DNA连接酶
非同源性末端接合
生物
结扎
核酸外切酶
DNA修复
分子生物学
DNA
聚合酶
细胞生物学
遗传学
作者
Marina Della,Phillip L. Palmbos,Hui-Min Tseng,Louise M. Tonkin,James M. Daley,Leana M. Topper,R. S. Pitcher,Alan E. Tomkinson,Thomas E. Wilson,Aidan J. Doherty
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2004-10-21
卷期号:306 (5696): 683-685
被引量:212
标识
DOI:10.1126/science.1099824
摘要
In mammalian cells, repair of DNA double-strand breaks (DSBs) by nonhomologous end-joining (NHEJ) is critical for genome stability. Although the end-bridging and ligation steps of NHEJ have been reconstituted in vitro, little is known about the end-processing reactions that occur before ligation. Recently, functionally homologous end-bridging and ligation activities have been identified in prokarya. Consistent with its homology to polymerases and nucleases, we demonstrate that DNA ligase D from Mycobacterium tuberculosis (Mt-Lig) possesses a unique variety of nucleotidyl transferase activities, including gap-filling polymerase, terminal transferase, and primase, and is also a 3' to 5' exonuclease. These enzyme activities allow the Mt-Ku and Mt-Lig proteins to join incompatible DSB ends in vitro, as well as to reconstitute NHEJ in vivo in yeast. These results demonstrate that prokaryotic Ku and ligase form a bona fide NHEJ system that encodes all the recognition, processing, and ligation activities required for DSB repair.
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