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Genetic Analysis and Molecular Mapping of Gene Associated with Dominant Genie Male Sterility in Rapeseed (Bmssica napus L)

机译:油菜(Bmssica napus L)主导显性雄性不育相关基因的遗传分析和分子定位

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摘要

Rsl046AB is a dominant genie male sterility (DGMS) line derived from a spontaneous mutant in Brassica napus. The sterihty of this mutant was previously regarded as to be eonditioned by the interaetion of a dominant male sterihty gene Ms and its non-allelie dominant restorer geneMf(or Rf in previous reports). Recent genetic analyses, however, indicated that Ms and Mf may be alleic In this research, we confirmed that a multiple allele model should be more appropriate to elucidate the heredity of DGMSline Rs1046AB. Based on this result, the present study emphasized on identifying DNA markers linked to Ms/Mf in an F_2 population constructed by crossing Rsl046A with a double haploid (DH) restorer hne (19514A). Twenty ampHfied fragment length polymorphism (AFLP) markers Unked to the Ms/Mflocus were identified by combination of bulked segregant analysis (BSA) with AFLP technique. The target locus was detected to be co-segregating with the marker S05T05 and bracketed by two nearest markers, E14M01 and E01M02, with a genetic distance of 0.1 cM and 1.2 cM, respectively. Furthermore, we successfully converted two AFLP markers into sequence characterized amphfied region (SCAR) markers. These findings provided direct molecular marker proofs on the inheritance model of this DGMS hne, and the high density molecular markers hnkage map aroimd the Ms/Mflocus will be more informative for both marker-assisted selection (MAS) of elite male sterile lines and isolation of the Ms/Mf genes by positional cloning in future.
机译:Rsl046AB是源自甘蓝型油菜的自发突变体的显性基因雄性不育(DGMS)品系。该突变体的无菌性以前被认为是由于显性雄性不育基因Ms和其非全性显性恢复基因Mf(或先前报道中的Rf)的相互作用而被取消。然而,最近的遗传分析表明,Ms和Mf可能是等位基因。在这项研究中,我们证实了多重等位基因模型应该更适合于阐明DGMSline Rs1046AB的遗传。基于此结果,本研究着重于鉴定通过将Rsl046A与双单倍体(DH)恢复子(19514A)杂交而构建的F_2群体中与Ms / Mf相关的DNA标记。 Ms / Mflocus的二十个扩增片段长度多态性(AFLP)标记是通过将大量分离物分析(BSA)与AFLP技术相结合而鉴定的。检测到目标基因座与标记S05T05共分离,并被两个最近的标记E14M01和E01M02包围,遗传距离分别为0.1 cM和1.2 cM。此外,我们成功地将两个AFLP标记转换为序列特征的两性区域(SCAR)标记。这些发现为该DGMS基因的遗传模型提供了直接的分子标记证据,而Ms / Mflocus的高密度分子标记hnkage图谱对于雄性雄性不育系的标记辅助选择(MAS)和分离Ms / Mflocus都将提供更多信息。将来通过位置克隆获得Ms / Mf基因。

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