Dobinson K F, Harris R E, Hamer J E
Department of Biological Sciences, Purdue University, West Lafayette, IN 47907.
Mol Plant Microbe Interact. 1993 Jan-Feb;6(1):114-26. doi: 10.1094/mpmi-6-114.
The fungal phytopathogen Magnaporthe grisea parasitizes a wide variety of gramineous hosts. In the course of investigating the genetic relationship between pathogen genotype and host specificity we identified a retroelement that is present in some strains of M. grisea that infect finger millet and goosegrass (members of the plant genus Eleusine). The element, designated grasshopper (grh), is present in multiple copies and dispersed throughout the genome. DNA sequence analysis showed that grasshopper contains 198 base pair direct, long terminal repeats (LTRs) with features characteristic of retroviral and retrotransposon LTRs. Within the element we identified an open reading frame with sequences homologous to the reverse transcriptase, RNaseH, and integrase domains of retroelement pol genes. Comparison of the open reading frame with sequences from other retroelements showed that grh is related to the gypsy family of retrotransposons. Comparisons of the distribution of the grasshopper element with other dispersed repeated DNA sequences in M. grisea indicated that grasshopper was present in a broadly dispersed subgroup of Eleusine pathogens, suggesting that the element was acquired subsequent to the evolution of this host-specific form. We present arguments that the amplification of different retroelements within populations of M. grisea is a consequence of the clonal organization of the fungal populations.
真菌植物病原体稻瘟病菌可寄生于多种禾本科宿主。在研究病原体基因型与宿主特异性之间的遗传关系过程中,我们鉴定出一种反转录元件,该元件存在于稻瘟病菌的一些感染龙爪稷和牛筋草(黍属植物成员)的菌株中。该元件被命名为grasshopper(grh),以多拷贝形式存在并分散于整个基因组中。DNA序列分析表明,grasshopper含有198个碱基对的直接长末端重复序列(LTRs),具有逆转录病毒和反转录转座子LTRs的特征。在该元件内部,我们鉴定出一个开放阅读框,其序列与反转录元件pol基因的逆转录酶、核糖核酸酶H和整合酶结构域同源。将该开放阅读框与其他反转录元件的序列进行比较表明,grh与反转录转座子的吉普赛家族相关。grasshopper元件的分布与稻瘟病菌中其他分散的重复DNA序列的比较表明,grasshopper存在于黍属病原体的一个广泛分散的亚组中,这表明该元件是在这种宿主特异性形式进化之后获得的。我们提出论据表明,稻瘟病菌群体中不同反转录元件的扩增是真菌群体克隆组织的结果。