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doi: 10.1242/10.1242/jcs.00139
Research Article |
1 Programme in Cell Biology The Hospital for Sick Children, University of
Toronto, 555 University Avenue, Toronto, Ontario M5G 1x8 Canada
2 Programme in Developmental Biology, The Hospital for Sick Children, University
of Toronto, 555 University Avenue, Toronto, Ontario M5G 1x8 Canada
3 Department of Biochemistry, University of Toronto, 555 University Avenue,
Toronto, Ontario M5G 1x8 Canada
4 Department of Molecular and Medical Genetics, University of Toronto, 555
University Avenue, Toronto, Ontario M5G 1x8 Canada
* Author for correspondence (e-mail: wtrimble{at}sickkids.on.ca)
Accepted 3 September 2002
SNARE isoforms appear to regulate specific intracellular membrane trafficking steps. To identify new SNARE proteins in Drosophila melanogaster we used a yeast two-hybrid screen to search for proteins that interact with SNAP. Here we report the identification of the Drosophila homologue of syntaxin 16. dsyntaxin 16 binds SNAP in a concentration-dependent fashion and genetically interacts with NSF2. Like its mammalian homologue, dsyntaxin 16 is ubiquitously expressed and appears to be localized to the Golgi apparatus. In addition, membranes containing dsyntaxin 16 become aggregated upon Brefeldin A treatment and are dispersed during meiosis. Inhibition of dsyntaxin 16 function by overexpression of truncated forms in cultured Schneider cells indicates that dsyntaxin 16 may selectively regulate Golgi dynamics.
Key words: Golgi, SNARE, Syntaxin, Membrane fusion, Drosophila
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