Kirkpatrick D T
Department of Biology, University of North Carolina at Chapel Hill 27599-3280, USA.
Cell Mol Life Sci. 1999 Mar;55(3):437-49. doi: 10.1007/s000180050300.
Numerous proteins are involved in the nucleotide excision repair (NER) and DNA mismatch repair (MMR) pathways. The function and specificity of these proteins during the mitotic cell cycle has been actively investigated, in large part due to the involvement of these systems in human diseases. In contrast, comparatively little is known about their functioning during meiosis. At least three repair pathways operate during meiosis in the yeast Saccharomyces cerevisiae to repair mismatches that occur as a consequence of heteroduplex formation in recombination. The first pathway is similar to the one acting during postreplicative mismatch repair in mitotically dividing cells, while two pathways are responsible for the repair of large loops during meiosis, using proteins from MMR and NER systems. Some MMR proteins also help prevent recombination between diverged sequences during meiosis, and act late in recombination to affect the resolution of crossovers. This review will discuss the current status of DNA mismatch repair and nucleotide excision repair proteins during meiosis, especially in the yeast S. cerevisiae.
许多蛋白质参与核苷酸切除修复(NER)和DNA错配修复(MMR)途径。这些蛋白质在有丝分裂细胞周期中的功能和特异性已得到积极研究,很大程度上是因为这些系统与人类疾病有关。相比之下,人们对它们在减数分裂过程中的功能了解较少。在酿酒酵母的减数分裂过程中,至少有三种修复途径发挥作用,以修复重组过程中由于异源双链形成而出现的错配。第一种途径类似于有丝分裂细胞中复制后错配修复过程中起作用的途径,而另外两种途径负责在减数分裂过程中利用MMR和NER系统的蛋白质修复大的环。一些MMR蛋白质还有助于防止减数分裂过程中分歧序列之间的重组,并在重组后期起作用以影响交叉的分辨率。本综述将讨论减数分裂过程中DNA错配修复和核苷酸切除修复蛋白质的现状,特别是在酿酒酵母中。