Identification of glutathione transferase gene associated with partial resistance to Sclerotinia stem rot of soybean using genome-wide association and linkage mapping

• DOI: 10.1007/s00122-021-03855-6
• Publication Date: 2021-05-31T05:02:52Z
• Authors: Zou Jianan; Wenjing Li; Yuting Zhang; Wei Song; Haipeng Jiang; Jingyun Zhao; Yuhang Zhan; Weili Teng; Lijuan Qiu; Xue Zhao; Yingpeng Han
• Keywords: 0301 basic medicine; 2. Zero hunger; Glycine max; Chromosome Mapping; Polymorphism, Single Nucleotide; Chromosomes, Plant; Linkage Disequilibrium; 03 medical and health sciences; Ascomycota; Gene Expression Regulation, Plant; Genome, Plant; Disease Resistance; Genome-Wide Association Study; Glutathione Transferase; Plant Diseases; Plant Proteins

Association and linkage mapping techniques were used to identify and verify single nucleotide polymorphisms (SNPs) associated with Sclerotinia sclerotiorum resistance. A novel resistant gene, GmGST , was cloned and shown to be involved in soybean resistance to SSR. Sclerotinia stem rot (SSR), caused by the fungus Sclerotinia sclerotiorum, is one of the most devastating diseases in soybean (Glycine max (Linn.) Merr.) However, the genetic architecture underlying soybean resistance to SSR is poorly understood, despite several mapping and gene mining studies. In the present study, the identification of quantitative trait loci (QTLs) involved in the resistance to S. sclerotiorum was conducted in two segregating populations: an association population that consisted of 261 diverse soybean germplasms, and the MH population, derived from a cross between a partially resistant cultivar (Maple arrow) and a susceptible cultivar (Hefeng25). Three and five genomic regions affecting resistance were detected by genome-wide association study to control the lesion length of stems (LLS) and the death rate of seedling (DRS), respectively. Four QTLs were detected to underlie LLS, and one QTL controlled DRS after SSR infection. A major locus on chromosome (Chr.) 13 (qDRS13-1), which affected both DRS and LLS, was detected in both the natural population and the MH population. GmGST, encoding a glutathione S-transferase, was cloned as a candidate gene in qDRS13-1. GmGST was upregulated by the induction of the partially resistant cultivar Maple arrow. Transgenic experiments showed that the overexpression of GmGST in soybean increased resistance to S. sclerotiorum and the content of soluble pigment in stems of soybean. The results increase our understanding of the genetic architecture of soybean resistance to SSR and provide a framework for the future marker-assisted breeding of resistant soybean cultivars.