The ubiquitin receptor Rad23: At the crossroads of nucleotide excision repair and proteasomal degradation

被引:122
作者
Dantuma, Nico P. [1 ]
Heinen, Christian [1 ]
Hoogstraten, Deborah [1 ]
机构
[1] Karolinska Inst, Med Nobel Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
DNA repair; Ubiquitin; Proteasome; Degradation; hHR23; Rad23; Dsk2; Ddi1; Xeroderma pigmentosum; Ultraviolet light; Photolesions; GROUP-C PROTEIN; NEWLY SYNTHESIZED PROTEINS; DAMAGE-INDUCIBLE PROTEINS; 19S REGULATORY PARTICLE; DNA-REPAIR; SACCHAROMYCES-CEREVISIAE; XERODERMA-PIGMENTOSUM; 26S PROTEASOME; UBA DOMAIN; TRANSCRIPTION FACTOR;
D O I
10.1016/j.dnarep.2009.01.005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A protein that exemplifies the intimate link between the ubiquitin/proteasome system (UPS) and DNA repair is the yeast nucleotide excision repair (NER) protein Rad23 and its human orthologs hHR23A and hHR23B. Rad23, which was originally identified as an important factor involved in the recognition of DNA lesions. also plays a central role in targeting ubiquitylated proteins for proteasomal degradation, an activity that it shares with other ubiquitin receptors like Dsk2 and Ddi1. Although the finding that Rad23 serves as a ubiquitin receptor explains to a large extent its importance in proteasomal degradation, the precise mode of action of Rad23 in NER and the possible link with the UPS is less clear. In this review, we discuss our present knowledge on the functions of Rad23 in protein degradation and DNA repair and speculate on the importance of the dual roles of Rad23 for the cell's ability to cope with stress conditions. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:449 / 460
页数:12
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