Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783555720098086912 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7343187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT grengalucia controlofmrnatranslationbydynamicribosomemodification AT littlerichardhoward controlofmrnatranslationbydynamicribosomemodification AT chandragovind controlofmrnatranslationbydynamicribosomemodification AT woodcockstuartdaniel controlofmrnatranslationbydynamicribosomemodification AT saalbachgerhard controlofmrnatranslationbydynamicribosomemodification AT morrisrichardjames controlofmrnatranslationbydynamicribosomemodification AT malonejacobgeorge controlofmrnatranslationbydynamicribosomemodification |