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The mechanism of mRNA activation
During translation initiation, messenger RNA molecules must be identified and activated for loading into a ribosome. In this rate-limiting step, the heterotrimeric protein eukaryotic initiation factor eIF4F must recognize and productively interact with the 7-methylguanosine cap at the 5’ end of the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680758/ https://www.ncbi.nlm.nih.gov/pubmed/38014128 http://dx.doi.org/10.1101/2023.11.15.567265 |
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author | Gentry, Riley C. Ide, Nicholas A. Comunale, Victoria M. Hartwick, Erik W. Kinz-Thompson, Colin D. Gonzalez, Ruben L. |
author_facet | Gentry, Riley C. Ide, Nicholas A. Comunale, Victoria M. Hartwick, Erik W. Kinz-Thompson, Colin D. Gonzalez, Ruben L. |
author_sort | Gentry, Riley C. |
collection | PubMed |
description | During translation initiation, messenger RNA molecules must be identified and activated for loading into a ribosome. In this rate-limiting step, the heterotrimeric protein eukaryotic initiation factor eIF4F must recognize and productively interact with the 7-methylguanosine cap at the 5’ end of the messenger RNA and subsequently activate the message. Despite its fundamental, regulatory role in gene expression, the molecular events underlying cap recognition and messenger RNA activation remain mysterious. Here, we generate a unique, single-molecule fluorescence imaging system to interrogate the dynamics with which eIF4F discriminates productive and non-productive locations on full-length, native messenger RNA molecules. At the single-molecule level, we observe stochastic sampling of eIF4F along the length of the messenger RNA and identify allosteric communication between the eIF4F subunits which ultimately drive cap-recognition and subsequent activation of the message. Our experiments uncover novel functions for each subunit of eIF4F and we conclude by presenting a model for messenger RNA activation which precisely defines the composition of the activated message. This model provides a general framework for understanding how messenger RNA molecules may be discriminated from one another, and how other RNA-binding proteins may control the efficiency of translation initiation. |
format | Online Article Text |
id | pubmed-10680758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106807582023-11-27 The mechanism of mRNA activation Gentry, Riley C. Ide, Nicholas A. Comunale, Victoria M. Hartwick, Erik W. Kinz-Thompson, Colin D. Gonzalez, Ruben L. bioRxiv Article During translation initiation, messenger RNA molecules must be identified and activated for loading into a ribosome. In this rate-limiting step, the heterotrimeric protein eukaryotic initiation factor eIF4F must recognize and productively interact with the 7-methylguanosine cap at the 5’ end of the messenger RNA and subsequently activate the message. Despite its fundamental, regulatory role in gene expression, the molecular events underlying cap recognition and messenger RNA activation remain mysterious. Here, we generate a unique, single-molecule fluorescence imaging system to interrogate the dynamics with which eIF4F discriminates productive and non-productive locations on full-length, native messenger RNA molecules. At the single-molecule level, we observe stochastic sampling of eIF4F along the length of the messenger RNA and identify allosteric communication between the eIF4F subunits which ultimately drive cap-recognition and subsequent activation of the message. Our experiments uncover novel functions for each subunit of eIF4F and we conclude by presenting a model for messenger RNA activation which precisely defines the composition of the activated message. This model provides a general framework for understanding how messenger RNA molecules may be discriminated from one another, and how other RNA-binding proteins may control the efficiency of translation initiation. Cold Spring Harbor Laboratory 2023-11-15 /pmc/articles/PMC10680758/ /pubmed/38014128 http://dx.doi.org/10.1101/2023.11.15.567265 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Gentry, Riley C. Ide, Nicholas A. Comunale, Victoria M. Hartwick, Erik W. Kinz-Thompson, Colin D. Gonzalez, Ruben L. The mechanism of mRNA activation |
title | The mechanism of mRNA activation |
title_full | The mechanism of mRNA activation |
title_fullStr | The mechanism of mRNA activation |
title_full_unstemmed | The mechanism of mRNA activation |
title_short | The mechanism of mRNA activation |
title_sort | mechanism of mrna activation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10680758/ https://www.ncbi.nlm.nih.gov/pubmed/38014128 http://dx.doi.org/10.1101/2023.11.15.567265 |
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