCR amplified HC- The fragment between the pro gene Nru I restriction site and the 6K2Xho I restriction site, the inventor named the fragment pHC-6K2; PCR amplification of the 6K2Xho I restriction site to the poly(A) tail Fragment, the inventor named the fragment p6K2-polyA (such as figure 1 shown).
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Embodiment 2
[0069] Example 2 Amplification of Tobacco Mosaic Virus Related Gene Fragments and Construction of Attenuated Vaccine
[0070] 1. Amplification of gene fragments related to tobacco mosaic virus
[0071] Using the cDNA genome of TMV as a template, each gene fragment was amplified by RT-PCR. The examples provided by the present invention are all according to conventional experimental conditions, wherein the primer sequences used are as follows:
[0072] Table 2 TMV gene fragment amplification primer sequence
[0073]
[0074] Primers 1 and 2 were used to amplify the TMV1 gene fragment, primers 3 and 4 were used to amplify the TMV 2 gene fragment, and primers 5 and 6 were used to amplify the TMV 3 gene fragment. The nucleotide sequence of the amplified TMV1 gene fragment is shown in Seq ID No.13, the nucleotide sequence of the TMV 2 gene fragment is shown in Seq ID No.14, and the nucleotide sequence of the TMV 3 gene fragment is shown in Seq ID Shown in No.15.
[0075] The ...
Embodiment 3
[0088] Embodiment three attenuated vaccine inoculation plant
[0089]The single attenuated vaccine vector constructed in Example 2 was transformed into Agrobacterium GV3101. After colony PCR verification, pick a single spot and inoculate it in liquid LB medium containing kanamycin (50 μg / mL), rifamycin (50 μg / mL), and tetracycline (50 μg / mL). Add 500 μL of bacterial liquid to 5 mL of LB medium containing 10 mmol / L 2-(N-morpholine)-ethanesulfonic acid (MES), 20 μmol / L acetosyringone (AS) and the above three antibiotics, at 28 °C Shake culture to logarithmic growth phase. Collect the bacteria by centrifugation and resuspend in 10mmol / L MgCl 2 , 10mmol / L MES, 150μmol / L AS, adjust the concentration so that its OD600 is about 0.5, and let stand at room temperature for 3 hours. Take a 5mL disposable syringe, remove the needle to absorb the Agrobacterium bacteria liquid, and infiltrate from the back of the leaves of ordinary tobacco (5-6 weeks old or 4-6 true leaves). Infiltrate ...
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