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Numb Is an Endocytic Protein

Numb is a protein that in Drosophila determines cell fate as a result of its asymmetric partitioning at mitosis. The function of Numb has been linked to its ability to bind and to biologically antagonize Notch, a membrane receptor that also specifies cell fate. The biochemical mechanisms underlying...

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Autores principales: Santolini, Elisa, Puri, Claudia, Salcini, Anna Elisabetta, Gagliani, Maria Cristina, Pelicci, Pier Giuseppe, Tacchetti, Carlo, Di Fiore, Pier Paolo
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190585/
https://www.ncbi.nlm.nih.gov/pubmed/11121447
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author Santolini, Elisa
Puri, Claudia
Salcini, Anna Elisabetta
Gagliani, Maria Cristina
Pelicci, Pier Giuseppe
Tacchetti, Carlo
Di Fiore, Pier Paolo
author_facet Santolini, Elisa
Puri, Claudia
Salcini, Anna Elisabetta
Gagliani, Maria Cristina
Pelicci, Pier Giuseppe
Tacchetti, Carlo
Di Fiore, Pier Paolo
author_sort Santolini, Elisa
collection PubMed
description Numb is a protein that in Drosophila determines cell fate as a result of its asymmetric partitioning at mitosis. The function of Numb has been linked to its ability to bind and to biologically antagonize Notch, a membrane receptor that also specifies cell fate. The biochemical mechanisms underlying the action of Numb, however, are still largely unknown. The wide pattern of expression of Numb suggests a general function in cellular homeostasis that could be additional to, or part of, its action in fate determination. Such a function could be endocytosis, as suggested by the interaction of Numb with Eps15, a component of the endocytic machinery. Here, we demonstrate that Numb is an endocytic protein. We found that Numb localizes to endocytic organelles and is cotrafficked with internalizing receptors. Moreover, it associates with the appendage domain of α adaptin, a subunit of AP2, a major component of clathrin-coated pits. Finally, fragments of Numb act as dominant negatives on both constitutive and ligand-regulated receptor-mediated internalization, suggesting a general role for Numb in the endocytic process.
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spelling pubmed-21905852008-05-01 Numb Is an Endocytic Protein Santolini, Elisa Puri, Claudia Salcini, Anna Elisabetta Gagliani, Maria Cristina Pelicci, Pier Giuseppe Tacchetti, Carlo Di Fiore, Pier Paolo J Cell Biol Report Numb is a protein that in Drosophila determines cell fate as a result of its asymmetric partitioning at mitosis. The function of Numb has been linked to its ability to bind and to biologically antagonize Notch, a membrane receptor that also specifies cell fate. The biochemical mechanisms underlying the action of Numb, however, are still largely unknown. The wide pattern of expression of Numb suggests a general function in cellular homeostasis that could be additional to, or part of, its action in fate determination. Such a function could be endocytosis, as suggested by the interaction of Numb with Eps15, a component of the endocytic machinery. Here, we demonstrate that Numb is an endocytic protein. We found that Numb localizes to endocytic organelles and is cotrafficked with internalizing receptors. Moreover, it associates with the appendage domain of α adaptin, a subunit of AP2, a major component of clathrin-coated pits. Finally, fragments of Numb act as dominant negatives on both constitutive and ligand-regulated receptor-mediated internalization, suggesting a general role for Numb in the endocytic process. The Rockefeller University Press 2000-12-11 /pmc/articles/PMC2190585/ /pubmed/11121447 Text en © 2000 The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Report
Santolini, Elisa
Puri, Claudia
Salcini, Anna Elisabetta
Gagliani, Maria Cristina
Pelicci, Pier Giuseppe
Tacchetti, Carlo
Di Fiore, Pier Paolo
Numb Is an Endocytic Protein
title Numb Is an Endocytic Protein
title_full Numb Is an Endocytic Protein
title_fullStr Numb Is an Endocytic Protein
title_full_unstemmed Numb Is an Endocytic Protein
title_short Numb Is an Endocytic Protein
title_sort numb is an endocytic protein
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190585/
https://www.ncbi.nlm.nih.gov/pubmed/11121447
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