Homologous recombination involves the formation of branched DNA molecules that may interfere with chromosome segregation. To resolve these persistent joint molecules, cells rely on the activation of structure-selective endonucleases (SSEs) during the late stages of the cell cycle. However, the premature activation of SSEs compromises genome integrity, due to untimely processing of replication and/or recombination intermediates. Here, we used a biochemical approach to show that the budding yeast SSEs Mus81 and Yen1 possess the ability to cleave the central recombination intermediate known as the displacement loop or D-loop. Moreover, we demonstrate that, consistently with previous genetic data, the simultaneous action of Mus81 and Yen1, followed by ligation, is sufficient to recreate the formation of a half-crossover precursor in vitro. Our results provide not only mechanistic explanation for the formation of a half-crossover, but also highlight the critical importance for precise regulation of these SSEs to prevent chromosomal rearrangements.
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机译:同源重组涉及可能干扰染色体分离的支链 DNA 分子的形成。为了解决这些顽固的关节分子,细胞依赖于在细胞周期后期激活结构选择性核酸内切酶 (SSE)。然而,由于复制和/或重组中间体的不及时加工,SSE 的过早激活会损害基因组完整性。在这里,我们使用生化方法表明出芽酵母 SSEs Mus81 和 Yen1 具有切割称为置换环或 D 环的中央重组中间体的能力。此外,我们证明,与以前的遗传数据一致,Mus81 和 Yen1 的同时作用,然后连接,足以在体外重建半交叉前体的形成。我们的结果不仅为半交叉的形成提供了机制解释,还强调了精确调节这些 SSE 以防止染色体重排的至关重要性。
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