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Pex14p Phosphorylation Modulates Import of Citrate Synthase 2 Into Peroxisomes in Saccharomyces cerevisiae

The peroxisomal biogenesis factor Pex14p is an essential component of the peroxisomal matrix protein import machinery. Together with Pex13p and Pex17p, it is part of the membrane-associated peroxisomal docking complex in yeast, facilitating the binding of cargo-loaded receptor proteins for transloca...

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Autores principales: Schummer, Andreas, Maier, Renate, Gabay-Maskit, Shiran, Hansen, Tobias, Mühlhäuser, Wignand W. D., Suppanz, Ida, Fadel, Amir, Schuldiner, Maya, Girzalsky, Wolfgang, Oeljeklaus, Silke, Zalckvar, Einat, Erdmann, Ralf, Warscheid, Bettina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522779/
https://www.ncbi.nlm.nih.gov/pubmed/33042991
http://dx.doi.org/10.3389/fcell.2020.549451
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author Schummer, Andreas
Maier, Renate
Gabay-Maskit, Shiran
Hansen, Tobias
Mühlhäuser, Wignand W. D.
Suppanz, Ida
Fadel, Amir
Schuldiner, Maya
Girzalsky, Wolfgang
Oeljeklaus, Silke
Zalckvar, Einat
Erdmann, Ralf
Warscheid, Bettina
author_facet Schummer, Andreas
Maier, Renate
Gabay-Maskit, Shiran
Hansen, Tobias
Mühlhäuser, Wignand W. D.
Suppanz, Ida
Fadel, Amir
Schuldiner, Maya
Girzalsky, Wolfgang
Oeljeklaus, Silke
Zalckvar, Einat
Erdmann, Ralf
Warscheid, Bettina
author_sort Schummer, Andreas
collection PubMed
description The peroxisomal biogenesis factor Pex14p is an essential component of the peroxisomal matrix protein import machinery. Together with Pex13p and Pex17p, it is part of the membrane-associated peroxisomal docking complex in yeast, facilitating the binding of cargo-loaded receptor proteins for translocation of cargo proteins into the peroxisome. Furthermore, Pex14p is part of peroxisomal import pores. The central role of Pex14p in peroxisomal matrix protein import processes renders it an obvious target for regulatory mechanisms such as protein phosphorylation. To explore this possibility, we examined the state of Pex14p phosphorylation in Saccharomyces cerevisiae. Phos-tag-SDS-PAGE of Pex14p affinity-purified from solubilized membranes revealed Pex14p as multi-phosphorylated protein. Using mass spectrometry, we identified 16 phosphorylation sites, with phosphorylation hot spots located in the N- and C-terminal regions of Pex14p. Analysis of phosphomimicking and non-phosphorylatable variants of Pex14p revealed a decreased import of GFP carrying a peroxisomal targeting signal type 1, indicating a functional relevance of Pex14p phosphorylation in peroxisomal matrix protein import. We show that this effect can be ascribed to the phosphomimicking mutation at serine 266 of Pex14p (Pex14p-S266D). We further screened the subcellular distribution of 23 native GFP-tagged peroxisomal matrix proteins by high-content fluorescence microscopy. Only Cit2p, the peroxisomal isoform of citrate synthase, was affected in the Pex14p-S266D mutant, showing increased cytosolic localization. Cit2p is part of the glyoxylate cycle, which is required for the production of essential carbohydrates when yeast is grown on non-fermentable carbon sources. Pex14p-S266 phosphosite mutants showed reversed growth phenotypes in oleic acid and ethanol with acetyl-CoA formed in peroxisomes and the cytosol, respectively. Overexpression of Cit2p rescued the growth phenotype of yeast cells expressing Pex14p-S266D in oleic acid. Our data indicate that phosphorylation of Pex14p at S266 provides a mechanism for controlling the peroxisomal import of Cit2p, which helps S. cerevisiae cells to adjust their carbohydrate metabolism according to the nutritional conditions.
