<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gorczyca D</submitter><funding>NINDS NIH HHS</funding><pagination>1033-44</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4664082</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(5)</volume><pubmed_abstract>Targeted membrane addition is a hallmark of many cellular functions. In the nervous system, modification of synaptic membrane size has a major impact on synaptic function. However, because of the complex shape of neurons and the need to target membrane addition to very small and polarized synaptic compartments, this process is poorly understood. Here, we show that Gtaxin (GTX), a Drosophila t-SNARE (target-soluble N-ethylmaleimide-sensitive factor attachment protein receptor), is required for expansion of postsynaptic membranes during new synapse formation. Mutations in gtx lead to drastic reductions in postsynaptic membrane surface, whereas gtx upregulation results in the formation of complex membrane structures at ectopic sites. Postsynaptic GTX activity depends on its direct interaction</pubmed_abstract><journal>The Journal of neuroscience : the official journal of the Society for Neuroscience</journal><pubmed_title>Postsynaptic membrane addition depends on the Discs-Large-interacting t-SNARE Gtaxin.</pubmed_title><pmcid>PMC4664082</pmcid><funding_grant_id>R01 NS042629</funding_grant_id><funding_grant_id>R01 NS030072</funding_grant_id><pubmed_authors>Ashley J</pubmed_authors><pubmed_authors>Gundelfinger E</pubmed_authors><pubmed_authors>Gorczyca D</pubmed_authors><pubmed_authors>Speese S</pubmed_authors><pubmed_authors>Thomas U</pubmed_authors><pubmed_authors>Gherbesi N</pubmed_authors><pubmed_authors>Gramates LS</pubmed_authors><pubmed_authors>Budnik V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Postsynaptic membrane addition depends on the Discs-Large-interacting t-SNARE Gtaxin.</name><description>Targeted membrane addition is a hallmark of many cellular functions. In the nervous system, modification of synaptic membrane size has a major impact on synaptic function. However, because of the complex shape of neurons and the need to target membrane addition to very small and polarized synaptic compartments, this process is poorly understood. Here, we show that Gtaxin (GTX), a Drosophila t-SNARE (target-soluble N-ethylmaleimide-sensitive factor attachment protein receptor), is required for expansion of postsynaptic membranes during new synapse formation. Mutations in gtx lead to drastic reductions in postsynaptic membrane surface, whereas gtx upregulation results in the formation of complex membrane structures at ectopic sites. Postsynaptic GTX activity depends on its direct interaction</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Jan</publication><modification>2025-04-04T20:26:09.889Z</modification><creation>2019-06-06T15:09:35Z</creation></dates><accession>S-EPMC4664082</accession><cross_references><pubmed>17267557</pubmed><doi>10.1523/JNEUROSCI.3160-06.2007</doi><doi>10.1523/jneurosci.3160-06.2007</doi></cross_references></HashMap>