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Association of a phosphatidylinositol-specific 3-kinase with a human trans-Golgi network resident protein.
Hickinson, D M; Lucocq, J M; Towler, M C; Clough, S; James, J; James, S R; Downes, C P; Ponnambalam, S.
Afiliación
  • Hickinson DM; Department of Biochemistry, Medical Sciences Institute, University of Dundee, Dundee DD1 4HN, UK.
Curr Biol ; 7(12): 987-90, 1997 Dec 01.
Article en En | MEDLINE | ID: mdl-9382841
ABSTRACT
The eukaryotic trans-Golgi network (TGN) is a key site for the formation of transport vesicles destined for different intracellular compartments [1]. A key marker for the mammalian TGN is TGN38/46 [2]. This integral membrane glycoprotein cycles between the TGN and the cell surface and is implicated in recruitment of cytosolic factors and regulation of at least one type of vesicle formation at the mammalian TGN [2] [3]. In this study, we have identified a phosphatidylinositol (PtdIns)-specific 3-kinase activity associated with the human orthologue (TGN46), which is sensitive to lipid kinase inhibitors. Treatment of HeLa cells with low levels of these inhibitors reveals subtle morphological changes in TGN46-positive compartments. Our findings suggest a role for PtdIns 3-kinases and presumably for the product, PtdIns 3-phosphate (PtdIns3P), in the formation of secretory transport vesicles by mechanisms conserved in yeast and mammals.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Glicoproteínas de Membrana / Glicoproteínas / Fosfatidilinositol 3-Quinasas / Aparato de Golgi / Proteínas de la Membrana Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Curr Biol Asunto de la revista: BIOLOGIA Año: 1997 Tipo del documento: Article País de afiliación: Reino Unido
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Glicoproteínas de Membrana / Glicoproteínas / Fosfatidilinositol 3-Quinasas / Aparato de Golgi / Proteínas de la Membrana Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Curr Biol Asunto de la revista: BIOLOGIA Año: 1997 Tipo del documento: Article País de afiliación: Reino Unido