Blanton H, Sekelsky J
Department of Biology and Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, NC 27599, USA.
Cytogenet Genome Res. 2004;107(3-4):172-9. doi: 10.1159/000080595.
To ensure the accurate disjunction of homologous chromosomes during meiosis, most eukaryotes rely on physical connections called chiasmata, which form at sites of crossing over. In the absence of crossing over, homologs may segregate randomly, resulting in high frequencies of aneuploid gametes. The process of meiotic recombination poses unique problems for the cell that must be overcome to ensure normal disjunction of homologous chromosomes. How is it ensured that crossovers occur between homologous chromosomes, rather than between sister chromatids? What determines the number and location of crossovers? The functions of DNA repair proteins hold some of the answers to these questions. In this review, we discuss DNA repair proteins that function in meiotic recombination in Drosophila melanogaster. We emphasize the processes of strand invasion and Holliday junction resolution in order to shed light on the questions raised above. Also, we compare the variety of ways several eukaryotes perform these processes and the different proteins they require.
为确保减数分裂过程中同源染色体的准确分离,大多数真核生物依赖于一种称为交叉的物理连接,交叉发生在基因交换的位点。在没有基因交换的情况下,同源染色体可能会随机分离,导致非整倍体配子的高频率出现。减数分裂重组过程给细胞带来了必须克服的独特问题,以确保同源染色体的正常分离。如何确保交叉发生在同源染色体之间,而不是姐妹染色单体之间?是什么决定了交叉的数量和位置?DNA修复蛋白的功能为这些问题提供了一些答案。在这篇综述中,我们讨论了在黑腹果蝇减数分裂重组中发挥作用的DNA修复蛋白。我们强调链侵入和霍利迪连接点解析过程,以便阐明上述问题。此外,我们比较了几种真核生物执行这些过程的多种方式以及它们所需的不同蛋白质。