Homer: A protein that selectively binds metabotropic glutamate receptors

被引:907
作者
Brakeman, PR
Lanahan, AA
OBrien, R
Roche, K
Barnes, CA
Huganir, RL
Worley, PF
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROSCI,BALTIMORE,MD 21205
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
[3] JOHNS HOPKINS UNIV,SCH MED,DEPT BIOCHEM,BALTIMORE,MD 21205
[4] JOHNS HOPKINS UNIV,SCH MED,HOWARD HUGHES MED INST,BALTIMORE,MD 21205
[5] NIH,BETHESDA,MD 20892
[6] UNIV ARIZONA,DEPT PSYCHOL & NEUROL,TUCSON,AZ
[7] UNIV ARIZONA,DIV NEURONAL SYST MEMORY & AGING,TUCSON,AZ
关键词
D O I
10.1038/386284a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Spatial localization and clustering of membrane proteins is critical to neuronal development and synaptic plasticity. Recent studies have identified a family of proteins, the PDZ proteins, that contain modular PDZ domains and interact with synaptic ionotropic glutamate receptors(1) and ion channels(2). PDZ proteins are thought to have a role in defining the cellular distribution of the proteins that interact with them, Here we report a novel dendritic protein, Homer, that contains a single, PDZ-like domain and binds specifically to the carboxy terminus of phosphoinositide-linked metabotropic glutamate receptors. Homer is highly divergent from known PDZ proteins and seems to represent a novel family. The Homer gene is also distinct from members of the PDZ family in that its expression is regulated as an immediate early gene and is dynamically responsive to physiological synaptic activity, particularly during cortical development. This dynamic transcriptional control suggests that Homer mediates a novel cellular mechanism that regulates metabotropic glutamate signalling.
引用
收藏
页码:284 / 288
页数:5
相关论文
共 28 条
  • [1] THE METABOTROPIC GLUTAMATE-RECEPTOR (MGLUR1-ALPHA) IS CONCENTRATED AT PERISYNAPTIC MEMBRANE OF NEURONAL SUBPOPULATIONS AS DETECTED BY IMMUNOGOLD REACTION
    BAUDE, A
    NUSSER, Z
    ROBERTS, JDB
    MULVIHILL, E
    MCILHINNEY, RAJ
    SOMOGYI, P
    [J]. NEURON, 1993, 11 (04) : 771 - 787
  • [2] BHAT RV, 1993, J PHARMACOL EXP THER, V267, P496
  • [3] PROTEIN-INTERACTION CLONING IN YEAST - IDENTIFICATION OF MAMMALIAN PROTEINS THAT REACT WITH THE LEUCINE ZIPPER OF JUN
    CHEVRAY, PM
    NATHANS, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (13) : 5789 - 5793
  • [4] GRIP: A synaptic PDZ domain-containing protein that interacts with AMPA receptors
    Dong, HL
    OBrien, RJ
    Fung, ET
    Lanahan, AA
    Worley, PF
    Huganir, RL
    [J]. NATURE, 1997, 386 (6622) : 279 - 284
  • [5] Crystal structures of a complexed and peptide-free membrane protein-binding domain: Molecular basis of peptide recognition by PDZ
    Doyle, DA
    Lee, A
    Lewis, J
    Kim, E
    Sheng, M
    MacKinnon, R
    [J]. CELL, 1996, 85 (07) : 1067 - 1076
  • [6] Flor PJ, 1996, J NEUROCHEM, V67, P58
  • [7] THE LONG AND THE SHORT OF LONG-TERM-MEMORY - A MOLECULAR FRAMEWORK
    GOELET, P
    CASTELLUCCI, VF
    SCHACHER, S
    KANDEL, ER
    [J]. NATURE, 1986, 322 (6078) : 419 - 422
  • [8] DOPAMINE REGULATION OF TRANSCRIPTION FACTOR-TARGET INTERACTIONS IN RAT STRIATUM
    HYMAN, SE
    COLE, RL
    KONRADI, C
    KOSOFSKY, BE
    [J]. CHEMICAL SENSES, 1995, 20 (02) : 257 - 260
  • [9] JOLY C, 1995, J NEUROSCI, V15, P3970
  • [10] CLUSTERING OF SHAKER-TYPE K+ CHANNELS BY INTERACTION WITH A FAMILY OF MEMBRANE-ASSOCIATED GUANYLATE KINASES
    KIM, E
    NIETHAMMER, M
    ROTHSCHILD, A
    JAN, YN
    SHENG, M
    [J]. NATURE, 1995, 378 (6552) : 85 - 88