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Riboswitch-inspired toehold riboregulators for gene regulation in Escherichia coli

Regulatory RNA molecules have been widely investigated as components for synthetic gene circuits, complementing the use of protein-based transcription factors. Among the potential advantages of RNA-based gene regulators are their comparatively simple design, sequence-programmability, orthogonality,...

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Autores principales: Wang, Tianhe, Simmel, Friedrich C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071393/
https://www.ncbi.nlm.nih.gov/pubmed/35446427
http://dx.doi.org/10.1093/nar/gkac275
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author Wang, Tianhe
Simmel, Friedrich C
author_facet Wang, Tianhe
Simmel, Friedrich C
author_sort Wang, Tianhe
collection PubMed
description Regulatory RNA molecules have been widely investigated as components for synthetic gene circuits, complementing the use of protein-based transcription factors. Among the potential advantages of RNA-based gene regulators are their comparatively simple design, sequence-programmability, orthogonality, and their relatively low metabolic burden. In this work, we developed a set of riboswitch-inspired riboregulators in Escherichia coli that combine the concept of toehold-mediated strand displacement (TMSD) with the switching principles of naturally occurring transcriptional and translational riboswitches. Specifically, for translational activation and repression, we sequestered anti-anti-RBS or anti-RBS sequences, respectively, inside the loop of a stable hairpin domain, which is equipped with a single-stranded toehold region at its 5′ end and is followed by regulated sequences on its 3′ side. A trigger RNA binding to the toehold region can invade the hairpin, inducing a structural rearrangement that results in translational activation or deactivation. We also demonstrate that TMSD can be applied in the context of transcriptional regulation by switching RNA secondary structure involved in Rho-dependent termination. Our designs expand the repertoire of available synthetic riboregulators by a set of RNA switches with no sequence limitation, which should prove useful for the development of robust genetic sensors and circuits.
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spelling pubmed-90713932022-05-06 Riboswitch-inspired toehold riboregulators for gene regulation in Escherichia coli Wang, Tianhe Simmel, Friedrich C Nucleic Acids Res Synthetic Biology and Bioengineering Regulatory RNA molecules have been widely investigated as components for synthetic gene circuits, complementing the use of protein-based transcription factors. Among the potential advantages of RNA-based gene regulators are their comparatively simple design, sequence-programmability, orthogonality, and their relatively low metabolic burden. In this work, we developed a set of riboswitch-inspired riboregulators in Escherichia coli that combine the concept of toehold-mediated strand displacement (TMSD) with the switching principles of naturally occurring transcriptional and translational riboswitches. Specifically, for translational activation and repression, we sequestered anti-anti-RBS or anti-RBS sequences, respectively, inside the loop of a stable hairpin domain, which is equipped with a single-stranded toehold region at its 5′ end and is followed by regulated sequences on its 3′ side. A trigger RNA binding to the toehold region can invade the hairpin, inducing a structural rearrangement that results in translational activation or deactivation. We also demonstrate that TMSD can be applied in the context of transcriptional regulation by switching RNA secondary structure involved in Rho-dependent termination. Our designs expand the repertoire of available synthetic riboregulators by a set of RNA switches with no sequence limitation, which should prove useful for the development of robust genetic sensors and circuits. Oxford University Press 2022-04-21 /pmc/articles/PMC9071393/ /pubmed/35446427 http://dx.doi.org/10.1093/nar/gkac275 Text en © The Author(s) 2022. 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 (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
Wang, Tianhe
Simmel, Friedrich C
Riboswitch-inspired toehold riboregulators for gene regulation in Escherichia coli
title Riboswitch-inspired toehold riboregulators for gene regulation in Escherichia coli
title_full Riboswitch-inspired toehold riboregulators for gene regulation in Escherichia coli
title_fullStr Riboswitch-inspired toehold riboregulators for gene regulation in Escherichia coli
title_full_unstemmed Riboswitch-inspired toehold riboregulators for gene regulation in Escherichia coli
title_short Riboswitch-inspired toehold riboregulators for gene regulation in Escherichia coli
title_sort riboswitch-inspired toehold riboregulators for gene regulation in escherichia coli
topic Synthetic Biology and Bioengineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071393/
https://www.ncbi.nlm.nih.gov/pubmed/35446427
http://dx.doi.org/10.1093/nar/gkac275
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