突触蛋白1
突触小泡
钙调蛋白
细胞生物学
基因亚型
小泡
囊泡融合
快照25
胞吐
突触蛋白I
化学
调节器
生物物理学
接吻奔跑融合
系统1
突触囊泡循环
STX1A型
生物
生物化学
基因
膜
酶
作者
Huisheng Liu,Hua Bai,Enfu Hui,Lu Yang,Chantell S. Evans,Xiaolong Yang,Sung Won Kwon,Edwin R. Chapman
出处
期刊:eLife
[eLife Sciences Publications, Ltd.]
日期:2014-02-25
卷期号:3
被引量:97
摘要
Synaptotagmin (syt) 7 is one of three syt isoforms found in all metazoans; it is ubiquitously expressed, yet its function in neurons remains obscure. Here, we resolved Ca2+-dependent and Ca2+-independent synaptic vesicle (SV) replenishment pathways, and found that syt 7 plays a selective and critical role in the Ca2+-dependent pathway. Mutations that disrupt Ca2+-binding to syt 7 abolish this function, suggesting that syt 7 functions as a Ca2+-sensor for replenishment. The Ca2+-binding protein calmodulin (CaM) has also been implicated in SV replenishment, and we found that loss of syt 7 was phenocopied by a CaM antagonist. Moreover, we discovered that syt 7 binds to CaM in a highly specific and Ca2+-dependent manner; this interaction requires intact Ca2+-binding sites within syt 7. Together, these data indicate that a complex of two conserved Ca2+-binding proteins, syt 7 and CaM, serve as a key regulator of SV replenishment in presynaptic nerve terminals.
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