Ehmsen Kirk T, Heyer Wolf-Dietrich
Section of Microbiology, University of California, Davis, One Shields Ave, Davis, CA 95616-8665, USA.
Genome Dyn Stab. 2008 Apr 5;3:91. doi: 10.1007/7050_2008_039.
Meiotic recombination ensures accurate chromosome segregation during the first meiotic division and provides a mechanism to increase genetic heterogeneity among the meiotic products. Unlike homologous recombination in somatic (vegetative) cells, where sister chromatid interactions prevail and crossover formation is avoided, meiotic recombination is targeted to involve homologs, resulting in crossovers to connect the homologs before anaphase of the first meiotic division. The mechanisms responsible for homolog choice and crossover control are poorly understood, but likely involve meiosis-specific recombination proteins, as well as meiosis-specific chromosome organization and architecture. Much progress has been made to identify and biochemically characterize many of the proteins acting during meiotic recombination. This review will focus on the proteins that generate and process heteroduplex DNA, as well as those that process DNA junctions during meiotic recombination, with particular attention to how recombination activities promote crossover resolution between homologs.
减数分裂重组确保了第一次减数分裂过程中染色体的准确分离,并提供了一种增加减数分裂产物之间遗传异质性的机制。与体细胞(营养细胞)中的同源重组不同,在体细胞中姐妹染色单体相互作用占主导且避免交叉形成,减数分裂重组的目标是涉及同源染色体,导致在第一次减数分裂后期之前交叉连接同源染色体。负责同源染色体选择和交叉控制的机制尚不清楚,但可能涉及减数分裂特异性重组蛋白,以及减数分裂特异性染色体组织和结构。在鉴定和生化表征许多在减数分裂重组过程中起作用的蛋白质方面已经取得了很大进展。本综述将重点关注在减数分裂重组过程中产生和处理异源双链DNA的蛋白质,以及那些处理DNA连接的蛋白质,特别关注重组活动如何促进同源染色体之间的交叉分辨率。