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Ribosome structure: revisiting the connection between translational accuracy and unconventional decoding

The ribosome is a molecular machine that converts genetic information in the form of RNA, into protein. Recent structural studies reveal a complex set of interactions between the ribosome and its ligands, mRNA and tRNA, that indicate ways in which the ribosome could avoid costly translational errors...

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Detalles Bibliográficos
Autores principales: Stahl, Guillaume, McCarty, Gregory P, Farabaugh, Philip J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd. 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126812/
https://www.ncbi.nlm.nih.gov/pubmed/11943544
http://dx.doi.org/10.1016/S0968-0004(02)02064-9
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author Stahl, Guillaume
McCarty, Gregory P
Farabaugh, Philip J
author_facet Stahl, Guillaume
McCarty, Gregory P
Farabaugh, Philip J
author_sort Stahl, Guillaume
collection PubMed
description The ribosome is a molecular machine that converts genetic information in the form of RNA, into protein. Recent structural studies reveal a complex set of interactions between the ribosome and its ligands, mRNA and tRNA, that indicate ways in which the ribosome could avoid costly translational errors. Ribosomes must decode each successive codon accurately, and structural data provide a clear indication of how ribosomes limit recruitment of the wrong tRNA (sense errors). In a triplet-based genetic code there are three potential forward reading frames, only one of which encodes the correct protein. Errors in which the ribosome reads a codon out of the normal reading frame (frameshift errors) occur less frequently than sense errors, although it is not clear from structural data how these errors are avoided. Some mRNA sequences, termed programmed-frameshift sites, cause the ribosome to change reading frame. Based on recent work on these sites, this article proposes that the ribosome uses the structure of the codon–anticodon complex formed by the peptidyl-tRNA, especially its wobble interaction, to constrain the incoming aminoacyl-tRNA to the correct reading frame.
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spelling pubmed-71268122020-04-08 Ribosome structure: revisiting the connection between translational accuracy and unconventional decoding Stahl, Guillaume McCarty, Gregory P Farabaugh, Philip J Trends Biochem Sci Opinion The ribosome is a molecular machine that converts genetic information in the form of RNA, into protein. Recent structural studies reveal a complex set of interactions between the ribosome and its ligands, mRNA and tRNA, that indicate ways in which the ribosome could avoid costly translational errors. Ribosomes must decode each successive codon accurately, and structural data provide a clear indication of how ribosomes limit recruitment of the wrong tRNA (sense errors). In a triplet-based genetic code there are three potential forward reading frames, only one of which encodes the correct protein. Errors in which the ribosome reads a codon out of the normal reading frame (frameshift errors) occur less frequently than sense errors, although it is not clear from structural data how these errors are avoided. Some mRNA sequences, termed programmed-frameshift sites, cause the ribosome to change reading frame. Based on recent work on these sites, this article proposes that the ribosome uses the structure of the codon–anticodon complex formed by the peptidyl-tRNA, especially its wobble interaction, to constrain the incoming aminoacyl-tRNA to the correct reading frame. Elsevier Science Ltd. 2002-04-01 2002-04-04 /pmc/articles/PMC7126812/ /pubmed/11943544 http://dx.doi.org/10.1016/S0968-0004(02)02064-9 Text en Copyright © 2002 Elsevier Science Ltd. 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 Opinion
Stahl, Guillaume
McCarty, Gregory P
Farabaugh, Philip J
Ribosome structure: revisiting the connection between translational accuracy and unconventional decoding
title Ribosome structure: revisiting the connection between translational accuracy and unconventional decoding
title_full Ribosome structure: revisiting the connection between translational accuracy and unconventional decoding
title_fullStr Ribosome structure: revisiting the connection between translational accuracy and unconventional decoding
title_full_unstemmed Ribosome structure: revisiting the connection between translational accuracy and unconventional decoding
title_short Ribosome structure: revisiting the connection between translational accuracy and unconventional decoding
title_sort ribosome structure: revisiting the connection between translational accuracy and unconventional decoding
topic Opinion
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7126812/
https://www.ncbi.nlm.nih.gov/pubmed/11943544
http://dx.doi.org/10.1016/S0968-0004(02)02064-9
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