Valent B, Farrall L, Chumley F G
Central Research and Development Department, Du Pont Company, Wilmington, Delaware 19880-0402.
Genetics. 1991 Jan;127(1):87-101. doi: 10.1093/genetics/127.1.87.
We have identified genes for pathogenicity toward rice (Oryza sativa) and genes for virulence toward specific rice cultivars in the plant pathogenic fungus Magnaporthe grisea. A genetic cross was conducted between the weeping lovegrass (Eragrostis curvula) pathogen 4091-5-8, a highly fertile, hermaphroditic laboratory strain, and the rice pathogen O-135, a poorly fertile, female-sterile field isolate that infects weeping lovegrass as well as rice. A six-generation backcrossing scheme was then undertaken with the rice pathogen as the recurrent parent. One goal of these crosses was to generate rice pathogenic progeny with the high fertility characteristic of strain 4091-5-8, which would permit rigorous genetic analysis of rice pathogens. Therefore, progeny strains to be used as parents for backcross generations were chosen only on the basis of fertility. The ratios of pathogenic to nonpathogenic (and virulent to avirulent) progeny through the backcross generations suggested that the starting parent strains differ in two types of genes that control the ability to infect rice. First, they differ by polygenic factors that determine the extent of lesion development achieved by those progeny that infect rice. These genes do not appear to play a role in infection of weeping lovegrass because both parents and all progeny infect weeping lovegrass. Second, the parents differ by simple Mendelian determinants, "avirulence genes," that govern virulence toward specific rice cultivars in all-or-none fashion. Several crosses confirm the segregation of three unlinked avirulence genes, Avr 1-CO39, Avr 1-M201 and Avr1-YAMO, alleles of which determine avirulence on rice cultivars CO39, M201, and Yashiro-mochi, respectively. Interestingly, avirulence alleles of Avr1-CO39, Avr1-M201 and Avr1-YAMO were inherited from the parent strain 4091-5-8, which is a nonpathogen of rice. Middle repetitive DNA sequences ("MGR sequences"), present in approximately 40-50 copies in the genome of the rice pathogen parent, and in very low copy number in the genome of the nonpathogen of rice, were used as physical markers to monitor restoration of the rice pathogen genetic background during introgression of fertility. The introgression of highest levels of fertility into the most successful rice pathogen progeny was incomplete by the sixth generation, perhaps a consequence of genetic linkage between genes for fertility and genes for rice pathogenicity. One chromosomal DNA segment with MGR sequence homology appeared to be linked to the gene Avr1-CO39. Finally, many of the crosses described in this paper exhibited a characteristic common to many crosses involving M. grisea rice pathogen field isolates.(ABSTRACT TRUNCATED AT 400 WORDS)
我们已经在植物致病真菌稻瘟病菌(Magnaporthe grisea)中鉴定出了对水稻(Oryza sativa)致病的基因以及对特定水稻品种具有毒性的基因。在垂穗草(Eragrostis curvula)病原菌4091 - 5 - 8(一种高度可育的雌雄同体实验室菌株)与水稻病原菌O - 135(一种育性差、雌性不育的田间分离株,能感染垂穗草和水稻)之间进行了遗传杂交。然后以水稻病原菌作为轮回亲本进行了六代回交实验。这些杂交的一个目标是培育出具有4091 - 5 - 8菌株高育性特征的水稻致病后代,这将有助于对水稻病原菌进行严格的遗传分析。因此,仅根据育性选择用作回交后代亲本的子代菌株。回交后代中致病与非致病(以及有毒与无毒)子代的比例表明,起始亲本菌株在控制感染水稻能力的两类基因上存在差异。首先,它们在多基因因素上存在差异,这些因素决定了感染水稻的子代所形成病斑的发展程度。这些基因似乎在感染垂穗草方面不起作用,因为亲本和所有子代都能感染垂穗草。其次,亲本在简单孟德尔决定因子(“无毒基因”)上存在差异,这些因子以全有或全无的方式控制对特定水稻品种的毒性。几次杂交证实了三个不连锁的无毒基因Avr 1 - CO39、Avr 1 - M201和Avr1 - YAMO的分离,它们的等位基因分别决定对水稻品种CO39、M201和八重穗的无毒。有趣的是,Avr1 - CO39、Avr1 - M201和Avr1 - YAMO的无毒等位基因是从亲本菌株4091 - 5 - 8遗传而来的,而该菌株是水稻的非病原菌。在水稻病原菌亲本基因组中大约有40 - 50个拷贝的中等重复DNA序列(“MGR序列”),在水稻非病原菌基因组中的拷贝数非常低,被用作物理标记来监测在导入育性过程中水稻病原菌遗传背景的恢复情况。到第六代时,将最高水平的育性导入最成功的水稻病原菌子代的过程并不完全,这可能是育性基因与水稻致病基因之间遗传连锁的结果。一个与MGR序列同源的染色体DNA片段似乎与基因Avr1 - CO39连锁。最后,本文描述的许多杂交都表现出了许多涉及稻瘟病菌水稻病原菌田间分离株的杂交所共有的一个特征。(摘要截断于400字)