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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....

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Detalles Bibliográficos
Autores principales: Marshall, E., Stansfield, I., Romano, M. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2014
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.
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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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AT romanomc ribosomerecyclinginducesoptimaltranslationrateatlowribosomalavailability