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An Optogenetic Platform for Real-Time, Single-Cell Interrogation of Stochastic Transcriptional Regulation

Transcription is a highly regulated and inherently stochastic process. The complexity of signal transduction and gene regulation makes it challenging to analyze how the dynamic activity of transcriptional regulators affects stochastic transcription. By combining a fast-acting, photo-regulatable tran...

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Detalles Bibliográficos
Autores principales: Rullan, Marc, Benzinger, Dirk, Schmidt, Gregor W., Milias-Argeitis, Andreas, Khammash, Mustafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5971206/
https://www.ncbi.nlm.nih.gov/pubmed/29775585
http://dx.doi.org/10.1016/j.molcel.2018.04.012
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author Rullan, Marc
Benzinger, Dirk
Schmidt, Gregor W.
Milias-Argeitis, Andreas
Khammash, Mustafa
author_facet Rullan, Marc
Benzinger, Dirk
Schmidt, Gregor W.
Milias-Argeitis, Andreas
Khammash, Mustafa
author_sort Rullan, Marc
collection PubMed
description Transcription is a highly regulated and inherently stochastic process. The complexity of signal transduction and gene regulation makes it challenging to analyze how the dynamic activity of transcriptional regulators affects stochastic transcription. By combining a fast-acting, photo-regulatable transcription factor with nascent RNA quantification in live cells and an experimental setup for precise spatiotemporal delivery of light inputs, we constructed a platform for the real-time, single-cell interrogation of transcription in Saccharomyces cerevisiae. We show that transcriptional activation and deactivation are fast and memoryless. By analyzing the temporal activity of individual cells, we found that transcription occurs in bursts, whose duration and timing are modulated by transcription factor activity. Using our platform, we regulated transcription via light-driven feedback loops at the single-cell level. Feedback markedly reduced cell-to-cell variability and led to qualitative differences in cellular transcriptional dynamics. Our platform establishes a flexible method for studying transcriptional dynamics in single cells.
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spelling pubmed-59712062018-06-01 An Optogenetic Platform for Real-Time, Single-Cell Interrogation of Stochastic Transcriptional Regulation Rullan, Marc Benzinger, Dirk Schmidt, Gregor W. Milias-Argeitis, Andreas Khammash, Mustafa Mol Cell Article Transcription is a highly regulated and inherently stochastic process. The complexity of signal transduction and gene regulation makes it challenging to analyze how the dynamic activity of transcriptional regulators affects stochastic transcription. By combining a fast-acting, photo-regulatable transcription factor with nascent RNA quantification in live cells and an experimental setup for precise spatiotemporal delivery of light inputs, we constructed a platform for the real-time, single-cell interrogation of transcription in Saccharomyces cerevisiae. We show that transcriptional activation and deactivation are fast and memoryless. By analyzing the temporal activity of individual cells, we found that transcription occurs in bursts, whose duration and timing are modulated by transcription factor activity. Using our platform, we regulated transcription via light-driven feedback loops at the single-cell level. Feedback markedly reduced cell-to-cell variability and led to qualitative differences in cellular transcriptional dynamics. Our platform establishes a flexible method for studying transcriptional dynamics in single cells. Cell Press 2018-05-17 /pmc/articles/PMC5971206/ /pubmed/29775585 http://dx.doi.org/10.1016/j.molcel.2018.04.012 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Rullan, Marc
Benzinger, Dirk
Schmidt, Gregor W.
Milias-Argeitis, Andreas
Khammash, Mustafa
An Optogenetic Platform for Real-Time, Single-Cell Interrogation of Stochastic Transcriptional Regulation
title An Optogenetic Platform for Real-Time, Single-Cell Interrogation of Stochastic Transcriptional Regulation
title_full An Optogenetic Platform for Real-Time, Single-Cell Interrogation of Stochastic Transcriptional Regulation
title_fullStr An Optogenetic Platform for Real-Time, Single-Cell Interrogation of Stochastic Transcriptional Regulation
title_full_unstemmed An Optogenetic Platform for Real-Time, Single-Cell Interrogation of Stochastic Transcriptional Regulation
title_short An Optogenetic Platform for Real-Time, Single-Cell Interrogation of Stochastic Transcriptional Regulation
title_sort optogenetic platform for real-time, single-cell interrogation of stochastic transcriptional regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5971206/
https://www.ncbi.nlm.nih.gov/pubmed/29775585
http://dx.doi.org/10.1016/j.molcel.2018.04.012
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