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增加控制菜豆角斑病主 QTL 周围标记的密度。

Increasing the density of markers around a major QTL controlling resistance to angular leaf spot in common bean.

机构信息

Departamento de Genética e Evolução e Bioagentes, Instituto de Biologia, Universidade Estadual de Campinas (UNICAMP), Campinas, São Paulo, 13083-970, Brazil,

出版信息

Theor Appl Genet. 2013 Oct;126(10):2451-65. doi: 10.1007/s00122-013-2146-1. Epub 2013 Jul 6.

DOI:10.1007/s00122-013-2146-1
PMID:23832048
Abstract

Angular leaf spot (ALS) causes major yield losses in the common bean (Phaseolus vulgaris L.), an important protein source in the human diet. This study describes the saturation around a major quantitative trait locus (QTL) region, ALS10.1, controlling resistance to ALS located on linkage group Pv10 and explores the genomic context of this region using available data from the P. vulgaris genome sequence. DArT-derived markers (STS-DArT) selected by bulk segregant analysis and SCAR and SSR markers were used to increase the resolution of the QTL, reducing the confidence interval of ALS10.1 from 13.4 to 3.0 cM. The position of the SSR ATA220 coincided with the maximum LOD score of the QTL. Moreover, a new QTL (ALS10.2(UC)) was identified at the end of the same linkage group. Sequence analysis using the P. vulgaris genome located ten SSRs and seven STS-DArT on chromosome 10 (Pv10). Coincident linkage and genome positions of five markers enabled the definition of a core region for ALS10.1 spanning 5.3 Mb. These markers are linked to putative genes related to disease resistance such as glycosyl transferase, ankyrin repeat-containing, phospholipase, and squamosa-promoter binding protein. Synteny analysis between ALS10.1 markers and the genome of soybean suggested a dynamic evolution of this locus in the common bean. The present study resulted in the identification of new candidate genes and markers closely linked to a major ALS disease resistance QTL, which can be used in marker-assisted selection, fine mapping and positional QTL cloning.

摘要

角斑病(ALS)会导致普通菜豆(Phaseolus vulgaris L.)严重减产,而普通菜豆是人类饮食中的一种重要蛋白质来源。本研究描述了 ALS10.1 这个主要数量性状位点(QTL)区域周围的饱和情况,该区域位于连锁群 Pv10 上,控制着 ALS 的抗性。利用来自 P. vulgaris 基因组序列的现有数据,探讨了该区域的基因组背景。通过 bulk segregant analysis 选择的 DArT 衍生标记(STS-DArT)、SCAR 和 SSR 标记被用来提高 QTL 的分辨率,将 ALS10.1 的置信区间从 13.4 厘摩缩小到 3.0 厘摩。SSR ATA220 的位置与 QTL 的最大 LOD 得分一致。此外,还在同一连锁群的末端鉴定到一个新的 QTL(ALS10.2(UC))。利用 P. vulgaris 基因组序列分析,在 10 号染色体(Pv10)上定位了 10 个 SSR 和 7 个 STS-DArT。五个标记的连锁和基因组位置一致,定义了 ALS10.1 的核心区域,跨度为 5.3Mb。这些标记与糖基转移酶、锚蛋白重复蛋白、磷酸脂酶和 squamosa 启动子结合蛋白等与抗病性相关的假定基因相连。ALS10.1 标记与大豆基因组之间的同线性分析表明,该基因座在普通菜豆中发生了动态进化。本研究确定了 ALS10.1 附近的新候选基因和紧密连锁的标记,这些标记可用于标记辅助选择、精细图谱绘制和定位 QTL 克隆。

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