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在紧张时刻放松身心:解旋酶在减数分裂重组中的作用机制。

Unwinding during stressful times: Mechanisms of helicases in meiotic recombination.

机构信息

Structural Biochemistry of Meiosis Group, Friedrich Miescher Laboratory of the Max Planck Society, Tuebingen, Germany.

Structural Biochemistry of Meiosis Group, Friedrich Miescher Laboratory of the Max Planck Society, Tuebingen, Germany.

出版信息

Curr Top Dev Biol. 2023;151:191-215. doi: 10.1016/bs.ctdb.2022.06.004. Epub 2022 Jul 18.

Abstract

Successful meiosis I requires that homologous chromosomes be correctly linked before they are segregated. In most organisms this physical linkage is achieved through the generation of crossovers between the homologs. Meiotic recombination co-opts and modifies the canonical homologous recombination pathway to successfully generate crossovers One of the central components of this pathway are a number of conserved DNA helicases. Helicases couple nucleic acid binding to nucleotide hydrolysis and use this activity to modify DNA or protein-DNA substrates. During meiosis I it is necessary for the cell to modulate the canonical DNA repair pathways in order to facilitate the generation of interhomolog crossovers. Many of these meiotic modulations take place in pathways involving DNA helicases, or with a meiosis specific helicase. This short review explores what is currently understood about these helicases, their interaction partners, and the role of regulatory modifications during meiosis I. We focus in particular on the molecular structure and mechanisms of these helicases.

摘要

减数分裂 I 的成功进行要求同源染色体在分离之前正确连接。在大多数生物体中,这种物理连接是通过同源之间的交叉生成来实现的。减数分裂重组采用并修饰了经典的同源重组途径,以成功生成交叉。该途径的核心组成部分之一是许多保守的 DNA 解旋酶。解旋酶将核酸结合与核苷酸水解偶联,并利用这种活性来修饰 DNA 或蛋白-DNA 底物。在减数分裂 I 期间,细胞有必要调节经典的 DNA 修复途径,以促进同源间交叉的生成。这些减数分裂调节中的许多发生在涉及 DNA 解旋酶的途径中,或与减数分裂特异性解旋酶有关。这篇简短的综述探讨了目前对这些解旋酶及其相互作用伙伴以及减数分裂 I 期间调节修饰的了解。我们特别关注这些解旋酶的分子结构和机制。

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