Role of yeast Rad5 and its human orthologs, HLTF and SHPRH in DNA damage tolerance

被引:145
|
作者
Unk, Ildiko [1 ]
Hajdu, Ildiko [1 ]
Blastyak, Andras [1 ]
Haracska, Lajos [1 ]
机构
[1] Hungarian Acad Sci, Biol Res Ctr, Inst Genet, H-6726 Szeged, Hungary
基金
英国惠康基金;
关键词
DNA translocase; SWI/SNF2; Damage bypass; Replication; Ubiquitin; DNA polymerase; CELL NUCLEAR ANTIGEN; UBIQUITIN-CONJUGATING-ENZYME; FREE POSTREPLICATION REPAIR; STALLED REPLICATION FORKS; SIMPLE REPETITIVE SEQUENCES; THYMINE-THYMINE DIMER; SACCHAROMYCES-CEREVISIAE; TRANSCRIPTION FACTOR; HOMOLOGOUS RECOMBINATION; GENOMIC INSTABILITY;
D O I
10.1016/j.dnarep.2009.12.013
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In the yeast Saccharomyces cerevisiae, the Rad6-Rad18 DNA damage tolerance pathway constitutes a major defense system against replication fork blocking DNA lesions. The Rad6-Rad18 ubiquitin-conjugating/ligase complex governs error-free and error-prone translesion synthesis by specialized DNA polymerases, as well as an error-free Rad5-dependent postreplicative repair pathway. For facilitating replication through DNA lesions, translesion synthesis polymerases copy directly from the damaged template, while the Rad5-dependent damage tolerance pathway obtains information from the newly synthesized strand of the undamaged sister duplex. Although genetic data demonstrate the importance of the Rad5-dependent pathway in tolerating DNA damages, there has been little understanding of its mechanism. Also, the conservation of the yeast Rad5-dependent pathway in higher order eukaryotic cells remained uncertain for a long time. Here we summarize findings published in recent years regarding the role of Rad5 in promoting error-free replication of damaged DNA, and we also discuss results obtained with its human orthologs, HLTF and SHPRH. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:257 / 267
页数:11
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