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The eps15 homology (EH) domain-based interaction between eps15 and hrb connects the molecular machinery of endocytosis to that of nucleocytosolic transport.
Doria, M; Salcini, A E; Colombo, E; Parslow, T G; Pelicci, P G; Di Fiore, P P.
Afiliação
  • Doria M; Department of Experimental Oncology, European Institute of Oncology, 20141 Milan, Italy.
J Cell Biol ; 147(7): 1379-84, 1999 Dec 27.
Article em En | MEDLINE | ID: mdl-10613896
ABSTRACT
The Eps15 homology (EH) module is a protein-protein interaction domain that establishes a network of connections involved in various aspects of endocytosis and sorting. The finding that EH-containing proteins bind to Hrb (a cellular cofactor of the Rev protein) and to the related protein Hrbl raised the possibility that the EH network might also influence the so-called Rev export pathway, which mediates nucleocytoplasmic transfer of proteins and RNAs. In this study, we demonstrate that Eps15 and Eps15R, two EH-containing proteins, synergize with Hrb and Hrbl to enhance the function of Rev in the export pathway. In addition, the EH-mediated association between Eps15 and Hrb is required for the synergistic effect. The interaction between Eps15 and Hrb occurs in the cytoplasm, thus pointing to an unexpected site of action of Hrb, and to a possible role of the Eps15-Hrb complex in regulating the stability of Rev.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfoproteínas / Proteínas de Ligação ao Cálcio / Proteínas Nucleares / Produtos do Gene rev / Núcleo Celular / Proteínas de Ligação a RNA / Citosol / Complexo de Proteínas Formadoras de Poros Nucleares / Endocitose Limite: Animals Idioma: En Ano de publicação: 1999 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fosfoproteínas / Proteínas de Ligação ao Cálcio / Proteínas Nucleares / Produtos do Gene rev / Núcleo Celular / Proteínas de Ligação a RNA / Citosol / Complexo de Proteínas Formadoras de Poros Nucleares / Endocitose Limite: Animals Idioma: En Ano de publicação: 1999 Tipo de documento: Article