Plant Genetic Group, Regional Service for Agrofood Research and Development (SERIDA), 33300, Villaviciosa, Asturias, Spain.
Theor Appl Genet. 2024 May 27;137(6):143. doi: 10.1007/s00122-024-04638-5.
Association analysis, colocation study with previously reported QTL, and differential expression analyses allowed the identification of the consistent QTLs and main candidate genes controlling seed traits. Common beans show wide seed variations in shape, size, water uptake, and coat proportion. This study aimed to identify consistent genomic regions and candidate genes involved in the genetic control of seed traits by combining association and differential expression analyses. In total, 298 lines from the Spanish Diversity Panel were genotyped with 4,658 SNP and phenotyped for seven seed traits in three seasons. Thirty-eight significant SNP-trait associations were detected, which were grouped into 23 QTL genomic regions with 1,605 predicted genes. The positions of the five QTL regions associated with seed weight were consistent with previously reported QTL. HCPC analysis using the SNP that tagged these five QTL regions revealed three main clusters with significantly different seed weights. This analysis also separated groups that corresponded well with the two gene pools described: Andean and Mesoamerican. Expression analysis was performed on the seeds of the cultivar 'Xana' in three seed development stages, and 1,992 differentially expressed genes (DEGs) were detected, mainly when comparing the early and late seed development stages (1,934 DEGs). Overall, 91 DEGs related to cell growth, signaling pathways, and transcriptomic factors underlying these 23 QTL were identified. Twenty-two DEGs were located in the five QTL regions associated with seed weight, suggesting that they are the main set of candidate genes controlling this character. The results confirmed that seed weight is the sum of the effects of a complex network of loci, and contributed to the understanding of seed phenotype control.
关联分析、与先前报道的 QTL 的共定位研究以及差异表达分析允许鉴定控制种子性状的一致 QTL 和主要候选基因。普通豆种在形状、大小、吸水率和种皮比例方面表现出广泛的种子变异。本研究旨在通过结合关联和差异表达分析,鉴定参与种子性状遗传控制的一致基因组区域和候选基因。总共对来自西班牙多样性小组的 298 个系进行了基因型分析,使用 4658 个 SNP 进行了表型分析,并在三个季节中对七个种子性状进行了表型分析。检测到 38 个显著的 SNP-性状关联,这些关联被分为 23 个 QTL 基因组区域,包含 1605 个预测基因。与种子重量相关的五个 QTL 区域的位置与先前报道的 QTL 一致。使用标记这五个 QTL 区域的 SNP 进行 HCPC 分析,揭示了三个具有显著不同种子重量的主要聚类。该分析还将组分为与描述的两个基因库(安第斯和中美洲)相对应的组。在三个种子发育阶段对 'Xana' 品种的种子进行表达分析,检测到 1992 个差异表达基因(DEGs),主要是在比较早期和晚期种子发育阶段(1934 个 DEGs)时。总体而言,鉴定出与这些 23 个 QTL 相关的细胞生长、信号通路和转录因子的 91 个 DEG。22 个 DEG 位于与种子重量相关的五个 QTL 区域,表明它们是控制该性状的主要候选基因。结果证实,种子重量是复杂基因座网络效应的总和,有助于理解种子表型控制。