Ashikawa Ikuo, Hayashi Nagao, Yamane Hiroko, Kanamori Hiroyuki, Wu Jianzhong, Matsumoto Takashi, Ono Kazuko, Yano Masahiro
QTL Genomics Research Center, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8602, Japan.
Genetics. 2008 Dec;180(4):2267-76. doi: 10.1534/genetics.108.095034. Epub 2008 Oct 20.
The rice blast resistance gene Pikm was cloned by a map-based cloning strategy. High-resolution genetic mapping and sequencing of the gene region in the Pikm-containing cultivar Tsuyuake narrowed down the candidate region to a 131-kb genomic interval. Sequence analysis predicted two adjacently arranged resistance-like genes, Pikm1-TS and Pikm2-TS, within this candidate region. These genes encoded proteins with a nucleotide-binding site (NBS) and leucine-rich repeats (LRRs) and were considered the most probable candidates for Pikm. However, genetic complementation analysis of transgenic lines individually carrying these two genes negated the possibility that either Pikm1-TS or Pikm2-TS alone was Pikm. Instead, it was revealed that transgenic lines carrying both of these genes expressed blast resistance. The results of the complementation analysis and an evaluation of the resistance specificity of the transgenic lines to blast isolates demonstrated that Pikm-specific resistance is conferred by cooperation of Pikm1-TS and Pikm2-TS. Although these two genes are not homologous with each other, they both contain all the conserved motifs necessary for an NBS-LRR class gene to function independently as a resistance gene.
通过图位克隆策略克隆了水稻抗稻瘟病基因Pikm。对含有Pikm的品种津轻早生中该基因区域进行高分辨率遗传定位和测序,将候选区域缩小到一个131 kb的基因组区间。序列分析预测在该候选区域内有两个相邻排列的类抗性基因,即Pikm1-TS和Pikm2-TS。这些基因编码具有核苷酸结合位点(NBS)和富含亮氨酸重复序列(LRR)的蛋白质,被认为是Pikm最有可能的候选基因。然而,对单独携带这两个基因的转基因系进行的遗传互补分析排除了Pikm1-TS或Pikm2-TS单独为Pikm的可能性。相反,结果表明携带这两个基因的转基因系表现出稻瘟病抗性。互补分析结果以及对转基因系对稻瘟病菌株抗性特异性的评估表明,Pikm特异性抗性是由Pikm1-TS和Pikm2-TS共同作用赋予的。尽管这两个基因彼此不具有同源性,但它们都包含NBS-LRR类基因独立作为抗性基因发挥功能所需的所有保守基序。