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The impact of ribosomal interference, codon usage, and exit tunnel interactions on translation elongation rate variation

Previous studies have shown that translation elongation is regulated by multiple factors, but the observed heterogeneity remains only partially explained. To dissect quantitatively the different determinants of elongation speed, we use probabilistic modeling to estimate initiation and local elongati...

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Autores principales: Dao Duc, Khanh, Song, Yun S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786338/
https://www.ncbi.nlm.nih.gov/pubmed/29337993
http://dx.doi.org/10.1371/journal.pgen.1007166
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author Dao Duc, Khanh
Song, Yun S.
author_facet Dao Duc, Khanh
Song, Yun S.
author_sort Dao Duc, Khanh
collection PubMed
description Previous studies have shown that translation elongation is regulated by multiple factors, but the observed heterogeneity remains only partially explained. To dissect quantitatively the different determinants of elongation speed, we use probabilistic modeling to estimate initiation and local elongation rates from ribosome profiling data. This model-based approach allows us to quantify the extent of interference between ribosomes on the same transcript. We show that neither interference nor the distribution of slow codons is sufficient to explain the observed heterogeneity. Instead, we find that electrostatic interactions between the ribosomal exit tunnel and specific parts of the nascent polypeptide govern the elongation rate variation as the polypeptide makes its initial pass through the tunnel. Once the N-terminus has escaped the tunnel, the hydropathy of the nascent polypeptide within the ribosome plays a major role in modulating the speed. We show that our results are consistent with the biophysical properties of the tunnel.
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spelling pubmed-57863382018-02-09 The impact of ribosomal interference, codon usage, and exit tunnel interactions on translation elongation rate variation Dao Duc, Khanh Song, Yun S. PLoS Genet Research Article Previous studies have shown that translation elongation is regulated by multiple factors, but the observed heterogeneity remains only partially explained. To dissect quantitatively the different determinants of elongation speed, we use probabilistic modeling to estimate initiation and local elongation rates from ribosome profiling data. This model-based approach allows us to quantify the extent of interference between ribosomes on the same transcript. We show that neither interference nor the distribution of slow codons is sufficient to explain the observed heterogeneity. Instead, we find that electrostatic interactions between the ribosomal exit tunnel and specific parts of the nascent polypeptide govern the elongation rate variation as the polypeptide makes its initial pass through the tunnel. Once the N-terminus has escaped the tunnel, the hydropathy of the nascent polypeptide within the ribosome plays a major role in modulating the speed. We show that our results are consistent with the biophysical properties of the tunnel. Public Library of Science 2018-01-16 /pmc/articles/PMC5786338/ /pubmed/29337993 http://dx.doi.org/10.1371/journal.pgen.1007166 Text en © 2018 Dao Duc, Song http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Dao Duc, Khanh
Song, Yun S.
The impact of ribosomal interference, codon usage, and exit tunnel interactions on translation elongation rate variation
title The impact of ribosomal interference, codon usage, and exit tunnel interactions on translation elongation rate variation
title_full The impact of ribosomal interference, codon usage, and exit tunnel interactions on translation elongation rate variation
title_fullStr The impact of ribosomal interference, codon usage, and exit tunnel interactions on translation elongation rate variation
title_full_unstemmed The impact of ribosomal interference, codon usage, and exit tunnel interactions on translation elongation rate variation
title_short The impact of ribosomal interference, codon usage, and exit tunnel interactions on translation elongation rate variation
title_sort impact of ribosomal interference, codon usage, and exit tunnel interactions on translation elongation rate variation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786338/
https://www.ncbi.nlm.nih.gov/pubmed/29337993
http://dx.doi.org/10.1371/journal.pgen.1007166
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