Marker primer and detection kit for detecting SNP mutation of rape ALS gene and application thereof
A technology of detection kits and marker primers is applied in the field of molecular genetic breeding of crops, which can solve the problems of decreased resistance effect of materials, long years of resistance breeding and high production costs, and achieves elimination of aerosol pollution, high specificity and high cost. Effect
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Embodiment 1
[0035] Example 1: Design of SNP molecular markers for detection of mutations at the Pro182Leu site of rapeseed ALS1 gene
[0036] DS3 is a new germplasm of rapeseed that is highly resistant to sulfonylurea herbicides, which we created through two rounds of EMS mutagenesis and years of directional selection. ) (Address: No. 3, Yard No. 1, Beichen West Road, Chaoyang District, Beijing, postcode: 100101, and the deposit number is CGMCC No. 14298). The germplasm has important application value in the breeding of herbicide-resistant rapeseed varieties, and has been introduced and applied by more than 20 rapeseed breeding units across the country for the breeding of herbicide-resistant rapeseed varieties. Through gene cloning and functional verification, it was found that there were two ALS gene mutations in DS3, namely Pro182Leu in the amino acid sequence of rapeseed ALS1 and Trp556Leu in the amino acid sequence of ALS3. In the process of breeding herbicide-resistant varieties usi...
Embodiment 2
[0046] Example 2: Establishment of KASP Molecular Marker Detection System for Pro182Leu Resistance Mutation Site of Rapeseed ALS1 Gene
[0047] Using the two sets of KASP primers designed above, select DS3 containing the resistance mutation site and its progeny derivatives, N131 and other rapeseed varieties (lines) without the resistance mutation site, and the F 1 A total of 30 rapeseed materials were generated, and the KASP reaction was verified on the LGCSNPline genotyping platform. The specific operation steps are as follows:
[0048] 1. Extraction of Rapeseed Genomic DNA:
[0049] Take an appropriate amount of leaf tissue of rape varieties (lines) to be tested, and use the CTAB method to extract whole-genome DNA (Murray MG, et al., Nucleic Acids Research, 1980, 8(19): 4321-4326). The quality of the extracted DNA was detected by agarose electrophoresis and Nanodrop2100 respectively, and it was found that the extracted genomic DNA all met the relevant quality requirements,...
Embodiment 3
[0082] Example 3: Validation of the detection effect of the molecular marker KBnALS1_1968545A in the isolated population
[0083] To verify the KASP molecular marker KBnALS1_1968545A in F 2 For the detection effect of the BnALS1 gene resistance mutation site (C / T) genotype of DS3 in the population, we used the MICMS double-low restorer lines N340 and N341 (Pu Huiming et al., Chinese Journal of Petroleum Science, 2011, 33 (1): 15-19) is the female parent, and the resistant germplasm DS3 is the male parent. Two hybrid combinations (N340×DS3 and N341×DS3) are arranged at the flowering stage of rape, F 1 Bagging selfing gets F 2 population, with the molecular marker KBnALS1_1968545A vs. F 2 The genotype of the BnALS1 gene resistance mutation site (C / T) of individual plants in the population was detected. Specific steps such as DNA extraction, PCR reaction, and KASP detection are the same as in Example 2 (using the detection kit of Example 2). Genotyping results showed that in ...
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