Karhoff Stephanie, Vargas-Garcia Christian, Lee Sungwoo, Mian M A Rouf, Graham Michelle A, Dorrance Anne E, McHale Leah K
Center for Applied Plant Sciences, The Ohio State University, Columbus, OH, United States.
Center for Soybean Research, The Ohio State University, Columbus, OH, United States.
Front Plant Sci. 2022 Jun 14;13:893652. doi: 10.3389/fpls.2022.893652. eCollection 2022.
Phytophthora root and stem rot is a yield-limiting soybean disease caused by the soil-borne oomycete . Although multiple quantitative disease resistance loci (QDRL) have been identified, most explain <10% of the phenotypic variation (PV). The major QDRL explaining up to 45% of the PV previously identified on chromosome 18 and represent a valuable source of resistance for soybean breeding programs. Resistance alleles from plant introductions 427105B and 427106 significantly increase yield in disease-prone fields and result in no significant yield difference in fields with less to no disease pressure. In this study, high-resolution mapping reduced the QDRL interval to 3.1 cm, and RNA-seq analysis of near-isogenic lines (NILs) varying at pinpointed a single gene of interest which was downregulated in inoculated NILs carrying the resistant allele compared to inoculated NILs with the susceptible allele. This gene of interest putatively encodes a serine-threonine kinase (STK) related to the family and may be acting as a susceptibility factor, based on the specific increase of jasmonic acid concentration in inoculated NILs. This work facilitates further functional analyses and marker-assisted breeding efforts by prioritizing candidate genes and narrowing the targeted region for introgression.
疫霉根腐病和茎腐病是一种由土壤传播的卵菌引起的限制大豆产量的病害。虽然已经鉴定出多个数量抗病位点(QDRL),但大多数解释的表型变异(PV)不到10%。先前在18号染色体上鉴定出的主要QDRL解释了高达45%的PV,是大豆育种计划的宝贵抗性来源。来自植物引进品种427105B和427106的抗性等位基因在病害易发田显著提高产量,而在病害压力较小或无病害压力的田块中产量差异不显著。在本研究中,高分辨率定位将QDRL区间缩小到3.1厘米,对在该区间存在差异的近等基因系(NIL)进行RNA测序分析,确定了一个感兴趣的基因,与携带感病等位基因的接种NIL相比,携带抗性等位基因的接种NIL中该基因表达下调。基于接种NIL中茉莉酸浓度的特异性增加,这个感兴趣的基因可能编码一种与该家族相关的丝氨酸-苏氨酸激酶(STK),并可能作为一个感病因子。这项工作通过确定候选基因的优先级和缩小导入的目标区域,促进了进一步的功能分析和标记辅助育种工作。