Rubin B P, Ferguson D O, Holloman W K
Department of Microbiology, Cornell University Medical College, New York, New York 10021.
Mol Cell Biol. 1994 Sep;14(9):6287-96. doi: 10.1128/mcb.14.9.6287-6296.1994.
Mutation in the REC2 gene of Ustilago maydis leads to defects in DNA repair, recombination, and meiosis. Analysis of the primary sequence of the Rec2 protein reveals a region with significant homology to bacterial RecA protein and to the yeast recombination proteins Dmc1, Rad51, and Rad57. This homologous region in the U. maydis Rec2 protein was found to be functionally sensitive to mutation, lending support to the hypothesis that Rec2 has a functional RecA-like domain essential for activity in recombination and repair. Homologous recombination between plasmid and chromosomal DNA sequences is reduced substantially in the rec2 mutant following transformation. The frequency can be restored to a level approaching, but not exceeding, that observed in the wild-type strain if transformation is performed with cells containing multiple copies of REC2.
玉米黑粉菌REC2基因的突变会导致DNA修复、重组和减数分裂出现缺陷。对Rec2蛋白一级序列的分析显示,有一个区域与细菌RecA蛋白以及酵母重组蛋白Dmc1、Rad51和Rad57具有显著同源性。发现玉米黑粉菌Rec2蛋白中的这个同源区域对突变在功能上敏感,这支持了以下假说:Rec2具有一个类似RecA的功能结构域,对重组和修复活性至关重要。转化后,rec2突变体中质粒与染色体DNA序列之间的同源重组大幅减少。如果用含有多个REC2拷贝的细胞进行转化,频率可以恢复到接近但不超过野生型菌株中观察到的水平。