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Antagonistic control of a dual-input mammalian gene switch by food additives

Synthetic biology has significantly advanced the design of mammalian trigger-inducible transgene-control devices that are able to programme complex cellular behaviour. Fruit-based benzoate derivatives licensed as food additives, such as flavours (e.g. vanillate) and preservatives (e.g. benzoate), ar...

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Autores principales: Xie, Mingqi, Ye, Haifeng, Hamri, Ghislaine Charpin-El, Fussenegger, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132709/
https://www.ncbi.nlm.nih.gov/pubmed/25030908
http://dx.doi.org/10.1093/nar/gku545
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author Xie, Mingqi
Ye, Haifeng
Hamri, Ghislaine Charpin-El
Fussenegger, Martin
author_facet Xie, Mingqi
Ye, Haifeng
Hamri, Ghislaine Charpin-El
Fussenegger, Martin
author_sort Xie, Mingqi
collection PubMed
description Synthetic biology has significantly advanced the design of mammalian trigger-inducible transgene-control devices that are able to programme complex cellular behaviour. Fruit-based benzoate derivatives licensed as food additives, such as flavours (e.g. vanillate) and preservatives (e.g. benzoate), are a particularly attractive class of trigger compounds for orthogonal mammalian transgene control devices because of their innocuousness, physiological compatibility and simple oral administration. Capitalizing on the genetic componentry of the soil bacterium Comamonas testosteroni, which has evolved to catabolize a variety of aromatic compounds, we have designed different mammalian gene expression systems that could be induced and repressed by the food additives benzoate and vanillate. When implanting designer cells engineered for gene switch-driven expression of the human placental secreted alkaline phosphatase (SEAP) into mice, blood SEAP levels of treated animals directly correlated with a benzoate-enriched drinking programme. Additionally, the benzoate-/vanillate-responsive device was compatible with other transgene control systems and could be assembled into higher-order control networks providing expression dynamics reminiscent of a lap-timing stopwatch. Designer gene switches using licensed food additives as trigger compounds to achieve antagonistic dual-input expression profiles and provide novel control topologies and regulation dynamics may advance future gene- and cell-based therapies.
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spelling pubmed-41327092014-12-01 Antagonistic control of a dual-input mammalian gene switch by food additives Xie, Mingqi Ye, Haifeng Hamri, Ghislaine Charpin-El Fussenegger, Martin Nucleic Acids Res Methods Online Synthetic biology has significantly advanced the design of mammalian trigger-inducible transgene-control devices that are able to programme complex cellular behaviour. Fruit-based benzoate derivatives licensed as food additives, such as flavours (e.g. vanillate) and preservatives (e.g. benzoate), are a particularly attractive class of trigger compounds for orthogonal mammalian transgene control devices because of their innocuousness, physiological compatibility and simple oral administration. Capitalizing on the genetic componentry of the soil bacterium Comamonas testosteroni, which has evolved to catabolize a variety of aromatic compounds, we have designed different mammalian gene expression systems that could be induced and repressed by the food additives benzoate and vanillate. When implanting designer cells engineered for gene switch-driven expression of the human placental secreted alkaline phosphatase (SEAP) into mice, blood SEAP levels of treated animals directly correlated with a benzoate-enriched drinking programme. Additionally, the benzoate-/vanillate-responsive device was compatible with other transgene control systems and could be assembled into higher-order control networks providing expression dynamics reminiscent of a lap-timing stopwatch. Designer gene switches using licensed food additives as trigger compounds to achieve antagonistic dual-input expression profiles and provide novel control topologies and regulation dynamics may advance future gene- and cell-based therapies. Oxford University Press 2014-08-18 2014-07-16 /pmc/articles/PMC4132709/ /pubmed/25030908 http://dx.doi.org/10.1093/nar/gku545 Text en © The Author(s) 2014. 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 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
Xie, Mingqi
Ye, Haifeng
Hamri, Ghislaine Charpin-El
Fussenegger, Martin
Antagonistic control of a dual-input mammalian gene switch by food additives
title Antagonistic control of a dual-input mammalian gene switch by food additives
title_full Antagonistic control of a dual-input mammalian gene switch by food additives
title_fullStr Antagonistic control of a dual-input mammalian gene switch by food additives
title_full_unstemmed Antagonistic control of a dual-input mammalian gene switch by food additives
title_short Antagonistic control of a dual-input mammalian gene switch by food additives
title_sort antagonistic control of a dual-input mammalian gene switch by food additives
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4132709/
https://www.ncbi.nlm.nih.gov/pubmed/25030908
http://dx.doi.org/10.1093/nar/gku545
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