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EF-G–induced ribosome sliding along the noncoding mRNA
Translational bypassing is a recoding event during which ribosomes slide over a noncoding region of the messenger RNA (mRNA) to synthesize one protein from two discontinuous reading frames. Structures in the mRNA orchestrate forward movement of the ribosome, but what causes ribosomes to start slidin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551183/ https://www.ncbi.nlm.nih.gov/pubmed/31183409 http://dx.doi.org/10.1126/sciadv.aaw9049 |
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author | Klimova, M. Senyushkina, T. Samatova, E. Peng, B. Z. Pearson, M. Peske, F. Rodnina, M. V. |
author_facet | Klimova, M. Senyushkina, T. Samatova, E. Peng, B. Z. Pearson, M. Peske, F. Rodnina, M. V. |
author_sort | Klimova, M. |
collection | PubMed |
description | Translational bypassing is a recoding event during which ribosomes slide over a noncoding region of the messenger RNA (mRNA) to synthesize one protein from two discontinuous reading frames. Structures in the mRNA orchestrate forward movement of the ribosome, but what causes ribosomes to start sliding remains unclear. Here, we show that elongation factor G (EF-G) triggers ribosome take-off by a pseudotranslocation event using a small mRNA stem-loop as an A-site transfer RNA mimic and requires hydrolysis of about two molecules of guanosine 5′-triphosphate per nucleotide of the noncoding gap. Bypassing ribosomes adopt a hyper-rotated conformation, also observed with ribosomes stalled by the SecM sequence, suggesting common ribosome dynamics during translation stalling. Our results demonstrate a new function of EF-G in promoting ribosome sliding along the mRNA, in contrast to codon-wise ribosome movement during canonical translation, and suggest a mechanism by which ribosomes could traverse untranslated parts of mRNAs. |
format | Online Article Text |
id | pubmed-6551183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-65511832019-06-10 EF-G–induced ribosome sliding along the noncoding mRNA Klimova, M. Senyushkina, T. Samatova, E. Peng, B. Z. Pearson, M. Peske, F. Rodnina, M. V. Sci Adv Research Articles Translational bypassing is a recoding event during which ribosomes slide over a noncoding region of the messenger RNA (mRNA) to synthesize one protein from two discontinuous reading frames. Structures in the mRNA orchestrate forward movement of the ribosome, but what causes ribosomes to start sliding remains unclear. Here, we show that elongation factor G (EF-G) triggers ribosome take-off by a pseudotranslocation event using a small mRNA stem-loop as an A-site transfer RNA mimic and requires hydrolysis of about two molecules of guanosine 5′-triphosphate per nucleotide of the noncoding gap. Bypassing ribosomes adopt a hyper-rotated conformation, also observed with ribosomes stalled by the SecM sequence, suggesting common ribosome dynamics during translation stalling. Our results demonstrate a new function of EF-G in promoting ribosome sliding along the mRNA, in contrast to codon-wise ribosome movement during canonical translation, and suggest a mechanism by which ribosomes could traverse untranslated parts of mRNAs. American Association for the Advancement of Science 2019-06-05 /pmc/articles/PMC6551183/ /pubmed/31183409 http://dx.doi.org/10.1126/sciadv.aaw9049 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Klimova, M. Senyushkina, T. Samatova, E. Peng, B. Z. Pearson, M. Peske, F. Rodnina, M. V. EF-G–induced ribosome sliding along the noncoding mRNA |
title | EF-G–induced ribosome sliding along the noncoding mRNA |
title_full | EF-G–induced ribosome sliding along the noncoding mRNA |
title_fullStr | EF-G–induced ribosome sliding along the noncoding mRNA |
title_full_unstemmed | EF-G–induced ribosome sliding along the noncoding mRNA |
title_short | EF-G–induced ribosome sliding along the noncoding mRNA |
title_sort | ef-g–induced ribosome sliding along the noncoding mrna |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551183/ https://www.ncbi.nlm.nih.gov/pubmed/31183409 http://dx.doi.org/10.1126/sciadv.aaw9049 |
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