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http://purl.uniprot.org/citations/18498733http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18498733http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18498733http://www.w3.org/2000/01/rdf-schema#comment"Regulation of synaptic growth is fundamental to the formation and plasticity of neural circuits. Here, we demonstrate that Nervous wreck (Nwk), a negative regulator of synaptic growth at Drosophila NMJs, interacts functionally and physically with components of the endocytic machinery, including dynamin and Dap160/intersectin, and negatively regulates retrograde BMP growth signaling through a direct interaction with the BMP receptor, thickveins. Synaptic overgrowth in nwk is sensitive to BMP signaling levels, and loss of Nwk facilitates BMP-induced overgrowth. Conversely, Nwk overexpression suppresses BMP-induced synaptic overgrowth. We observe analogous genetic interactions between dap160 and the BMP pathway, confirming that endocytosis regulates BMP signaling at NMJs. Finally, we demonstrate a correlation between synaptic growth and pMAD levels and show that Nwk regulates these levels. We propose that Nwk functions at the interface of endocytosis and BMP signaling to ensure proper synaptic growth by negatively regulating Tkv to set limits on this positive growth signal."xsd:string
http://purl.uniprot.org/citations/18498733http://purl.org/dc/terms/identifier"doi:10.1016/j.neuron.2008.03.007"xsd:string
http://purl.uniprot.org/citations/18498733http://purl.org/dc/terms/identifier"doi:10.1016/j.neuron.2008.03.007"xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/author"Ganetzky B."xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/author"Ganetzky B."xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/author"Ho L.L."xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/author"Ho L.L."xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/author"O'Connor-Giles K.M."xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/author"O'Connor-Giles K.M."xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/name"Neuron"xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/name"Neuron"xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/pages"507-518"xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/pages"507-518"xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/title"Nervous wreck interacts with thickveins and the endocytic machinery to attenuate retrograde BMP signaling during synaptic growth."xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/title"Nervous wreck interacts with thickveins and the endocytic machinery to attenuate retrograde BMP signaling during synaptic growth."xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/volume"58"xsd:string
http://purl.uniprot.org/citations/18498733http://purl.uniprot.org/core/volume"58"xsd:string
http://purl.uniprot.org/citations/18498733http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18498733
http://purl.uniprot.org/citations/18498733http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18498733
http://purl.uniprot.org/citations/18498733http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18498733
http://purl.uniprot.org/citations/18498733http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18498733