Wang Qun, Li Jinbin, Lu Lin, He Chengxing, Li Chengyun
Agricultural Environment and Resource Research Institute, Yunnan Academy of Agricultural Sciences, Kunming, China.
Flower Research Institute, Yunnan Academy of Agricultural Sciences, Kunming, China.
Front Genet. 2020 Aug 28;11:746. doi: 10.3389/fgene.2020.00746. eCollection 2020.
The product of the avirulence () gene of can be detected by the product of the corresponding resistance () gene of rice and activates immunity to rice mediated by the gene. The high degree of variability of isolates in pathogenicity makes the control of rice blast difficult. That resistance of the gene in rice has been lost has been ascribed to the instability of the gene in . Further study on the variation of the genes in field isolates may yield valuable information on the durable and effective deployment of genes in rice production areas. and are a pair of valuable genes in the Rice- pathosystem. is detectable by and determines the effectiveness of . To effectively deploy the gene , the distribution, variation, and evolution of the corresponding gene were found among 312 isolates collected from Yunnan rice production areas of China. PCR amplification and pathogenicity assays of showed that 202 isolates (64.7%) held alleles and were avirulent to IRBLzt-T (holding ). There were 42.3-83.3% avirulent isolates containing among seven regions in Yunnan Province. Meanwhile, 11 haplotypes of encoding three novel variants were identified among 100 isolates. A 198 bps insertion homologous to solo-LTR of the retrotransposon inago2 in the promoter region of in one isolate and a frameshift mutation of CDS in another isolate were identified among 100 isolates, and those two isolates had evolved to virulent from avirulent. Synonymous mutation and non-AUG-initiated N-terminal extensions keeps the gene avirulence function in field isolates in Yunnan. A haplotype network showed that H3 was an ancestral haplotype. Structure variance for absence (28.2%) or partial fragment loss (71.8%) of was found among 39 virulent isolates and may cause the avirulence function to be lost. Overall, evolved to virulent from avirulent forms via point mutation, retrotransposon, shift mutation, and structure variance under field conditions.
稻瘟病菌无毒基因的产物可被水稻相应抗性基因的产物检测到,并激活由该基因介导的对水稻的免疫反应。稻瘟病菌株致病性的高度变异性使得稻瘟病的防治变得困难。水稻中该抗性基因抗性的丧失被归因于稻瘟病菌中该基因的不稳定性。对稻瘟病菌田间分离株中该基因变异的进一步研究可能会为在水稻产区持久有效地部署该基因提供有价值的信息。该基因和该基因是水稻-稻瘟病菌系统中的一对重要基因。该基因可被该基因检测到,并决定该基因的有效性。为了有效地部署该基因,在中国云南水稻产区收集的312株稻瘟病菌株中发现了相应基因的分布、变异和进化情况。该基因的PCR扩增和致病性分析表明,202株分离株(64.7%)携带该等位基因,对携带该基因的IRBLzt-T无毒。云南省七个地区中,含有该基因的无毒分离株比例为42.3%-83.3%。同时,在100株分离株中鉴定出11种该基因的单倍型,编码三种新的该基因变体。在100株分离株中,有一株该基因启动子区域存在与反转录转座子inago2的单拷贝长末端重复序列同源的198bp插入,另一株存在编码区移码突变,这两株已从无毒进化为有毒。同义突变和非AUG起始的N端延伸使该基因在云南稻瘟病菌田间分离株中保持无毒功能。单倍型网络显示H3是祖先单倍型。在39株有毒分离株中发现该基因存在缺失(28.2%)或部分片段丢失(71.8%)的结构变异,可能导致该基因无毒功能丧失。总体而言,在田间条件下,该基因通过点突变、反转录转座子、移码突变和结构变异从无毒形式进化为有毒形式。