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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Ltd.
2002
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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. |
format | Online Article Text |
id | pubmed-7126812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | Elsevier Science Ltd. |
record_format | MEDLINE/PubMed |
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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