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Ribosome profiling analysis of eEF3-depleted Saccharomyces cerevisiae

In addition to the standard set of translation factors common in eukaryotic organisms, protein synthesis in the yeast Saccharomyces cerevisiae requires an ABCF ATPase factor eEF3, eukaryotic Elongation Factor 3. eEF3 is an E-site binder that was originally identified as an essential factor involved...

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Autores principales: Kasari, Villu, Margus, Tõnu, Atkinson, Gemma C., Johansson, Marcus J. O., Hauryliuk, Vasili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395859/
https://www.ncbi.nlm.nih.gov/pubmed/30816176
http://dx.doi.org/10.1038/s41598-019-39403-y
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author Kasari, Villu
Margus, Tõnu
Atkinson, Gemma C.
Johansson, Marcus J. O.
Hauryliuk, Vasili
author_facet Kasari, Villu
Margus, Tõnu
Atkinson, Gemma C.
Johansson, Marcus J. O.
Hauryliuk, Vasili
author_sort Kasari, Villu
collection PubMed
description In addition to the standard set of translation factors common in eukaryotic organisms, protein synthesis in the yeast Saccharomyces cerevisiae requires an ABCF ATPase factor eEF3, eukaryotic Elongation Factor 3. eEF3 is an E-site binder that was originally identified as an essential factor involved in the elongation stage of protein synthesis. Recent biochemical experiments suggest an additional function of eEF3 in ribosome recycling. We have characterised the global effects of eEF3 depletion on translation using ribosome profiling. Depletion of eEF3 results in decreased ribosome density at the stop codon, indicating that ribosome recycling does not become rate limiting when eEF3 levels are low. Consistent with a defect in translation elongation, eEF3 depletion causes a moderate redistribution of ribosomes towards the 5′ part of the open reading frames. We observed no E-site codon- or amino acid-specific ribosome stalling upon eEF3 depletion, supporting its role as a general elongation factor. Surprisingly, depletion of eEF3 leads to a relative decrease in P-site proline stalling, which we hypothesise is a secondary effect of generally decreased translation and/or decreased competition for the E-site with eIF5A.
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spelling pubmed-63958592019-03-05 Ribosome profiling analysis of eEF3-depleted Saccharomyces cerevisiae Kasari, Villu Margus, Tõnu Atkinson, Gemma C. Johansson, Marcus J. O. Hauryliuk, Vasili Sci Rep Article In addition to the standard set of translation factors common in eukaryotic organisms, protein synthesis in the yeast Saccharomyces cerevisiae requires an ABCF ATPase factor eEF3, eukaryotic Elongation Factor 3. eEF3 is an E-site binder that was originally identified as an essential factor involved in the elongation stage of protein synthesis. Recent biochemical experiments suggest an additional function of eEF3 in ribosome recycling. We have characterised the global effects of eEF3 depletion on translation using ribosome profiling. Depletion of eEF3 results in decreased ribosome density at the stop codon, indicating that ribosome recycling does not become rate limiting when eEF3 levels are low. Consistent with a defect in translation elongation, eEF3 depletion causes a moderate redistribution of ribosomes towards the 5′ part of the open reading frames. We observed no E-site codon- or amino acid-specific ribosome stalling upon eEF3 depletion, supporting its role as a general elongation factor. Surprisingly, depletion of eEF3 leads to a relative decrease in P-site proline stalling, which we hypothesise is a secondary effect of generally decreased translation and/or decreased competition for the E-site with eIF5A. Nature Publishing Group UK 2019-02-28 /pmc/articles/PMC6395859/ /pubmed/30816176 http://dx.doi.org/10.1038/s41598-019-39403-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kasari, Villu
Margus, Tõnu
Atkinson, Gemma C.
Johansson, Marcus J. O.
Hauryliuk, Vasili
Ribosome profiling analysis of eEF3-depleted Saccharomyces cerevisiae
title Ribosome profiling analysis of eEF3-depleted Saccharomyces cerevisiae
title_full Ribosome profiling analysis of eEF3-depleted Saccharomyces cerevisiae
title_fullStr Ribosome profiling analysis of eEF3-depleted Saccharomyces cerevisiae
title_full_unstemmed Ribosome profiling analysis of eEF3-depleted Saccharomyces cerevisiae
title_short Ribosome profiling analysis of eEF3-depleted Saccharomyces cerevisiae
title_sort ribosome profiling analysis of eef3-depleted saccharomyces cerevisiae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395859/
https://www.ncbi.nlm.nih.gov/pubmed/30816176
http://dx.doi.org/10.1038/s41598-019-39403-y
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