Sansam Christopher L, Pezza Roberto J
Cell Cycle and Cancer Biology Program, Oklahoma Medical Research Foundation and the Department of Cell Biology, University of Oklahoma Health Science Center, Oklahoma City, OK, USA.
FEBS J. 2015 Jul;282(13):2444-57. doi: 10.1111/febs.13317. Epub 2015 May 20.
During prophase of meiosis I, homologous chromosomes interact and undergo recombination. Successful completion of these processes is required in order for the homologous chromosomes to mount the meiotic spindle as a pair. The organization of the chromosomes into pairs ensures orderly segregation to opposite poles of the dividing cell, such that each gamete receives one copy of each chromosome. Chiasmata, the cytological manifestation of crossover products of recombination, physically connect the homologs in pairs, providing a linkage that facilitates their segregation. Consequently, mutations that reduce the level of recombination are invariably associated with increased errors in meiotic chromosome segregation. In this review, we focus on recent biochemical and genetic advances in elucidating the mechanisms of meiotic DNA strand exchange catalyzed by the Dmc1 protein. We also discuss the mode by which two recombination mediators, Hop2 and Mnd1, facilitate rate-limiting steps of DNA strand exchange catalyzed by Dmc1.
在减数分裂I的前期,同源染色体相互作用并发生重组。为了使同源染色体作为一对附着到减数分裂纺锤体上,这些过程需要成功完成。染色体配对排列可确保它们有序地分离到分裂细胞的相对两极,从而使每个配子获得每条染色体的一个拷贝。交叉,即重组交换产物的细胞学表现,将同源染色体物理性地成对连接起来,提供一种便于它们分离的连接。因此,降低重组水平的突变总是与减数分裂染色体分离中错误的增加相关。在这篇综述中,我们重点关注在阐明由Dmc1蛋白催化减数分裂DNA链交换机制方面的最新生化和遗传学进展。我们还讨论了两种重组介质Hop2和Mnd1促进由Dmc1催化的DNA链交换限速步骤的方式。