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Adaptive tuning of cell sensory diversity without changes in gene expression
In the face of uncertainty, cell populations tend to diversify to enhance survival and growth. Previous studies established that cells can optimize such bet hedging upon environmental change by modulating gene expression to adapt both the average and diversity of phenotypes. Here, we demonstrate tha...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673753/ https://www.ncbi.nlm.nih.gov/pubmed/33188019 http://dx.doi.org/10.1126/sciadv.abc1087 |
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author | Kamino, K. Keegstra, J. M. Long, J. Emonet, T. Shimizu, T. S. |
author_facet | Kamino, K. Keegstra, J. M. Long, J. Emonet, T. Shimizu, T. S. |
author_sort | Kamino, K. |
collection | PubMed |
description | In the face of uncertainty, cell populations tend to diversify to enhance survival and growth. Previous studies established that cells can optimize such bet hedging upon environmental change by modulating gene expression to adapt both the average and diversity of phenotypes. Here, we demonstrate that cells can tune phenotypic diversity also using posttranslational modifications. In the chemotaxis network of Escherichia coli, we find, for both major chemoreceptors Tar and Tsr, that cell-to-cell variation in response sensitivity is dynamically modulated depending on the presence or absence of their cognate chemoeffector ligands in the environment. Combining experiments with mathematical modeling, we show that this diversity tuning requires only the environment-dependent covalent modification of chemoreceptors and a standing cell-to-cell variation in their allosteric coupling. Thus, when environmental cues are unavailable, phenotypic diversity enhances the population’s readiness for many signals. However, once a signal is perceived, the population focuses on tracking that signal. |
format | Online Article Text |
id | pubmed-7673753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-76737532020-11-24 Adaptive tuning of cell sensory diversity without changes in gene expression Kamino, K. Keegstra, J. M. Long, J. Emonet, T. Shimizu, T. S. Sci Adv Research Articles In the face of uncertainty, cell populations tend to diversify to enhance survival and growth. Previous studies established that cells can optimize such bet hedging upon environmental change by modulating gene expression to adapt both the average and diversity of phenotypes. Here, we demonstrate that cells can tune phenotypic diversity also using posttranslational modifications. In the chemotaxis network of Escherichia coli, we find, for both major chemoreceptors Tar and Tsr, that cell-to-cell variation in response sensitivity is dynamically modulated depending on the presence or absence of their cognate chemoeffector ligands in the environment. Combining experiments with mathematical modeling, we show that this diversity tuning requires only the environment-dependent covalent modification of chemoreceptors and a standing cell-to-cell variation in their allosteric coupling. Thus, when environmental cues are unavailable, phenotypic diversity enhances the population’s readiness for many signals. However, once a signal is perceived, the population focuses on tracking that signal. American Association for the Advancement of Science 2020-11-13 /pmc/articles/PMC7673753/ /pubmed/33188019 http://dx.doi.org/10.1126/sciadv.abc1087 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 Kamino, K. Keegstra, J. M. Long, J. Emonet, T. Shimizu, T. S. Adaptive tuning of cell sensory diversity without changes in gene expression |
title | Adaptive tuning of cell sensory diversity without changes in gene expression |
title_full | Adaptive tuning of cell sensory diversity without changes in gene expression |
title_fullStr | Adaptive tuning of cell sensory diversity without changes in gene expression |
title_full_unstemmed | Adaptive tuning of cell sensory diversity without changes in gene expression |
title_short | Adaptive tuning of cell sensory diversity without changes in gene expression |
title_sort | adaptive tuning of cell sensory diversity without changes in gene expression |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7673753/ https://www.ncbi.nlm.nih.gov/pubmed/33188019 http://dx.doi.org/10.1126/sciadv.abc1087 |
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