spo11介导的DNA切割的体外重建为减数分裂重组的启动提供了新的思路。

IF 2.6
DNA and cell biology Pub Date : 2025-08-01 Epub Date: 2025-05-19 DOI:10.1089/dna.2025.0091
Cédric Oger, Corentin Claeys Bouuaert
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引用次数: 0

摘要

最近的三项研究报道了由SPO11(拓扑异构酶衍生的酯交换酶,在有性生殖生物中启动减数分裂重组)形成的DNA双链断裂(DSB)的首次生化重建。这些研究的一个中心结论是,SPO11在体外足以催化dsb,但由于SPO11二聚化倾向较差,裂解受到限制,从而提供了有效的机制来防止不受控制的断裂。这些研究为DNA DSB的形成机制提供了新的见解,并对SPO11伴侣的功能、DNA底物的影响、裂解事件之间的协调以及反应的可逆性提出了新的问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Vitro Reconstitution of SPO11-Mediated DNA Cleavage Sheds New Light on the Initiation of Meiotic Recombination.

Three recent studies report the first biochemical reconstitution of DNA double-strand break (DSB) formation by SPO11, the topoisomerase-derived transesterase that initiates meiotic recombination in sexually reproducing organisms. A central conclusion of these studies is that SPO11 is sufficient to catalyze DSBs in vitro, but cleavage is limited by the poor propensity of SPO11 to dimerize, thereby providing an effective mechanism to prevent uncontrolled breaks. The studies yield new insights into the mechanism of DNA DSB formation and raise new questions regarding the functions of SPO11 partners, the impact of the DNA substrate, the coordination between cleavage events, and the reversibility of the reaction.

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