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Stochastic tuning of gene expression enables cellular adaptation in the absence of pre-existing regulatory circuitry
Cells adapt to familiar changes in their environment by activating predefined regulatory programs that establish adaptive gene expression states. These hard-wired pathways, however, may be inadequate for adaptation to environments never encountered before. Here, we reveal evidence for an alternative...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919758/ https://www.ncbi.nlm.nih.gov/pubmed/29620524 http://dx.doi.org/10.7554/eLife.31867 |
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author | Freddolino, Peter L Yang, Jamie Momen-Roknabadi, Amir Tavazoie, Saeed |
author_facet | Freddolino, Peter L Yang, Jamie Momen-Roknabadi, Amir Tavazoie, Saeed |
author_sort | Freddolino, Peter L |
collection | PubMed |
description | Cells adapt to familiar changes in their environment by activating predefined regulatory programs that establish adaptive gene expression states. These hard-wired pathways, however, may be inadequate for adaptation to environments never encountered before. Here, we reveal evidence for an alternative mode of gene regulation that enables adaptation to adverse conditions without relying on external sensory information or genetically predetermined cis-regulation. Instead, individual genes achieve optimal expression levels through a stochastic search for improved fitness. By focusing on improving the overall health of the cell, the proposed stochastic tuning mechanism discovers global gene expression states that are fundamentally new and yet optimized for novel environments. We provide experimental evidence for stochastic tuning in the adaptation of Saccharomyces cerevisiae to laboratory-engineered environments that are foreign to its native gene-regulatory network. Stochastic tuning operates locally at individual gene promoters, and its efficacy is modulated by perturbations to chromatin modification machinery. |
format | Online Article Text |
id | pubmed-5919758 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59197582018-04-30 Stochastic tuning of gene expression enables cellular adaptation in the absence of pre-existing regulatory circuitry Freddolino, Peter L Yang, Jamie Momen-Roknabadi, Amir Tavazoie, Saeed eLife Computational and Systems Biology Cells adapt to familiar changes in their environment by activating predefined regulatory programs that establish adaptive gene expression states. These hard-wired pathways, however, may be inadequate for adaptation to environments never encountered before. Here, we reveal evidence for an alternative mode of gene regulation that enables adaptation to adverse conditions without relying on external sensory information or genetically predetermined cis-regulation. Instead, individual genes achieve optimal expression levels through a stochastic search for improved fitness. By focusing on improving the overall health of the cell, the proposed stochastic tuning mechanism discovers global gene expression states that are fundamentally new and yet optimized for novel environments. We provide experimental evidence for stochastic tuning in the adaptation of Saccharomyces cerevisiae to laboratory-engineered environments that are foreign to its native gene-regulatory network. Stochastic tuning operates locally at individual gene promoters, and its efficacy is modulated by perturbations to chromatin modification machinery. eLife Sciences Publications, Ltd 2018-04-05 /pmc/articles/PMC5919758/ /pubmed/29620524 http://dx.doi.org/10.7554/eLife.31867 Text en © 2018, Freddolino et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Freddolino, Peter L Yang, Jamie Momen-Roknabadi, Amir Tavazoie, Saeed Stochastic tuning of gene expression enables cellular adaptation in the absence of pre-existing regulatory circuitry |
title | Stochastic tuning of gene expression enables cellular adaptation in the absence of pre-existing regulatory circuitry |
title_full | Stochastic tuning of gene expression enables cellular adaptation in the absence of pre-existing regulatory circuitry |
title_fullStr | Stochastic tuning of gene expression enables cellular adaptation in the absence of pre-existing regulatory circuitry |
title_full_unstemmed | Stochastic tuning of gene expression enables cellular adaptation in the absence of pre-existing regulatory circuitry |
title_short | Stochastic tuning of gene expression enables cellular adaptation in the absence of pre-existing regulatory circuitry |
title_sort | stochastic tuning of gene expression enables cellular adaptation in the absence of pre-existing regulatory circuitry |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919758/ https://www.ncbi.nlm.nih.gov/pubmed/29620524 http://dx.doi.org/10.7554/eLife.31867 |
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