Physiological consequences of defects in ERCC1-XPF DNA repair endonuclease

被引:126
作者
Gregg, Siobhan Q. [1 ,2 ]
Robinson, Andria Rasile [2 ,3 ]
Niedernhofer, Laura J. [1 ,2 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Microbiol & Mol Genet, Pittsburgh, PA 15219 USA
[2] Univ Pittsburgh, Inst Canc, Hillman Canc Ctr, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15261 USA
基金
美国国家卫生研究院;
关键词
Genetic diseases; Knockout mice; Endogenous damage; Progeria; Cancer; NUCLEOTIDE EXCISION-REPAIR; COMPLEMENTATION GROUP-F; DOUBLE-STRAND BREAKS; PIGMENTOSUM GROUP-F; FACIO-SKELETAL SYNDROME; CROSS-LINK REPAIR; STRUCTURE-SPECIFIC NUCLEASES; HOLLIDAY JUNCTION RESOLVASE; XERODERMA-PIGMENTOSUM; GENE ERCC1;
D O I
10.1016/j.dnarep.2011.04.026
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
ERCC1-XPF is a structure-specific endonuclease required for nucleotide excision repair, interstrand crosslink repair, and the repair of some double-strand breaks. Mutations in ERCC1 or XPF cause xeroderma pigmentosum, XFE progeroid syndrome or cerebro-oculo-facio-skeletal syndrome, characterized by increased risk of cancer, accelerated aging and severe developmental abnormalities, respectively. This review provides a comprehensive overview of the health impact of ERCC1-XPF deficiency, based on these rare diseases and mouse models of them. This offers an understanding of the tremendous health impact of DNA damage derived from environmental and endogenous sources. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:781 / 791
页数:11
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