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A tunable dual-input system for on-demand dynamic gene expression regulation

Cellular systems have evolved numerous mechanisms to adapt to environmental stimuli, underpinned by dynamic patterns of gene expression. In addition to gene transcription regulation, modulation of protein levels, dynamics and localization are essential checkpoints governing cell functions. The intro...

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Autores principales: Pedone, Elisa, Postiglione, Lorena, Aulicino, Francesco, Rocca, Dan L., Montes-Olivas, Sandra, Khazim, Mahmoud, di Bernardo, Diego, Pia Cosma, Maria, Marucci, Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775159/
https://www.ncbi.nlm.nih.gov/pubmed/31578371
http://dx.doi.org/10.1038/s41467-019-12329-9
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author Pedone, Elisa
Postiglione, Lorena
Aulicino, Francesco
Rocca, Dan L.
Montes-Olivas, Sandra
Khazim, Mahmoud
di Bernardo, Diego
Pia Cosma, Maria
Marucci, Lucia
author_facet Pedone, Elisa
Postiglione, Lorena
Aulicino, Francesco
Rocca, Dan L.
Montes-Olivas, Sandra
Khazim, Mahmoud
di Bernardo, Diego
Pia Cosma, Maria
Marucci, Lucia
author_sort Pedone, Elisa
collection PubMed
description Cellular systems have evolved numerous mechanisms to adapt to environmental stimuli, underpinned by dynamic patterns of gene expression. In addition to gene transcription regulation, modulation of protein levels, dynamics and localization are essential checkpoints governing cell functions. The introduction of inducible promoters has allowed gene expression control using orthogonal molecules, facilitating its rapid and reversible manipulation to study gene function. However, differing protein stabilities hinder the generation of protein temporal profiles seen in vivo. Here, we improve the Tet-On system integrating conditional destabilising elements at the post-translational level and permitting simultaneous control of gene expression and protein stability. We show, in mammalian cells, that adding protein stability control allows faster response times, fully tunable and enhanced dynamic range, and improved in silico feedback control of gene expression. Finally, we highlight the effectiveness of our dual-input system to modulate levels of signalling pathway components in mouse Embryonic Stem Cells.
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spelling pubmed-67751592019-10-04 A tunable dual-input system for on-demand dynamic gene expression regulation Pedone, Elisa Postiglione, Lorena Aulicino, Francesco Rocca, Dan L. Montes-Olivas, Sandra Khazim, Mahmoud di Bernardo, Diego Pia Cosma, Maria Marucci, Lucia Nat Commun Article Cellular systems have evolved numerous mechanisms to adapt to environmental stimuli, underpinned by dynamic patterns of gene expression. In addition to gene transcription regulation, modulation of protein levels, dynamics and localization are essential checkpoints governing cell functions. The introduction of inducible promoters has allowed gene expression control using orthogonal molecules, facilitating its rapid and reversible manipulation to study gene function. However, differing protein stabilities hinder the generation of protein temporal profiles seen in vivo. Here, we improve the Tet-On system integrating conditional destabilising elements at the post-translational level and permitting simultaneous control of gene expression and protein stability. We show, in mammalian cells, that adding protein stability control allows faster response times, fully tunable and enhanced dynamic range, and improved in silico feedback control of gene expression. Finally, we highlight the effectiveness of our dual-input system to modulate levels of signalling pathway components in mouse Embryonic Stem Cells. Nature Publishing Group UK 2019-10-02 /pmc/articles/PMC6775159/ /pubmed/31578371 http://dx.doi.org/10.1038/s41467-019-12329-9 Text en © Crown 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pedone, Elisa
Postiglione, Lorena
Aulicino, Francesco
Rocca, Dan L.
Montes-Olivas, Sandra
Khazim, Mahmoud
di Bernardo, Diego
Pia Cosma, Maria
Marucci, Lucia
A tunable dual-input system for on-demand dynamic gene expression regulation
title A tunable dual-input system for on-demand dynamic gene expression regulation
title_full A tunable dual-input system for on-demand dynamic gene expression regulation
title_fullStr A tunable dual-input system for on-demand dynamic gene expression regulation
title_full_unstemmed A tunable dual-input system for on-demand dynamic gene expression regulation
title_short A tunable dual-input system for on-demand dynamic gene expression regulation
title_sort tunable dual-input system for on-demand dynamic gene expression regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775159/
https://www.ncbi.nlm.nih.gov/pubmed/31578371
http://dx.doi.org/10.1038/s41467-019-12329-9
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