Qu Shaohong, Liu Guifu, Zhou Bo, Bellizzi Maria, Zeng Lirong, Dai Liangying, Han Bin, Wang Guo-Liang
Department of Plant Pathology, Ohio State University, Columbus 43210, USA.
Genetics. 2006 Mar;172(3):1901-14. doi: 10.1534/genetics.105.044891. Epub 2005 Dec 30.
The broad-spectrum rice blast resistance gene Pi9 was cloned using a map-based cloning strategy. Sequencing of a 76-kb bacterial artificial chromosome (BAC) contig spanning the Pi9 locus led to identification of six tandemly arranged resistance-like genes with a nucleotide-binding site (NBS) and leucine-rich repeats (LRRs) (Nbs1-Pi9-Nbs6-Pi9). Analysis of selected Pi9 deletion mutants and transformation of a 45-kb fragment from the BAC contig into the susceptible rice cultivar TP309 narrowed down Pi9 to the candidate genes Nbs2-Pi9 and Nbs3-Pi9. Disease evaluation of the transgenic lines carrying the individual candidate genes confirmed that Nbs2-Pi9 is the Pi9 gene. Sequence comparison analysis revealed that the six paralogs at the Pi9 locus belong to four classes and gene duplication might be one of the major evolutionary forces contributing to the formation of the NBS-LRR gene cluster. Semiquantitative reverse transcriptase (RT)-PCR analysis showed that Pi9 was constitutively expressed in the Pi9-resistant plants and was not induced by blast infection. The cloned Pi9 gene provides a starting point to elucidate the molecular basis of the broad-spectrum disease resistance and the evolutionary mechanisms of blast resistance gene clusters in rice.
利用图位克隆策略克隆了广谱稻瘟病抗性基因Pi9。对跨越Pi9基因座的一个76 kb细菌人工染色体(BAC)重叠群进行测序,鉴定出6个串联排列的类抗性基因,这些基因具有核苷酸结合位点(NBS)和富含亮氨酸重复序列(LRR)(Nbs1-Pi9-Nbs6-Pi9)。对选定的Pi9缺失突变体进行分析,并将BAC重叠群中的一个45 kb片段转化到感病水稻品种TP309中,将Pi9定位到候选基因Nbs2-Pi9和Nbs3-Pi9。对携带单个候选基因的转基因系进行病害评估,证实Nbs2-Pi9就是Pi9基因。序列比较分析表明,Pi9基因座上的6个旁系同源基因属于4类,基因复制可能是导致NBS-LRR基因簇形成的主要进化力量之一。半定量逆转录酶(RT)-PCR分析表明,Pi9在Pi9抗性植株中组成型表达,不受稻瘟病菌感染诱导。克隆的Pi9基因为阐明水稻广谱抗病性的分子基础和稻瘟病抗性基因簇的进化机制提供了一个起点。