State Key Laboratory of Hybrid Rice, College of Life Sciences, Wuhan University, Wuhan, 430072, China.
Mol Genet Genomics. 2021 Jul;296(4):939-952. doi: 10.1007/s00438-021-01795-w. Epub 2021 May 9.
Plant major resistance (R) genes are effective in detecting pathogen signal molecules and triggering robust defense responses. Investigating the natural variation in R genes will allow identification of the critical amino acid residues determining recognition specificity in R protein and the discovery of novel R alleles. The rice blast resistance gene Pike, comprising of two adjacent CC-NBS-LRR genes, namely, Pike-1 and Pike-2, confers broad-spectrum resistance to Magnaporthe oryzae. Here, we demonstrated that Pike-1 determined Pike-specific resistance through direct interaction with the pathogen signal molecule AvrPik. Analysis of natural variation in 79 Pike-1 variants in the Asian cultivated rice Oryza sativa and its wild relatives revealed that the CC and NBS regions, particularly the CC region of the Pike-1 protein were the most diversified. We also found that balancing selection had occurred in O. sativa and O. rufipogon to maintain the genetic diversity of the Pike-1 alleles. By analysis of amino acid sequences, we identified 40 Pike-1 variants in these rice germplasms. These variants were divided into three major groups that corresponded to their respective clades. A new Pike allele, designated Pikg, that differed from Pike by a single amino acid substitution (D229E) in the Pike-1 CC region of the Pike protein was identified from wild rice relatives. Pathogen assays of Pikg transgenic plants revealed a unique reaction pattern that was different from that of the previously identified Pike alleles, namely, Pik, Pikh, Pikm, Pikp, Piks and Pi1. These findings suggest that minor amino acid residues in Pike-1/Pikg-1 determine pathogen recognition specificity and plant resistance. As a new blast R gene derived from rice wild relatives, Pikg has potential applications in rice breeding.
植物主要抗性 (R) 基因在检测病原体信号分子和触发强大的防御反应方面非常有效。研究 R 基因的自然变异将允许识别决定 R 蛋白识别特异性的关键氨基酸残基,并发现新的 R 等位基因。水稻稻瘟病抗性基因 Pike 由两个相邻的 CC-NBS-LRR 基因组成,即 Pike-1 和 Pike-2,赋予对 Magnaporthe oryzae 的广谱抗性。在这里,我们证明 Pike-1 通过与病原体信号分子 AvrPik 的直接相互作用决定了 Pike 特异性抗性。对亚洲栽培稻 Oryza sativa 及其野生近缘种中的 79 个 Pike-1 变体的自然变异分析表明,CC 和 NBS 区域,特别是 Pike-1 蛋白的 CC 区域是最多样化的。我们还发现,在 O. sativa 和 O. rufipogon 中发生了平衡选择,以维持 Pike-1 等位基因的遗传多样性。通过对氨基酸序列的分析,我们在这些水稻种质资源中鉴定出 40 个 Pike-1 变体。这些变体分为三个主要组,与各自的分支相对应。从野生稻亲缘关系中鉴定出一个新的 Pike 等位基因,命名为 Pikg,它在 Pike 蛋白的 Pike-1 CC 区域与 Pike 不同,只有一个氨基酸替换 (D229E)。对 Pikg 转基因植物的病原体测定表明,其反应模式与之前鉴定的 Pike 等位基因不同,即 Pik、Pikh、Pikm、Pikp、Piks 和 Pi1。这些发现表明,Pike-1/Pikg-1 中的微小氨基酸残基决定了病原体的识别特异性和植物的抗性。作为一个源自水稻野生近缘种的新的稻瘟病 R 基因,Pikg 在水稻育种中有潜在的应用。