IDENTIFICATION AND CHARACTERIZATION OF DROSOPHILA GENES FOR SYNAPTIC VESICLE PROTEINS

Citation
A. Diantonio et al., IDENTIFICATION AND CHARACTERIZATION OF DROSOPHILA GENES FOR SYNAPTIC VESICLE PROTEINS, The Journal of neuroscience, 13(11), 1993, pp. 4924-4935
Citations number
51
Categorie Soggetti
Neurosciences
Journal title
ISSN journal
02706474
Volume
13
Issue
11
Year of publication
1993
Pages
4924 - 4935
Database
ISI
SICI code
0270-6474(1993)13:11<4924:IACODG>2.0.ZU;2-J
Abstract
Proteins associated with synaptic vesicles are likely to control the r elease of neurotransmitter. Because synaptic transmission is fundament ally similar between vertebrates and invertebrates, vesicle proteins f rom vertebrates that are important for synaptic transmission should be present in Drosophila as well. This investigation describes Drosophil a homologs of vamp, synaptotagmin, and rab3 that are expressed in a pa ttern consistent with a function in Drosophila neurotransmission. One previously reported candidate (syb), a Drosophila homolog of the vamp or synaptobrevin proteins, has been shown to be expressed at very low levels in neurons and is most abundant in the gut. A neuronal Drosophi la vamp (n-syb) is described here and is localized to chromosome band 62A. Northern analysis and in situ hybridizations to mRNA indicate tha t the novel vamp, as well as the genes for synaptotagmin (syt) and rab 3 (drab3), is expressed in the Drosophila nervous system. These genes are widely (perhaps ubiquitously) expressed in the nervous system and we have no evidence of additional neuronal isoforms of synaptotagmin, vamp, or rab3. Immunoreactivity for synaptotagmin and vamp is located in synaptic regions of the nervous system. This distribution suggests that these molecules are components of synaptic vesicles in Drosophila . The conserved structure and neuronal expression pattern of these gen es indicate that they may function in processes that are required for both vertebrate and invertebrate synaptic transmission. Because of the ir distribution in the nervous system and because n-syb, synaptotagmin , and drab3 do not appear to be in a family of functionally redundant homologs, we predict that mutation of these genes will have a profound neurological phenotype and that they are therefore good candidates fo r a genetic dissection in Drosophila.