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spelling pubmed-75227792020-10-09 Pex14p Phosphorylation Modulates Import of Citrate Synthase 2 Into Peroxisomes in Saccharomyces cerevisiae Schummer, Andreas Maier, Renate Gabay-Maskit, Shiran Hansen, Tobias Mühlhäuser, Wignand W. D. Suppanz, Ida Fadel, Amir Schuldiner, Maya Girzalsky, Wolfgang Oeljeklaus, Silke Zalckvar, Einat Erdmann, Ralf Warscheid, Bettina Front Cell Dev Biol Cell and Developmental Biology The peroxisomal biogenesis factor Pex14p is an essential component of the peroxisomal matrix protein import machinery. Together with Pex13p and Pex17p, it is part of the membrane-associated peroxisomal docking complex in yeast, facilitating the binding of cargo-loaded receptor proteins for translocation of cargo proteins into the peroxisome. Furthermore, Pex14p is part of peroxisomal import pores. The central role of Pex14p in peroxisomal matrix protein import processes renders it an obvious target for regulatory mechanisms such as protein phosphorylation. To explore this possibility, we examined the state of Pex14p phosphorylation in Saccharomyces cerevisiae. Phos-tag-SDS-PAGE of Pex14p affinity-purified from solubilized membranes revealed Pex14p as multi-phosphorylated protein. Using mass spectrometry, we identified 16 phosphorylation sites, with phosphorylation hot spots located in the N- and C-terminal regions of Pex14p. Analysis of phosphomimicking and non-phosphorylatable variants of Pex14p revealed a decreased import of GFP carrying a peroxisomal targeting signal type 1, indicating a functional relevance of Pex14p phosphorylation in peroxisomal matrix protein import. We show that this effect can be ascribed to the phosphomimicking mutation at serine 266 of Pex14p (Pex14p-S266D). We further screened the subcellular distribution of 23 native GFP-tagged peroxisomal matrix proteins by high-content fluorescence microscopy. Only Cit2p, the peroxisomal isoform of citrate synthase, was affected in the Pex14p-S266D mutant, showing increased cytosolic localization. Cit2p is part of the glyoxylate cycle, which is required for the production of essential carbohydrates when yeast is grown on non-fermentable carbon sources. Pex14p-S266 phosphosite mutants showed reversed growth phenotypes in oleic acid and ethanol with acetyl-CoA formed in peroxisomes and the cytosol, respectively. Overexpression of Cit2p rescued the growth phenotype of yeast cells expressing Pex14p-S266D in oleic acid. Our data indicate that phosphorylation of Pex14p at S266 provides a mechanism for controlling the peroxisomal import of Cit2p, which helps S. cerevisiae cells to adjust their carbohydrate metabolism according to the nutritional conditions. Frontiers Media S.A. 2020-09-15 /pmc/articles/PMC7522779/ /pubmed/33042991 http://dx.doi.org/10.3389/fcell.2020.549451 Text en Copyright © 2020 Schummer, Maier, Gabay-Maskit, Hansen, Mühlhäuser, Suppanz, Fadel, Schuldiner, Girzalsky, Oeljeklaus, Zalckvar, Erdmann and Warscheid. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Schummer, Andreas
Maier, Renate
Gabay-Maskit, Shiran
Hansen, Tobias
Mühlhäuser, Wignand W. D.
Suppanz, Ida
Fadel, Amir
Schuldiner, Maya
Girzalsky, Wolfgang
Oeljeklaus, Silke
Zalckvar, Einat
Erdmann, Ralf
Warscheid, Bettina
Pex14p Phosphorylation Modulates Import of Citrate Synthase 2 Into Peroxisomes in Saccharomyces cerevisiae
title Pex14p Phosphorylation Modulates Import of Citrate Synthase 2 Into Peroxisomes in Saccharomyces cerevisiae
title_full Pex14p Phosphorylation Modulates Import of Citrate Synthase 2 Into Peroxisomes in Saccharomyces cerevisiae
title_fullStr Pex14p Phosphorylation Modulates Import of Citrate Synthase 2 Into Peroxisomes in Saccharomyces cerevisiae
title_full_unstemmed Pex14p Phosphorylation Modulates Import of Citrate Synthase 2 Into Peroxisomes in Saccharomyces cerevisiae
title_short Pex14p Phosphorylation Modulates Import of Citrate Synthase 2 Into Peroxisomes in Saccharomyces cerevisiae
title_sort pex14p phosphorylation modulates import of citrate synthase 2 into peroxisomes in saccharomyces cerevisiae
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522779/
https://www.ncbi.nlm.nih.gov/pubmed/33042991
http://dx.doi.org/10.3389/fcell.2020.549451
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