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突触结合蛋白II。一种新型的分布有差异的突触结合蛋白形式。

Synaptotagmin II. A novel differentially distributed form of synaptotagmin.

作者信息

Geppert M, Archer B T, Südhof T C

机构信息

Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas 75235.

出版信息

J Biol Chem. 1991 Jul 25;266(21):13548-52.

PMID:1856191
Abstract

Synaptotagmin is a synaptic vesicle membrane protein with properties suggestive of a role in synaptic vesicle exocytosis (Perin, M. S., Fried, V. A., Mignery, G. A., Jahn, R., and Südhof, T. C. (1990) Nature 345, 260-263). Here, we report the structure of a novel form of synaptotagmin named synaptotagmin II that is highly homologous to the originally described synaptotagmin, now referred to as synaptotagmin I. Synaptotagmins I and II exhibit the same overall structure, containing a small intravesicular sequence that is glycosylated, a single transmembrane region, and a large carboxyl-terminal cytoplasmic sequence that includes two copies of an internal repeat homologous to the regulatory region of protein kinase C. The homology between synaptotagmins I and II is not uniformly distributed across the molecule but is highest in their carboxyl-terminal regulatory repeats (88% sequence identity) and lowest in their amino-terminal intravesicular sequences (46% sequence identity). RNA blots demonstrate complementary patterns of expression for synaptotagmins I and II, with synaptotagmin I preferentially expressed in rostral, phylogenetically younger brain regions, and synaptotagmin II predominantly expressed in caudal, phylogenetically older brain regions. With this description of two forms of synaptotagmin, all major synaptic vesicle proteins implicated in membrane traffic have now been shown to be present in several isoforms with differential distributions, suggesting that this is a general organizational principle of the mammalian brain.

摘要

突触结合蛋白是一种突触小泡膜蛋白,其特性表明它在突触小泡胞吐作用中发挥作用(佩林,M. S.,弗里德,V. A.,米涅里,G. A.,亚恩,R.,和苏多霍夫,T. C.(1990年)《自然》345卷,260 - 263页)。在此,我们报告一种新型突触结合蛋白的结构,名为突触结合蛋白II,它与最初描述的突触结合蛋白(现称为突触结合蛋白I)高度同源。突触结合蛋白I和II具有相同的整体结构,包含一个经糖基化修饰的小泡内序列、一个单一跨膜区域以及一个大的羧基末端细胞质序列,该序列包含两个与蛋白激酶C调节区域同源的内部重复序列拷贝。突触结合蛋白I和II之间的同源性并非均匀分布于整个分子,而是在其羧基末端调节重复序列中最高(序列同一性为88%),在其氨基末端小泡内序列中最低(序列同一性为46%)。RNA印迹显示突触结合蛋白I和II的表达模式互补,突触结合蛋白I优先表达于前端、系统发育上较年轻的脑区,而突触结合蛋白II主要表达于后端、系统发育上较古老的脑区。随着对两种形式突触结合蛋白的描述,所有与膜转运相关的主要突触小泡蛋白现已被证明以几种具有差异分布的同工型存在,这表明这是哺乳动物脑的一种普遍组织原则。

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