National Key Laboratory of Crop Genetics and Germplasm Enhancement, National Center for Soybean Improvement, Key Laboratory for Biology and Genetic Improvement of Soybean (General, Ministry of Agriculture), Jiangsu Collaborative Innovation Center for Modern Crop Production, Nanjing Agricultural University, Nanjing, China.
Theor Appl Genet. 2023 Jan;136(1):22. doi: 10.1007/s00122-023-04299-w. Epub 2023 Jan 23.
Four major quantitative trait loci for 100-seed weight were identified in a soybean RIL population under five environments, and the most likely candidate genes underlying these loci were identified. Seed weight is an important target of soybean breeding. However, the genes underlying the major quantitative trait loci (QTL) controlling seed weight remain largely unknown. In this study, a soybean population of 300 recombinant inbred lines (RILs) derived from a cross between PI595843 (PI) and WH was used to map the QTL and identify candidate genes for seed weight. The RIL population was genotyped through whole genome resequencing, and phenotyped for 100-seed weight under five environments. A total of 38 QTL were detected, and four major QTL, each explained at least 10% of the variation in 100-seed weight, were identified. Six candidate genes within these four major QTL regions were identified by analyses of their tissue expression patterns, gene annotations, and differential gene expression levels in soybean seeds during four developmental stages between two parental lines. Further sequence variation analyses revealed a C to T substitution in the first exon of the Glyma.19G143300, resulting in an amino acid change between PI and WH, and thus leading to a different predicted kinase domain, which might affect its protein function. Glyma.19G143300 is highly expressed in soybean seeds and encodes a leucine-rich repeat receptor-like protein kinase (LRR-RLK). Its predicted protein has typical domains of LRR-RLK family, and phylogenetic analyses reveled its similarity with the known LRR-RLK protein XIAO (LOC_Os04g48760), which is involved in controlling seed size. The major QTL and candidate genes identified in this study provide useful information for molecular breeding of new soybean cultivars with desirable seed weight.
四个控制百粒重的大豆数量性状位点在五个环境下被鉴定,并且鉴定了这些位点最可能的候选基因。种子重量是大豆育种的一个重要目标。然而,控制种子重量的主要数量性状位点(QTL)的基因仍然很大程度上未知。在这项研究中,使用 PI595843(PI)和 WH 杂交产生的 300 个重组自交系(RIL)群体来定位 QTL,并鉴定种子重量的候选基因。通过全基因组重测序对 RIL 群体进行了基因型分析,并在五个环境下对百粒重进行了表型分析。共检测到 38 个 QTL,鉴定出四个主要 QTL,每个 QTL至少解释了 10%的百粒重变异。通过分析这四个主要 QTL 区域内的组织表达模式、基因注释和两个亲本系之间四个发育阶段的大豆种子中差异表达水平,鉴定出 6 个候选基因。进一步的序列变异分析显示,Glyma.19G143300 的第一个外显子中存在 C 到 T 的替换,导致 PI 和 WH 之间的氨基酸变化,从而导致不同的预测激酶结构域,这可能影响其蛋白功能。Glyma.19G143300 在大豆种子中高度表达,编码富含亮氨酸重复受体样蛋白激酶(LRR-RLK)。其预测蛋白具有 LRR-RLK 家族的典型结构域,系统发育分析表明它与已知的 LRR-RLK 蛋白 XIAO(LOC_Os04g48760)相似,后者参与控制种子大小。本研究中鉴定的主要 QTL 和候选基因为具有理想种子重量的新大豆品种的分子育种提供了有用信息。