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Optimization of Ribosome Structure and Function by rRNA Base Modification
BACKGROUND: Translating mRNA sequences into functional proteins is a fundamental process necessary for the viability of organisms throughout all kingdoms of life. The ribosome carries out this process with a delicate balance between speed and accuracy. This work investigates how ribosome structure a...
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1766470/ https://www.ncbi.nlm.nih.gov/pubmed/17245450 http://dx.doi.org/10.1371/journal.pone.0000174 |
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author | Baxter-Roshek, Jennifer L. Petrov, Alexey N. Dinman, Jonathan D. |
author_facet | Baxter-Roshek, Jennifer L. Petrov, Alexey N. Dinman, Jonathan D. |
author_sort | Baxter-Roshek, Jennifer L. |
collection | PubMed |
description | BACKGROUND: Translating mRNA sequences into functional proteins is a fundamental process necessary for the viability of organisms throughout all kingdoms of life. The ribosome carries out this process with a delicate balance between speed and accuracy. This work investigates how ribosome structure and function are affected by rRNA base modification. The prevailing view is that rRNA base modifications serve to fine tune ribosome structure and function. METHODOLOGY/PRINCIPAL FINDINGS: To test this hypothesis, yeast strains deficient in rRNA modifications in the ribosomal peptidyltransferase center were monitored for changes in and translational fidelity. These studies revealed allele-specific sensitivity to translational inhibitors, changes in reading frame maintenance, nonsense suppression and aa-tRNA selection. Ribosomes isolated from two mutants with the most pronounced phenotypic changes had increased affinities for aa-tRNA, and surprisingly, increased rates of peptidyltransfer as monitored by the puromycin assay. rRNA chemical analyses of one of these mutants identified structural changes in five specific bases associated with the ribosomal A-site. CONCLUSIONS/SIGNIFICANCE: Together, the data suggest that modification of these bases fine tune the structure of the A-site region of the large subunit so as to assure correct positioning of critical rRNA bases involved in aa-tRNA accommodation into the PTC, of the eEF-1A•aa-tRNA•GTP ternary complex with the GTPase associated center, and of the aa-tRNA in the A-site. These findings represent a direct demonstration in support of the prevailing hypothesis that rRNA modifications serve to optimize rRNA structure for production of accurate and efficient ribosomes. |
format | Text |
id | pubmed-1766470 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-17664702007-01-24 Optimization of Ribosome Structure and Function by rRNA Base Modification Baxter-Roshek, Jennifer L. Petrov, Alexey N. Dinman, Jonathan D. PLoS One Research Article BACKGROUND: Translating mRNA sequences into functional proteins is a fundamental process necessary for the viability of organisms throughout all kingdoms of life. The ribosome carries out this process with a delicate balance between speed and accuracy. This work investigates how ribosome structure and function are affected by rRNA base modification. The prevailing view is that rRNA base modifications serve to fine tune ribosome structure and function. METHODOLOGY/PRINCIPAL FINDINGS: To test this hypothesis, yeast strains deficient in rRNA modifications in the ribosomal peptidyltransferase center were monitored for changes in and translational fidelity. These studies revealed allele-specific sensitivity to translational inhibitors, changes in reading frame maintenance, nonsense suppression and aa-tRNA selection. Ribosomes isolated from two mutants with the most pronounced phenotypic changes had increased affinities for aa-tRNA, and surprisingly, increased rates of peptidyltransfer as monitored by the puromycin assay. rRNA chemical analyses of one of these mutants identified structural changes in five specific bases associated with the ribosomal A-site. CONCLUSIONS/SIGNIFICANCE: Together, the data suggest that modification of these bases fine tune the structure of the A-site region of the large subunit so as to assure correct positioning of critical rRNA bases involved in aa-tRNA accommodation into the PTC, of the eEF-1A•aa-tRNA•GTP ternary complex with the GTPase associated center, and of the aa-tRNA in the A-site. These findings represent a direct demonstration in support of the prevailing hypothesis that rRNA modifications serve to optimize rRNA structure for production of accurate and efficient ribosomes. Public Library of Science 2007-01-24 /pmc/articles/PMC1766470/ /pubmed/17245450 http://dx.doi.org/10.1371/journal.pone.0000174 Text en Baxter-Roshek et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Baxter-Roshek, Jennifer L. Petrov, Alexey N. Dinman, Jonathan D. Optimization of Ribosome Structure and Function by rRNA Base Modification |
title | Optimization of Ribosome Structure and Function by rRNA Base Modification |
title_full | Optimization of Ribosome Structure and Function by rRNA Base Modification |
title_fullStr | Optimization of Ribosome Structure and Function by rRNA Base Modification |
title_full_unstemmed | Optimization of Ribosome Structure and Function by rRNA Base Modification |
title_short | Optimization of Ribosome Structure and Function by rRNA Base Modification |
title_sort | optimization of ribosome structure and function by rrna base modification |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1766470/ https://www.ncbi.nlm.nih.gov/pubmed/17245450 http://dx.doi.org/10.1371/journal.pone.0000174 |
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