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Programmed –1 Frameshifting by Kinetic Partitioning during Impeded Translocation

Programmed –1 ribosomal frameshifting (−1PRF) is an mRNA recoding event utilized by cells to enhance the information content of the genome and to regulate gene expression. The mechanism of –1PRF and its timing during translation elongation are unclear. Here, we identified the steps that govern –1PRF...

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Detalles Bibliográficos
Autores principales: Caliskan, Neva, Katunin, Vladimir I., Belardinelli, Riccardo, Peske, Frank, Rodnina, Marina V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112342/
https://www.ncbi.nlm.nih.gov/pubmed/24949973
http://dx.doi.org/10.1016/j.cell.2014.04.041
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author Caliskan, Neva
Katunin, Vladimir I.
Belardinelli, Riccardo
Peske, Frank
Rodnina, Marina V.
author_facet Caliskan, Neva
Katunin, Vladimir I.
Belardinelli, Riccardo
Peske, Frank
Rodnina, Marina V.
author_sort Caliskan, Neva
collection PubMed
description Programmed –1 ribosomal frameshifting (−1PRF) is an mRNA recoding event utilized by cells to enhance the information content of the genome and to regulate gene expression. The mechanism of –1PRF and its timing during translation elongation are unclear. Here, we identified the steps that govern –1PRF by following the stepwise movement of the ribosome through the frameshifting site of a model mRNA derived from the IBV 1a/1b gene in a reconstituted in vitro translation system from Escherichia coli. Frameshifting occurs at a late stage of translocation when the two tRNAs are bound to adjacent slippery sequence codons of the mRNA. The downstream pseudoknot in the mRNA impairs the closing movement of the 30S subunit head, the dissociation of EF-G, and the release of tRNA from the ribosome. The slippage of the ribosome into the –1 frame accelerates the completion of translocation, thereby further favoring translation in the new reading frame.
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spelling pubmed-71123422020-04-02 Programmed –1 Frameshifting by Kinetic Partitioning during Impeded Translocation Caliskan, Neva Katunin, Vladimir I. Belardinelli, Riccardo Peske, Frank Rodnina, Marina V. Cell Article Programmed –1 ribosomal frameshifting (−1PRF) is an mRNA recoding event utilized by cells to enhance the information content of the genome and to regulate gene expression. The mechanism of –1PRF and its timing during translation elongation are unclear. Here, we identified the steps that govern –1PRF by following the stepwise movement of the ribosome through the frameshifting site of a model mRNA derived from the IBV 1a/1b gene in a reconstituted in vitro translation system from Escherichia coli. Frameshifting occurs at a late stage of translocation when the two tRNAs are bound to adjacent slippery sequence codons of the mRNA. The downstream pseudoknot in the mRNA impairs the closing movement of the 30S subunit head, the dissociation of EF-G, and the release of tRNA from the ribosome. The slippage of the ribosome into the –1 frame accelerates the completion of translocation, thereby further favoring translation in the new reading frame. Elsevier Inc. 2014-06-19 2014-06-19 /pmc/articles/PMC7112342/ /pubmed/24949973 http://dx.doi.org/10.1016/j.cell.2014.04.041 Text en Copyright © 2014 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Caliskan, Neva
Katunin, Vladimir I.
Belardinelli, Riccardo
Peske, Frank
Rodnina, Marina V.
Programmed –1 Frameshifting by Kinetic Partitioning during Impeded Translocation
title Programmed –1 Frameshifting by Kinetic Partitioning during Impeded Translocation
title_full Programmed –1 Frameshifting by Kinetic Partitioning during Impeded Translocation
title_fullStr Programmed –1 Frameshifting by Kinetic Partitioning during Impeded Translocation
title_full_unstemmed Programmed –1 Frameshifting by Kinetic Partitioning during Impeded Translocation
title_short Programmed –1 Frameshifting by Kinetic Partitioning during Impeded Translocation
title_sort programmed –1 frameshifting by kinetic partitioning during impeded translocation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112342/
https://www.ncbi.nlm.nih.gov/pubmed/24949973
http://dx.doi.org/10.1016/j.cell.2014.04.041
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