鉴定 Sesamum indicum L 的镰刀菌枯萎病抗性基因 SiRLK1

Yinghui Duan, Wenwen Qu, Shuxian Chang, Ming Ju, Cuiying Wang, Cong Mu, Hengchun Cao, Guiting Li, Qiuzhen Tian, Qin Ma, Zhanyou Zhang, Haiyang Zhang, Hongmei Miao
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引用次数: 0

摘要

由 Fusarium oxysporum f. sp. sesami(Fos)引起的芝麻镰刀菌枯萎病(SFW)是影响芝麻种植的最具破坏性的病害之一。破译SFW抗性的遗传控制是有效管理芝麻病害的关键。利用 Fos 致病性组 1 分离物对高抗品种玉芝 11 和高感品种 Sp1 进行的杂交遗传研究表明,抗性是由单个显性等位基因赋予的。通过跨群体关联图谱和大量分离分析,目标基因座被定位在 3 号染色体上的 1.24 Mb 区间。精细基因图谱进一步缩小了 21,350 和 21,401 kb 之间的间隔。Sindi_0812400基因座被确定为SFW抗性基因,并正式命名为SiRLK1。该基因编码一种特异的麦芽糖蛋白/受体样蛋白激酶,具有三个假定的串联激酶结构域,被认为是一种激酶融合蛋白。序列分析表明,该基因位点上很大比例(49.44%)的变异位于激酶结构域III,其中几个变异明显与SFW反应的多样性有关,表明激酶结构域III在抗病性表达中起着关键作用。这些发现为芝麻抗SFW基因的进一步功能分析和标记辅助抗性育种提供了有价值的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Fusarium wilt resistance gene SiRLK1 in Sesamum indicum L

Sesame Fusarium wilt (SFW), caused by Fusarium oxysporum f. sp. sesami (Fos), is one of the most devastating diseases affecting sesame cultivation. Deciphering the genetic control of SFW resistance is pivotal for effective disease management in sesame. An inheritance study on a cross between the highly resistant variety Yuzhi 11 and the highly susceptible accession Sp1 using a Fos pathogenicity group 1 isolate indicated that resistance was conferred by a single dominant allele. The target locus was located in a 1.24 Mb interval on chromosome 3 using a combination of cross-population association mapping and bulked segregant analysis. Fine genetic mapping further narrowed the interval between 21,350 and 21,401 kb. The locus Sindi_0812400 was identified as the SFW resistance gene and officially designated SiRLK1. This gene encodes a specific malectin/receptor-like protein kinase with three putative tandem kinase domains and is considered a kinase fusion protein. Sequence analysis revealed that a high proportion (49.44%) of variants within the locus was located within the kinase domain III, and several of which were evidently associated with the diversity in SFW response, indicating the critical role of kinase domain III in expression of disease resistance. These findings provide valuable information for further functional analysis of SFW resistance genes and marker-assisted resistance breeding in sesame.

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