The emerging role of deubiquitination in nucleotide excision repair

被引:6
|
作者
Zhang, Ling [1 ]
Gong, Feng [1 ]
机构
[1] Univ Miami, Miller Sch Med, Dept Biochem & Mol Biol, Miami, FL 33136 USA
关键词
Ubiquitination; Deubiquitination; GG-NER; TC-NER; E3 ubiquitin ligase; DUBs; Ubiquitin linkage specificity; Segregase; UV-SENSITIVE SYNDROME; UBIQUITIN LIGASE COMPLEX; PIGMENTOSUM GROUP-E; DNA-DAMAGE; XPC PROTEIN; MOLECULAR-MECHANISMS; GENE-PRODUCT; HISTONE H2A; DDB2; UBIQUITYLATION;
D O I
10.1016/j.dnarep.2016.05.035
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Nucleotide excision repair (NER) protects genome stability by eliminating DNA helix distorting lesions, such as those induced by UV radiation. The addition and removal of ubiquitin, namely, ubiquitination and deubiquitination, have recently been demonstrated as general mechanisms to regulate protein functions. Accumulating evidence shows that several NER factors are subjected to extensive regulation by ubiquitination and deubiquitination. Thus, the balance between E3 ligases and deubiquitinating enzyme activities can dynamically alter the ubiquitin landscape at DNA damage sites, thereby regulating NER efficiency. Current knowledge about XPC ubiquitination by different ubiquitin E3 ligases highlights the importance of ubiquitin linkage types in regulating XPC binding and release from damaged DNA. Here, we discuss the emerging roles of deubiquitinating enzymes and their ubiquitin linkage specificities in NER. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:118 / 122
页数:5
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