Rudolph C, Kunz C, Parisi S, Lehmann E, Hartsuiker E, Fartmann B, Kramer W, Kohli J, Fleck O
Institute of General Microbiology, University of Bern, CH-3012 Bern, Switzerland.
Mol Cell Biol. 1999 Jan;19(1):241-50. doi: 10.1128/MCB.19.1.241.
We have identified in the fission yeast Schizosaccharomyces pombe a MutS homolog that shows highest homology to the Msh2 subgroup. msh2 disruption gives rise to increased mitotic mutation rates and increased levels of postmeiotic segregation of genetic markers. In bandshift assays performed with msh2Delta cell extracts, a general mismatch-binding activity is absent. By complementation assays, we showed that S. pombe msh2 is allelic with the previously identified swi8 and mut3 genes, which are involved in mating-type switching. The swi8-137 mutant has a mutation in the msh2 gene which causes a truncated Msh2 peptide lacking a putative DNA-binding domain. Cytological analysis revealed that during meiotic prophase of msh2-defective cells, chromosomal structures were frequently formed; such structures are rarely found in the wild type. Our data show that besides having a function in mismatch repair, S. pombe msh2 is required for correct termination of copy synthesis during mating-type switching as well as for proper organization of chromosomes during meiosis.
我们在裂殖酵母粟酒裂殖酵母中鉴定出一种MutS同源物,它与Msh2亚组具有最高的同源性。msh2基因的破坏导致有丝分裂突变率增加以及遗传标记的减数分裂后分离水平升高。在用msh2Δ细胞提取物进行的凝胶迁移实验中,缺乏一般的错配结合活性。通过互补实验,我们表明粟酒裂殖酵母msh2与先前鉴定的参与交配型转换的swi8和mut3基因等位。swi8-137突变体在msh2基因中有一个突变,该突变导致截短的Msh2肽,缺少一个假定的DNA结合结构域。细胞学分析表明,在msh2缺陷细胞的减数分裂前期,经常形成染色体结构;而在野生型中很少发现这种结构。我们的数据表明,粟酒裂殖酵母msh2除了在错配修复中起作用外,在交配型转换过程中正确终止复制合成以及减数分裂过程中染色体的正确组织方面也是必需的。