Wheat disease resistance protein taafrk and its related biomaterials and applications
A biomaterial and protein technology, applied in wheat disease-resistant protein TaAFRK and its related biomaterials and applications, can solve the problems of slow progress in breeding of wheat disease-resistant varieties, difficulty in field identification, and shortage
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Embodiment 1
[0100] Embodiment 1, the cloning of wheat disease resistance protein TaAFRK and its coding gene
[0101] 1. Cloning of TaAFRK gene
[0102] The inventors of the present invention isolated and cloned a wheat disease resistance-related protein from sheath blight resistant wheat germplasm CI12633, the amino acid sequence of which is shown in SEQ ID No.2, and named it TaAFRK protein. The gene encoding the TaAFRK protein is named TaAFRK gene, as shown in SEQ ID No.1, and the specific cloning method is as follows:
[0103] Total RNA was extracted from the stems of wheat CI12633 inoculated with wheat sheath blight (Rhizoctonia graminearum strain WK207), and the extracted RNA samples were reverse-transcribed to synthesize the first cDNA Strand cDNA was used as a template for gene cloning, using TaAFRK-OF and TaAFRK-OR as primers, and TOYOBO's high-fidelity TAQ enzyme (KOD FX), KOD FX Buffer, and dNTPs for PCR amplification.
[0104] TaAFRK-OF: 5'-CGCGGTTAGGTAGCTAGCAT-3';
[0105] T...
Embodiment 2
[0122] Example 2, TaAFRK gene expression level is closely related to wheat sheath blight resistance
[0123] 1. Analysis of the expression characteristics of TaAFRK gene in different varieties
[0124] Inoculate wheat sheath blight bacteria (Rhizoctonia graminearum WK207) for two days, and take sheath blight-resistant wheat varieties / lines (CI12633, Shanhong wheat), moderately resistant wheat varieties (Shannong 0431 and Xifeng) and susceptible wheat Wheat leaf sheaths and stem tissues at the inoculation sites of varieties (Wenmai No. 6 and Yangmai No. 9) were quick-frozen in liquid nitrogen. The RNA of the above six wheat materials was extracted with TRIZOL and purified.
[0125] About 5 μg of total RNA from each sample was reverse-transcribed into cDNA according to the procedure of the first-strand cDNA synthesis kit of Tiangen Biochemical Company. The cDNA concentrations of the samples were normalized using the constitutively expressed actin gene as an internal reference....
Embodiment 3
[0130] Example 3. Reverse verification of TaAFRK gene function by cultivating wheat with reduced resistance to sheath blight
[0131] 1. Silencing the TaAFRK gene in wheat CI12633 using virus-mediated gene silencing technology
[0132] 1. The two ends of the DNA fragment shown in nucleotides 1588-1817 of SEQ ID No.1 (ie, SEQ ID No.3) are respectively provided with NheI recognition sequences. After NheI digestion, the DNA fragment (230bp) shown in the 1588-1817th nucleotide of SEQ ID No.1 (ie SEQID No.3) is inserted into the NheI digestion of the BSMV-γ chain by reverse insertion site, to obtain the recombinant vector BSMV-γ: antiTaAFRK, so that the DNA molecule (antiTaAFRK) reverse complementary to the DNA fragment shown in the 1588-1817 positions (ie SEQ ID No.3) of SEQ ID No.1 is γ The vector is driven by a T7 promoter.
[0133] 2. Preparation of transcription reaction solution
[0134] (1) Take the BSMV-α plasmid, digest it with the restriction endonuclease MluI, recover...
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