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首页> 外文期刊>Acta Horticulturae >Identification of SRAP markers linked to the restorer gene of CMS7311 in heading Chinese cabbage [Brassica rapal. subsp. pekinensis(Lour.) Olsson]
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Identification of SRAP markers linked to the restorer gene of CMS7311 in heading Chinese cabbage [Brassica rapal. subsp. pekinensis(Lour.) Olsson]

机译:大白菜抽穗期与CMS7311恢复基因连锁的SRAP标记的鉴定。亚种pekinensis(Lour。)奥尔森]

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摘要

In order to map the restorer gene BrRfp of the polima (poI)-like cytoplasmic male sterility (CMS) 06)45 line of heading Chinese cabbage, a segregating population consisting of 258 F2 progeny of CMS06J45 and the restorer line 01S325 was tested by sequence-related amplified polymorphism (SRAP) combined with the bulked segregant analysis method. As a result, two SRAP markers, me3em3.366 and pm88bg5.263, linked with the BrRfp gene were identified from 463 SRAP primer pairs. By cloning, sequencing, and basic local alignment search tool analysis, the two markers were targeted to the BGIScaffold000053 of Brassica rapa in the Brassica database. Linkage analysis showed that these markers were distributed on either side of the BrRfp gene, the linkage distances of the two markers were 1.30 and 0.54 cM, respectively, and the BrRfp gene was restricted to the chromosome A09 genomic region of B. rapa. Moreover, the special me3em3.366 marker was a co-dominant marker and was successfully converted into a SCAR dominant marker. These specific markers provide basic information for map-based cloning of the BrRfp gene and will be very valuable for marker-assisted selection of a new restorer line of heading Chinese cabbage.
机译:为了定位大白菜的polima(poI)样细胞质雄性不育(CMS)06)45系的恢复基因BrRfp,按序列测试了由258个F2后代CMS06J45和恢复系01S325组成的分离群体相关扩增多态性(SRAP)结合大量分离物分析方法。结果,从463个SRAP引物对中鉴定了两个与BrRfp基因连接的SRAP标记me3em3.366和pm88bg5.263。通过克隆,测序和基本的局部比对搜索工具分析,将两个标记物定位于芸苔数据库中的芸苔属的BGIScaffold000053。连锁分析表明,这些标记分布在BrRfp基因的两侧,两个标记的连锁距离分别为1.30和0.54 cM,并且BrRfp基因被限制在B. rapa的A09染色体基因组区域。而且,特殊的me3em3.366标记是共显性标记,已成功转换为SCAR显性标记。这些特异性标记为BrRfp基因的基于图谱的克隆提供了基础信息,对于标记辅助选择新的大白菜恢复系将非常有价值。

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