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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....
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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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. |
format | Online Article Text |
id | pubmed-5747351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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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