Regulation of proteasome activity in health and disease

被引:353
作者
Schmidt, Marion [1 ]
Finley, Daniel [2 ]
机构
[1] Albert Einstein Coll Med, Dept Biochem, Bronx, NY 10461 USA
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2014年 / 1843卷 / 01期
关键词
Proteasome; Ubiquitin; Protein degradation; UBIQUITIN-INDEPENDENT DEGRADATION; 26S PROTEASOME; TRANSCRIPTION FACTOR; OXIDATIVE-STRESS; 20S PROTEASOME; NUCLEAR PROTEASOME; CONSTITUTIVE PROTEASOMES; PROTEIN-DEGRADATION; SELECTIVE INHIBITOR; HYBRID PROTEASOMES;
D O I
10.1016/j.bbamcr.2013.08.012
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 ubiquitin-proteasome system (UPS) is the primary selective degradation system in the nuclei and cytoplasm of eukaryotic cells, required for the turnover of myriad soluble proteins. The hundreds of factors that comprise the UPS include an enzymatic cascade that tags proteins for degradation via the covalent attachment of a poly-ubiquitin chain, and a large multimeric enzyme that degrades ubiquitinated proteins, the proteasome. Protein degradation by the UPS regulates many pathways and is a crucial component of the cellular proteostasis network. Dysfunction of the ubiquitination machinery or the proteolytic activity of the proteasome is associated with numerous human diseases. In this review we discuss the contributions of the proteasome to human pathology, describe mechanisms that regulate the proteolytic capacity of the proteasome, and discuss strategies to modulate proteasome function as a therapeutic approach to ameliorate diseases associated with altered UPS function. This article is part of a Special Issue entitled: Ubiquitin-Proteasome System. Guest Editors: Thomas Sommer and Dieter H. Wolf. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:13 / 25
页数:13
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