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首页> 外文期刊>Crop Improvement >Microsatellite marker based linkage map construction and mapping of granule bound starch synthase (GBSS) in rice using recombinant inbred lines of the cross Basmati370 / ASD16
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Microsatellite marker based linkage map construction and mapping of granule bound starch synthase (GBSS) in rice using recombinant inbred lines of the cross Basmati370 / ASD16

机译:基于杂交Basmati370 / ASD16的自交系,基于微卫星标记的连锁图谱构建和颗粒结合淀粉合酶(GBSS)的作图

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摘要

In the present investigation, a framework linkage map of Basmati370 / ASD16 recombinant inbred population (F_9) based on microsatellite markers and candidate genes was constructed. Parental polymorphism survey with 471 SSR primer pairs identified about 357 pairs (markers) to be polymorphic between the parental lines. A subset of polymorphic markers was surveyed across the 182 RILs of the mapping population and the marker segregation data was used for the construction of a framework linkage map with 101 loci. Mapping of the candidate genes involved in nitrogen metabolism as well as in grain quality parameters was also taken up. Parental polymorphism survey with 22 candidate gene based primer pairs resulted in successful amplification of only nine primer pairs of which six were polymorphic and 3 were monomorphic between the parents. Three polymorphic primer pairs, each representing the genes encoding glutamate synthase (GOP5), starch branching enzyme (SBE12) and granule bound starch synthase (GBSSI)were surveyed across the RILs. Analysis of the marker segregation data from candidate gene primers resulted in successful mapping of only the gene GBSS (Wx) on the linkage group 6. The GBSS1 marker was positioned between the microsatellite markers RM4923and RM253 in the linkage group 6 of the framework genetic map.
机译:在本研究中,构建了基于微卫星标记和候选基因的Basmati370 / ASD16重组近交种群(F_9)的框架连锁图。用471对SSR引物对进行的父母多态性调查确定,大约357对(标记)在亲本系之间是多态的。在映射人群的182个RIL中调查了多态性标记的子集,并将标记分离数据用于构建具有101个基因座的框架连锁图。还对涉及氮代谢以及谷物质量参数的候选基因进行了定位。父母对22个基于候选基因的引物对进行多态性调查,结果成功扩增了9对引物,其中6对为多态,3对为单态。在整个RIL中对三个多态性引物对进行了研究,每个引物对代表编码谷氨酸合酶(GOP5),淀粉分支酶(SBE12)和颗粒结合淀粉合酶(GBSSI)的基因。分析来自候选基因引物的标记分离数据导致仅成功将基因GBSS(Wx)定位在连锁群6上。GBSS1标记位于框架遗传图的连锁群6中的微卫星标记RM4923和RM253之间。

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