Zhong Chao, Sun Suli, Li Yinping, Duan Canxing, Zhu Zhendong
National Key Facility for Crop Gene Resources and Genetic Improvement, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing, 100081, China.
Theor Appl Genet. 2018 Mar;131(3):525-538. doi: 10.1007/s00122-017-3016-z. Epub 2017 Nov 14.
A novel Phytophthora sojae resistance gene RpsHC18 was identified and finely mapped on soybean chromosome 3. Two NBS-LRR candidate genes were identified and two diagnostic markers of RpsHC18 were developed. Phytophthora root rot caused by Phytophthora sojae is a destructive disease of soybean. The most effective disease-control strategy is to deploy resistant cultivars carrying Phytophthora-resistant Rps genes. The soybean cultivar Huachun 18 has a broad and distinct resistance spectrum to 12 P. sojae isolates. Quantitative trait loci sequencing (QTL-seq), based on the whole-genome resequencing (WGRS) of two extreme resistant and susceptible phenotype bulks from an F population, was performed, and one 767-kb genomic region with ΔSNP-index ≥ 0.9 on chromosome 3 was identified as the RpsHC18 candidate region in Huachun 18. The candidate region was reduced to a 146-kb region by fine mapping. Nonsynonymous SNP and haplotype analyses were carried out in the 146-kb region among ten soybean genotypes using WGRS. Four specific nonsynonymous SNPs were identified in two nucleotide-binding sites-leucine-rich repeat (NBS-LRR) genes, RpsHC18-NBL1 and RpsHC18-NBL2, which were considered to be the candidate genes. Finally, one specific SNP marker in each candidate gene was successfully developed using a tetra-primer ARMS-PCR assay, and the two markers were verified to be specific for RpsHC18 and to effectively distinguish other known Rps genes. In this study, we applied an integrated genomic-based strategy combining WGRS with traditional genetic mapping to identify RpsHC18 candidate genes and develop diagnostic markers. These results suggest that next-generation sequencing is a precise, rapid and cost-effective way to identify candidate genes and develop diagnostic markers, and it can accelerate Rps gene cloning and marker-assisted selection for breeding of P. sojae-resistant soybean cultivars.
鉴定出一个新的大豆疫霉抗性基因RpsHC18,并将其精细定位在大豆3号染色体上。鉴定出两个NBS-LRR候选基因,并开发了RpsHC18的两个诊断标记。由大豆疫霉引起的大豆疫霉根腐病是大豆的一种毁灭性病害。最有效的病害防控策略是种植携带抗大豆疫霉Rps基因的抗性品种。大豆品种华春18对12个大豆疫霉菌株具有广泛且独特的抗性谱。基于F群体中两个极端抗感表型混合池的全基因组重测序(WGRS)进行数量性状位点测序(QTL-seq),在3号染色体上鉴定出一个ΔSNP-index≥0.9的767 kb基因组区域作为华春18中RpsHC18的候选区域。通过精细定位将候选区域缩小到146 kb区域。利用WGRS在10个大豆基因型的146 kb区域内进行非同义SNP和单倍型分析。在两个核苷酸结合位点富含亮氨酸重复序列(NBS-LRR)基因RpsHC18-NBL1和RpsHC18-NBL2中鉴定出四个特定的非同义SNP,它们被认为是候选基因。最后,使用四引物ARMS-PCR分析成功开发了每个候选基因中的一个特定SNP标记,并且验证这两个标记对RpsHC18具有特异性,并能有效区分其他已知的Rps基因。在本研究中,我们应用了一种基于基因组的综合策略,将WGRS与传统遗传定位相结合,以鉴定RpsHC18候选基因并开发诊断标记。这些结果表明,下一代测序是鉴定候选基因和开发诊断标记的一种精确、快速且经济高效的方法,它可以加速Rps基因克隆以及抗大豆疫霉大豆品种育种的标记辅助选择。