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Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunit
In eukaryotic translation the 60S ribosome subunit has not been proposed to interact with mRNA or closed-loop factors eIF4E, eIF4G, and PAB1. Using analytical ultracentrifugation with fluorescent detection system, we have identified a 57S translation complex that contains the 60S ribosome, mRNA, and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068138/ https://www.ncbi.nlm.nih.gov/pubmed/30065356 http://dx.doi.org/10.1038/s41598-018-29832-6 |
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author | Denis, Clyde L. Laue, Thomas M. Wang, Xin |
author_facet | Denis, Clyde L. Laue, Thomas M. Wang, Xin |
author_sort | Denis, Clyde L. |
collection | PubMed |
description | In eukaryotic translation the 60S ribosome subunit has not been proposed to interact with mRNA or closed-loop factors eIF4E, eIF4G, and PAB1. Using analytical ultracentrifugation with fluorescent detection system, we have identified a 57S translation complex that contains the 60S ribosome, mRNA, and the closed-loop factors. Previously published data by others also indicate the presence of a 50S-60S translation complex containing these same components. We have found that the abundance of this complex increased upon translational cessation, implying formation after ribosomal dissociation. Stoichiometric analyses of the abundances of the closed-loop components in the 57S complex indicate this complex is most similar to polysomal and monosomal translation complexes at the end of translation rather than at the beginning or middle of translation. In contrast, a 39S complex containing the 40S ribosome bound to mRNA and closed-loop factors was also identified with stoichiometries most similar to polysomal complexes engaged in translation, suggesting that the 39S complex is the previously studied 48S translation initiation complex. These results indicate that the 60S ribosome can associate with the closed-loop mRNA structure and plays a previously undetected role in the translation process. |
format | Online Article Text |
id | pubmed-6068138 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60681382018-08-03 Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunit Denis, Clyde L. Laue, Thomas M. Wang, Xin Sci Rep Article In eukaryotic translation the 60S ribosome subunit has not been proposed to interact with mRNA or closed-loop factors eIF4E, eIF4G, and PAB1. Using analytical ultracentrifugation with fluorescent detection system, we have identified a 57S translation complex that contains the 60S ribosome, mRNA, and the closed-loop factors. Previously published data by others also indicate the presence of a 50S-60S translation complex containing these same components. We have found that the abundance of this complex increased upon translational cessation, implying formation after ribosomal dissociation. Stoichiometric analyses of the abundances of the closed-loop components in the 57S complex indicate this complex is most similar to polysomal and monosomal translation complexes at the end of translation rather than at the beginning or middle of translation. In contrast, a 39S complex containing the 40S ribosome bound to mRNA and closed-loop factors was also identified with stoichiometries most similar to polysomal complexes engaged in translation, suggesting that the 39S complex is the previously studied 48S translation initiation complex. These results indicate that the 60S ribosome can associate with the closed-loop mRNA structure and plays a previously undetected role in the translation process. Nature Publishing Group UK 2018-07-31 /pmc/articles/PMC6068138/ /pubmed/30065356 http://dx.doi.org/10.1038/s41598-018-29832-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Denis, Clyde L. Laue, Thomas M. Wang, Xin Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunit |
title | Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunit |
title_full | Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunit |
title_fullStr | Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunit |
title_full_unstemmed | Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunit |
title_short | Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunit |
title_sort | identification of a 57s translation complex containing closed-loop factors and the 60s ribosome subunit |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068138/ https://www.ncbi.nlm.nih.gov/pubmed/30065356 http://dx.doi.org/10.1038/s41598-018-29832-6 |
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