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Control of mRNA translation by dynamic ribosome modification

Control of mRNA translation is a crucial regulatory mechanism used by bacteria to respond to their environment. In the soil bacterium Pseudomonas fluorescens, RimK modifies the C-terminus of ribosomal protein RpsF to influence important aspects of rhizosphere colonisation through proteome remodellin...

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Autores principales: Grenga, Lucia, Little, Richard Howard, Chandra, Govind, Woodcock, Stuart Daniel, Saalbach, Gerhard, Morris, Richard James, Malone, Jacob George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343187/
https://www.ncbi.nlm.nih.gov/pubmed/32584816
http://dx.doi.org/10.1371/journal.pgen.1008837
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author Grenga, Lucia
Little, Richard Howard
Chandra, Govind
Woodcock, Stuart Daniel
Saalbach, Gerhard
Morris, Richard James
Malone, Jacob George
author_facet Grenga, Lucia
Little, Richard Howard
Chandra, Govind
Woodcock, Stuart Daniel
Saalbach, Gerhard
Morris, Richard James
Malone, Jacob George
author_sort Grenga, Lucia
collection PubMed
description Control of mRNA translation is a crucial regulatory mechanism used by bacteria to respond to their environment. In the soil bacterium Pseudomonas fluorescens, RimK modifies the C-terminus of ribosomal protein RpsF to influence important aspects of rhizosphere colonisation through proteome remodelling. In this study, we show that RimK activity is itself under complex, multifactorial control by the co-transcribed phosphodiesterase trigger enzyme (RimA) and a polyglutamate-specific protease (RimB). Furthermore, biochemical experimentation and mathematical modelling reveal a role for the nucleotide second messenger cyclic-di-GMP in coordinating these activities. Active ribosome regulation by RimK occurs by two main routes: indirectly, through changes in the abundance of the global translational regulator Hfq and directly, with translation of surface attachment factors, amino acid transporters and key secreted molecules linked specifically to RpsF modification. Our findings show that post-translational ribosomal modification functions as a rapid-response mechanism that tunes global gene translation in response to environmental signals.
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spelling pubmed-73431872020-07-17 Control of mRNA translation by dynamic ribosome modification Grenga, Lucia Little, Richard Howard Chandra, Govind Woodcock, Stuart Daniel Saalbach, Gerhard Morris, Richard James Malone, Jacob George PLoS Genet Research Article Control of mRNA translation is a crucial regulatory mechanism used by bacteria to respond to their environment. In the soil bacterium Pseudomonas fluorescens, RimK modifies the C-terminus of ribosomal protein RpsF to influence important aspects of rhizosphere colonisation through proteome remodelling. In this study, we show that RimK activity is itself under complex, multifactorial control by the co-transcribed phosphodiesterase trigger enzyme (RimA) and a polyglutamate-specific protease (RimB). Furthermore, biochemical experimentation and mathematical modelling reveal a role for the nucleotide second messenger cyclic-di-GMP in coordinating these activities. Active ribosome regulation by RimK occurs by two main routes: indirectly, through changes in the abundance of the global translational regulator Hfq and directly, with translation of surface attachment factors, amino acid transporters and key secreted molecules linked specifically to RpsF modification. Our findings show that post-translational ribosomal modification functions as a rapid-response mechanism that tunes global gene translation in response to environmental signals. Public Library of Science 2020-06-25 /pmc/articles/PMC7343187/ /pubmed/32584816 http://dx.doi.org/10.1371/journal.pgen.1008837 Text en © 2020 Grenga 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Grenga, Lucia
Little, Richard Howard
Chandra, Govind
Woodcock, Stuart Daniel
Saalbach, Gerhard
Morris, Richard James
Malone, Jacob George
Control of mRNA translation by dynamic ribosome modification
title Control of mRNA translation by dynamic ribosome modification
title_full Control of mRNA translation by dynamic ribosome modification
title_fullStr Control of mRNA translation by dynamic ribosome modification
title_full_unstemmed Control of mRNA translation by dynamic ribosome modification
title_short Control of mRNA translation by dynamic ribosome modification
title_sort control of mrna translation by dynamic ribosome modification
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7343187/
https://www.ncbi.nlm.nih.gov/pubmed/32584816
http://dx.doi.org/10.1371/journal.pgen.1008837
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