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QTL‐seq for rapid identification of candidate genes for 100‐seed weight and root/total plant dry weight ratio under rainfed conditions in chickpea

机译:QTL-seq用于快速鉴定鹰嘴豆在雨育条件下100种子重量和根/总植物干重比的候选基因

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摘要

Terminal drought is a major constraint to chickpea productivity. Two component traits responsible for reduction in yield under drought stress include reduction in seeds size and root length/root density. QTL-seq approach, therefore, was used to identify candidate genomic regions for 100-seed weight (100SDW) and total dry root weight to total plant dry weight ratio (RTR) under rainfed conditions. Genomewide SNP profiling of extreme phenotypic bulks from the ICC 4958 × ICC 1882 population identified two significant genomic regions, one on CaLG01 (1.08 Mb) and another on CaLG04 (2.7 Mb) linkage groups for 100SDW. Similarly, one significant genomic region on CaLG04 (1.10 Mb) was identified for RTR. Comprehensive analysis revealed four and five putative candidate genes associated with 100SDW and RTR, respectively. Subsequently, two genes (Ca_04364 and Ca_04607) for 100SDW and one gene (Ca_04586) for RTR were validated using CAPS/dCAPS markers. Identified candidate genomic regions and genes may be useful for molecular breeding for chickpea improvement.
机译:终末干旱是鹰嘴豆生产力的主要制约因素。干旱胁迫下导致产量降低的两个组成特征包括种子大小和根长/根密度的减少。因此,在雨育条件下,使用QTL-seq方法来鉴定100种子重量(100SDW)的候选基因组区域以及总干根重量与总植物干重之比(RTR)。从ICC 4958×ICC 1882人群的极端表型基因组的全基因组SNP分析中,鉴定出两个重要的基因组区域,一个位于CaLG01(1.08 Mb),另一个位于CaLG04(2.7 Mb)连锁组,适用于100SDW。同样,在CaLG04上一个重要的基因组区域(1.10 Mb)被确定用于RTR。综合分析显示,分别有四个和五个推定的候选基因与100SDW和RTR相关。随后,使用CAPS / dCAPS标记验证了100SDW的两个基因(Ca_04364和Ca_04607)和RTR的一个基因(Ca_04586)。确定的候选基因组区域和基因可能有助于鹰嘴豆改良的分子育种。

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