Deubiquitinating enzymes: Their roles in development, differentiation, and disease

被引:22
作者
Fischer, JA [1 ]
机构
[1] Univ Texas, Inst Cellular & Mol Biol, Sect Mol Cell & Dev Biol, Austin, TX 78712 USA
来源
INTERNATIONAL REVIEW OF CYTOLOGY - A SURVEY OF CELL BIOLOGY, VOL 229 | 2003年 / 229卷
关键词
deubiquitinating enzyme; ubiquitin; Ubp; Uch; Dub; proteolysis; UBIQUITIN-SPECIFIC PROTEASE; DROSOPHILA EYE DEVELOPMENT; FAT-FACETS GENE; TUMOR-SUPPRESSOR PROTEIN; FREE POLYUBIQUITIN CHAINS; SACCHAROMYCES-CEREVISIAE; TERMINAL HYDROLASE; PARKINSONS-DISEASE; EMBRYO DEVELOPMENT; IN-VIVO;
D O I
10.1016/S0074-7696(03)29002-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ubiquitin-mediated proteolysis pathway has come a long way in the past decade. At first thought to be an unglamorous garbage dump for damaged proteins, the ubiquitin pathway has been shown to regulate virtually everything that occurs in the cell. Deubiquitinating enzymes, which cleave ubiquitin-protein bonds, are the largest group of enzymes in the pathway, yet they are the least well understood. Deubiquitinating enzymes have two kinds of functions: housekeeping and regulatory. The housekeeping enzymes facilitate the proteolytic pathway. By contrast, the regulatory enzymes control the ubiquitination of specific protein substrates; their relationship to ubiquitination is analgous to that of phosphatases with respect to phosphorylation. Here, I review the current state of knowledge of the deubiquitinating enzymes. I focus particularly on the known regulatory enzymes, and also on the housekeeping enzymes that are implicated in development of disease. © 2003 Elsevier Inc.
引用
收藏
页码:43 / 72
页数:30
相关论文
共 104 条
[1]   Analysis of the deubiquitinating enzymes of the yeast Saccharomyces cerevisiae [J].
Amerik, AY ;
Li, SJ ;
Hochstrasser, M .
BIOLOGICAL CHEMISTRY, 2000, 381 (9-10) :981-992
[2]  
Amerik AY, 1997, EMBO J, V16, P4826
[3]   The Doa4 deubiquitinating enzyme is functionally linked to the vacuolar protein-sorting and endocytic pathways [J].
Amerik, AY ;
Nowak, J ;
Swaminathan, S ;
Hochstrasser, M .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (10) :3365-3380
[4]   Regulation of p53 stability [J].
Ashcroft, M ;
Vousden, KH .
ONCOGENE, 1999, 18 (53) :7637-7643
[5]  
BAKER RT, 1992, J BIOL CHEM, V267, P23364
[6]   Isolation of UBP3, encoding a de-ubiquitinating enzyme, as a multicopy suppressor of a heat-shock mutant strain of S-cerevisiae [J].
Baxter, BK ;
Craig, EA .
CURRENT GENETICS, 1998, 33 (06) :412-419
[7]   Identification of the familial cylindromatosis tumour-suppressor gene [J].
Bignell, GR ;
Warren, W ;
Seal, S ;
Takahashi, M ;
Rapley, E ;
Barfoot, R ;
Green, H ;
Brown, C ;
Biggs, PJ ;
Lakhani, SR ;
Jones, C ;
Hansen, J ;
Blair, E ;
Hofmann, B ;
Siebert, R ;
Turner, G ;
Evans, DG ;
Schrander-Stumpel, C ;
Beemer, FA ;
van den Ouweland, A ;
Halley, D ;
Delpech, B ;
Cleveland, MG ;
Leigh, I ;
Leisti, J ;
Rasmussen, S ;
Wallace, MR ;
Fenske, C ;
Banerjee, P ;
Oiso, N ;
Chaggar, R ;
Merrett, S ;
Leonard, N ;
Huber, M ;
Hohl, D ;
Chapman, P ;
Burn, J ;
Swift, S ;
Smith, A ;
Ashworth, A ;
Stratton, MR .
NATURE GENETICS, 2000, 25 (02) :160-165
[8]   Chemistry-based functional proteomics reveals novel members of the deubiquitinating enzyme [J].
Borodovsky, A ;
Ovaa, H ;
Kolli, N ;
Gan-Erdene, T ;
Wilkinson, KD ;
Ploegh, HL ;
Kessler, BM .
CHEMISTRY & BIOLOGY, 2002, 9 (10) :1149-1159
[9]   Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and manning to the Sxrb interval of the mouse Y chromosome of the Dffry gene [J].
Brown, GM ;
Furlong, RA ;
Sargent, CA ;
Erickson, RP ;
Longepied, G ;
Mitchell, M ;
Jones, MH ;
Hargreave, TB ;
Cooke, HJ ;
Affara, NA .
HUMAN MOLECULAR GENETICS, 1998, 7 (01) :97-107
[10]  
Cadavid ALM, 2000, DEVELOPMENT, V127, P1727