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Sensitive mutant detection by concentrating mutant DNA with allele-specific capture and its application to analysis of contaminated grains in rice

机译:用等位基因特异性捕获浓缩突变DNA敏感突变体检测及其在水稻中分析污染粒度的应用

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摘要

Many techniques for SNP analysis have been developed, but most of these techniques are not so sensitive to be used for detection of mutants in a large number of plants. Although some highly sensitive methods of SNP analysis have been reported, they are costly. In the present study, a method for concentrating mutant DNA was examined for sensitive detection of an SNP allele in a bulked DNA sample. PCR products of mutant alleles were captured by biotin-labeled oligonucleotide conjugated with streptavidin-coated magnetic beads. By repeated captures of each strand and combining both strands, mutant alleles with a concentration of 1/1000 in wild-type alleles were detectable by CAPS or dCAPS analysis. Indirect capture of a mutant allele was possible, but efficiency was slightly lower than that of the direct capture. The developed method was applied to detection of contamination of rice grains by grains of a different cultivar. Possible applications of this method are discussed.
机译:已经开发出许多SNP分析技术,但大多数这些技术对用于检测大量植物中的突变体是如此敏感。 虽然已经报告了SNP分析的一些高度敏感的方法,但它们昂贵。 在本研究中,检查用于浓缩突变体DNA的方法,用于敏感的DNA样品中的SNP等位基因的敏感检测。 通过与链霉蛋白涂覆的磁珠缀合的生物素标记的寡核苷酸捕获突变等位基因的PCR产物。 通过每条链的重复捕获并将两条链组合,通过帽或DCAP分析可检测野生型等位基因中浓度为1/1000的突变等位基因。 间接捕获突变等位基因,但效率略低于直接捕获。 应用了不同品种谷物的粒子污染的开发方法。 讨论了这种方法的可能应用。

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