Hollingsworth N M, Ponte L, Halsey C
Department of Biochemistry and Cell Biology, State University of New York, Stony Brook 11794-5215, USA.
Genes Dev. 1995 Jul 15;9(14):1728-39. doi: 10.1101/gad.9.14.1728.
Using a screen designed to identify yeast mutants specifically defective in recombination between homologous chromosomes during meiosis, we have obtained new alleles of the meiosis-specific genes, HOP1, RED1, and MEK1. In addition, the screen identified a novel gene designated MSH5 (MutS Homolog 5). Although Msh5p exhibits strong homology to the MutS family of proteins, it is not involved in DNA mismatch repair. Diploids lacking the MSH5 gene display decreased levels of spore viability, increased levels of meiosis I chromosome nondisjuction, and decreased levels of reciprocal exchange between, but not within, homologs. Gene conversion is not reduced. Msh5 mutants are phenotypically similar to mutants in the meiosis-specific gene MSH4 (Ross-Macdonald and Roeder 1994). Double mutant analysis using msh4 msh5 diploids demonstrates that the two genes are in the same epistasis group and therefore are likely to function in a similar process--namely, the facilitation of interhomolog crossovers during meiosis.
利用一个旨在鉴定在减数分裂过程中同源染色体间重组存在特异性缺陷的酵母突变体的筛选系统,我们获得了减数分裂特异性基因HOP1、RED1和MEK1的新等位基因。此外,该筛选系统还鉴定出一个名为MSH5(MutS同源物5)的新基因。尽管Msh5p与MutS蛋白家族具有很强的同源性,但它不参与DNA错配修复。缺失MSH5基因的二倍体表现出孢子活力水平降低、减数分裂I染色体不分离水平增加以及同源染色体之间而非同源染色体内的相互交换水平降低。基因转换没有减少。Msh5突变体在表型上与减数分裂特异性基因MSH4的突变体相似(罗斯 - 麦克唐纳和罗德,1994年)。使用msh4 msh5二倍体进行的双突变分析表明,这两个基因处于同一上位性组,因此可能在一个相似的过程中发挥作用,即在减数分裂过程中促进同源染色体间的交叉互换。