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Identification of parents of F1 hybrids through SSR profiling of maternal and hybrid tissue

机译:通过对母体和杂种组织进行SSR分析来鉴定F1杂种的亲本

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The ability of maternally inherited pericarp tissue to be useful as a source from which molecular marker profiles of the inbred parents can be generated was investigated, using pericarp and kernel tissue from reciprocal crosses of five maize (Zea mays L.) hybrids and their parental inbred lines. Genotypes were examined using ten SSR loci for each hybrid and their parents. SSR loci were selected that could distinguish between all parental genotypes for each hybrid. One hundred SSR profiles were generated using pericarp tissue (10 hybrids x 10 SSR loci). Ninety-four percent of amplifications from pericarp tissue resulted in the SSR profile of the female inbred parent of the hybrid. Five percent of the profiles showed both female and male contributions to the hybrid and would therefore immediately lead to suspicions that pericarp tissue was contaminated with other tissues from the kernel. One percent showed only the contribution of the male parent, possibly due to a failure of SSRs to always report all heterozygote alleles. These results show that SSR technology can be reliably used to genotype the female parent of a maize hybrid and thus to also determine the profile of the male parent from comparison of hybrid and female parent profiles.
机译:利用来自五个玉米(Zea mays L.)杂种及其亲本近交的互交后代的果皮和果仁组织,研究了母本遗传的果皮组织用作产生近交亲本分子标记图谱来源的能力。线。使用每个杂种及其亲本的十个SSR基因座检查基因型。选择了可以区分每种杂种的所有亲本基因型的SSR基因座。使用果皮组织(10个杂种x 10个SSR基因座)生成了一百个SSR谱。来自果皮组织的94%的扩增导致杂种的雌性近交亲本的SSR谱。 5%的轮廓显示出雌性和雄性对杂种的贡献,因此将立即引起怀疑果皮组织被籽粒中的其他组织污染。 1%的人仅表现出男性亲本的贡献,这可能是由于SSR无法始终报告所有杂合子等位基因所致。这些结果表明,SSR技术可以可靠地用于对玉米杂交种的雌性亲本进行基因分型,从而通过比较杂种和雌性亲本来确定雄性亲本。

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