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Ribosome recycling induces optimal translation rate at low ribosomal availability
During eukaryotic cellular protein synthesis, ribosomal translation is made more efficient through interaction between the two ends of the messenger RNA (mRNA). Ribosomes reaching the 3′ end of the mRNA can thus recycle and begin translation again on the same mRNA, the so-called ‘closed-loop’ model....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4233708/ https://www.ncbi.nlm.nih.gov/pubmed/25008084 http://dx.doi.org/10.1098/rsif.2014.0589 |
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author | Marshall, E. Stansfield, I. Romano, M. C. |
author_facet | Marshall, E. Stansfield, I. Romano, M. C. |
author_sort | Marshall, E. |
collection | PubMed |
description | During eukaryotic cellular protein synthesis, ribosomal translation is made more efficient through interaction between the two ends of the messenger RNA (mRNA). Ribosomes reaching the 3′ end of the mRNA can thus recycle and begin translation again on the same mRNA, the so-called ‘closed-loop’ model. Using a driven diffusion lattice model of translation, we study the effects of ribosome recycling on the dynamics of ribosome flow and density on the mRNA. We show that ribosome recycling induces a substantial increase in ribosome current. Furthermore, for sufficiently large values of the recycling rate, the lattice does not transition directly from low to high ribosome density, as seen in lattice models without recycling. Instead, a maximal current phase becomes accessible for much lower values of the initiation rate, and multiple phase transitions occur over a wide region of the phase plane. Crucially, we show that in the presence of ribosome recycling, mRNAs can exhibit a peak in protein production at low values of the initiation rate, beyond which translation rate decreases. This has important implications for translation of certain mRNAs, suggesting that there is an optimal concentration of ribosomes at which protein synthesis is maximal, and beyond which translational efficiency is impaired. |
format | Online Article Text |
id | pubmed-4233708 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42337082014-11-21 Ribosome recycling induces optimal translation rate at low ribosomal availability Marshall, E. Stansfield, I. Romano, M. C. J R Soc Interface Research Articles During eukaryotic cellular protein synthesis, ribosomal translation is made more efficient through interaction between the two ends of the messenger RNA (mRNA). Ribosomes reaching the 3′ end of the mRNA can thus recycle and begin translation again on the same mRNA, the so-called ‘closed-loop’ model. Using a driven diffusion lattice model of translation, we study the effects of ribosome recycling on the dynamics of ribosome flow and density on the mRNA. We show that ribosome recycling induces a substantial increase in ribosome current. Furthermore, for sufficiently large values of the recycling rate, the lattice does not transition directly from low to high ribosome density, as seen in lattice models without recycling. Instead, a maximal current phase becomes accessible for much lower values of the initiation rate, and multiple phase transitions occur over a wide region of the phase plane. Crucially, we show that in the presence of ribosome recycling, mRNAs can exhibit a peak in protein production at low values of the initiation rate, beyond which translation rate decreases. This has important implications for translation of certain mRNAs, suggesting that there is an optimal concentration of ribosomes at which protein synthesis is maximal, and beyond which translational efficiency is impaired. The Royal Society 2014-09-06 /pmc/articles/PMC4233708/ /pubmed/25008084 http://dx.doi.org/10.1098/rsif.2014.0589 Text en http://creativecommons.org/licenses/by/4.0/ © 2014 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Articles Marshall, E. Stansfield, I. Romano, M. C. Ribosome recycling induces optimal translation rate at low ribosomal availability |
title | Ribosome recycling induces optimal translation rate at low ribosomal availability |
title_full | Ribosome recycling induces optimal translation rate at low ribosomal availability |
title_fullStr | Ribosome recycling induces optimal translation rate at low ribosomal availability |
title_full_unstemmed | Ribosome recycling induces optimal translation rate at low ribosomal availability |
title_short | Ribosome recycling induces optimal translation rate at low ribosomal availability |
title_sort | ribosome recycling induces optimal translation rate at low ribosomal availability |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4233708/ https://www.ncbi.nlm.nih.gov/pubmed/25008084 http://dx.doi.org/10.1098/rsif.2014.0589 |
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