The COP9 signalosome is involved in the regulation of lipid metabolism and of transition metals uptake inSaccharomyces cerevisiae
Autor: | Benedetta Mattei, Laylan Bramasole, Valerio Licursi, Chiara Salvi, Rodolfo Negri, Martin Bard, Giovanna Serino, Jacob Z. Zimbler, Claudia Fabbri, Brett M. Barnes, Teresa Rinaldi, Virginia De Cesare, Elah Pick |
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Přispěvatelé: | Department of Biology and Biotechnology 'Charles Darwin', Institut Pasteur, Fondation Cenci Bolognetti - Istituto Pasteur Italia, Fondazione Cenci Bolognetti, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome], Department of Biology, Faculty of Sciences and Science Education, University of Haifa [Haifa], Department of Evolutionary and Environmental Biology, Department of Biology, Indiana University - Purdue University Indianapolis (IUPUI), Indiana University System-Indiana University System, This work was supported by FIRB 2011-2013 (grantno. RBIN06E9Z8) ‘Molecular Bases of Diseases’,PRIN 2009 ‘Role ofS. cerevisiaeGeneral RegulatoryFactors (GRF) in Chromatin Organization andDynamics’ and Progetti di Ricerca di Ateneo (grantno. C26A1139XY) to RN, Israel Ministry of Scienceand Technology (MOST)–Italy Ministry of ForeignAffairs (MAE) grant 3-9022 to RN, TR, GS and EP, and Israel Science Foundation grant (EP355/10) forEP, Progetto di Ricerca C26A1089CJ (2010), SapienzaUniversita’ di Roma, to RN, TR and GS. VL’s fellowship is supported by a grant from Regione Lazio, Università degli Studi di Roma 'La Sapienza' [Rome] - Réseau International des Instituts Pasteur - Institut Pasteur - Fondation Cenci Bolognetti, Indiana University - Purdue University |
Rok vydání: | 2013 |
Předmět: |
medicine.disease_cause
MESH: Zinc Biochemistry MESH: Ergosterol chemistry.chemical_compound neddylation MESH: Saccharomyces cerevisiae Proteins cop9 signalosome Ubiquitin Tandem Mass Spectrometry Ergosterol MESH: Reverse Transcriptase Polymerase Chain Reaction Transition Elements Oligonucleotide Array Sequence Analysis MESH: Lipid Metabolism 0303 health sciences Mutation biology Reverse Transcriptase Polymerase Chain Reaction MESH: Real-Time Polymerase Chain Reaction MESH: Chromatography Gas 030302 biochemistry & molecular biology zinc uptake Metalloendopeptidases Cullin Proteins MESH: Saccharomyces cerevisiae Zinc Cullin Chromatography Gas Saccharomyces cerevisiae Proteins MESH: Peptide Hydrolases Protein subunit Blotting Western ergosterol biosynthesis lipid metabolism Saccharomyces cerevisiae MESH: Metalloendopeptidases Real-Time Polymerase Chain Reaction MESH: Cullin Proteins MESH: Transition Elements MESH: Gene Expression Profiling 03 medical and health sciences [SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular Biology medicine MESH: Blotting Western [SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology RNA Messenger COP9 signalosome Molecular Biology Gene MESH: RNA Messenger 030304 developmental biology COP9 Signalosome Complex Gene Expression Profiling MESH: Biological Markers MESH: Tandem Mass Spectrometry Cell Biology MESH: Multiprotein Complexes Lipid Metabolism biology.organism_classification chemistry Multiprotein Complexes MESH: Oligonucleotide Array Sequence Analysis biology.protein MESH: Chromatography Liquid Biomarkers Chromatography Liquid Peptide Hydrolases |
Zdroj: | FEBS Journal FEBS Journal, Wiley, 2013, 281 (1), pp.175-90. ⟨10.1111/febs.12584⟩ FEBS Journal, Wiley, 2013, 281 (1), pp.175-90. <10.1111/febs.12584> |
ISSN: | 1742-464X 1742-4658 |
DOI: | 10.1111/febs.12584 |
Popis: | International audience; The COP9 signalosome (CSN) is a highly conserved eukaryotic protein complex which regulates the cullin RING family of ubiquitin ligases and carries out a deneddylase activity that resides in subunit 5 (CSN5). Whereas CSN activity is essential for the development of higher eukaryotes, several unicellular fungi including the budding yeast Saccharomyces cerevisiae can survive without a functional CSN. Nevertheless, the budding yeast CSN is biochemically active and deletion mutants of each of its subunits exhibit deficiency in cullins deneddylation, although the biological context of this activity is still unknown in this organism. To further characterize CSN function in budding yeast, we present here a transcriptomic and proteomic analysis of a S. cerevisiae strain deleted in the CSN5/RRI1 gene (hereafter referred to as CSN5), coding for the only canonical subunit of the complex. We show that Csn5 is involved in modulation of the genes controlling amino acid and lipid metabolism and especially ergosterol biosynthesis. These alterations in gene expression correlate with the lower ergosterol levels and increased intracellular zinc content which we observed in csn5 null mutant cells. We show that some of these regulatory effects of Csn5, in particular the control of isoprenoid biosynthesis, are conserved through evolution, since similar transcriptomic and/or proteomic effects of csn5 mutation were previously observed in other eukaryotic organisms such as Aspergillus nidulans, Arabidopsis thaliana and Drosophila melanogaster. Our results suggest that the diverged budding yeast CSN is more conserved than was previously thought. |
Databáze: | OpenAIRE |
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