Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunit

Abstract 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,...

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Main Authors: Clyde L. Denis, Thomas M. Laue, Xin Wang
Format: Article
Language:English
Published: Nature Publishing Group 2018-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-018-29832-6
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spelling doaj-f913d2dae08f435f983fd4a9a50939cb2020-12-08T04:59:50ZengNature Publishing GroupScientific Reports2045-23222018-07-018111210.1038/s41598-018-29832-6Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunitClyde L. Denis0Thomas M. Laue1Xin Wang2Department of Molecular, Cellular, and Biomedical Sciences, University of New HampshireDepartment of Molecular, Cellular, and Biomedical Sciences, University of New HampshireDepartment of Molecular, Cellular, and Biomedical Sciences, University of New HampshireAbstract 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.https://doi.org/10.1038/s41598-018-29832-6
collection DOAJ
language English
format Article
sources DOAJ
author Clyde L. Denis
Thomas M. Laue
Xin Wang
spellingShingle Clyde L. Denis
Thomas M. Laue
Xin Wang
Identification of a 57S translation complex containing closed-loop factors and the 60S ribosome subunit
Scientific Reports
author_facet Clyde L. Denis
Thomas M. Laue
Xin Wang
author_sort Clyde L. Denis
title 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_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_sort identification of a 57s translation complex containing closed-loop factors and the 60s ribosome subunit
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2018-07-01
description Abstract 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.
url https://doi.org/10.1038/s41598-018-29832-6
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AT thomasmlaue identificationofa57stranslationcomplexcontainingclosedloopfactorsandthe60sribosomesubunit
AT xinwang identificationofa57stranslationcomplexcontainingclosedloopfactorsandthe60sribosomesubunit
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