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Development of a PCR marker tightly linked to mollis, the gene that controls seed dormancy in Lupinus angustifolius L

机译:开发与mollis紧密连锁的PCR标记,mollis是控制羽扇豆L种子休眠的基因

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Wild plants of Lupinus angustifolius avoid extinction in a drought year by production of seeds with coats that are impermeable to water, preventing germination of a large percentage of the seed in any given year. Domesticated cultivars of this species carry the recessive gene mollis, making the seed coat permeable to water and, in turn promoting good crop establishment in the year of sowing. A dominant microsatellite-anchored fragment length polymorphism candidate marker was identified as being tightly linked to mollis in a population of recombinant inbred lines derived from domesticated and wild-type parents. The candidate marker was excised from the gel, amplified by PCR, sequenced and extended beyond the SSR end of the original MseI-SSR fragment. Two single nucleotide polymorphisms were found within this extended sequence. Specific primers were designed to create a marker 209 bp long. PCR products of these primers run on a single strand conformation polymorphism gel resolved in a co-dominant fashion. This marker will be used in marker-assisted selection for mollis when introgressing wild material into lupin breeding programmes.
机译:干旱年份羽扇豆的野生植物通过产生带有不透水的被膜的种子来避免在干旱年份灭绝,从而防止了任何一年中大部分种子的发芽。该物种的驯化品种携带隐性基因mollis,使种皮可透水,从而在播种之年促进了良好的作物生长。优势微卫星锚定的片段长度多态性候选标记被确定为紧密耦合到从驯养和野生型亲本的重组自交系群体中的mollis。从凝胶上切下候选标记,通过PCR扩增,测序并延伸到原始MseI-SSR片段的SSR末端之外。在该扩展序列内发现了两个单核苷酸多态性。设计特异性引物以产生长209 bp的标记。这些引物的PCR产物在单链构象多态性凝胶上电泳,该凝胶以共同优势方式解析。当将野生材料渗入羽扇豆育种程序时,该标记物将用于标记的软体动物选择。

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