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Ubiquitination of the peroxisomal import receptor Pex5p is required for its recycling
Pex5p, which is the import receptor for peroxisomal matrix proteins harboring a type I signal sequence (PTS1), is mono- and polyubiquitinated in Saccharomyces cerevisiae. We identified Pex5p as a molecular target for Pex4p-dependent monoubiquitination and demonstrated that either poly- or monoubiqui...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064128/ https://www.ncbi.nlm.nih.gov/pubmed/17452527 http://dx.doi.org/10.1083/jcb.200611012 |
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author | Platta, Harald W. Magraoui, Fouzi El Schlee, Daniel Grunau, Silke Girzalsky, Wolfgang Erdmann, Ralf |
author_facet | Platta, Harald W. Magraoui, Fouzi El Schlee, Daniel Grunau, Silke Girzalsky, Wolfgang Erdmann, Ralf |
author_sort | Platta, Harald W. |
collection | PubMed |
description | Pex5p, which is the import receptor for peroxisomal matrix proteins harboring a type I signal sequence (PTS1), is mono- and polyubiquitinated in Saccharomyces cerevisiae. We identified Pex5p as a molecular target for Pex4p-dependent monoubiquitination and demonstrated that either poly- or monoubiquitination of the receptor is required for the ATP-dependent release of the protein from the peroxisomal membrane to the cytosol as part of the receptor cycle. Therefore, the energy requirement of the peroxisomal import pathway has to be extended by a second ATP-dependent step, namely receptor monoubiquitination. |
format | Text |
id | pubmed-2064128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-20641282007-11-29 Ubiquitination of the peroxisomal import receptor Pex5p is required for its recycling Platta, Harald W. Magraoui, Fouzi El Schlee, Daniel Grunau, Silke Girzalsky, Wolfgang Erdmann, Ralf J Cell Biol Research Articles Pex5p, which is the import receptor for peroxisomal matrix proteins harboring a type I signal sequence (PTS1), is mono- and polyubiquitinated in Saccharomyces cerevisiae. We identified Pex5p as a molecular target for Pex4p-dependent monoubiquitination and demonstrated that either poly- or monoubiquitination of the receptor is required for the ATP-dependent release of the protein from the peroxisomal membrane to the cytosol as part of the receptor cycle. Therefore, the energy requirement of the peroxisomal import pathway has to be extended by a second ATP-dependent step, namely receptor monoubiquitination. The Rockefeller University Press 2007-04-23 /pmc/articles/PMC2064128/ /pubmed/17452527 http://dx.doi.org/10.1083/jcb.200611012 Text en Copyright © 2007, 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 | Research Articles Platta, Harald W. Magraoui, Fouzi El Schlee, Daniel Grunau, Silke Girzalsky, Wolfgang Erdmann, Ralf Ubiquitination of the peroxisomal import receptor Pex5p is required for its recycling |
title | Ubiquitination of the peroxisomal import receptor Pex5p is required for its recycling |
title_full | Ubiquitination of the peroxisomal import receptor Pex5p is required for its recycling |
title_fullStr | Ubiquitination of the peroxisomal import receptor Pex5p is required for its recycling |
title_full_unstemmed | Ubiquitination of the peroxisomal import receptor Pex5p is required for its recycling |
title_short | Ubiquitination of the peroxisomal import receptor Pex5p is required for its recycling |
title_sort | ubiquitination of the peroxisomal import receptor pex5p is required for its recycling |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2064128/ https://www.ncbi.nlm.nih.gov/pubmed/17452527 http://dx.doi.org/10.1083/jcb.200611012 |
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