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Topologies of synthetic gene circuit for optimal fold change activation
Computations widely exist in biological systems for functional regulations. Recently, incoherent feedforward loop and integral feedback controller have been implemented into Escherichia coli to achieve a robust adaptation. Here, we demonstrate that an indirect coherent feedforward loop and mutual in...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8136830/ https://www.ncbi.nlm.nih.gov/pubmed/34009384 http://dx.doi.org/10.1093/nar/gkab253 |
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author | Litovco, Phyana Barger, Natalia Li, Ximing Daniel, Ramez |
author_facet | Litovco, Phyana Barger, Natalia Li, Ximing Daniel, Ramez |
author_sort | Litovco, Phyana |
collection | PubMed |
description | Computations widely exist in biological systems for functional regulations. Recently, incoherent feedforward loop and integral feedback controller have been implemented into Escherichia coli to achieve a robust adaptation. Here, we demonstrate that an indirect coherent feedforward loop and mutual inhibition designs can experimentally improve the fold change of promoters, by reducing the basal level while keeping the maximum activity high. We applied both designs to six different promoters in E. coli, starting with synthetic inducible promoters as a proof-of-principle. Then, we examined native promoters that are either functionally specific or systemically involved in complex pathways such as oxidative stress and SOS response. Both designs include a cascade having a repressor and a construct of either transcriptional interference or antisense transcription. In all six promoters, an improvement of up to ten times in the fold change activation was observed. Theoretically, our unitless models show that when regulation strength matches promoter basal level, an optimal fold change can be achieved. We expect that this methodology can be applied in various biological systems for biotechnology and therapeutic applications. |
format | Online Article Text |
id | pubmed-8136830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81368302021-05-25 Topologies of synthetic gene circuit for optimal fold change activation Litovco, Phyana Barger, Natalia Li, Ximing Daniel, Ramez Nucleic Acids Res Synthetic Biology and Bioengineering Computations widely exist in biological systems for functional regulations. Recently, incoherent feedforward loop and integral feedback controller have been implemented into Escherichia coli to achieve a robust adaptation. Here, we demonstrate that an indirect coherent feedforward loop and mutual inhibition designs can experimentally improve the fold change of promoters, by reducing the basal level while keeping the maximum activity high. We applied both designs to six different promoters in E. coli, starting with synthetic inducible promoters as a proof-of-principle. Then, we examined native promoters that are either functionally specific or systemically involved in complex pathways such as oxidative stress and SOS response. Both designs include a cascade having a repressor and a construct of either transcriptional interference or antisense transcription. In all six promoters, an improvement of up to ten times in the fold change activation was observed. Theoretically, our unitless models show that when regulation strength matches promoter basal level, an optimal fold change can be achieved. We expect that this methodology can be applied in various biological systems for biotechnology and therapeutic applications. Oxford University Press 2021-05-01 /pmc/articles/PMC8136830/ /pubmed/34009384 http://dx.doi.org/10.1093/nar/gkab253 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Synthetic Biology and Bioengineering Litovco, Phyana Barger, Natalia Li, Ximing Daniel, Ramez Topologies of synthetic gene circuit for optimal fold change activation |
title | Topologies of synthetic gene circuit for optimal fold change activation |
title_full | Topologies of synthetic gene circuit for optimal fold change activation |
title_fullStr | Topologies of synthetic gene circuit for optimal fold change activation |
title_full_unstemmed | Topologies of synthetic gene circuit for optimal fold change activation |
title_short | Topologies of synthetic gene circuit for optimal fold change activation |
title_sort | topologies of synthetic gene circuit for optimal fold change activation |
topic | Synthetic Biology and Bioengineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8136830/ https://www.ncbi.nlm.nih.gov/pubmed/34009384 http://dx.doi.org/10.1093/nar/gkab253 |
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