Cargando…

Extrinsic noise prevents the independent tuning of gene expression noise and protein mean abundance in bacteria

It is generally accepted that prokaryotes can tune gene expression noise independently of protein mean abundance by varying the relative levels of transcription and translation. Here, we address this question quantitatively, using a custom-made library of 40 Bacillus subtilis strains expressing a fl...

Descripción completa

Detalles Bibliográficos
Autores principales: Deloupy, A., Sauveplane, V., Robert, J., Aymerich, S., Jules, M., Robert, L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541070/
https://www.ncbi.nlm.nih.gov/pubmed/33028528
http://dx.doi.org/10.1126/sciadv.abc3478
_version_ 1783591328814202880
author Deloupy, A.
Sauveplane, V.
Robert, J.
Aymerich, S.
Jules, M.
Robert, L.
author_facet Deloupy, A.
Sauveplane, V.
Robert, J.
Aymerich, S.
Jules, M.
Robert, L.
author_sort Deloupy, A.
collection PubMed
description It is generally accepted that prokaryotes can tune gene expression noise independently of protein mean abundance by varying the relative levels of transcription and translation. Here, we address this question quantitatively, using a custom-made library of 40 Bacillus subtilis strains expressing a fluorescent protein under the control of different transcription and translation control elements. We quantify noise and mean protein abundance by fluorescence microscopy and show that for most of the natural transcription range of B. subtilis, expression noise is equally sensitive to variations in the transcription or translation rate because of the prevalence of extrinsic noise. In agreement, analysis of whole-genome transcriptomic and proteomic datasets suggests that noise optimization through transcription and translation tuning during evolution may only occur in a regime of weak transcription. Therefore, independent control of mean abundance and noise can rarely be achieved, which has strong implications for both genome evolution and biological engineering.
format Online
Article
Text
id pubmed-7541070
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher American Association for the Advancement of Science
record_format MEDLINE/PubMed
spelling pubmed-75410702020-10-20 Extrinsic noise prevents the independent tuning of gene expression noise and protein mean abundance in bacteria Deloupy, A. Sauveplane, V. Robert, J. Aymerich, S. Jules, M. Robert, L. Sci Adv Research Articles It is generally accepted that prokaryotes can tune gene expression noise independently of protein mean abundance by varying the relative levels of transcription and translation. Here, we address this question quantitatively, using a custom-made library of 40 Bacillus subtilis strains expressing a fluorescent protein under the control of different transcription and translation control elements. We quantify noise and mean protein abundance by fluorescence microscopy and show that for most of the natural transcription range of B. subtilis, expression noise is equally sensitive to variations in the transcription or translation rate because of the prevalence of extrinsic noise. In agreement, analysis of whole-genome transcriptomic and proteomic datasets suggests that noise optimization through transcription and translation tuning during evolution may only occur in a regime of weak transcription. Therefore, independent control of mean abundance and noise can rarely be achieved, which has strong implications for both genome evolution and biological engineering. American Association for the Advancement of Science 2020-10-07 /pmc/articles/PMC7541070/ /pubmed/33028528 http://dx.doi.org/10.1126/sciadv.abc3478 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Deloupy, A.
Sauveplane, V.
Robert, J.
Aymerich, S.
Jules, M.
Robert, L.
Extrinsic noise prevents the independent tuning of gene expression noise and protein mean abundance in bacteria
title Extrinsic noise prevents the independent tuning of gene expression noise and protein mean abundance in bacteria
title_full Extrinsic noise prevents the independent tuning of gene expression noise and protein mean abundance in bacteria
title_fullStr Extrinsic noise prevents the independent tuning of gene expression noise and protein mean abundance in bacteria
title_full_unstemmed Extrinsic noise prevents the independent tuning of gene expression noise and protein mean abundance in bacteria
title_short Extrinsic noise prevents the independent tuning of gene expression noise and protein mean abundance in bacteria
title_sort extrinsic noise prevents the independent tuning of gene expression noise and protein mean abundance in bacteria
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541070/
https://www.ncbi.nlm.nih.gov/pubmed/33028528
http://dx.doi.org/10.1126/sciadv.abc3478
work_keys_str_mv AT deloupya extrinsicnoisepreventstheindependenttuningofgeneexpressionnoiseandproteinmeanabundanceinbacteria
AT sauveplanev extrinsicnoisepreventstheindependenttuningofgeneexpressionnoiseandproteinmeanabundanceinbacteria
AT robertj extrinsicnoisepreventstheindependenttuningofgeneexpressionnoiseandproteinmeanabundanceinbacteria
AT aymerichs extrinsicnoisepreventstheindependenttuningofgeneexpressionnoiseandproteinmeanabundanceinbacteria
AT julesm extrinsicnoisepreventstheindependenttuningofgeneexpressionnoiseandproteinmeanabundanceinbacteria
AT robertl extrinsicnoisepreventstheindependenttuningofgeneexpressionnoiseandproteinmeanabundanceinbacteria