Ent5p Is Required with Ent3p and Vps27p for Ubiquitin-dependent Protein Sorting into the Multivesicular Body

DOI 被引用文献2件
  • Anne Eugster
    Laboratoire de Transport et Compartimentation Intracellulaire
  • Eve-Isabelle Pécheur
    Laboratoire de RMN et Bioinformatique Structurales
  • Fabrice Michel
    Laboratoire de BioCristallographie, Institut de Biologie et Chimie des Protéines, UMR5086 Centre National de la Recherche Scientifique, Institut Fédératif de Recherche 128 BioSciences Lyon-Gerland, 69367 Lyon, France
  • Barbara Winsor
    Laboratoire Modèles Levure de Pathologies Humaines, IBMC, FRE2375 Centre National de la Recherche Scientifique, 67084 Strasbourg, France
  • François Letourneur
    Laboratoire de Transport et Compartimentation Intracellulaire
  • Sylvie Friant
    Laboratoire Modèles Levure de Pathologies Humaines, IBMC, FRE2375 Centre National de la Recherche Scientifique, 67084 Strasbourg, France

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<jats:p> At the late endosomes, cargoes destined for the interior of the vacuole are sorted into invaginating vesicles of the multivesicular body. Both PtdIns(3,5)P<jats:sub>2</jats:sub> and ubiquitin are necessary for proper sorting of some of these cargoes. We show that Ent5p, a yeast protein of the epsin family homologous to Ent3p, localizes to endosomes and specifically binds to PtdIns(3,5)P<jats:sub>2</jats:sub> via its ENTH domain. In cells lacking Ent3p and Ent5p, ubiquitin-dependent sorting of biosynthetic and endocytic cargo into the multivesicular body is disrupted, whereas other trafficking routes to the vacuole are not affected. Ent3p and Ent5p are associated with Vps27p, a FYVE domain containing protein that interacts with ubiquitinated cargoes and is required for protein sorting into the multivesicular body. Therefore, Ent3p and Ent5p are the first proteins shown to be connectors between PtdIns(3,5)P<jats:sub>2</jats:sub>- and the Vps27p-ubiquitin-driven sorting machinery at the multivesicular body. </jats:p>

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