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植物减数分裂中DNA双链断裂的修复:真核生物RecA重组酶及其调节剂的作用

Repair of DNA double-strand breaks in plant meiosis: role of eukaryotic RecA recombinases and their modulators.

作者信息

Emmenecker Côme, Mézard Christine, Kumar Rajeev

机构信息

Institut Jean-Pierre Bourgin (IJPB), Université Paris-Saclay, INRAE, AgroParisTech, 78000, Versailles, France.

University of Paris-Sud, Université Paris-Saclay, 91405, Orsay, France.

出版信息

Plant Reprod. 2023 Mar;36(1):17-41. doi: 10.1007/s00497-022-00443-6. Epub 2022 Jun 1.

Abstract

Homologous recombination during meiosis is crucial for the DNA double-strand breaks (DSBs) repair that promotes the balanced segregation of homologous chromosomes and enhances genetic variation. In most eukaryotes, two recombinases RAD51 and DMC1 form nucleoprotein filaments on single-stranded DNA generated at DSB sites and play a central role in the meiotic DSB repair and genome stability. These nucleoprotein filaments perform homology search and DNA strand exchange to initiate repair using homologous template-directed sequences located elsewhere in the genome. Multiple factors can regulate the assembly, stability, and disassembly of RAD51 and DMC1 nucleoprotein filaments. In this review, we summarize the current understanding of the meiotic functions of RAD51 and DMC1 and the role of their positive and negative modulators. We discuss the current models and regulators of homology searches and strand exchange conserved during plant meiosis. Manipulation of these repair factors during plant meiosis also holds a great potential to accelerate plant breeding for crop improvements and productivity.

摘要

减数分裂期间的同源重组对于DNA双链断裂(DSB)修复至关重要,该修复促进同源染色体的平衡分离并增强遗传变异。在大多数真核生物中,两种重组酶RAD51和DMC1在DSB位点产生的单链DNA上形成核蛋白丝,并在减数分裂DSB修复和基因组稳定性中起核心作用。这些核蛋白丝进行同源性搜索和DNA链交换,以利用位于基因组其他位置的同源模板导向序列启动修复。多种因素可调节RAD51和DMC1核蛋白丝的组装、稳定性和解聚。在这篇综述中,我们总结了目前对RAD51和DMC1减数分裂功能及其正负调节剂作用的理解。我们讨论了植物减数分裂期间保守的同源性搜索和链交换的当前模型和调节剂。在植物减数分裂期间操纵这些修复因子也具有加速植物育种以改善作物和提高生产力的巨大潜力。

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