Yoshihara Motojiro, Montana Enrico Sakai
The Picower Center for Learning and Memory, Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Neuroscientist. 2004 Dec;10(6):566-74. doi: 10.1177/1073858404268770.
The synaptotagmin family of vesicle proteins is believed to mediate calcium-dependent regulation of membrane trafficking. Detailed biochemical and in vivo studies of the most characterized isoform, synaptotagmin 1 (syt 1), have provided compelling evidence that it functions as a calcium sensor for fast neurotransmitter release at synapses. However, the function of the remaining isoforms is unclear, and multiple roles have been hypothesized for several of these. Recent evidence in Drosophila has given insight into the function of some of the remaining synaptotagmin family members. Of the five evolutionarily conserved isoforms in Drosophila, only two, syt 1 and syt 4, localize to most, if not all, synapses. The former is localized to presynaptic terminals, whereas the latter is predominantly postsynaptic. This suggests an intriguing possibility that syt 4 may mediate a postsynaptic vesicle trafficking pathway, providing a molecular basis for an evolutionarily conserved bidirectional vesicular trafficking communication system at synapses.
囊泡蛋白的突触结合蛋白家族被认为介导膜转运的钙依赖性调节。对最具特征的异构体突触结合蛋白1(syt 1)进行的详细生化和体内研究提供了令人信服的证据,表明它作为一种钙传感器,在突触处介导快速神经递质释放。然而,其余异构体的功能尚不清楚,并且已对其中几种异构体的多种作用进行了假设。果蝇中的最新证据为其余一些突触结合蛋白家族成员的功能提供了深入了解。在果蝇的五种进化保守异构体中,只有两种,即syt 1和syt 4,定位于大多数(如果不是全部)突触。前者定位于突触前终末,而后者主要位于突触后。这表明了一种有趣的可能性,即syt 4可能介导突触后囊泡转运途径,为突触处进化保守的双向囊泡转运通信系统提供分子基础。