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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...

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Autores principales: Mahilkar, Anjali, Venkataraman, Pavithra, Mall, Akshat, Saini, Supreet
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
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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.
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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
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