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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...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2010
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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. |
format | Text |
id | pubmed-2828926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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