UMR1095, Genetics Diversity and Ecophysiology of Cereals, INRA,Clermont Auvergne University, 63000, Clermont-Ferrand, France.
Theor Appl Genet. 2020 Mar;133(3):751-770. doi: 10.1007/s00122-019-03505-y. Epub 2020 Jan 6.
A set of eight SNP markers was developed to facilitate the early selection of HMW-GS alleles in breeding programmes. In bread wheat (Triticum aestivum), the high molecular weight glutenin subunits (HMW-GSs) are the most important determinants of technological quality. Known to be very diverse, HMW-GSs are encoded by the tightly linked genes Glu-1-1 and Glu-1-2. Alleles that improve the quality of dough have been identified. Up to now, sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) of grain proteins is the most widely used for their identification. To facilitate the early selection of HMW-GS alleles in breeding programmes, we developed DNA-based molecular markers. For each accession of a core collection (n = 364 lines) representative of worldwide bread wheat diversity, HMW-GSs were characterized by both genotyping and SDS-PAGE. Based on electrophoresis, we observed at least 8, 22 and 9 different alleles at the Glu-A1, Glu-B1 and Glu-D1 loci, respectively, including new variants. We designed a set of 17 single-nucleotide polymorphism (SNP) markers that were representative of the most frequent SDS-PAGE alleles at each locus. At Glu-A1 and Glu-D1, two and three marker-based haplotypes, respectively, captured the diversity of the SDS-PAGE alleles rather well. Discrepancies were found mainly for the Glu-B1 locus. However, statistical tests revealed that two markers at each Glu-B1 gene and their corresponding haplotypes were more significantly associated with the rheological properties of the dough than were the relevant SDS-PAGE alleles. To conclude, this study demonstrates that the SNP markers developed provide additional information on HMW-GS diversity. Two markers at Glu-A1, four at Glu-B1 and two at Glu-D1 constitute a useful toolbox for breeding wheat to improve end-use value.
开发了一套 8 个 SNP 标记,以促进在育种计划中 HMW-GS 等位基因的早期选择。在普通小麦(Triticum aestivum)中,高分子量谷蛋白亚基(HMW-GS)是决定面团加工品质的最重要因素。已知 HMW-GS 具有高度多样性,由紧密连锁的基因 Glu-1-1 和 Glu-1-2 编码。已经鉴定出了能够提高面团品质的等位基因。到目前为止,谷物蛋白的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)是最广泛用于鉴定 HMW-GS 的方法。为了在育种计划中促进 HMW-GS 等位基因的早期选择,我们开发了基于 DNA 的分子标记。对于核心种质库(n=364 条系)的每个品系,我们通过基因分型和 SDS-PAGE 对 HMW-GS 进行了特征分析。基于电泳,我们在 Glu-A1、Glu-B1 和 Glu-D1 位点分别观察到至少 8、22 和 9 种不同的等位基因,包括新的变异体。我们设计了一套 17 个单核苷酸多态性(SNP)标记,这些标记代表了每个位点最常见的 SDS-PAGE 等位基因。在 Glu-A1 和 Glu-D1 位点,分别有两个和三个基于标记的单倍型很好地捕获了 SDS-PAGE 等位基因的多样性。在 Glu-B1 位点发现了一些差异。然而,统计检验表明,每个 Glu-B1 基因的两个标记及其相应的单倍型与面团的流变特性的相关性比相关的 SDS-PAGE 等位基因更为显著。综上所述,本研究表明,开发的 SNP 标记提供了 HMW-GS 多样性的额外信息。Glu-A1 有两个标记,Glu-B1 有四个标记,Glu-D1 有两个标记,构成了一个用于改良小麦加工品质的有用工具包。