DNA连接酶
Ku80型
非同源性末端接合
生物
DNA修复
同源重组
DNA修复蛋白XRCC4
DNA
枯草芽孢杆菌
复制蛋白A
遗传学
细胞生物学
dna连接酶
DNA结合蛋白
细菌
核苷酸切除修复
基因
转录因子
作者
Geoffrey R. Weller,Boris Kysela,Rajat Roy,Louise M. Tonkin,Elizabeth Scanlan,Marina Della,Susanne Krogh Devine,Jonathan P. Day,Adam C. Wilkinson,Fabrizio d’Adda di Fagagna,Kevin M. Devine,Richard P. Bowater,Penny A. Jeggo,Stephen P. Jackson,Aidan J. Doherty
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2002-09-05
卷期号:297 (5587): 1686-1689
被引量:334
标识
DOI:10.1126/science.1074584
摘要
In eukaryotic cells, double-strand breaks (DSBs) in DNA are generally repaired by the pathway of homologous recombination or by DNA nonhomologous end joining (NHEJ). Both pathways have been highly conserved throughout eukaryotic evolution, but no equivalent NHEJ system has been identified in prokaryotes. The NHEJ pathway requires a DNA end-binding component called Ku. We have identified bacterial Ku homologs and show that these proteins retain the biochemical characteristics of the eukaryotic Ku heterodimer. Furthermore, we show that bacterial Ku specifically recruits DNA ligase to DNA ends and stimulates DNA ligation. Loss of these proteins leads to hypersensitivity to ionizing radiation in Bacillus subtilis. These data provide evidence that many bacteria possess a DNA DSB repair apparatus that shares many features with the NHEJ system of eukarya and suggest that this DNA repair pathway arose before the prokaryotic and eukaryotic lineages diverged.
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