A tripartite protein complex with the potential to couple synaptic vesicle exocytosis to cell adhesion in brain

被引:461
作者
Butz, S [1 ]
Okamoto, M [1 ]
Südhof, TC [1 ]
机构
[1] Univ Texas, SW Med Ctr, Howard Hughes Med Inst, Dept Mol Genet,Ctr Basic Neurosci, Dallas, TX 75235 USA
关键词
D O I
10.1016/S0092-8674(00)81736-5
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
We identify a complex of three proteins in brain that has the potential to couple synaptic vesicle exocytosis to neuronal cell adhesion. The three proteins are: (1) CASK, a protein related to MAGUKs (membrane-associated guanylate kinases); (2) Mint1, a putative vesicular trafficking protein; and (3) Veli1, -2, and -3, vertebrate homologs of C. elegans LIN-7. CASK, Mint1, and Velis form a tight, salt-resistant complex that can be readily isolated. CASK, Mint1, and Velis contain PDZ domains in addition to other modules. However, no PDZ domains are involved in complex formation, leaving them free to recruit cell adhesion molecules, receptors, and channels to the complex. We propose that the tripartite complex acts as a nucleation site for the assembly of proteins involved in synaptic vesicle exocytosis and synaptic junctions.
引用
收藏
页码:773 / 782
页数:10
相关论文
共 42 条
[1]   CHARACTERIZATION OF ZO-1, A PROTEIN-COMPONENT OF THE TIGHT JUNCTION FROM MOUSE-LIVER AND MADIN-DARBY CANINE KIDNEY-CELLS [J].
ANDERSON, JM ;
STEVENSON, BR ;
JESAITIS, LA ;
GOODENOUGH, DA ;
MOOSEKER, MS .
JOURNAL OF CELL BIOLOGY, 1988, 106 (04) :1141-1149
[2]   IMPROVED SILVER STAINING OF PLANT-PROTEINS, RNA AND DNA IN POLYACRYLAMIDE GELS [J].
BLUM, H ;
BEIER, H ;
GROSS, HJ .
ELECTROPHORESIS, 1987, 8 (02) :93-99
[3]   THE RAT-BRAIN POSTSYNAPTIC DENSITY FRACTION CONTAINS A HOMOLOG OF THE DROSOPHILA DISKS-LARGE TUMOR SUPPRESSOR PROTEIN [J].
CHO, KO ;
HUNT, CA ;
KENNEDY, MB .
NEURON, 1992, 9 (05) :929-942
[4]  
COHEN AR, 1998, IN PRESS J CELL BIOL
[5]   Crystal structure of the hCASK PDZ domain reveals the structural basis of class II PDZ domain target recognition [J].
Daniels, DL ;
Cohen, AR ;
Anderson, JM ;
Brünger, AT .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (04) :317-325
[6]   Molecular structure and assembly of the tight junction [J].
Denker, BM ;
Nigam, SK .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1998, 274 (01) :F1-F9
[7]   GENE IN THE REGION OF THE FRIEDREICH ATAXIA LOCUS ENCODES A PUTATIVE TRANSMEMBRANE PROTEIN EXPRESSED IN THE NERVOUS-SYSTEM [J].
DUCLOS, F ;
BOSCHERT, U ;
SIRUGO, G ;
MANDEL, JL ;
HEN, R ;
KOENIG, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (01) :109-113
[8]   COMPARISON OF PRIMARY STRUCTURE OF A NEURON-SPECIFIC PROTEIN, X11, BETWEEN HUMAN AND MOUSE [J].
DUCLOS, F ;
KOENIG, M .
MAMMALIAN GENOME, 1995, 6 (01) :57-58
[9]   Sec6/8 complex is recruited to cell-cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells [J].
Grindstaff, KK ;
Yeaman, C ;
Anandasabapathy, N ;
Hsu, SC ;
Rodriguez-Boulan, E ;
Scheller, RH ;
Nelson, WJ .
CELL, 1998, 93 (05) :731-740
[10]   EUKARYOTIC PROTEINS EXPRESSED IN ESCHERICHIA-COLI - AN IMPROVED THROMBIN CLEAVAGE AND PURIFICATION PROCEDURE OF FUSION PROTEINS WITH GLUTATHIONE-S-TRANSFERASE [J].
GUAN, KL ;
DIXON, JE .
ANALYTICAL BIOCHEMISTRY, 1991, 192 (02) :262-267