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Yes-Associated Protein 65 Localizes P62(c-Yes) to the Apical Compartment of Airway Epithelia by Association with Ebp50

We recently showed that the COOH terminus of the cystic fibrosis transmembrane conductance regulator associates with the submembranous scaffolding protein EBP50 (ERM-binding phosphoprotein 50 kD; also called Na(+)/H(+) exchanger regulatory factor). Since EBP50 associates with ezrin, this interaction...

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Autores principales: Mohler, Peter J., Kreda, Silvia M., Boucher, Richard C., Sudol, Marius, Stutts, M. Jackson, Milgram, Sharon L.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2156157/
https://www.ncbi.nlm.nih.gov/pubmed/10562288
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author Mohler, Peter J.
Kreda, Silvia M.
Boucher, Richard C.
Sudol, Marius
Stutts, M. Jackson
Milgram, Sharon L.
author_facet Mohler, Peter J.
Kreda, Silvia M.
Boucher, Richard C.
Sudol, Marius
Stutts, M. Jackson
Milgram, Sharon L.
author_sort Mohler, Peter J.
collection PubMed
description We recently showed that the COOH terminus of the cystic fibrosis transmembrane conductance regulator associates with the submembranous scaffolding protein EBP50 (ERM-binding phosphoprotein 50 kD; also called Na(+)/H(+) exchanger regulatory factor). Since EBP50 associates with ezrin, this interaction links the cystic fibrosis transmembrane conductance regulator (CFTR) to the cortical actin cytoskeleton. EBP50 has two PDZ domains, and CFTR binds with high affinity to the first PDZ domain. Here, we report that Yes-associated protein 65 (YAP65) binds with high affinity to the second EBP50 PDZ domain. YAP65 is concentrated at the apical membrane in airway epithelia and interacts with EBP50 in cells. The COOH terminus of YAP65 is necessary and sufficient to mediate association with EBP50. The EBP50–YAP65 interaction is involved in the compartmentalization of YAP65 at the apical membrane since mutant YAP65 proteins lacking the EBP50 interaction motif are mislocalized when expressed in airway epithelial cells. In addition, we show that the nonreceptor tyrosine kinase c-Yes is contained within EBP50 protein complexes by association with YAP65. Subapical EBP50 protein complexes, containing the nonreceptor tyrosine kinase c-Yes, may regulate apical signal transduction pathways leading to changes in ion transport, cytoskeletal organization, or gene expression in epithelial cells.
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spelling pubmed-21561572008-05-01 Yes-Associated Protein 65 Localizes P62(c-Yes) to the Apical Compartment of Airway Epithelia by Association with Ebp50 Mohler, Peter J. Kreda, Silvia M. Boucher, Richard C. Sudol, Marius Stutts, M. Jackson Milgram, Sharon L. J Cell Biol Original Article We recently showed that the COOH terminus of the cystic fibrosis transmembrane conductance regulator associates with the submembranous scaffolding protein EBP50 (ERM-binding phosphoprotein 50 kD; also called Na(+)/H(+) exchanger regulatory factor). Since EBP50 associates with ezrin, this interaction links the cystic fibrosis transmembrane conductance regulator (CFTR) to the cortical actin cytoskeleton. EBP50 has two PDZ domains, and CFTR binds with high affinity to the first PDZ domain. Here, we report that Yes-associated protein 65 (YAP65) binds with high affinity to the second EBP50 PDZ domain. YAP65 is concentrated at the apical membrane in airway epithelia and interacts with EBP50 in cells. The COOH terminus of YAP65 is necessary and sufficient to mediate association with EBP50. The EBP50–YAP65 interaction is involved in the compartmentalization of YAP65 at the apical membrane since mutant YAP65 proteins lacking the EBP50 interaction motif are mislocalized when expressed in airway epithelial cells. In addition, we show that the nonreceptor tyrosine kinase c-Yes is contained within EBP50 protein complexes by association with YAP65. Subapical EBP50 protein complexes, containing the nonreceptor tyrosine kinase c-Yes, may regulate apical signal transduction pathways leading to changes in ion transport, cytoskeletal organization, or gene expression in epithelial cells. The Rockefeller University Press 1999-11-15 /pmc/articles/PMC2156157/ /pubmed/10562288 Text en © 1999 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 Original Article
Mohler, Peter J.
Kreda, Silvia M.
Boucher, Richard C.
Sudol, Marius
Stutts, M. Jackson
Milgram, Sharon L.
Yes-Associated Protein 65 Localizes P62(c-Yes) to the Apical Compartment of Airway Epithelia by Association with Ebp50
title Yes-Associated Protein 65 Localizes P62(c-Yes) to the Apical Compartment of Airway Epithelia by Association with Ebp50
title_full Yes-Associated Protein 65 Localizes P62(c-Yes) to the Apical Compartment of Airway Epithelia by Association with Ebp50
title_fullStr Yes-Associated Protein 65 Localizes P62(c-Yes) to the Apical Compartment of Airway Epithelia by Association with Ebp50
title_full_unstemmed Yes-Associated Protein 65 Localizes P62(c-Yes) to the Apical Compartment of Airway Epithelia by Association with Ebp50
title_short Yes-Associated Protein 65 Localizes P62(c-Yes) to the Apical Compartment of Airway Epithelia by Association with Ebp50
title_sort yes-associated protein 65 localizes p62(c-yes) to the apical compartment of airway epithelia by association with ebp50
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2156157/
https://www.ncbi.nlm.nih.gov/pubmed/10562288
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