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Asymmetry between Activation and Deactivation during a Transcriptional Pulse

Transcription in eukaryotic cells occurs in gene-specific bursts or pulses of activity. Recent studies identified a spectrum of transcriptionally active “on-states,” interspersed with periods of inactivity, but these “off-states” and the process of transcriptional deactivation are poorly understood....

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Autores principales: Dunham, Lee S.S., Momiji, Hiroshi, Harper, Claire V., Downton, Polly J., Hey, Kirsty, McNamara, Anne, Featherstone, Karen, Spiller, David G., Rand, David A., Finkenstädt, Bärbel, White, Michael R.H., Davis, Julian R.E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5747351/
https://www.ncbi.nlm.nih.gov/pubmed/29153839
http://dx.doi.org/10.1016/j.cels.2017.10.013
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author Dunham, Lee S.S.
Momiji, Hiroshi
Harper, Claire V.
Downton, Polly J.
Hey, Kirsty
McNamara, Anne
Featherstone, Karen
Spiller, David G.
Rand, David A.
Finkenstädt, Bärbel
White, Michael R.H.
Davis, Julian R.E.
author_facet Dunham, Lee S.S.
Momiji, Hiroshi
Harper, Claire V.
Downton, Polly J.
Hey, Kirsty
McNamara, Anne
Featherstone, Karen
Spiller, David G.
Rand, David A.
Finkenstädt, Bärbel
White, Michael R.H.
Davis, Julian R.E.
author_sort Dunham, Lee S.S.
collection PubMed
description Transcription in eukaryotic cells occurs in gene-specific bursts or pulses of activity. Recent studies identified a spectrum of transcriptionally active “on-states,” interspersed with periods of inactivity, but these “off-states” and the process of transcriptional deactivation are poorly understood. To examine what occurs during deactivation, we investigate the dynamics of switching between variable rates. We measured live single-cell expression of luciferase reporters from human growth hormone or human prolactin promoters in a pituitary cell line. Subsequently, we applied a statistical variable-rate model of transcription, validated by single-molecule FISH, to estimate switching between transcriptional rates. Under the assumption that transcription can switch to any rate at any time, we found that transcriptional activation occurs predominantly as a single switch, whereas deactivation occurs with graded, stepwise decreases in transcription rate. Experimentally altering cAMP signalling with forskolin or chromatin remodelling with histone deacetylase inhibitor modifies the duration of defined transcriptional states. Our findings reveal transcriptional activation and deactivation as mechanistically independent, asymmetrical processes.
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spelling pubmed-57473512018-01-09 Asymmetry between Activation and Deactivation during a Transcriptional Pulse Dunham, Lee S.S. Momiji, Hiroshi Harper, Claire V. Downton, Polly J. Hey, Kirsty McNamara, Anne Featherstone, Karen Spiller, David G. Rand, David A. Finkenstädt, Bärbel White, Michael R.H. Davis, Julian R.E. Cell Syst Article Transcription in eukaryotic cells occurs in gene-specific bursts or pulses of activity. Recent studies identified a spectrum of transcriptionally active “on-states,” interspersed with periods of inactivity, but these “off-states” and the process of transcriptional deactivation are poorly understood. To examine what occurs during deactivation, we investigate the dynamics of switching between variable rates. We measured live single-cell expression of luciferase reporters from human growth hormone or human prolactin promoters in a pituitary cell line. Subsequently, we applied a statistical variable-rate model of transcription, validated by single-molecule FISH, to estimate switching between transcriptional rates. Under the assumption that transcription can switch to any rate at any time, we found that transcriptional activation occurs predominantly as a single switch, whereas deactivation occurs with graded, stepwise decreases in transcription rate. Experimentally altering cAMP signalling with forskolin or chromatin remodelling with histone deacetylase inhibitor modifies the duration of defined transcriptional states. Our findings reveal transcriptional activation and deactivation as mechanistically independent, asymmetrical processes. Cell Press 2017-12-27 /pmc/articles/PMC5747351/ /pubmed/29153839 http://dx.doi.org/10.1016/j.cels.2017.10.013 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Dunham, Lee S.S.
Momiji, Hiroshi
Harper, Claire V.
Downton, Polly J.
Hey, Kirsty
McNamara, Anne
Featherstone, Karen
Spiller, David G.
Rand, David A.
Finkenstädt, Bärbel
White, Michael R.H.
Davis, Julian R.E.
Asymmetry between Activation and Deactivation during a Transcriptional Pulse
title Asymmetry between Activation and Deactivation during a Transcriptional Pulse
title_full Asymmetry between Activation and Deactivation during a Transcriptional Pulse
title_fullStr Asymmetry between Activation and Deactivation during a Transcriptional Pulse
title_full_unstemmed Asymmetry between Activation and Deactivation during a Transcriptional Pulse
title_short Asymmetry between Activation and Deactivation during a Transcriptional Pulse
title_sort asymmetry between activation and deactivation during a transcriptional pulse
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5747351/
https://www.ncbi.nlm.nih.gov/pubmed/29153839
http://dx.doi.org/10.1016/j.cels.2017.10.013
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