THE SYNTAXIN FAMILY OF VESICULAR TRANSPORT RECEPTORS

被引:614
作者
BENNETT, MK
GARCIAARRARAS, JE
ELFERINK, LA
PETERSON, K
FLEMING, AM
HAZUKA, CD
SCHELLER, RH
机构
[1] Department of Molecular, Cellular Physiology Howard Hughes Medical Institute Stanford University Medical Center Stanford
基金
美国国家科学基金会;
关键词
D O I
10.1016/0092-8674(93)90466-4
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
Syntaxins A and B are nervous system-specific proteins implicated in the docking of synaptic vesicles with the presynaptic plasma membrane. A family of syntaxin-related proteins from rat has been identified that shares 23%-84% amino acid identity. Each of the six syntaxins terminate with a carboxy-terminal hydrophobic domain that anchors the protein on the cytoplasmic surface of cellular membranes. The syntaxins display a broad tissue distribution and, when expressed in COS cells, are targeted to different subcellular compartments. Microinjection studies suggest that the nervous system-specific syntaxin 1A is important for calcium-regulated secretion from neuroendocrine PC12 cells. These results indicate that the syntaxins are a family of receptors for intracellular transport vesicles and that each target membrane may be identified by a specific member of the syntaxin family.
引用
收藏
页码:863 / 873
页数:11
相关论文
共 41 条
  • [1] ANDERSSON S, 1989, J BIOL CHEM, V264, P8222
  • [2] SYNAPTOBREVIN - AN INTEGRAL MEMBRANE-PROTEIN OF 18000 DALTONS PRESENT IN SMALL SYNAPTIC VESICLES OF RAT-BRAIN
    BAUMERT, M
    MAYCOX, PR
    NAVONE, F
    DECAMILLI, P
    JAHN, R
    [J]. EMBO JOURNAL, 1989, 8 (02) : 379 - 384
  • [3] THE MOLECULAR MACHINERY FOR SECRETION IS CONSERVED FROM YEAST TO NEURONS
    BENNETT, MK
    SCHELLER, RH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) : 2559 - 2563
  • [4] SYNTAXIN - A SYNAPTIC PROTEIN IMPLICATED IN DOCKING OF SYNAPTIC VESICLES AT PRESYNAPTIC ACTIVE ZONES
    BENNETT, MK
    CALAKOS, N
    SCHELLER, RH
    [J]. SCIENCE, 1992, 257 (5067) : 255 - 259
  • [5] DO GTPASES DIRECT MEMBRANE TRAFFIC IN SECRETION
    BOURNE, HR
    [J]. CELL, 1988, 53 (05) : 669 - 671
  • [6] INTERACTIONS OF 3 DOMAINS DISTINGUISHING THE RAS-RELATED GTP-BINDING PROTEINS YPT1 AND SEC4
    BRENNWALD, P
    NOVICK, P
    [J]. NATURE, 1993, 362 (6420) : 560 - 563
  • [7] THE SMALL GTPASE RAB5 FUNCTIONS AS A REGULATORY FACTOR IN THE EARLY ENDOCYTIC PATHWAY
    BUCCI, C
    PARTON, RG
    MATHER, IH
    STUNNENBERG, H
    SIMONS, K
    HOFLACK, B
    ZERIAL, M
    [J]. CELL, 1992, 70 (05) : 715 - 728
  • [8] CAIN CC, 1992, J BIOL CHEM, V267, P11681
  • [9] LOCALIZATION OF LOW-MOLECULAR-WEIGHT GTP BINDING-PROTEINS TO EXOCYTIC AND ENDOCYTIC COMPARTMENTS
    CHAVRIER, P
    PARTON, RG
    HAURI, HP
    SIMONS, K
    ZERIAL, M
    [J]. CELL, 1990, 62 (02) : 317 - 329
  • [10] CHIN A, 1993, IN PRESS GENE