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http://purl.uniprot.org/citations/26218657http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/26218657http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/26218657http://www.w3.org/2000/01/rdf-schema#comment"ADAMTS9 is a metalloprotease that cleaves components of the extracellular matrix and is also implicated in transport from the endoplasmic reticulum (ER) to the Golgi. It has been reported that an ADAMTS9 gene variant is associated with type 2 diabetes. The underlying pathology of type 2 diabetes is insulin resistance and beta-cell dysfunction. However, the molecular mechanisms underlying ADAMTS9 function in beta cells and peripheral tissues are unknown. We show that loss of C. elegans GON-1, an ADAMTS9 homolog, alters lifespan and dauer formation. GON-1 loss impairs secretion of proteins such as insulin orthologs and TGF-beta, and additionally impacts insulin/IGF-1 signaling in peripheral tissues. The function of the GON domain, but not the protease domain, is essential for normal lifespan and dauer formation in these scenarios. We conclude that the GON domain is critical for ADAMTS9/GON-1 function across species, which should help the understanding of type 2 diabetes in humans."xsd:string
http://purl.uniprot.org/citations/26218657http://purl.org/dc/terms/identifier"doi:10.1371/journal.pone.0133966"xsd:string
http://purl.uniprot.org/citations/26218657http://purl.org/dc/terms/identifier"doi:10.1371/journal.pone.0133966"xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/author"Mitani S."xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/author"Mitani S."xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/author"Yoshina S."xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/author"Yoshina S."xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/name"PLoS ONE"xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/name"PLoS ONE"xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/pages"E0133966"xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/pages"E0133966"xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/title"Loss of C. elegans GON-1, an ADAMTS9 Homolog, decreases secretion resulting in altered lifespan and dauer formation."xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/title"Loss of C. elegans GON-1, an ADAMTS9 Homolog, decreases secretion resulting in altered lifespan and dauer formation."xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/volume"10"xsd:string
http://purl.uniprot.org/citations/26218657http://purl.uniprot.org/core/volume"10"xsd:string
http://purl.uniprot.org/citations/26218657http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/26218657
http://purl.uniprot.org/citations/26218657http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/26218657
http://purl.uniprot.org/citations/26218657http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/26218657
http://purl.uniprot.org/citations/26218657http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/26218657
http://purl.uniprot.org/uniprot/Q19791http://purl.uniprot.org/core/citationhttp://purl.uniprot.org/citations/26218657
http://purl.uniprot.org/uniprot/P92172#attribution-150FDF1D9C5F660EF675A8AC209B1B91http://purl.uniprot.org/core/sourcehttp://purl.uniprot.org/citations/26218657