A novel ubiquitin-specific protease, synUSP, is localized at the post-synaptic density and post-synaptic lipid raft

被引:27
作者
Tian, QB
Okano, A
Nakayama, K
Miyazawa, S
Endo, S
Suzuki, T
机构
[1] Shinshu Univ, Grad Sch Med, Res Inst Aging & Adaptat, Dept Neuroplast, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Grad Sch Med, Dept Anat, Matsumoto, Nagano 390, Japan
[3] RIKEN, Brain Sci Inst, Neuronal Circuit Mech Res Grp, Wako, Saitama 35101, Japan
关键词
de-ubiquitination; lipid raft; post-synaptic density; synapse; ubiquitin; ubiquitin-specific protease;
D O I
10.1046/j.1471-4159.2003.02024.x
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
Recent reports suggest an important role for protein ubiquitination in synaptic plasticity. We cloned, from the rat brain, a novel gene that encoded an ubiquitin-specific protease (USP), and termed this protein synaptic ubiquitin-specific protease (synUSP, GenBank(TM) Accession no. AB073880). The homologous human gene was mapped to a locus on chromosome 1p36.12. The deduced synUSP protein consisted of 1036 amino acids, and possessed an ubiquitin-like domain at the C-terminus, Cys- and His-boxes, leucine zipper motifs, and six amino acid-repeats of L/ILCPHG. The protein possessed de-ubiquitinating activity toward a model substrate, as expected from its sequence. The protein of 125 kDa was present in the rat brain; in particular, it was enriched in the post-synaptic density and the dendritic lipid raft fractions. The immunostaining of cortical neurons confirmed the post-synaptic localization. The mRNA for synUSP was localized to dendrites, as well as somas, of neuronal cells. Thus, both the mRNA and the protein were localized in the post-synaptic compartments. These results suggest a regulatory mechanism for the ubiquitin-related system at the post-synaptic sites.
引用
收藏
页码:665 / 675
页数:11
相关论文
共 51 条
[31]   EFFECT OF A GAMMA-AMINOBUTYRIC-ACID UPTAKE INHIBITOR, NNC-711, ON SPONTANEOUS POSTSYNAPTIC CURRENTS IN CULTURED RAT HIPPOCAMPAL-NEURONS - IMPLICATIONS FOR ANTIEPILEPTIC DRUG DEVELOPMENT [J].
OH, DJ ;
DICHTER, MA .
EPILEPSIA, 1994, 35 (02) :426-430
[32]   THE YEAST DOA4 GENE ENCODES A DEUBIQUITINATING ENZYME RELATED TO A PRODUCT OF THE HUMAN TRE-2 ONCOGENE [J].
PAPA, FR ;
HOCHSTRASSER, M .
NATURE, 1993, 366 (6453) :313-319
[33]  
Paradies MA, 1997, J NEUROBIOL, V33, P473, DOI 10.1002/(SICI)1097-4695(199710)33:4<473::AID-NEU10>3.0.CO
[34]  
2-D
[35]   INHIBITORS OF THE PROTEASOME BLOCK THE DEGRADATION OF MOST CELL-PROTEINS AND THE GENERATION OF PEPTIDES PRESENTED ON MHC CLASS-I MOLECULES [J].
ROCK, KL ;
GRAMM, C ;
ROTHSTEIN, L ;
CLARK, K ;
STEIN, R ;
DICK, L ;
HWANG, D ;
GOLDBERG, AL .
CELL, 1994, 78 (05) :761-771
[36]   Intragenic deletion in the gene encoding ubiquitin carboxy-terminal hydrolase in gad mice [J].
Saigoh, K ;
Wang, YL ;
Suh, TG ;
Yamanishi, T ;
Sakai, Y ;
Kiyosawa, H ;
Harada, T ;
Ichihara, N ;
Wakana, S ;
Kikuchi, T ;
Wada, K .
NATURE GENETICS, 1999, 23 (01) :47-51
[37]   DNA SEQUENCING WITH CHAIN-TERMINATING INHIBITORS [J].
SANGER, F ;
NICKLEN, S ;
COULSON, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (12) :5463-5467
[38]   Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase [J].
Shimura, H ;
Hattori, N ;
Kubo, S ;
Mizuno, Y ;
Asakawa, S ;
Minoshima, S ;
Shimizu, N ;
Iwai, K ;
Chiba, T ;
Tanaka, K ;
Suzuki, T .
NATURE GENETICS, 2000, 25 (03) :302-305
[39]   Characterization and chromosomal localization of USP3, a novel human ubiquitin-specific protease [J].
Sloper-Mould, KE ;
Eyre, HJ ;
Wang, XW ;
Sutherland, GR ;
Baker, RT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (38) :26878-26884
[40]  
SUZUKI T, 1994, INT J BIOCHEM, V26, P735