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A Statistical Approach Reveals Designs for the Most Robust Stochastic Gene Oscillators

[Image: see text] The engineering of transcriptional networks presents many challenges due to the inherent uncertainty in the system structure, changing cellular context, and stochasticity in the governing dynamics. One approach to address these problems is to design and build systems that can funct...

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Autores principales: Woods, Mae L., Leon, Miriam, Perez-Carrasco, Ruben, Barnes, Chris P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914944/
https://www.ncbi.nlm.nih.gov/pubmed/26835539
http://dx.doi.org/10.1021/acssynbio.5b00179
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author Woods, Mae L.
Leon, Miriam
Perez-Carrasco, Ruben
Barnes, Chris P.
author_facet Woods, Mae L.
Leon, Miriam
Perez-Carrasco, Ruben
Barnes, Chris P.
author_sort Woods, Mae L.
collection PubMed
description [Image: see text] The engineering of transcriptional networks presents many challenges due to the inherent uncertainty in the system structure, changing cellular context, and stochasticity in the governing dynamics. One approach to address these problems is to design and build systems that can function across a range of conditions; that is they are robust to uncertainty in their constituent components. Here we examine the parametric robustness landscape of transcriptional oscillators, which underlie many important processes such as circadian rhythms and the cell cycle, plus also serve as a model for the engineering of complex and emergent phenomena. The central questions that we address are: Can we build genetic oscillators that are more robust than those already constructed? Can we make genetic oscillators arbitrarily robust? These questions are technically challenging due to the large model and parameter spaces that must be efficiently explored. Here we use a measure of robustness that coincides with the Bayesian model evidence, combined with an efficient Monte Carlo method to traverse model space and concentrate on regions of high robustness, which enables the accurate evaluation of the relative robustness of gene network models governed by stochastic dynamics. We report the most robust two and three gene oscillator systems, plus examine how the number of interactions, the presence of autoregulation, and degradation of mRNA and protein affects the frequency, amplitude, and robustness of transcriptional oscillators. We also find that there is a limit to parametric robustness, beyond which there is nothing to be gained by adding additional feedback. Importantly, we provide predictions on new oscillator systems that can be constructed to verify the theory and advance design and modeling approaches to systems and synthetic biology.
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spelling pubmed-49149442016-06-22 A Statistical Approach Reveals Designs for the Most Robust Stochastic Gene Oscillators Woods, Mae L. Leon, Miriam Perez-Carrasco, Ruben Barnes, Chris P. ACS Synth Biol [Image: see text] The engineering of transcriptional networks presents many challenges due to the inherent uncertainty in the system structure, changing cellular context, and stochasticity in the governing dynamics. One approach to address these problems is to design and build systems that can function across a range of conditions; that is they are robust to uncertainty in their constituent components. Here we examine the parametric robustness landscape of transcriptional oscillators, which underlie many important processes such as circadian rhythms and the cell cycle, plus also serve as a model for the engineering of complex and emergent phenomena. The central questions that we address are: Can we build genetic oscillators that are more robust than those already constructed? Can we make genetic oscillators arbitrarily robust? These questions are technically challenging due to the large model and parameter spaces that must be efficiently explored. Here we use a measure of robustness that coincides with the Bayesian model evidence, combined with an efficient Monte Carlo method to traverse model space and concentrate on regions of high robustness, which enables the accurate evaluation of the relative robustness of gene network models governed by stochastic dynamics. We report the most robust two and three gene oscillator systems, plus examine how the number of interactions, the presence of autoregulation, and degradation of mRNA and protein affects the frequency, amplitude, and robustness of transcriptional oscillators. We also find that there is a limit to parametric robustness, beyond which there is nothing to be gained by adding additional feedback. Importantly, we provide predictions on new oscillator systems that can be constructed to verify the theory and advance design and modeling approaches to systems and synthetic biology. American Chemical Society 2016-02-02 2016-06-17 /pmc/articles/PMC4914944/ /pubmed/26835539 http://dx.doi.org/10.1021/acssynbio.5b00179 Text en Copyright © 2016 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Woods, Mae L.
Leon, Miriam
Perez-Carrasco, Ruben
Barnes, Chris P.
A Statistical Approach Reveals Designs for the Most Robust Stochastic Gene Oscillators
title A Statistical Approach Reveals Designs for the Most Robust Stochastic Gene Oscillators
title_full A Statistical Approach Reveals Designs for the Most Robust Stochastic Gene Oscillators
title_fullStr A Statistical Approach Reveals Designs for the Most Robust Stochastic Gene Oscillators
title_full_unstemmed A Statistical Approach Reveals Designs for the Most Robust Stochastic Gene Oscillators
title_short A Statistical Approach Reveals Designs for the Most Robust Stochastic Gene Oscillators
title_sort statistical approach reveals designs for the most robust stochastic gene oscillators
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914944/
https://www.ncbi.nlm.nih.gov/pubmed/26835539
http://dx.doi.org/10.1021/acssynbio.5b00179
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