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对来自大豆PI 230970的亚洲大豆锈病抗性基因Rpp2进行精细定位。

Fine mapping of the Asian soybean rust resistance gene Rpp2 from soybean PI 230970.

作者信息

Yu Neil, Kim Myungsik, King Zachary R, Harris Donna K, Buck James W, Li Zenglu, Diers Brian W

机构信息

Department of Crop Sciences, University of Illinois, 1101 W. Peabody Drive, Urbana, IL, 61801, USA.

出版信息

Theor Appl Genet. 2015 Mar;128(3):387-96. doi: 10.1007/s00122-014-2438-0. Epub 2014 Dec 12.

Abstract

Asian soybean rust (ASR) resistance gene Rpp2 has been fine mapped into a 188.1 kb interval on Glyma.Wm82.a2, which contains a series of plant resistance ( R ) genes. Asian soybean rust (ASR), caused by the fungus Phakopsora pachyrihizi Syd. & P. Syd., is a serious disease in major soybean [Glycine max (L.) Merr.] production countries worldwide and causes yield losses up to 75 %. Defining the exact chromosomal position of ASR resistance genes is critical for improving the effectiveness of marker-assisted selection (MAS) for resistance and for cloning these genes. The objective of this study was to fine map the ASR resistance gene Rpp2 from the plant introduction (PI) 230970. Rpp2 was previously mapped within a 12.9-cM interval on soybean chromosome 16. The fine mapping was initiated by identifying recombination events in F2 and F3 plants using simple sequence repeat (SSR) and single nucleotide polymorphism (SNP) markers that flank the gene. Seventeen recombinant plants were identified and then tested with additional genetic markers saturating the gene region to localize the positions of each recombination. The progeny of these selected plants were tested for resistance to ASR and with SSR markers resulting in the mapping of Rpp2 to a 188.1 kb interval on the Williams 82 reference genome (Glyma.Wm82.a2). Twelve genes including ten toll/interleukin-1 receptor (TIR)-nucleotide-binding site (NBS)-leucine-rich repeat (LRR) genes were predicted to exist in this interval on the Glyma.Wm82.a2.v1 gene model map. Eight of these ten genes were homologous to the Arabidopsis TIR-NBS-LRR gene AT5G17680.1. The identified SSR and SNP markers close to Rpp2 and the candidate gene information presented in this study will be significant resources for MAS and gene cloning research.

摘要

亚洲大豆锈病(ASR)抗性基因Rpp2已被精细定位到Glyma.Wm82.a2上一个188.1 kb的区间内,该区间包含一系列植物抗性(R)基因。由真菌大豆锈病菌(Phakopsora pachyrihizi Syd. & P. Syd.)引起的亚洲大豆锈病,是全球主要大豆[Glycine max (L.) Merr.]生产国的一种严重病害,可导致高达75%的产量损失。确定ASR抗性基因的确切染色体位置,对于提高抗性标记辅助选择(MAS)的有效性以及克隆这些基因至关重要。本研究的目的是对来自植物引进种(PI)230970的ASR抗性基因Rpp2进行精细定位。Rpp2先前被定位在大豆第16号染色体上一个12.9厘摩的区间内。精细定位通过使用位于该基因两侧的简单序列重复(SSR)和单核苷酸多态性(SNP)标记,在F2和F3植株中鉴定重组事件来启动。鉴定出17株重组植株,然后用使基因区域饱和的其他遗传标记进行测试,以定位每个重组的位置。对这些选定植株的后代进行ASR抗性测试,并使用SSR标记,从而将Rpp2定位到威廉姆斯82参考基因组(Glyma.Wm82.a2)上一个188.1 kb的区间内。在Glyma.Wm82.a2.v1基因模型图谱的这个区间内,预计存在12个基因,其中包括10个 toll/白细胞介素-1受体(TIR)-核苷酸结合位点(NBS)-富含亮氨酸重复序列(LRR)基因。这10个基因中的8个与拟南芥TIR-NBS-LRR基因AT5G17680.1同源。本研究中鉴定出的与Rpp2紧密连锁的SSR和SNP标记以及候选基因信息,将是MAS和基因克隆研究的重要资源。

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