Wang Yanyan, Xiang Xianyu, Huang Fan, Yu Wenlin, Zhou Xueqing, Li Baojun, Zhang Yunyun, Chen Peng, Zhang Chunyu
College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, China.
Hybrid Rape Research Center of Shaanxi Province, Shaanxi Rapeseed Branch of National Centre for Oil Crops Genetic Improvement, Yangling, China.
Front Plant Sci. 2022 May 6;13:898108. doi: 10.3389/fpls.2022.898108. eCollection 2022.
Clubroot is caused by , which threatens crop production worldwide. In recent years, there has been an outbreak and rapid spread of clubroot in many major cruciferous crop-producing areas of China. In this study, we identified a cabbage material DingWen (DW) with different resistant capabilities from Huashuang5R (H5R) and Huayouza62R of , which are currently used as the main resistant cultivars for clubroot management in China. We used a next-generation sequencing-based bulked segregant analysis approach, combined with genetic mapping to identify clubroot-resistant (CR) genes from F population generated from a cross between the DW (CR) and HZSX (clubroot susceptible). The CR locus of DW (named ) was mapped to a region between markers A08-4346 and A08-4853, which contains two different loci and after fine mapping. The loci contain a fragment of 395 kb between markers A08-4624 and A08-4853 on A08 chromosome, and it is responsible for the resistance to and isolates. However, together with , corresponding to a 765-kb region between markers A08-4346 and A08-4624, then it can confer resistance to . Finally, through expression analysis between resistant and susceptible materials, two genes encoding TIR-NBS-LRR proteins ( and ) and one gene encoding an RLP protein () were identified to be the most likely CR candidates for the peculiar resistance in DW.
根肿病是由[病原体名称未给出]引起的,它威胁着全球的作物生产。近年来,中国许多主要十字花科作物产区根肿病爆发并迅速传播。在本研究中,我们鉴定出一种甘蓝材料丁文(DW),其抗性能力与华双5R(H5R)和华油杂62R不同,而H5R和华油杂62R目前是中国用于根肿病防治的主要抗性品种。我们采用基于二代测序的混合分组分析法,并结合遗传图谱构建,从DW(抗病)与HZSX(感根肿病)杂交产生的F群体中鉴定根肿病抗性(CR)基因。DW的CR位点(命名为[具体名称未给出])被定位到标记A08 - 4346和A08 - 4853之间的区域,精细定位后该区域包含两个不同的位点[具体名称未给出]和[具体名称未给出]。[具体名称未给出]位点在A08染色体上标记A08 - 4624和A08 - 4853之间包含一个395 kb的片段,它负责对[病原体名称未给出]和[病原体名称未给出]分离株的抗性。然而,与[具体名称未给出]一起,对应于标记A08 - 4346和A08 - 4624之间765 - kb的区域,则可赋予对[病原体名称未给出]的抗性。最后,通过抗性和感病材料之间的表达分析,鉴定出两个编码TIR - NBS - LRR蛋白的基因([具体基因名称未给出]和[具体基因名称未给出])以及一个编码RLP蛋白([具体基因名称未给出])的基因是DW中独特抗性最有可能的CR候选基因。