The National Key Facility for Gene Resources and Genetic Improvement/Key Laboratory of Crop Germplasm Utilization, Institute of Crop Sciences, Chinese Academy of Agricultural Science, Beijing, 100081, People's Republic of China.
Soybean Research Institute, Heilongjiang Academy of Agricultural Sciences, Harbin, 150086, China.
Theor Appl Genet. 2023 Mar 13;136(3):50. doi: 10.1007/s00122-023-04268-3.
IBD analysis clarified the dynamics of chromosomal recombination during the ZP pedigree breeding process and identified ten genomic regions resistant to SCN race3 combining association mapping. Soybean cyst nematode (SCN, Heterodera glycines Ichinohe) is one of the most devastating pathogens for soybean production worldwide. The cultivar Zhongpin03-5373 (ZP), derived from SCN-resistant progenitor parents, Peking, PI 437654 and Huipizhi Heidou, is an elite line with high resistance to SCN race3. In the current study, a pedigree variation map was generated for ZP and its ten progenitors using 3,025,264 high-quality SNPs identified from an average of 16.2 × re-sequencing for each genome. Through identity by decent (IBD) tracking, we showed the dynamic change of genome and detected important IBD fragments, which revealed the comprehensively artificial selection of important traits during ZP breeding process. A total of 2,353 IBD fragments related to SCN resistance including SCN-resistant genes rhg1, rhg4 and NSF were identified based on the resistant-related genetic paths. Moreover, 23 genomic regions underlying resistance to SCN race3 were identified by genome-wide association study (GWAS) in 481 re-sequenced cultivated soybeans. Ten common loci were found by both IBD tracking and GWAS analysis. Haplotype analysis of 16 potential candidate genes suggested a causative SNP (C/T, - 1065) located in the promoter of Glyma.08G096500 and encoding a predicted TIFY5b-related protein on chr8 was highly correlated with SCN race3 resistance. Our results more thoroughly elucidated the dynamics of genomic fragments during ZP pedigree breeding and the genetic basis of SCN resistance, which will provide useful information for gene cloning and the development of resistant soybean cultivars using a marker-assisted selection approach.
IBD 分析阐明了 ZP 系谱育种过程中染色体重组的动态,并确定了 10 个对 SCN 抗性的基因组区域,这些区域与 SCN 抗性 3 号结合关联作图。大豆胞囊线虫(SCN,Heterodera glycines Ichinohe)是全球范围内对大豆生产危害最大的病原体之一。中黄 03-5373(ZP)是一种由 SCN 抗性亲本亲本北京、PI 437654 和槐皮黑豆衍生而来的品种,是一种对 SCN 抗性 3 号具有高度抗性的优秀品系。在本研究中,使用从每个基因组平均 16.2×重测序中鉴定出的 3,025,264 个高质量 SNP,为 ZP 及其 10 个亲本生成了系谱变异图谱。通过身份由血统(IBD)跟踪,我们展示了基因组的动态变化,并检测到重要的 IBD 片段,这揭示了 ZP 育种过程中对重要性状的全面人工选择。基于抗性相关遗传途径,共鉴定出 2,353 个与 SCN 抗性相关的 IBD 片段,包括 rhg1、rhg4 和 NSF 等 SCN 抗性基因。此外,通过对 481 个重测序栽培大豆进行全基因组关联研究(GWAS),鉴定出 23 个与 SCN 抗性 3 号相关的基因组区域。通过 IBD 跟踪和 GWAS 分析发现了 10 个共同的位点。对 16 个潜在候选基因的单倍型分析表明,位于 chr8 上 Glyma.08G096500 启动子内的一个推定的 TIFY5b 相关蛋白的候选基因上的一个功能 SNP(C/T,-1065)与 SCN 抗性 3 号高度相关。我们的结果更全面地阐明了 ZP 系谱育种过程中基因组片段的动态变化以及 SCN 抗性的遗传基础,这将为利用标记辅助选择方法克隆基因和开发抗性大豆品种提供有用信息。