Molecular Biology of Vegetable Laboratory, College of Horticulture, Shenyang Agricultural University, Shenyang 110866, China.
Guangdong Key Laboratory for New Technology Research of Vegetables, Vegetable Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China.
Int J Mol Sci. 2024 Sep 28;25(19):10462. doi: 10.3390/ijms251910462.
Clubroot, a significant soil-borne disease, severely impacts the productivity of cruciferous crops. The identification and development of clubroot resistance (CR) genes are crucial for mitigating this disease. This study investigated the genetic inheritance of clubroot resistance within an F progeny derived from the cross of a resistant parent, designated "377", and a susceptible parent, designated "12A". Notably, "377" exhibited robust resistance to the "KEL-23" strain of , the causative agent of clubroot. Genetic analyses suggested that the observed resistance is controlled by a single dominant gene. Through Bulked Segregant Analysis sequencing (BSA-seq) and preliminary gene mapping, we localized the CR gene locus, designated as , to a 1.30 Mb genomic segment on chromosome A08, flanked by the markers "333" and "sau332-1". Further fine mapping precisely narrowed down the position of to a 173.8 kb region between the markers "srt8-65" and "srt8-25", where we identified 22 genes, including with a TIR-NBS-LRR domain and with an LRR domain. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) analyses confirmed that both and exhibit increased expression levels in the resistant parent "377" following inoculation with , thereby underscoring their potential as key genes implicated in -mediated clubroot resistance. This study not only identifies molecular markers associated with but also enriches the genetic resources available for breeding programs aimed at enhancing resistance to clubroot.
根肿病是一种严重影响十字花科作物生产力的土壤传播疾病。鉴定和开发根肿病抗性(CR)基因对于减轻这种疾病至关重要。本研究调查了抗性亲本“377”和感病亲本“12A”杂交产生的 F 后代中根肿病抗性的遗传。值得注意的是,“377”对根肿病的“KEL-23”菌株表现出强大的抗性。遗传分析表明,观察到的抗性由单个显性基因控制。通过 bulked segregant analysis sequencing(BSA-seq)和初步基因定位,我们将 CR 基因座定位到染色体 A08 上一个 1.30 Mb 的基因组片段上,该片段由标记“333”和“sau332-1”侧翼。进一步的精细定位将 的位置精确缩小到标记“srt8-65”和“srt8-25”之间的 173.8 kb 区域,在该区域我们鉴定了 22 个基因,包括具有 TIR-NBS-LRR 结构域的 和具有 LRR 结构域的 。定量逆转录聚合酶链反应(qRT-PCR)分析证实,在接种后,抗性亲本“377”中 和 均表现出表达水平的增加,这表明它们作为与介导的根肿病抗性相关的关键基因具有潜力。本研究不仅鉴定了与 相关的分子标记,还丰富了用于培育抗根肿病品种的遗传资源。