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Variable cellular decision-making behavior in a constant synthetic network topology
BACKGROUND: Modules of interacting components arranged in specific network topologies have evolved to perform a diverse array of cellular functions. For a network with a constant topological structure, its function within a cell may still be tuned by changing the number of instances of a particular...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515661/ https://www.ncbi.nlm.nih.gov/pubmed/31088350 http://dx.doi.org/10.1186/s12859-019-2866-6 |
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author | Shah, Najaf A. Sarkar, Casim A. |
author_facet | Shah, Najaf A. Sarkar, Casim A. |
author_sort | Shah, Najaf A. |
collection | PubMed |
description | BACKGROUND: Modules of interacting components arranged in specific network topologies have evolved to perform a diverse array of cellular functions. For a network with a constant topological structure, its function within a cell may still be tuned by changing the number of instances of a particular component (e.g., gene copy number) or by modulating the intrinsic biochemical properties of a component (e.g., binding strength or catalytic efficiency). How such perturbations affect cellular response dynamics remains poorly understood. Here, we explored these effects in a common decision-making motif, cross-antagonism with autoregulation, by synthetically constructing this network in yeast. RESULTS: We employed the engineering design strategy of reuse to build this topology with a single protein building block, TetR, creating necessary components through TetR mutations and fusion partners. We then studied the impact of several topology-preserving perturbations – strength of cross-antagonism, number of operator sites in a promoter, and gene dosage – on decision-making behavior. We found that reducing TetR repression strength, which hinders cross-antagonism, resulted in a loss of mutually exclusive cell responses. Unexpectedly, increasing the number of operator sites also impeded decision-making exclusivity, which may be a consequence of the averaging effect that arises when multiple transcriptional activators and repressors are accommodated at a given locus. Stochastic simulations of this topology revealed that, even for networks with high TetR repression strength and a low number of operator sites, increasing gene dosage can reduce exclusivity in response dynamics. We further demonstrated this result experimentally by quantifying gene copy numbers in selected yeast clones with differing phenotypic responses. CONCLUSIONS: Our study illustrates how parameters that do not change the topological structure of a decision-making network can nonetheless exert significant influence on its response dynamics. These findings should further inform the study of native motifs, including the effects of topology-preserving mutations, and the robust engineering of synthetic networks. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-2866-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6515661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65156612019-05-21 Variable cellular decision-making behavior in a constant synthetic network topology Shah, Najaf A. Sarkar, Casim A. BMC Bioinformatics Research Article BACKGROUND: Modules of interacting components arranged in specific network topologies have evolved to perform a diverse array of cellular functions. For a network with a constant topological structure, its function within a cell may still be tuned by changing the number of instances of a particular component (e.g., gene copy number) or by modulating the intrinsic biochemical properties of a component (e.g., binding strength or catalytic efficiency). How such perturbations affect cellular response dynamics remains poorly understood. Here, we explored these effects in a common decision-making motif, cross-antagonism with autoregulation, by synthetically constructing this network in yeast. RESULTS: We employed the engineering design strategy of reuse to build this topology with a single protein building block, TetR, creating necessary components through TetR mutations and fusion partners. We then studied the impact of several topology-preserving perturbations – strength of cross-antagonism, number of operator sites in a promoter, and gene dosage – on decision-making behavior. We found that reducing TetR repression strength, which hinders cross-antagonism, resulted in a loss of mutually exclusive cell responses. Unexpectedly, increasing the number of operator sites also impeded decision-making exclusivity, which may be a consequence of the averaging effect that arises when multiple transcriptional activators and repressors are accommodated at a given locus. Stochastic simulations of this topology revealed that, even for networks with high TetR repression strength and a low number of operator sites, increasing gene dosage can reduce exclusivity in response dynamics. We further demonstrated this result experimentally by quantifying gene copy numbers in selected yeast clones with differing phenotypic responses. CONCLUSIONS: Our study illustrates how parameters that do not change the topological structure of a decision-making network can nonetheless exert significant influence on its response dynamics. These findings should further inform the study of native motifs, including the effects of topology-preserving mutations, and the robust engineering of synthetic networks. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-2866-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-14 /pmc/articles/PMC6515661/ /pubmed/31088350 http://dx.doi.org/10.1186/s12859-019-2866-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Shah, Najaf A. Sarkar, Casim A. Variable cellular decision-making behavior in a constant synthetic network topology |
title | Variable cellular decision-making behavior in a constant synthetic network topology |
title_full | Variable cellular decision-making behavior in a constant synthetic network topology |
title_fullStr | Variable cellular decision-making behavior in a constant synthetic network topology |
title_full_unstemmed | Variable cellular decision-making behavior in a constant synthetic network topology |
title_short | Variable cellular decision-making behavior in a constant synthetic network topology |
title_sort | variable cellular decision-making behavior in a constant synthetic network topology |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6515661/ https://www.ncbi.nlm.nih.gov/pubmed/31088350 http://dx.doi.org/10.1186/s12859-019-2866-6 |
work_keys_str_mv | AT shahnajafa variablecellulardecisionmakingbehaviorinaconstantsyntheticnetworktopology AT sarkarcasima variablecellulardecisionmakingbehaviorinaconstantsyntheticnetworktopology |