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比较基因组学在开发与大豆抗病毒基因Rsv4紧密连锁的分子标记中的应用。

Application of comparative genomics in developing molecular markers tightly linked to the virus resistance gene Rsv4 in soybean.

作者信息

Hwang Tae-Young, Moon Jung-Kyung, Yu Seok, Yang Kiwoung, Mohankumar Subbarayalu, Yu Yong Hwan, Lee Yeong Ho, Kim Hong Sig, Kim Hwan Mook, Maroof M A Saghai, Jeong Soon-Chun

机构信息

BioEvaluation Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-806, Republic of Korea.

出版信息

Genome. 2006 Apr;49(4):380-8. doi: 10.1139/g05-111.

Abstract

The Rsv4 gene confers resistance to all the known strain groups of soybean mosaic virus in soybean (Glycine max (L.) Merr.). To construct a fine genetic map near Rsv4 in soybean, we employed a comparative genomics approach that used genome sequence information of the model legume Lotus japonicus. Sequences of the soybean expressed sequence tags (ESTs) AI856415 and BF070293 mapping to one side of the Rsv4 gene showed high similarity with gene sequences of the transformation-competent artificial chromosome (TAC) clone LjT32P24 of Lotus. LjT32P24 is tightly linked to another sequenced TAC clone, LjT26I01, in Lotus. A new marker, AW307114A, developed from soybean EST AW307114, which is homologous to a Lotus gene within LjT26I01, was mapped to the other side of the Rsv4 gene. The identification of the microsyntenic relationship facilitated the development of additional 2 EST markers between BF070293-S and AW307114A bracketing the Rsv4 gene. Several other markers developed in this study were mapped to putative homoeologous or duplicated chromosomal regions in soybean. Alignment between the soybean maps indicated that Rsv4 is located near a local chromosomal rearrangement. This targeted comparative mapping serves to provide a foundation for marker-assisted selection and cloning of the Rsv4 gene.

摘要

Rsv4基因赋予大豆(Glycine max (L.) Merr.)对所有已知大豆花叶病毒株系的抗性。为了构建大豆中Rsv4附近的精细遗传图谱,我们采用了一种比较基因组学方法,该方法利用了模式豆科植物百脉根的基因组序列信息。定位到Rsv4基因一侧的大豆表达序列标签(EST)AI856415和BF070293的序列与百脉根的可转化人工染色体(TAC)克隆LjT32P24的基因序列高度相似。LjT32P24与百脉根中另一个已测序的TAC克隆LjT26I01紧密连锁。从大豆EST AW307114开发的一个新标记AW307114A,与LjT26I01内的一个百脉根基因同源,被定位到Rsv4基因的另一侧。微共线性关系的确定促进了在BF070293 - S和AW307114A之间开发另外2个EST标记,将Rsv4基因包围起来。本研究中开发的其他几个标记被定位到大豆中假定的同源或重复染色体区域。大豆图谱之间的比对表明,Rsv4位于局部染色体重排附近。这种有针对性的比较图谱绘制为Rsv4基因的标记辅助选择和克隆提供了基础。

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