Ubiquitin, proteasome and parkin

被引:85
作者
Tanaka, K
Suzuki, T
Hattori, N
Mizuno, Y
机构
[1] Tokyo Metropolitan Inst Med Sci, Dept Mol Oncol, Bunkyo Ku, Tokyo 1130021, Japan
[2] Juntendo Univ, Sch Med, Dept Neurol, Bunkyo Ku, Tokyo 1130033, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2004年 / 1695卷 / 1-3期
关键词
neurodegeneration; parkin; Parkinson's disease; proteasome; quality control; ubiquitin;
D O I
10.1016/j.bbamcr.2004.09.026
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 important for intracellular proteolysis. and is responsible for a diverse array of biologically important cellular processes, such as cell-cycle progression, signaling cascades and developmental programs. This system is also involved in the protein quality control, which maintains the health of the cell. Thus, the UPS provides a clue for understanding of the molecular mechanisms underlying various neurodegenerative diseases. In the last decade. we witnessed a tremendous progress in uncovering the mechanisms of Parkinson's disease (PD). Of the several genes that can cause familial PD, park-in. the causative gene of autosomal recessive juvenile parkinsonism (ARJP), is of a special interest because it encodes an ubiquitin-protein ligase. which covalently attaches ubiquitin to target proteins, designating them for destruction by the proteasome. This review summarizes recent studies on the UPS pathway with a special reference to parkin, focusing on how parkin is linked to the pathogenesis of ARJP. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:235 / 247
页数:13
相关论文
共 79 条
[1]   A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe [J].
Abbas, N ;
Lücking, CB ;
Ricard, S ;
Dürr, A ;
Bonifati, V ;
De Michele, G ;
Bouley, S ;
Vaughan, JR ;
Gasser, T ;
Marconi, R ;
Broussolle, E ;
Brefel-Courbon, C ;
Harhangi, BS ;
Oostra, AB ;
Fabrizio, E ;
Böhme, GA ;
Pradier, L ;
Wood, NW ;
Filla, A ;
Meco, G ;
Denefle, P ;
Agid, Y ;
Brice, A .
HUMAN MOLECULAR GENETICS, 1999, 8 (04) :567-574
[2]   The U box is a modified RING finger - a common domain in ubiquitination [J].
Aravind, L ;
Koonin, EV .
CURRENT BIOLOGY, 2000, 10 (04) :R132-R134
[3]   The proteasome:: Paradigm of a self-compartmentalizing protease [J].
Baumeister, W ;
Walz, J ;
Zühl, F ;
Seemuller, E .
CELL, 1998, 92 (03) :367-380
[4]   The proteasome [J].
Bochtler, M ;
Ditzel, L ;
Groll, M ;
Hartmann, C ;
Huber, R .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 1999, 28 :295-+
[5]   RING domains: Master builders of molecular scaffolds? [J].
Borden, KLB .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 295 (05) :1103-1112
[6]   Parkin ubiquitinates the α-synuclein-interacting protein, synphilin-1:: implications for Lewy-body formation in Parkinson disease [J].
Chung, KKK ;
Zhang, Y ;
Lim, KL ;
Tanaka, Y ;
Huang, H ;
Gao, J ;
Ross, CA ;
Dawson, VL ;
Dawson, TM .
NATURE MEDICINE, 2001, 7 (10) :1144-1150
[7]   Neurodegeneration: How does Parkin prevent Parkinson's disease? [J].
Cookson, MR .
CURRENT BIOLOGY, 2003, 13 (13) :R522-R524
[8]   Pathways to parkinsonism [J].
Cookson, MR .
NEURON, 2003, 37 (01) :7-10
[9]   The p38 subunit of the aminoacyl-tRNA synthetase complex is a Parkin substrate: linking protein biosynthesis and neurodegeneration [J].
Corti, O ;
Hampe, C ;
Koutnikova, H ;
Darios, F ;
Jacquier, S ;
Prigent, A ;
Robinson, JC ;
Pradier, L ;
Ruberg, M ;
Mirande, M ;
Hirsch, E ;
Rooney, T ;
Fournier, A ;
Brice, A .
HUMAN MOLECULAR GENETICS, 2003, 12 (12) :1427-1437
[10]   Structure and functions of the 20S and 26S proteasomes [J].
Coux, O ;
Tanaka, K ;
Goldberg, AL .
ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 :801-847