Warsame Ahmed O, Balk Janneke, Domoney Claire
Department of Biochemistry and Metabolism, John Innes Centre, Norwich, UK.
Plant Genome. 2025 Jun;18(2):e70051. doi: 10.1002/tpg2.70051.
Pulses are a valuable source of plant proteins for human and animal nutrition and have various industrial applications. Understanding the genetic basis for the relative abundance of different seed storage proteins is crucial for developing cultivars with improved protein quality and functional properties. In this study, we employed two complementary approaches, genome-wide association study (GWAS) and quantitative trait locus (QTL) mapping, to identify genetic loci underlying seed protein composition in pea (Pisum sativum L.). Sodium dodecyl sulfate-polyacrylamide gel electrophoresis was used to separate the seed proteins, and their relative abundance was quantified using densitometric analysis. For GWAS, we analyzed a diverse panel of 209 accessions genotyped with an 84,691 single-nucleotide polymorphism (SNP) array and identified genetic loci significantly associated with globulins, such as convicilin, vicilin, legumins, and non-globulins, including lipoxygenase, late embryogenesis abundant protein, and annexin-like protein. Additionally, using QTL mapping with 96 recombinant inbred lines, we mapped 11 QTL, including five that overlapped with regions identified by GWAS for the same proteins. Some of the significant SNPs were within or near the genes encoding seed proteins and other genes with predicted functions in protein biosynthesis, trafficking, and modification. This comprehensive genetic mapping study serves as a foundation for future breeding efforts to improve protein quality in pea and other legumes.
豆类是人类和动物营养中植物蛋白的宝贵来源,并且有多种工业应用。了解不同种子贮藏蛋白相对丰度的遗传基础对于培育具有改良蛋白质品质和功能特性的品种至关重要。在本研究中,我们采用了两种互补方法,即全基因组关联研究(GWAS)和数量性状位点(QTL)定位,来鉴定豌豆(Pisum sativum L.)种子蛋白质组成的潜在遗传位点。使用十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳分离种子蛋白,并通过光密度分析对其相对丰度进行定量。对于GWAS,我们分析了一个由209份材料组成的多样化群体,这些材料用84,691个单核苷酸多态性(SNP)阵列进行了基因分型,并鉴定出与球蛋白(如伴刀豆球蛋白、豌豆球蛋白、豆球蛋白)以及非球蛋白(包括脂氧合酶、胚胎后期丰富蛋白和类膜联蛋白)显著相关的遗传位点。此外,利用96个重组自交系进行QTL定位,我们定位了11个QTL,其中5个与GWAS鉴定的相同蛋白质区域重叠。一些显著的SNP位于编码种子蛋白的基因内部或附近,以及其他在蛋白质生物合成、运输和修饰方面具有预测功能的基因中。这项全面的遗传图谱研究为未来提高豌豆和其他豆类蛋白质品质的育种工作奠定了基础。