Functional interaction of the active zone proteins Munc13-1 and RIM1 in synaptic vesicle priming

被引:314
作者
Betz, A
Thakur, P
Junge, HJ
Ashery, U
Rhee, JS
Scheuss, V
Rosenmund, C
Rettig, J
Brose, N
机构
[1] Max Planck Inst Biophys Chem, Abt Membranbiophys, D-37077 Gottingen, Germany
[2] Max Planck Inst Expt Med, Abt Neurogenet, D-37075 Gottingen, Germany
[3] Univ Saarland, Inst Physiol, D-66421 Homburg, Germany
关键词
D O I
10.1016/S0896-6273(01)00272-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Synaptic neurotransmitter release is restricted to active zones, where the processes of synaptic vesicle tethering, priming to fusion competence, and Ca2+-triggered fusion are taking place in a highly coordinated manner, We show that the active zone components Munc13-1, an essential vesicle priming protein, and RIM1, a Rab3 effector with a putative role in vesicle tethering, interact functionally. Disruption of this interaction causes a loss of fusion-competent synaptic vesicles, creating a phenocopy of Munc13-1-deficient neurons. RIM1 binding and Vesicle priming are mediated by two distinct structural modules of Munc13-1. The Munc13-1/RIM1 interaction may create a functional link between synaptic vesicle tethering and priming, or it may regulate the priming reaction itself, thereby determining the number of fusion-competent vesicles.
引用
收藏
页码:183 / 196
页数:14
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