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Plakophilin 1 stimulates translation by promoting eIF4A1 activity

Plakophilins 1–3 (PKP1–3) are desmosomal proteins of the p120(ctn) family of armadillo-related proteins that are essential for organizing the desmosomal plaque. Recent findings identified PKPs in stress granules, suggesting an association with the translational machinery. However, a role of PKPs in...

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Autores principales: Wolf, Annika, Krause-Gruszczynska, Malgorzata, Birkenmeier, Olaf, Ostareck-Lederer, Antje, Hüttelmaier, Stefan, Hatzfeld, Mechthild
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2828926/
https://www.ncbi.nlm.nih.gov/pubmed/20156963
http://dx.doi.org/10.1083/jcb.200908135
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author Wolf, Annika
Krause-Gruszczynska, Malgorzata
Birkenmeier, Olaf
Ostareck-Lederer, Antje
Hüttelmaier, Stefan
Hatzfeld, Mechthild
author_facet Wolf, Annika
Krause-Gruszczynska, Malgorzata
Birkenmeier, Olaf
Ostareck-Lederer, Antje
Hüttelmaier, Stefan
Hatzfeld, Mechthild
author_sort Wolf, Annika
collection PubMed
description Plakophilins 1–3 (PKP1–3) are desmosomal proteins of the p120(ctn) family of armadillo-related proteins that are essential for organizing the desmosomal plaque. Recent findings identified PKPs in stress granules, suggesting an association with the translational machinery. However, a role of PKPs in controlling translation remained elusive so far. In this study, we show a direct association of PKP1 with the eukaryotic translation initiation factor 4A1 (eIF4A1). PKP1 stimulated eIF4A1-dependent translation via messenger RNA cap and encephalomyocarditis virus internal ribosomal entry site (IRES) structures, whereas eIF4A1-independent translation via hepatitis C virus IRES was not affected. PKP1 copurified with eIF4A1 in the cap complex, and its overexpression stimulated eIF4A1 recruitment into cap-binding complexes. At the molecular level, PKP1 directly promoted eIF4A1 adenosine triphosphatase activity. The stimulation of translation upon PKP1 overexpression correlated with the up-regulation of proliferation and cell size. In conclusion, these findings identify PKP1 as a regulator of translation and proliferation via modulation of eIF4A1 activity and suggest that PKP1 controls cell growth in physiological and pathological conditions.
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spelling pubmed-28289262010-08-22 Plakophilin 1 stimulates translation by promoting eIF4A1 activity Wolf, Annika Krause-Gruszczynska, Malgorzata Birkenmeier, Olaf Ostareck-Lederer, Antje Hüttelmaier, Stefan Hatzfeld, Mechthild J Cell Biol Research Articles Plakophilins 1–3 (PKP1–3) are desmosomal proteins of the p120(ctn) family of armadillo-related proteins that are essential for organizing the desmosomal plaque. Recent findings identified PKPs in stress granules, suggesting an association with the translational machinery. However, a role of PKPs in controlling translation remained elusive so far. In this study, we show a direct association of PKP1 with the eukaryotic translation initiation factor 4A1 (eIF4A1). PKP1 stimulated eIF4A1-dependent translation via messenger RNA cap and encephalomyocarditis virus internal ribosomal entry site (IRES) structures, whereas eIF4A1-independent translation via hepatitis C virus IRES was not affected. PKP1 copurified with eIF4A1 in the cap complex, and its overexpression stimulated eIF4A1 recruitment into cap-binding complexes. At the molecular level, PKP1 directly promoted eIF4A1 adenosine triphosphatase activity. The stimulation of translation upon PKP1 overexpression correlated with the up-regulation of proliferation and cell size. In conclusion, these findings identify PKP1 as a regulator of translation and proliferation via modulation of eIF4A1 activity and suggest that PKP1 controls cell growth in physiological and pathological conditions. The Rockefeller University Press 2010-02-22 /pmc/articles/PMC2828926/ /pubmed/20156963 http://dx.doi.org/10.1083/jcb.200908135 Text en © 2010 Wolf et al. 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.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Wolf, Annika
Krause-Gruszczynska, Malgorzata
Birkenmeier, Olaf
Ostareck-Lederer, Antje
Hüttelmaier, Stefan
Hatzfeld, Mechthild
Plakophilin 1 stimulates translation by promoting eIF4A1 activity
title Plakophilin 1 stimulates translation by promoting eIF4A1 activity
title_full Plakophilin 1 stimulates translation by promoting eIF4A1 activity
title_fullStr Plakophilin 1 stimulates translation by promoting eIF4A1 activity
title_full_unstemmed Plakophilin 1 stimulates translation by promoting eIF4A1 activity
title_short Plakophilin 1 stimulates translation by promoting eIF4A1 activity
title_sort plakophilin 1 stimulates translation by promoting eif4a1 activity
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2828926/
https://www.ncbi.nlm.nih.gov/pubmed/20156963
http://dx.doi.org/10.1083/jcb.200908135
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