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历史重组在硬粒小麦育种群体中实现了对赤霉病抗性数量性状位点的高分辨率图谱绘制。

Historic recombination in a durum wheat breeding panel enables high-resolution mapping of Fusarium head blight resistance quantitative trait loci.

机构信息

Aquatic and Crop Resource Development Centre, National Research Council, Saskatoon, SK, Canada.

Department of Plant Sciences, University of Saskatchewan, Saskatoon, SK, Canada.

出版信息

Sci Rep. 2020 May 5;10(1):7567. doi: 10.1038/s41598-020-64399-1.

Abstract

The durum wheat line DT696 is a source of moderate Fusarium head blight (FHB) resistance. Previous analysis using a bi-parental population identified two FHB resistance quantitative trait loci (QTL) on chromosome 5A: 5A1 was co-located with a plant height QTL, and 5A2 with a major maturity QTL. A Genome-Wide Association Study (GWAS) of DT696 derivative lines from 72 crosses based on multi-environment FHB resistance, plant height, and maturity phenotypic data was conducted to improve the mapping resolution and further elucidate the genetic relationship of height and maturity with FHB resistance. The Global Tetraploid Wheat Collection (GTWC) was exploited to identify durum wheat lines with DT696 allele and additional recombination events. The 5A2 QTL was confirmed in the derivatives, suggesting the expression stability of the 5A2 QTL in various genetic backgrounds. The GWAS led to an improved mapping resolution rendering the 5A2 interval 10 Mbp shorter than the bi-parental QTL mapping interval. Haplotype analysis using SNPs within the 5A2 QTL applied to the GTWC identified novel haplotypes and recombination breakpoints, which could be exploited for further improvement of the mapping resolution. This study suggested that GWAS of derivative breeding lines is a credible strategy for improving mapping resolution.

摘要

硬粒小麦品系 DT696 是中度赤霉病(FHB)抗性的来源。先前使用双亲群体进行的分析在 5A 染色体上确定了两个 FHB 抗性数量性状位点(QTL):5A1 与株高 QTL 共定位,5A2 与主要成熟 QTL 共定位。对基于多环境 FHB 抗性、株高和成熟表型数据的 72 个杂交后代 DT696 衍生系进行了全基因组关联研究(GWAS),以提高作图分辨率,并进一步阐明高度和成熟度与 FHB 抗性的遗传关系。利用全球四倍体小麦集合(GTWC)鉴定出具有 DT696 等位基因和其他重组事件的硬粒小麦品系。在衍生系中证实了 5A2 QTL 的存在,表明 5A2 QTL 在各种遗传背景下的表达稳定性。GWAS 提高了作图分辨率,使 5A2 区间比双亲作图区间缩短了 10 Mbp。在 GTWC 中使用 5A2 QTL 内的 SNP 进行的单倍型分析确定了新的单倍型和重组断点,可用于进一步提高作图分辨率。本研究表明,衍生系的 GWAS 是提高作图分辨率的可靠策略。

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