Clevinger Elizabeth M, Biyashev Ruslan, Schmidt Clarice, Song Qijian, Batnini Amine, Bolaños-Carriel Carlos, Robertson Alison E, Dorrance Anne E, Saghai Maroof M A
School of Plant and Environmental Sciences, Virginia Tech, Blacksburg, VA, United States.
Department of Plant Pathology, Entomology and Microbiology, Iowa State University, Ames, IA, United States.
Front Plant Sci. 2024 Jul 1;15:1394676. doi: 10.3389/fpls.2024.1394676. eCollection 2024.
For soybean, novel single dominant ( genes are sought to manage Phytophthora root and stem rot. In this study, resistance to was mapped individually in four recombinant inbred line (RIL) populations derived from crosses of the susceptible cultivar Williams with PI 407985, PI 408029, PI 408097, and PI424477 previously identified as putative novel sources of disease resistance. Each population was screened for resistance with five to seven isolates of separately over multiple F-F generations. Additionally, three of the populations were screened with inoculum from the combination of three isolates (PPR), which comprised virulence to 14 genes. Over 2,300 single-nucleotide polymorphism markers were used to construct genetic maps in each population to identify chromosomal regions associated with resistance to . Resistance segregated as one or two genes to the individual isolates and one gene toward PPR in each population and mapped to chromosomes 3, 13, or 18 in one or more of the four RIL populations. Resistance to five isolates mapped to the same chromosome 3 region are as follows: OH7 (PI 424477 and PI408029), OH12168, OH7/8, PPR (PI 407985), and 1.S.1.1 (PI408029). The resistance regions on chromosome 13 also overlapped for OH1, OH25, OH-MIA (PI424477), PPR (PI 424477, PI 407985, and PI 408097), PPR and OH0217 (PI 408097), and OH4 (PI 408029), but were distinct for each population suggesting multiple genes confer resistance. Two regions were identified on chromosome 18 but all appear to map to known loci; notably, resistance to the combined inoculum (PPR) did not map at this locus. However, there are putative new alleles in three of four populations, three on chromosome 3 and two on chromosome 13 based on mapping location but also known virulence in the isolate used. This characterization of all the genes segregating in these populations to these isolates will be informative for breeding, but the combined inoculum was able to map a novel loci. Furthermore, within each of these isolates, there was virulence to more than the described genes, and the effectiveness of the novel genes requires testing in larger populations.
对于大豆,人们正在寻找新的单一显性基因来防治疫霉根腐病和茎腐病。在本研究中,分别在四个重组自交系(RIL)群体中对疫霉根腐病抗性进行了定位,这些群体来源于感病品种Williams与PI 407985、PI 408029、PI 408097和PI424477的杂交,PI 407985、PI 408029、PI 408097和PI424477先前被鉴定为假定的新抗病源。每个群体在多个F - F世代中分别用5至7个疫霉菌株进行抗性筛选。此外,其中三个群体还用来自三种疫霉菌株组合(PPR)的接种物进行了筛选,该组合对14个疫霉基因具有毒力。使用了超过2300个单核苷酸多态性标记来构建每个群体的遗传图谱,以鉴定与疫霉根腐病抗性相关的染色体区域。在每个群体中,对单个菌株的抗性分离为一个或两个基因,对PPR的抗性分离为一个基因,并在四个RIL群体中的一个或多个群体中定位到染色体3、13或18上。对五个菌株的抗性定位到同一染色体3区域的情况如下:OH7(PI 424477和PI408029)、OH12168、OH7/8、PPR(PI 407985)和1.S.1.1(PI408029)。染色体13上的抗性区域在OH1、OH25、OH - MIA(PI424477)、PPR(PI 424477、PI 407985和PI 408097)、PPR和OH0217(PI 408097)以及OH4(PI 408029)之间也有重叠,但每个群体的抗性区域不同,表明有多个基因赋予抗性。在染色体18上鉴定出了两个区域,但似乎都映射到已知位点;值得注意的是,对混合接种物(PPR)的抗性并未映射到该位点。然而,根据定位位置以及所用菌株中已知的毒力情况,在四个群体中的三个群体中存在假定的新等位基因,三个在染色体3上,两个在染色体13上。对这些群体中分离到这些菌株的所有疫霉基因进行的这种表征将为育种提供信息,但混合接种物能够定位一个新位点。此外,在这些疫霉菌株中的每一个中,其毒力针对的基因都超过了所描述的疫霉基因,新基因的有效性需要在更大的群体中进行测试。