p53 and regulation of DNA damage recognition during nucleotide excision repair

被引:138
作者
Adimoolam, S
Ford, JM
机构
[1] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Oncol, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
关键词
p53; nucleotide excision repair; global genornic repair; XPC; DDB2; DNA damage;
D O I
10.1016/S1568-7864(03)00087-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In response to a variety of types of DNA damage, the p53 tumor suppressor gene product is activated and regulates a number of downstream cellular processes such as cell cycle arrest, apoptosis and DNA repair. Recent discoveries concerning the regulation of DNA repair processes by p53, such as nucleotide excision repair (NER) and base excision repair (BER) have paved the way for studies to understand the mechanisms governing p53-dependent DNA repair. Although several theories have been proposed, accumulating evidence points to a transcriptional regulatory role for p53 in NER, mediating expression of the global genomic repair (GGR)-specific damage recognition genes, DDB2 and XPC. In BER, a more direct role for p53 has been proposed, potentially acting through protein-protein interactions with BER specific factors. These advances have greatly enhanced our understanding of the role of p53 in DNA repair and this review comprehensively summarizes current opinions on the mechanisms of p53-dependent DNA repair. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:947 / 954
页数:8
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