| Literature DB >> 27002143 |
Ji Won Um1, Gayoung Choii2, Dongseok Park3, Dongwook Kim3, Sangmin Jeon2, Hyeyeon Kang3, Takuma Mori4, Theofilos Papadopoulos5, Taesun Yoo6, Yeunkum Lee7, Eunjoon Kim8, Katsuhiko Tabuchi9, Jaewon Ko10.
Abstract
Gephyrin is a central scaffold protein that mediates development, function, and plasticity of mammalian inhibitory synapses by interacting with various inhibitory synaptic proteins. Here, we show that IQSEC3, a guanine nucleotide exchange factor for ARF6, directly interacts with gephyrin, an interaction that is critical for the inhibitory synapse localization of IQSEC3. Overexpression of IQSEC3 increases inhibitory, but not excitatory, synapse density in a guanine nucleotide exchange factor activity-dependent manner. Conversely, knockdown of IQSEC3 decreases size of gephyrin cluster without altering gephyrin puncta density. Collectively, these data reveal that IQSEC3 acts together with gephyrin to regulate inhibitory synapse development.Entities:
Keywords: BRAG3; IQSEC3; SynARFGEF; gephyrin; inhibition mechanism; inhibitory synapse; protein-protein interaction; scaffold protein; synapse; γ-aminobutyric acid (GABA)
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Year: 2016 PMID: 27002143 PMCID: PMC4858964 DOI: 10.1074/jbc.M115.712893
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157