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http://purl.uniprot.org/citations/19590496http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19590496http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19590496http://www.w3.org/2000/01/rdf-schema#comment"The majority of studies on autophagy, a cytoplasmic homeostasis pathway of broad biological and medical significance, have been hitherto focused on the phosphatidylinositol 3-kinases as the regulators of autophagy. Here, we addressed the reverse process driven by phosphoinositide phosphatases and uncovered a key negative regulatory role in autophagy of a phosphatidylinositol 3-phosphate (PI3P) phosphatase Jumpy (MTMR14). Jumpy associated with autophagic isolation membranes and early autophagosomes, defined by the key factor Atg16 necessary for proper localization and development of autophagic organelles. Jumpy orchestrated orderly succession of Atg factors by controlling recruitment to autophagic membranes of the sole mammalian Atg factor that interacts with PI3P, WIPI-1 (Atg18), and by affecting the distribution of Atg9 and LC3, the two Atg factors controlling organization and growth of autophagic membranes. A catalytically inactive Jumpy mutant, R336Q, found in congenital disease centronuclear myopathy, lost the ability to negatively regulate autophagy. This work reports for the first time that initiation of autophagy is controlled not only by the forward reaction of generating PI3P through a lipid kinase but that its levels are controlled by a specific PI3P phosphatase, which when defective can lead to human disease."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.org/dc/terms/identifier"doi:10.1038/emboj.2009.159"xsd:string
http://purl.uniprot.org/citations/19590496http://purl.org/dc/terms/identifier"doi:10.1038/emboj.2009.159"xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Deretic V."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Deretic V."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Proikas-Cezanne T."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Proikas-Cezanne T."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Laporte J."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Laporte J."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Roberts E."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Roberts E."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Tosch V."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Tosch V."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Delgado M.A."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Delgado M.A."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Vergne I."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Vergne I."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Elmaoued R.A."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/author"Elmaoued R.A."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/date"2009"xsd:gYear
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/date"2009"xsd:gYear
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/name"EMBO J."xsd:string
http://purl.uniprot.org/citations/19590496http://purl.uniprot.org/core/name"EMBO J."xsd:string