Cargando…
Deep mutational scanning reveals the molecular determinants of RNA polymerase-mediated adaptation and tradeoffs
RNA polymerase (RNAP) is emblematic of complex biological systems that control multiple traits involving trade-offs such as growth versus maintenance. Laboratory evolution has revealed that mutations in RNAP subunits, including RpoB, are frequently selected. However, we lack a systems view of how mu...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562459/ https://www.ncbi.nlm.nih.gov/pubmed/37813857 http://dx.doi.org/10.1038/s41467-023-41882-7 |
_version_ | 1785118133561851904 |
---|---|
author | Choudhury, Alaksh Gachet, Benoit Dixit, Zoya Faure, Roland Gill, Ryan T. Tenaillon, Olivier |
author_facet | Choudhury, Alaksh Gachet, Benoit Dixit, Zoya Faure, Roland Gill, Ryan T. Tenaillon, Olivier |
author_sort | Choudhury, Alaksh |
collection | PubMed |
description | RNA polymerase (RNAP) is emblematic of complex biological systems that control multiple traits involving trade-offs such as growth versus maintenance. Laboratory evolution has revealed that mutations in RNAP subunits, including RpoB, are frequently selected. However, we lack a systems view of how mutations alter the RNAP molecular functions to promote adaptation. We, therefore, measured the fitness of thousands of mutations within a region of rpoB under multiple conditions and genetic backgrounds, to find that adaptive mutations cluster in two modules. Mutations in one module favor growth over maintenance through a partial loss of an interaction associated with faster elongation. Mutations in the other favor maintenance over growth through a destabilized RNAP-DNA complex. The two molecular handles capture the versatile RNAP-mediated adaptations. Combining both interaction losses simultaneously improved maintenance and growth, challenging the idea that growth-maintenance tradeoff resorts only from limited resources, and revealing how compensatory evolution operates within RNAP. |
format | Online Article Text |
id | pubmed-10562459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105624592023-10-11 Deep mutational scanning reveals the molecular determinants of RNA polymerase-mediated adaptation and tradeoffs Choudhury, Alaksh Gachet, Benoit Dixit, Zoya Faure, Roland Gill, Ryan T. Tenaillon, Olivier Nat Commun Article RNA polymerase (RNAP) is emblematic of complex biological systems that control multiple traits involving trade-offs such as growth versus maintenance. Laboratory evolution has revealed that mutations in RNAP subunits, including RpoB, are frequently selected. However, we lack a systems view of how mutations alter the RNAP molecular functions to promote adaptation. We, therefore, measured the fitness of thousands of mutations within a region of rpoB under multiple conditions and genetic backgrounds, to find that adaptive mutations cluster in two modules. Mutations in one module favor growth over maintenance through a partial loss of an interaction associated with faster elongation. Mutations in the other favor maintenance over growth through a destabilized RNAP-DNA complex. The two molecular handles capture the versatile RNAP-mediated adaptations. Combining both interaction losses simultaneously improved maintenance and growth, challenging the idea that growth-maintenance tradeoff resorts only from limited resources, and revealing how compensatory evolution operates within RNAP. Nature Publishing Group UK 2023-10-09 /pmc/articles/PMC10562459/ /pubmed/37813857 http://dx.doi.org/10.1038/s41467-023-41882-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Choudhury, Alaksh Gachet, Benoit Dixit, Zoya Faure, Roland Gill, Ryan T. Tenaillon, Olivier Deep mutational scanning reveals the molecular determinants of RNA polymerase-mediated adaptation and tradeoffs |
title | Deep mutational scanning reveals the molecular determinants of RNA polymerase-mediated adaptation and tradeoffs |
title_full | Deep mutational scanning reveals the molecular determinants of RNA polymerase-mediated adaptation and tradeoffs |
title_fullStr | Deep mutational scanning reveals the molecular determinants of RNA polymerase-mediated adaptation and tradeoffs |
title_full_unstemmed | Deep mutational scanning reveals the molecular determinants of RNA polymerase-mediated adaptation and tradeoffs |
title_short | Deep mutational scanning reveals the molecular determinants of RNA polymerase-mediated adaptation and tradeoffs |
title_sort | deep mutational scanning reveals the molecular determinants of rna polymerase-mediated adaptation and tradeoffs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562459/ https://www.ncbi.nlm.nih.gov/pubmed/37813857 http://dx.doi.org/10.1038/s41467-023-41882-7 |
work_keys_str_mv | AT choudhuryalaksh deepmutationalscanningrevealsthemoleculardeterminantsofrnapolymerasemediatedadaptationandtradeoffs AT gachetbenoit deepmutationalscanningrevealsthemoleculardeterminantsofrnapolymerasemediatedadaptationandtradeoffs AT dixitzoya deepmutationalscanningrevealsthemoleculardeterminantsofrnapolymerasemediatedadaptationandtradeoffs AT faureroland deepmutationalscanningrevealsthemoleculardeterminantsofrnapolymerasemediatedadaptationandtradeoffs AT gillryant deepmutationalscanningrevealsthemoleculardeterminantsofrnapolymerasemediatedadaptationandtradeoffs AT tenaillonolivier deepmutationalscanningrevealsthemoleculardeterminantsofrnapolymerasemediatedadaptationandtradeoffs |