枯草芽孢杆菌ku介导的DNA突触复合体的结构。

IF 13.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Whan-Jong Kim,Jieun Kim,Mingyu Jo,Youngjin Kim,Min-Sung Kim
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引用次数: 0

摘要

DNA双链断裂(DSBs)对基因组完整性构成严重威胁,细胞的修复主要依赖于两种途径:同源重组和非同源末端连接(NHEJ)。真核生物的NHEJ需要包括Ku70/80异源二聚体在内的多组分组装,而细菌的NHEJ使用一个更简单的工具包,包括Ku同源二聚体和多功能的LigD。尽管如此简单,但在细菌NHEJ中,断裂的DNA末端连接在一起的机制仍不清楚。在这里,我们展示了枯草芽孢杆菌Ku (bsKu)-DNA复合物的低温电镜结构,分辨率为2.74 Å,捕获了两个由Ku蛋白单独桥接的钝DNA末端。在进一步生化分析的支持下,我们提出了一个整合模型,其中Ku同型二聚体的寡聚阵列连接并稳定了两个DNA末端,促进了枯草芽孢杆菌DSB的有效修复。这项工作揭示了bsku介导的DNA桥接机制不同于真核系统,并为原核DNA修复提供了关键的结构见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structure of Bacillus subtilis Ku-mediated DNA synaptic complex.
DNA double-strand breaks (DSBs) pose a severe threat to genomic integrity, and cells rely on two major pathways for repair: homologous recombination and non-homologous end joining (NHEJ). While eukaryotic NHEJ requires a multi-component assembly including the Ku70/80 heterodimer, bacterial NHEJ operates with a simpler toolkit comprising a Ku homodimer and the multifunctional LigD. Despite this simplicity, the mechanism by which broken DNA ends are bridged together has remained unclear in bacterial NHEJ. Here, we present a cryo-electron microscopy structure of the Bacillus subtilis Ku (bsKu)-DNA complex at 2.74 Å resolution, capturing two blunt DNA ends bridged by a Ku protein alone. Supported by further biochemical assays, we propose an integrated model in which oligomeric arrays of Ku homodimers bridge and stabilize two DNA ends, facilitating efficient DSB repair in Bacillus subtilis. This work reveals a bsKu-mediated DNA bridging mechanism distinct from the eukaryotic system and provides critical structural insight into prokaryotic DNA repair.
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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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