DUBs, the regulation of cell identity and disease

被引:64
作者
Heideker, Johanna [1 ]
Wertz, Ingrid E. [1 ]
机构
[1] Genentech Inc, Dept Mol Oncol, San Francisco, CA 94080 USA
关键词
deubiquitinase; drug discovery; signalling; post-translational modification; ubiquitin; NF-KAPPA-B; UBIQUITIN-SPECIFIC PROTEASE; SMALL-MOLECULE INHIBITOR; TUMOR-SUPPRESSOR CYLD; PAPAIN-LIKE PROTEASE; FATTY-ACID SYNTHASE; DNA-DAMAGE RESPONSE; LOOP-HELIX PROTEINS; DEUBIQUITINATING ENZYME; HISTONE H2A;
D O I
10.1042/BJ20140496
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The post-translational modification of proteins with ubiquitin represents a complex signalling system that co-ordinates essential cellular functions, including proteolysis, DNA repair, receptor signalling and cell communication. DUBs (deubiquitinases), the enzymes that disassemble ubiquitin chains and remove ubiquitin from proteins, are central to this system. Reflecting the complexity and versatility of ubiquitin signalling, DUB activity is controlled in multiple ways. Although several lines of evidence indicate that aberrant DUB function may promote human disease, the underlying molecular mechanisms are often unclear. Notwithstanding, considerable interest in DUBs as potential drug targets has emerged over the past years. The future success of DUB-based therapy development will require connecting the basic science of DUB function and enzymology with drug discovery. In the present review, we discuss new insights into DUB activity regulation and their links to disease, focusing on the role of DUBs as regulators of cell identity and differentiation, and discuss their potential as emerging drug targets.
引用
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页码:1 / 26
页数:26
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