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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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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. |
format | Online Article Text |
id | pubmed-5786338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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