SYNTAXIN AND SYNAPTOBREVIN FUNCTION DOWNSTREAM OF VESICLE DOCKING IN DROSOPHILA

被引:304
作者
BROADIE, K
PROKOP, A
BELLEN, HJ
OKANE, CJ
SCHULZE, KL
SWEENEY, ST
机构
[1] UNIV CAMBRIDGE,DEPT GENET,CAMBRIDGE CB2 3EJ,ENGLAND
[2] BAYLOR COLL MED,HOWARD HUGHES MED INST,DIV NEUROSCI,HOUSTON,TX 77030
[3] BAYLOR COLL MED,DEPT HUMAN MOLEC GENET,HOUSTON,TX 77030
[4] BAYLOR COLL MED,DEPT MOLEC & HUMAN GENET,HOUSTON,TX 77030
基金
英国惠康基金;
关键词
D O I
10.1016/0896-6273(95)90154-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In synaptic transmission, vesicles are proposed to dock at presynaptic active zones by the association of synaptobrevin (V-SNARE) with syntaxin (t-SNARE). We test this hypothesis in Drosophila strains lacking neural synaptobrevin (n-synaptobrevin) or syntaxin, We showed previously that loss of either protein completely blocks synaptic transmission, Here, we attempt to establish the level of this blockade. Ultrastructurally, vesicles are still targeted to the presynaptic membrane and dock normally at specialized release sites, These vesicles are mature and functional since spontaneous vesicle fusion persists in the absence of n-synaptobrevin and since vesicle fusion is triggered by hyperosmotic saline in the absence of syntaxin, We conclude that the SNARE hypothesis cannot fully explain the role of these proteins in synaptic transmission, Instead, both proteins play distinct roles downstream of docking.
引用
收藏
页码:663 / 673
页数:11
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