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http://purl.uniprot.org/citations/25771894http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/25771894http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/25771894http://www.w3.org/2000/01/rdf-schema#comment"We investigate how outgrowth at the basolateral cell membrane is coordinated with apical lumen formation in the development of a biological tube by characterizing exc-6, a gene required for C. elegans excretory cell (EC) tubulogenesis. We show that EXC-6 is orthologous to the human formin INF2, which polymerizes filamentous actin (F-actin) and binds microtubules (MTs) in vitro. Dominant INF2 mutations cause focal segmental glomerulosclerosis (FSGS), a kidney disease, and FSGS+Charcot-Marie-Tooth neuropathy. We show that activated INF2 can substitute for EXC-6 in C. elegans and that disease-associated mutations cause constitutive activity. Using genetic analysis and live imaging, we show that exc-6 regulates MT and F-actin accumulation at EC tips and dynamics of basolateral-localized MTs, indicating that EXC-6 organizes F-actin and MT cytoskeletons during tubulogenesis. The pathology associated with INF2 mutations is believed to reflect misregulation of F-actin, but our results suggest alternative or additional mechanisms via effects on MT dynamics."xsd:string
http://purl.uniprot.org/citations/25771894http://purl.org/dc/terms/identifier"doi:10.1016/j.devcel.2015.01.009"xsd:string
http://purl.uniprot.org/citations/25771894http://purl.org/dc/terms/identifier"doi:10.1016/j.devcel.2015.01.009"xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/author"Greenwald I."xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/author"Greenwald I."xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/author"Shaye D.D."xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/author"Shaye D.D."xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/name"Dev. Cell"xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/name"Dev. Cell"xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/pages"743-755"xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/pages"743-755"xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/title"The disease-associated formin INF2/EXC-6 organizes lumen and cell outgrowth during tubulogenesis by regulating F-actin and microtubule cytoskeletons."xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/title"The disease-associated formin INF2/EXC-6 organizes lumen and cell outgrowth during tubulogenesis by regulating F-actin and microtubule cytoskeletons."xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/volume"32"xsd:string
http://purl.uniprot.org/citations/25771894http://purl.uniprot.org/core/volume"32"xsd:string
http://purl.uniprot.org/citations/25771894http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/25771894
http://purl.uniprot.org/citations/25771894http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/25771894
http://purl.uniprot.org/citations/25771894http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/25771894
http://purl.uniprot.org/citations/25771894http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/25771894
http://purl.uniprot.org/uniprot/Q9TYU9http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/25771894
http://purl.uniprot.org/uniprot/Q9TYU9#attribution-3DDB608F8E03FD87B6731082EF07B595http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/25771894