The State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, South China Agricultural University, Guangzhou, Guangdong, 510642, People's Republic of China.
The Key Laboratory of Plant Molecular Breeding of Guangdong Province, College of Agriculture, South China Agricultural University, Guangzhou, Guangdong, 510642, People's Republic of China.
BMC Genomics. 2020 Apr 3;21(1):280. doi: 10.1186/s12864-020-6668-z.
Phytophthora root rot (PRR) caused by Phytophthora sojae (P. sojae) is one of the most serious limitations to soybean production worldwide. The identification of resistance gene(s) and their incorporation into elite varieties is an effective approach for breeding to prevent soybean from being harmed by this disease. A valuable mapping population of 228 F recombinant inbred lines (RILs) derived from a cross of the resistant cultivar Guizao1 and the susceptible cultivar BRSMG68 and a high-density genetic linkage map with an average distance of 0.81 centimorgans (cM) between adjacent bin markers in this population were used to map and explore candidate gene(s).
PRR resistance in Guizao1 was found to be controlled by a single Mendelian locus and was finely mapped to a 367.371-kb genomic region on chromosome 3 harbouring 19 genes, including 7 disease resistance (R)-like genes, in the reference Willliams 82 genome. Quantitative real-time PCR assays of possible candidate genes revealed that Glyma.03 g05300 was likely involved in PRR resistance.
These findings from the fine mapping of a novel Rps locus will serve as a basis for the cloning and transfer of resistance genes in soybean and the breeding of P. sojae-resistant soybean cultivars through marker-assisted selection.
由大豆疫霉(Phytophthora sojae,P. sojae)引起的疫霉根腐病(Phytophthora root rot,PRR)是全球范围内大豆生产的最严重限制因素之一。鉴定抗性基因(s)并将其整合到优良品种中是一种有效的育种方法,可防止大豆受到这种疾病的侵害。利用一个由抗性品种 Guizao1 和易感品种 BRSMG68 杂交产生的 228 个 F2 重组自交系(recombinant inbred lines,RILs)的宝贵作图群体,以及该群体中相邻 bin 标记之间平均距离为 0.81 厘摩(centimorgans,cM)的高密度遗传连锁图谱,对其进行了定位和候选基因(s)的探索。
Guizao1 的 PRR 抗性被发现由单个孟德尔基因控制,并被精细定位到包含 19 个基因的染色体 3 上的 367.371kb 基因组区域,参考 Williams 82 基因组中的 7 个抗病(R)类似基因。对可能的候选基因进行定量实时 PCR 检测表明,Glyma.03g05300 可能参与了 PRR 抗性。
对一个新的 Rps 基因座的精细定位的这些发现将为大豆中抗性基因的克隆和转移以及通过标记辅助选择培育抗大豆疫霉的大豆品种提供基础。