Cheng Yanbo, Ma Qibin, Ren Hailong, Xia Qiuju, Song Enliang, Tan Zhiyuan, Li Shuxian, Zhang Gengyun, Nian Hai
The State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China.
The Key Laboratory of Plant Molecular Breeding of Guangdong Province, College of Agriculture, South China Agricultural University, Guangzhou, 510642, Guangdong, People's Republic of China.
Theor Appl Genet. 2017 May;130(5):1041-1051. doi: 10.1007/s00122-017-2869-5. Epub 2017 Feb 28.
Using a combination of phenotypic screening, genetic and statistical analyses, and high-throughput genome-wide sequencing, we have finely mapped a dominant Phytophthora resistance gene in soybean cultivar Wayao. Phytophthora root rot (PRR) caused by Phytophthora sojae is one of the most important soil-borne diseases in many soybean-production regions in the world. Identification of resistant gene(s) and incorporating them into elite varieties are an effective way for breeding to prevent soybean from being harmed by this disease. Two soybean populations of 191 F individuals and 196 F recombinant inbred lines (RILs) were developed to map Rps gene by crossing a susceptible cultivar Huachun 2 with the resistant cultivar Wayao. Genetic analysis of the F population indicated that PRR resistance in Wayao was controlled by a single dominant gene, temporarily named RpsWY, which was mapped on chromosome 3. A high-density genetic linkage bin map was constructed using 3469 recombination bins of the RILs to explore the candidate genes by the high-throughput genome-wide sequencing. The results of genotypic analysis showed that the RpsWY gene was located in bin 401 between 4466230 and 4502773 bp on chromosome 3 through line 71 and 100 of the RILs. Four predicted genes (Glyma03g04350, Glyma03g04360, Glyma03g04370, and Glyma03g04380) were found at the narrowed region of 36.5 kb in bin 401. These results suggest that the high-throughput genome-wide resequencing is an effective method to fine map PRR candidate genes.
通过结合表型筛选、遗传和统计分析以及高通量全基因组测序,我们精细定位了大豆品种洼腰中的一个显性疫霉抗性基因。由大豆疫霉引起的疫霉根腐病(PRR)是世界上许多大豆产区最重要的土传病害之一。鉴定抗性基因并将其整合到优良品种中是培育防止大豆受此病危害的有效途径。通过将感病品种华春2与抗病品种洼腰杂交,构建了两个由191个F个体和196个F重组自交系(RILs)组成的大豆群体,用于定位Rps基因。F群体的遗传分析表明,洼腰对PRR的抗性由一个单显性基因控制,暂命名为RpsWY,该基因位于3号染色体上。利用RILs的3469个重组区间构建了高密度遗传连锁区间图谱,通过高通量全基因组测序探索候选基因。基因型分析结果表明,通过RILs的71号和100号线,RpsWY基因位于3号染色体上4466230至4502773 bp之间的401区间。在401区间36.5 kb的狭窄区域发现了四个预测基因(Glyma03g04350、Glyma03g04360、Glyma03g04370和Glyma03g04380)。这些结果表明,高通量全基因组重测序是精细定位PRR候选基因的有效方法。