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Regulostat Inferelator: a novel network biology platform to uncover molecular devices that predetermine cellular response phenotypes

With the emergence of genome editing technologies and synthetic biology, it is now possible to engineer genetic circuits driving a cell's phenotypic response to a stressor. However, capturing a continuous response, rather than simply a binary ‘on’ or ‘off’ response, remains a bioengineering cha...

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Detalles Bibliográficos
Autores principales: Ung, Choong Yong, Ghanat Bari, Mehrab, Zhang, Cheng, Liang, Jingjing, Correia, Cristina, Li, Hu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698671/
https://www.ncbi.nlm.nih.gov/pubmed/31114928
http://dx.doi.org/10.1093/nar/gkz417
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author Ung, Choong Yong
Ghanat Bari, Mehrab
Zhang, Cheng
Liang, Jingjing
Correia, Cristina
Li, Hu
author_facet Ung, Choong Yong
Ghanat Bari, Mehrab
Zhang, Cheng
Liang, Jingjing
Correia, Cristina
Li, Hu
author_sort Ung, Choong Yong
collection PubMed
description With the emergence of genome editing technologies and synthetic biology, it is now possible to engineer genetic circuits driving a cell's phenotypic response to a stressor. However, capturing a continuous response, rather than simply a binary ‘on’ or ‘off’ response, remains a bioengineering challenge. No tools currently exist to identify gene candidates responsible for predetermining and fine-tuning cell response phenotypes. To address this gap, we devised a novel Regulostat Inferelator (RSI) algorithm to decipher intrinsic molecular devices or networks that predetermine cellular phenotypic responses. The RSI algorithm is designed to extract gene expression patterns from basal transcriptomic data in order to identify ‘regulostat’ constituent gene pairs, which exhibit rheostat-like mode-of-cooperation capable of fine-tuning cellular response. Our proof-of-concept study provides computational evidence for the existence of regulostats and that these networks predetermine cellular response prior to exposure to a stressor or drug. In addition, our work, for the first time, provides evidence of context-specific, drug–regulostat interactions in predetermining drug response phenotypes in cancer cells. Given RSI-inferred regulostat networks offer insights for prioritizing gene candidates capable of rendering a resistant phenotype sensitive to a given drug, we envision that this tool will be of great value in bioengineering and medicine.
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spelling pubmed-66986712019-08-22 Regulostat Inferelator: a novel network biology platform to uncover molecular devices that predetermine cellular response phenotypes Ung, Choong Yong Ghanat Bari, Mehrab Zhang, Cheng Liang, Jingjing Correia, Cristina Li, Hu Nucleic Acids Res Methods Online With the emergence of genome editing technologies and synthetic biology, it is now possible to engineer genetic circuits driving a cell's phenotypic response to a stressor. However, capturing a continuous response, rather than simply a binary ‘on’ or ‘off’ response, remains a bioengineering challenge. No tools currently exist to identify gene candidates responsible for predetermining and fine-tuning cell response phenotypes. To address this gap, we devised a novel Regulostat Inferelator (RSI) algorithm to decipher intrinsic molecular devices or networks that predetermine cellular phenotypic responses. The RSI algorithm is designed to extract gene expression patterns from basal transcriptomic data in order to identify ‘regulostat’ constituent gene pairs, which exhibit rheostat-like mode-of-cooperation capable of fine-tuning cellular response. Our proof-of-concept study provides computational evidence for the existence of regulostats and that these networks predetermine cellular response prior to exposure to a stressor or drug. In addition, our work, for the first time, provides evidence of context-specific, drug–regulostat interactions in predetermining drug response phenotypes in cancer cells. Given RSI-inferred regulostat networks offer insights for prioritizing gene candidates capable of rendering a resistant phenotype sensitive to a given drug, we envision that this tool will be of great value in bioengineering and medicine. Oxford University Press 2019-08-22 2019-05-22 /pmc/articles/PMC6698671/ /pubmed/31114928 http://dx.doi.org/10.1093/nar/gkz417 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Methods Online
Ung, Choong Yong
Ghanat Bari, Mehrab
Zhang, Cheng
Liang, Jingjing
Correia, Cristina
Li, Hu
Regulostat Inferelator: a novel network biology platform to uncover molecular devices that predetermine cellular response phenotypes
title Regulostat Inferelator: a novel network biology platform to uncover molecular devices that predetermine cellular response phenotypes
title_full Regulostat Inferelator: a novel network biology platform to uncover molecular devices that predetermine cellular response phenotypes
title_fullStr Regulostat Inferelator: a novel network biology platform to uncover molecular devices that predetermine cellular response phenotypes
title_full_unstemmed Regulostat Inferelator: a novel network biology platform to uncover molecular devices that predetermine cellular response phenotypes
title_short Regulostat Inferelator: a novel network biology platform to uncover molecular devices that predetermine cellular response phenotypes
title_sort regulostat inferelator: a novel network biology platform to uncover molecular devices that predetermine cellular response phenotypes
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6698671/
https://www.ncbi.nlm.nih.gov/pubmed/31114928
http://dx.doi.org/10.1093/nar/gkz417
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