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从花生(Arachis hypogaea L.)表达序列标签中鉴定表达的抗性基因类似物。

Identification of expressed resistance gene analogs from peanut (Arachis hypogaea L.) expressed sequence tags.

机构信息

University of Georgia, Department of Plant Pathology, Tifton, GA 31793, USA.

出版信息

J Integr Plant Biol. 2013 May;55(5):453-61. doi: 10.1111/jipb.12037. Epub 2013 Mar 18.

DOI:10.1111/jipb.12037
PMID:23384141
Abstract

Low genetic diversity makes peanut (Arachis hypogaea L.) very vulnerable to plant pathogens, causing severe yield loss and reduced seed quality. Several hundred partial genomic DNA sequences as nucleotide-binding-site leucine-rich repeat (NBS-LRR) resistance genes (R) have been identified, but a small portion with expressed transcripts has been found. We aimed to identify resistance gene analogs (RGAs) from peanut expressed sequence tags (ESTs) and to develop polymorphic markers. The protein sequences of 54 known R genes were used to identify homologs from peanut ESTs from public databases. A total of 1,053 ESTs corresponding to six different classes of known R genes were recovered, and assembled 156 contigs and 229 singletons as peanut-expressed RGAs. There were 69 that encoded for NBS-LRR proteins, 191 that encoded for protein kinases, 82 that encoded for LRR-PK/transmembrane proteins, 28 that encoded for Toxin reductases, 11 that encoded for LRR-domain containing proteins and four that encoded for TM-domain containing proteins. Twenty-eight simple sequence repeats (SSRs) were identified from 25 peanut expressed RGAs. One SSR polymorphic marker (RGA121) was identified. Two polymerase chain reaction-based markers (Ahsw-1 and Ahsw-2) developed from RGA013 were homologous to the Tomato Spotted Wilt Virus (TSWV) resistance gene. All three markers were mapped on the same linkage group AhIV. These expressed RGAs are the source for RGA-tagged marker development and identification of peanut resistance genes.

摘要

低遗传多样性使花生(Arachis hypogaea L.)极易受到植物病原体的侵害,导致严重的产量损失和种子质量下降。已经鉴定出数百个部分基因组 DNA 序列作为核苷酸结合位点富含亮氨酸重复(NBS-LRR)抗性基因(R),但发现具有表达转录本的只有一小部分。我们旨在从花生表达序列标签(EST)中鉴定抗性基因类似物(RGA)并开发多态性标记。使用 54 个已知 R 基因的蛋白质序列,从公共数据库中的花生 EST 中鉴定同源物。总共回收了对应于 6 个已知 R 基因类别的 1,053 个 EST,并组装了 156 个 contigs 和 229 个 singletons 作为花生表达的 RGA。其中有 69 个编码 NBS-LRR 蛋白,191 个编码蛋白激酶,82 个编码 LRR-PK/跨膜蛋白,28 个编码 Toxin reductases,11 个编码 LRR 结构域蛋白,4 个编码 TM 结构域蛋白。从 25 个花生表达的 RGA 中鉴定出 28 个简单序列重复(SSR)。鉴定出一个 SSR 多态性标记(RGA121)。从 RGA013 开发的两个基于聚合酶链反应的标记(Ahsw-1 和 Ahsw-2)与番茄斑点萎蔫病毒(TSWV)抗性基因同源。这三个标记都被映射到相同的连锁群 AhIV 上。这些表达的 RGA 是 RGA 标记开发和鉴定花生抗性基因的来源。

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BMC Genet. 2016 Sep 6;17(1):128. doi: 10.1186/s12863-016-0435-9.
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