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−1 Programmed Ribosomal Frameshifting as a Force-Dependent Process

−1 Programmed ribosomal frameshifting is a translational recoding event in which ribosomes slip backward along messenger RNA presumably due to increased tension disrupting the codon–anticodon interaction at the ribosome's coding site. Single-molecule physical methods and recent experiments char...

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Detalles Bibliográficos
Autor principal: Visscher, Koen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102820/
https://www.ncbi.nlm.nih.gov/pubmed/26970190
http://dx.doi.org/10.1016/bs.pmbts.2015.11.003
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author Visscher, Koen
author_facet Visscher, Koen
author_sort Visscher, Koen
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description −1 Programmed ribosomal frameshifting is a translational recoding event in which ribosomes slip backward along messenger RNA presumably due to increased tension disrupting the codon–anticodon interaction at the ribosome's coding site. Single-molecule physical methods and recent experiments characterizing the physical properties of mRNA's slippery sequence as well as the mechanical stability of downstream mRNA structure motifs that give rise to frameshifting are discussed. Progress in technology, experimental assays, and data analysis methods hold promise for accurate physical modeling and quantitative understanding of −1 programmed ribosomal frameshifting.
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spelling pubmed-71028202020-03-31 −1 Programmed Ribosomal Frameshifting as a Force-Dependent Process Visscher, Koen Prog Mol Biol Transl Sci Article −1 Programmed ribosomal frameshifting is a translational recoding event in which ribosomes slip backward along messenger RNA presumably due to increased tension disrupting the codon–anticodon interaction at the ribosome's coding site. Single-molecule physical methods and recent experiments characterizing the physical properties of mRNA's slippery sequence as well as the mechanical stability of downstream mRNA structure motifs that give rise to frameshifting are discussed. Progress in technology, experimental assays, and data analysis methods hold promise for accurate physical modeling and quantitative understanding of −1 programmed ribosomal frameshifting. Elsevier Inc. 2016 2016-02-02 /pmc/articles/PMC7102820/ /pubmed/26970190 http://dx.doi.org/10.1016/bs.pmbts.2015.11.003 Text en Copyright © 2016 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
Visscher, Koen
−1 Programmed Ribosomal Frameshifting as a Force-Dependent Process
title −1 Programmed Ribosomal Frameshifting as a Force-Dependent Process
title_full −1 Programmed Ribosomal Frameshifting as a Force-Dependent Process
title_fullStr −1 Programmed Ribosomal Frameshifting as a Force-Dependent Process
title_full_unstemmed −1 Programmed Ribosomal Frameshifting as a Force-Dependent Process
title_short −1 Programmed Ribosomal Frameshifting as a Force-Dependent Process
title_sort −1 programmed ribosomal frameshifting as a force-dependent process
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7102820/
https://www.ncbi.nlm.nih.gov/pubmed/26970190
http://dx.doi.org/10.1016/bs.pmbts.2015.11.003
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