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Robust landscapes of ribosome dwell times and aminoacyl-tRNAs in response to nutrient stress in liver
Translation depends on messenger RNA (mRNA)-specific initiation, elongation, and termination rates. While translation elongation is well studied in bacteria and yeast, less is known in higher eukaryotes. Here we combined ribosome and transfer RNA (tRNA) profiling to investigate the relations between...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196831/ https://www.ncbi.nlm.nih.gov/pubmed/32295881 http://dx.doi.org/10.1073/pnas.1918145117 |
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author | Gobet, Cédric Weger, Benjamin Dieter Marquis, Julien Martin, Eva Neelagandan, Nagammal Gachon, Frédéric Naef, Felix |
author_facet | Gobet, Cédric Weger, Benjamin Dieter Marquis, Julien Martin, Eva Neelagandan, Nagammal Gachon, Frédéric Naef, Felix |
author_sort | Gobet, Cédric |
collection | PubMed |
description | Translation depends on messenger RNA (mRNA)-specific initiation, elongation, and termination rates. While translation elongation is well studied in bacteria and yeast, less is known in higher eukaryotes. Here we combined ribosome and transfer RNA (tRNA) profiling to investigate the relations between translation elongation rates, (aminoacyl-) tRNA levels, and codon usage in mammals. We modeled codon-specific ribosome dwell times from ribosome profiling, considering codon pair interactions between ribosome sites. In mouse liver, the model revealed site- and codon-specific dwell times that differed from those in yeast, as well as pairs of adjacent codons in the P and A site that markedly slow down or speed up elongation. While translation efficiencies vary across diurnal time and feeding regimen, codon dwell times were highly stable and conserved in human. Measured tRNA levels correlated with codon usage and several tRNAs showed reduced aminoacylation, which was conserved in fasted mice. Finally, we uncovered that the longest codon dwell times could be explained by aminoacylation levels or high codon usage relative to tRNA abundance. |
format | Online Article Text |
id | pubmed-7196831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-71968312020-05-06 Robust landscapes of ribosome dwell times and aminoacyl-tRNAs in response to nutrient stress in liver Gobet, Cédric Weger, Benjamin Dieter Marquis, Julien Martin, Eva Neelagandan, Nagammal Gachon, Frédéric Naef, Felix Proc Natl Acad Sci U S A Biological Sciences Translation depends on messenger RNA (mRNA)-specific initiation, elongation, and termination rates. While translation elongation is well studied in bacteria and yeast, less is known in higher eukaryotes. Here we combined ribosome and transfer RNA (tRNA) profiling to investigate the relations between translation elongation rates, (aminoacyl-) tRNA levels, and codon usage in mammals. We modeled codon-specific ribosome dwell times from ribosome profiling, considering codon pair interactions between ribosome sites. In mouse liver, the model revealed site- and codon-specific dwell times that differed from those in yeast, as well as pairs of adjacent codons in the P and A site that markedly slow down or speed up elongation. While translation efficiencies vary across diurnal time and feeding regimen, codon dwell times were highly stable and conserved in human. Measured tRNA levels correlated with codon usage and several tRNAs showed reduced aminoacylation, which was conserved in fasted mice. Finally, we uncovered that the longest codon dwell times could be explained by aminoacylation levels or high codon usage relative to tRNA abundance. National Academy of Sciences 2020-04-28 2020-04-15 /pmc/articles/PMC7196831/ /pubmed/32295881 http://dx.doi.org/10.1073/pnas.1918145117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Gobet, Cédric Weger, Benjamin Dieter Marquis, Julien Martin, Eva Neelagandan, Nagammal Gachon, Frédéric Naef, Felix Robust landscapes of ribosome dwell times and aminoacyl-tRNAs in response to nutrient stress in liver |
title | Robust landscapes of ribosome dwell times and aminoacyl-tRNAs in response to nutrient stress in liver |
title_full | Robust landscapes of ribosome dwell times and aminoacyl-tRNAs in response to nutrient stress in liver |
title_fullStr | Robust landscapes of ribosome dwell times and aminoacyl-tRNAs in response to nutrient stress in liver |
title_full_unstemmed | Robust landscapes of ribosome dwell times and aminoacyl-tRNAs in response to nutrient stress in liver |
title_short | Robust landscapes of ribosome dwell times and aminoacyl-tRNAs in response to nutrient stress in liver |
title_sort | robust landscapes of ribosome dwell times and aminoacyl-trnas in response to nutrient stress in liver |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196831/ https://www.ncbi.nlm.nih.gov/pubmed/32295881 http://dx.doi.org/10.1073/pnas.1918145117 |
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