A. Diantonio et al., IDENTIFICATION AND CHARACTERIZATION OF DROSOPHILA GENES FOR SYNAPTIC VESICLE PROTEINS, The Journal of neuroscience, 13(11), 1993, pp. 4924-4935
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.