Membrane-associated guanylate kinases regulate adhesion and plasticity at cell junctions

被引:371
作者
Funke, L [1 ]
Dakoji, S [1 ]
Bredt, DS [1 ]
机构
[1] Univ Calif San Francisco, Dept Physiol, San Francisco, CA 94143 USA
关键词
PDZ domain; SH3; domain; synapse; tight junction; signal transduction;
D O I
10.1146/annurev.biochem.74.082803.133339
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
Tissue development, differentiation, and physiology require specialized cellular adhesion and signal transduction at sites of cell-cell contact. Scaffolding proteins that tether adhesion molecules, receptors, and intracellular signaling enzymes organize macromolecular protein complexes at cellular junctions to integrate these functions. One family of such scaffolding proteins is the large group of membrane-associated guanylate kinases (MAGUKs). Genetic studies have highlighted critical roles for MAGUK proteins in the development and physiology of numerous tissues from a variety of metazoan organisms. Mutation of Drosophila discs large (dlg) disrupts epithelial septate junctions and causes overgrowth of imaginal discs. Similarly, mutation of lin-2, a related MAGUK in Caenorhabditis elegans, blocks vulval development, and mutation of the postsynaptic density protein PSD-95 impairs synaptic plasticity in mammalian brain. These diverse roles are explained by recent biochemical and structural analyses of MAGUKs, which demonstrate their capacity to assemble well-defined-yet adaptable-protein complexes at cellular junctions.
引用
收藏
页码:219 / 245
页数:27
相关论文
共 175 条
[71]  
Hoskins R, 1996, DEVELOPMENT, V122, P97
[72]   Organizing a functional junctional complex requires specific domains of the Drosophila MAGUK Discs large [J].
Hough, CD ;
Woods, DF ;
Park, S ;
Bryant, PJ .
GENES & DEVELOPMENT, 1997, 11 (23) :3242-3253
[73]   Nuclear translocation and transcription regulation by the membrane-associated guanylate kinase CASK/LIN-2 [J].
Hsueh, YP ;
Wang, TF ;
Yang, FC ;
Sheng, M .
NATURE, 2000, 404 (6775) :298-302
[74]   Direct interaction of CASK/LIN-2 and syndecan heparan sulfate proteoglycan and their overlapping distribution in neuronal synapses [J].
Hsueh, YP ;
Yang, FC ;
Kharazia, V ;
Naisbitt, S ;
Cohen, AR ;
Weinberg, RJ ;
Sheng, M .
JOURNAL OF CELL BIOLOGY, 1998, 142 (01) :139-151
[75]   Dlg, Scribble and Lgl in cell polarity, cell proliferation and cancer [J].
Humbert, P ;
Russell, S ;
Richardson, H .
BIOESSAYS, 2003, 25 (06) :542-553
[76]   Direct interaction of two polarity complexes implicated in epithelial tight junction assembly [J].
Hurd, TW ;
Gao, L ;
Roh, MH ;
Macara, IG ;
Margolis, B .
NATURE CELL BIOLOGY, 2003, 5 (02) :137-142
[77]   EVIDENCE FOR SILENT SYNAPSES - IMPLICATIONS FOR THE EXPRESSION OF LTP [J].
ISAAC, JTR ;
NICOLL, RA ;
MALENKA, RC .
NEURON, 1995, 15 (02) :427-434
[78]   The LIN-2/LIN-7/LIN-10 complex mediates basolateral membrane localization of the C-elegans EGF receptor LET-23 in vulval epithelial cells [J].
Kaech, SM ;
Whitfield, CW ;
Kim, SK .
CELL, 1998, 94 (06) :761-771
[79]   GKAP, a novel synaptic protein that interacts with the guanylate kinase-like domain of the PSD-95/SAP90 family of channel clustering molecules [J].
Kim, E ;
Naisbitt, S ;
Hsueh, YP ;
Rao, A ;
Rothschild, A ;
Craig, AM ;
Sheng, M .
JOURNAL OF CELL BIOLOGY, 1997, 136 (03) :669-678
[80]   CLUSTERING OF SHAKER-TYPE K+ CHANNELS BY INTERACTION WITH A FAMILY OF MEMBRANE-ASSOCIATED GUANYLATE KINASES [J].
KIM, E ;
NIETHAMMER, M ;
ROTHSCHILD, A ;
JAN, YN ;
SHENG, M .
NATURE, 1995, 378 (6552) :85-88