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大豆F3H基因InDel标记的开发及定位

n InDel marker and mapping of F3H gene in soybean

中文摘要英文摘要

为研究大豆异黄酮合成途径关键酶中F3H基因标记和遗传定位信息,以亲本科丰1号(P1)、南农1138-2(P2)及其衍生的重组自交系(RIL)群体NJRIKY为材料构建遗传连锁图谱, 根据大豆F3H基因序列设计引物进行PCR扩增,获得约2600 bp的片段包括部分5'-UTR,完整的编码区(含三个外显子),两个内含子和部分3'-UTR序列。通过克隆测序分析发现RIL群体两亲本间F3H存在3碱基的InDel,因此开发了与此相关的F3H的InDel标记。通过在RIL群体中扩增检测,将该标记即F3H基因定位于大豆G8-D1b+W连锁群,与大豆花叶病毒抗性基因Rsc-7处于同一连锁群,位于SSR标记Satt698和Sat_351之间,遗传距离分别为38.5和9.4 cM。

In order to develop and map F3H gene, a key enzymes in isoflavone synthesis pathway of soybean, a recombinant inbred line (RIL) population, NJRIKY, which was derived from the cross Kefeng 1 ×Nannong 1138-2, was used to constructed the genetic linkage map. Using gene specific primer pair designed according to the sequence of F3H gene from soybean, a fragment about of 2600 bp was generated. Sequencing of fragments revealed there were 3bp insertion/deletion(InDel)differences among the parents of NJRIKY, and an InDel marker was developed for F3H gene based on the sequence variation. The InDel marker, namely F3H gene was mapped on linkage group G8-D1b+W by PCR amplification detection in the RIL population NJRIKY. The F3H gene and Rsc-7 locus, which is resistant to SMV, were mapped on the same linkage group and located to between Satt698 and Sat_351 of SSR makers with distances of 38.5 and 9.4 cM, respectively.

喻德跃、程浩、付三雄

农业科学研究遗传学植物学

大豆、黄烷酮-3-羟化酶InDel标记定位

SoybeanF3HInDel markermapping

喻德跃,程浩,付三雄.大豆F3H基因InDel标记的开发及定位[EB/OL].(2012-12-28)[2025-05-01].http://www.paper.edu.cn/releasepaper/content/201212-1161.点此复制

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