Double-stranded RNA molecule for targeted silence of phytophthora capsici cellulose synthase 3 and application of double-stranded RNA molecule
A technology of cellulose synthase and Phytophthora capsici, which is applied in the field of agricultural biology, can solve problems such as undiscovered plant diseases, and achieve the effects of delaying the emergence of drug resistance, inhibiting infection, and reducing the amount of use
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Embodiment 1
[0031] Example 1 Source of double-stranded RNA molecule for inhibiting the expression of Phytophthora capsicum cellulose synthase 3 gene involved in the present invention
[0032] (1) The sequence of the double-stranded RNA molecule of the present invention is derived from the cDNA of PcCesA3. The cDNA sequence of PcCesA3 was derived from the gene numbered JX905357 in the database (GenBank) of Phytophthora capsici.
[0033] (2) A total of 555 base sequences numbered JX905357, Nos. 3005-3559 in the cDNA sequence database (GenBank) of PcCesA3 were selected as the sequence of the double-stranded RNA molecule involved in the present invention. Its sense strand sequence is shown in sequence 1 in the sequence listing, and its antisense strand is shown in sequence 2 in the sequence listing.
[0034](3) The above sequences were compared with the genome sequences (NCBI) of common hosts of Phytophthora capsicum such as tobacco, tomato, and pepper, respectively, to detect the possibilit...
Embodiment 2
[0035] Example 2 Preparation of double-stranded RNA molecule of the present invention
[0036] (1) Double-stranded RNA expression plasmid L4440 contains two bidirectional T7 promoters, which can be transcribed in RNaseⅢ-deficient Escherichia coli to generate double-stranded RNA. The target fragment was amplified by PCR, and the amplification primers were shown in Table 1. Using the cDNA of Phytophthora capsici standard strain LT1534 (doi: 10.1094 / MPMI-02-12-0028-R) as a template, the amplified fragment was inserted between the two T7 promoters of the L4440 plasmid by enzymatic ligation (Between the recognition sites of Sac II and Xba I enzymes), after verification by PCR and sequencing, a plasmid capable of expressing double-stranded RNA molecules is obtained.
[0037] Table 1 Sequences of primers for constructing double-stranded RNA molecules
[0038]
[0039] (2) Transform the plasmid capable of expressing double-stranded RNA molecules obtained in step (1) into RNaseIII...
Embodiment 3
[0046] Example 3. Evaluation of disease resistance of plants to which the double-stranded RNA molecule of the present invention is applied to Phytophthora capsici
[0047] In this patent, a. double-stranded RNA molecules are directly sprayed on the surface of the host plant (in vitro leaves of Nicotiana benthamiana and pepper) for 1 day and then inoculated with Phytophthora capsicum zoospores, and the diameter of leaf lesions is observed and measured after 3 days. b. First irrigate the root plants with double-stranded RNA molecules, and then inoculate the pepper seedlings with zoospores in a simulated field environment to determine the disease index of the pepper seedlings. According to the above two evaluation methods, the effect of double-stranded RNA on the growth, development and pathogenicity of Phytophthora capsicum was clarified.
[0048] Phytophthora capsicum BYA5 (isolated by the Laboratory of Fungicide Pharmacology and Pathogen Resistance of China Agricultural Univer...
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