Controlling Meiotic Double-Strand Break Formation in Mice: A Web of Multivalent Protein–Protein Interactions

IF 3.3 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
BioEssays Pub Date : 2026-09-30 DOI:10.1002/bies.70190
Jiaqi Xu, Scott Keeney
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引用次数: 0

Abstract

A complex network of protein interactions promotes the cooperative assembly of biomolecular condensates that control the formation of meiotic DNA double-strand breaks (DSBs). In many species, programmed DSBs made by SPO11 are required for the faithful pairing and segregation of homologous chromosomes during meiosis I. DSBs must be tightly regulated to support their intended function but also to minimize the risk of genomic damage from mutation or defective DSB repair. Multiple chromosome axis-associated proteins are important for the control of meiotic DSB formation and recombination, but the underlying mechanisms of those proteins remain poorly understood. Here, we present a current view of how these proteins work together in mice, based on recent advances in the characterization of their function and structure.

控制小鼠减数分裂双链断裂的形成:一个多价蛋白相互作用的网络。
一个复杂的蛋白质相互作用网络促进生物分子凝聚物的合作组装,控制减数分裂DNA双链断裂(DSBs)的形成。在许多物种中,由SPO11制造的程序化DSB在减数分裂i期间对同源染色体的忠实配对和分离是必需的。DSB必须被严格调节以支持其预期功能,同时也要将DSB突变或缺陷修复带来的基因组损伤风险降至最低。多染色体轴相关蛋白对减数分裂DSB的形成和重组的控制很重要,但这些蛋白的潜在机制尚不清楚。在这里,我们提出了这些蛋白质如何在小鼠中协同工作的当前观点,基于其功能和结构表征的最新进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BioEssays
BioEssays 生物-生化与分子生物学
CiteScore
7.30
自引率
2.50%
发文量
167
审稿时长
4-8 weeks
期刊介绍: molecular – cellular – biomedical – physiology – translational research – systems - hypotheses encouraged BioEssays is a peer-reviewed, review-and-discussion journal. Our aims are to publish novel insights, forward-looking reviews and commentaries in contemporary biology with a molecular, genetic, cellular, or physiological dimension, and serve as a discussion forum for new ideas in these areas. An additional goal is to encourage transdisciplinarity and integrative biology in the context of organismal studies, systems approaches, through to ecosystems, where appropriate.
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