Doc2γ, a third isoform of double C2 protein, lacking calcium-dependent phospholipid binding activity

被引:37
作者
Fukuda, M
Mikoshiba, K
机构
[1] RIKEN, Brain Sci Inst, Lab Dev Neurobiol, Wako, Saitama 3510198, Japan
[2] Univ Tokyo, Inst Med Sci, Dept Basic Med Sci, Div Mol Neurobiol,Minato Ku, Tokyo 1088639, Japan
基金
日本科学技术振兴机构;
关键词
Doc2; synaptotagmin; rabphilin; C2; domain; exocytosis; phospholipid binding;
D O I
10.1006/bbrc.2000.3520
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
The Doc2 (double C2) family consists of two isoforms (Doc2 alpha and Doc2 beta) characterized by an N-terminal Munc13-1 interacting domain (Mid) and two C2 domains that interact with Ca2+ and phospholipid at the C-terminus. This Ca2+-binding property is thought to be important to the regulation of neurotransmitter release. In this paper, we report a third isoform of mouse Doc2, named Doc2 gamma. Doc2 gamma also contains a putative Mid domain and two C2 domains, and it is 45.6 and 43.2% identical to mouse Doc2 alpha: and Doc2 beta, respectively, at the amino acid level. In contrast to the other Doca isoforms, the C2 domains of Doc2 gamma impair Ca2+-dependent phospholipid binding activity. The highest expression of Doc2 gamma mRNA was found in the heart, but occurs ubiquitously, the same as Doc2 beta. These findings indicate that Doc2 gamma may also function as an effector for Munc13-1 and that it may be involved in the regulation of vesicular trafficking. (C) 2000 Academic Press.
引用
收藏
页码:626 / 632
页数:7
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