Cargando…
Experimental Evolution of Anticipatory Regulation in Escherichia coli
Environmental cues in an ecological niche are often temporal in nature. For instance, in temperate climates, temperature is higher in daytime compared to during night. In response to these temporal cues, bacteria have been known to exhibit anticipatory regulation, whereby triggering response to a ye...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787300/ https://www.ncbi.nlm.nih.gov/pubmed/35087497 http://dx.doi.org/10.3389/fmicb.2021.796228 |
_version_ | 1784639331797827584 |
---|---|
author | Mahilkar, Anjali Venkataraman, Pavithra Mall, Akshat Saini, Supreet |
author_facet | Mahilkar, Anjali Venkataraman, Pavithra Mall, Akshat Saini, Supreet |
author_sort | Mahilkar, Anjali |
collection | PubMed |
description | Environmental cues in an ecological niche are often temporal in nature. For instance, in temperate climates, temperature is higher in daytime compared to during night. In response to these temporal cues, bacteria have been known to exhibit anticipatory regulation, whereby triggering response to a yet to appear cue. Such an anticipatory response in known to enhance Darwinian fitness, and hence, is likely an important feature of regulatory networks in microorganisms. However, the conditions under which an anticipatory response evolves as an adaptive response are not known. In this work, we develop a quantitative model to study response of a population to two temporal environmental cues, and predict variables which are likely important for evolution of anticipatory regulatory response. We follow this with experimental evolution of Escherichia coli in alternating environments of rhamnose and paraquat for ∼850 generations. We demonstrate that growth in this cyclical environment leads to evolution of anticipatory regulation. As a result, pre-exposure to rhamnose leads to a greater fitness in paraquat environment. Genome sequencing reveals that this anticipatory regulation is encoded via mutations in global regulators. Overall, our study contributes to understanding of how environment shapes the topology of regulatory networks in an organism. |
format | Online Article Text |
id | pubmed-8787300 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87873002022-01-26 Experimental Evolution of Anticipatory Regulation in Escherichia coli Mahilkar, Anjali Venkataraman, Pavithra Mall, Akshat Saini, Supreet Front Microbiol Microbiology Environmental cues in an ecological niche are often temporal in nature. For instance, in temperate climates, temperature is higher in daytime compared to during night. In response to these temporal cues, bacteria have been known to exhibit anticipatory regulation, whereby triggering response to a yet to appear cue. Such an anticipatory response in known to enhance Darwinian fitness, and hence, is likely an important feature of regulatory networks in microorganisms. However, the conditions under which an anticipatory response evolves as an adaptive response are not known. In this work, we develop a quantitative model to study response of a population to two temporal environmental cues, and predict variables which are likely important for evolution of anticipatory regulatory response. We follow this with experimental evolution of Escherichia coli in alternating environments of rhamnose and paraquat for ∼850 generations. We demonstrate that growth in this cyclical environment leads to evolution of anticipatory regulation. As a result, pre-exposure to rhamnose leads to a greater fitness in paraquat environment. Genome sequencing reveals that this anticipatory regulation is encoded via mutations in global regulators. Overall, our study contributes to understanding of how environment shapes the topology of regulatory networks in an organism. Frontiers Media S.A. 2022-01-11 /pmc/articles/PMC8787300/ /pubmed/35087497 http://dx.doi.org/10.3389/fmicb.2021.796228 Text en Copyright © 2022 Mahilkar, Venkataraman, Mall and Saini. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Mahilkar, Anjali Venkataraman, Pavithra Mall, Akshat Saini, Supreet Experimental Evolution of Anticipatory Regulation in Escherichia coli |
title | Experimental Evolution of Anticipatory Regulation in Escherichia coli |
title_full | Experimental Evolution of Anticipatory Regulation in Escherichia coli |
title_fullStr | Experimental Evolution of Anticipatory Regulation in Escherichia coli |
title_full_unstemmed | Experimental Evolution of Anticipatory Regulation in Escherichia coli |
title_short | Experimental Evolution of Anticipatory Regulation in Escherichia coli |
title_sort | experimental evolution of anticipatory regulation in escherichia coli |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787300/ https://www.ncbi.nlm.nih.gov/pubmed/35087497 http://dx.doi.org/10.3389/fmicb.2021.796228 |
work_keys_str_mv | AT mahilkaranjali experimentalevolutionofanticipatoryregulationinescherichiacoli AT venkataramanpavithra experimentalevolutionofanticipatoryregulationinescherichiacoli AT mallakshat experimentalevolutionofanticipatoryregulationinescherichiacoli AT sainisupreet experimentalevolutionofanticipatoryregulationinescherichiacoli |