Wang Junyou, Yang Chenkang, Zhao Wenjia, Wang Ying, Qiao Ling, Wu Bangbang, Zhao Jiajia, Zheng Xingwei, Wang Juanling, Zheng Jun
Shanxi Key Laboratory of Crop Genetics and Molecular Improvement, College of Agronomy, Shanxi Agricultural University, Jinzhong, 030801 China.
State Key Laboratory of Sustainable Dryland Agriculture, Institute of Wheat Research, Shanxi Agricultural University, Linfen, 041000 China.
Mol Breed. 2022 Jun 29;42(7):40. doi: 10.1007/s11032-022-01303-x. eCollection 2022 Jul.
Grain hardness (HI) is a key trait for wheat milling and end-use quality. genes () are the major genes responsible for grain hardness, but other QTLs also contribute to the trait. Therefore, it is essential to identify loci associated with the HI and allelic variations of in wheat. In the present study, 287 accessions from Shanxi province representing 70 years of wheat breeding were grown in one rainfed and two irrigated conditions to study grain hardness. Genome-wide association analysis (GWAS) was performed using the 15 K array, and the variability of alleles was investigated. Among the accessions, hard wheat was most common. The broad-sense heritability () among the three environments was 99.5%, suggesting HI was mainly affected by heredity. GWAS identified nine significant marker-trait associations (MTAs), including that , which explained 7.03% to 17.70% of phenotypic variation. Four MTAs on chromosome 2A, 2B, 5A, and 7A were novel loci. As for diversity of , a total of 11 haplotypes were detected, composed of 12 allelic variations of the gene. The most frequent haplotypes were / (43.9%) and / (18.8%), and both the frequency of / and the HI value increased with breeding years were related to local dietary habits probably. A novel double deletion allele of the haplotype was found in Donghei1206. These results will be useful not only in understanding of the genetics of the HI but also in breeding for improved grain texture.
The online version contains supplementary material available at 10.1007/s11032-022-01303-x.
籽粒硬度(HI)是小麦制粉和最终用途品质的关键性状。Puroindoline基因(Pin)是决定籽粒硬度的主要基因,但其他数量性状位点(QTL)也对该性状有贡献。因此,鉴定与小麦籽粒硬度相关的位点以及Pin基因的等位变异至关重要。在本研究中,种植了来自山西省的287份代表70年小麦育种历程的材料,分别在一种雨养条件和两种灌溉条件下研究籽粒硬度。使用15K芯片进行全基因组关联分析(GWAS),并研究Pin等位基因的变异性。在这些材料中,硬粒小麦最为常见。三种环境下的广义遗传力(H²)为99.5%,表明籽粒硬度主要受遗传影响。GWAS鉴定出9个显著的标记-性状关联(MTA),其中PinB解释了7.03%至17.70%的表型变异。位于2A、2B、5A和7A染色体上的4个MTA是新位点。至于Pin基因的多样性,共检测到11种单倍型,由该基因的12个等位变异组成。最常见的单倍型是PinBd/PinBj(43.9%)和PinBc/PinBj(18.8%),PinBd/PinBj的频率和籽粒硬度值都随育种年份增加,这可能与当地饮食习惯有关。在东黑1206中发现了一种新的PinB单倍型双缺失等位基因。这些结果不仅有助于理解籽粒硬度的遗传机制,也有助于改良籽粒质地的育种。
在线版本包含可在10.1007/s11032-022-01303-x获取的补充材料。