Linking stochastic fluctuations in chromatin structure and gene expression.

The number of mRNA and protein molecules expressed from a single gene molecule fluctuates over time. These fluctuations have been attributed, in part, to the random transitioning of promoters between transcriptionally active and inactive states, causing transcription to occur in bursts. However, the...

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Main Authors: Christopher R Brown, Changhui Mao, Elena Falkovskaia, Melissa S Jurica, Hinrich Boeger
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS Biology
Online Access:http://europepmc.org/articles/PMC3735467?pdf=render
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spelling doaj-62f4973d25724669b7cafb93aa7e0d7e2021-07-02T11:26:59ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852013-01-01118e100162110.1371/journal.pbio.1001621Linking stochastic fluctuations in chromatin structure and gene expression.Christopher R BrownChanghui MaoElena FalkovskaiaMelissa S JuricaHinrich BoegerThe number of mRNA and protein molecules expressed from a single gene molecule fluctuates over time. These fluctuations have been attributed, in part, to the random transitioning of promoters between transcriptionally active and inactive states, causing transcription to occur in bursts. However, the molecular basis of transcriptional bursting remains poorly understood. By electron microscopy of single PHO5 gene molecules from yeast, we show that the "activated" promoter assumes alternative nucleosome configurations at steady state, including the maximally repressive, fully nucleosomal, and the maximally non-repressive, nucleosome-free, configuration. We demonstrate that the observed probabilities of promoter nucleosome configurations are obtained from a simple, intrinsically stochastic process of nucleosome assembly, disassembly, and position-specific sliding; and we show that gene expression and promoter nucleosome configuration can be mechanistically coupled, relating promoter nucleosome dynamics and gene expression fluctuations. Together, our findings suggest a structural basis for transcriptional bursting, and offer new insights into the mechanism of transcriptional regulation and the kinetics of promoter nucleosome transitions.http://europepmc.org/articles/PMC3735467?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Christopher R Brown
Changhui Mao
Elena Falkovskaia
Melissa S Jurica
Hinrich Boeger
spellingShingle Christopher R Brown
Changhui Mao
Elena Falkovskaia
Melissa S Jurica
Hinrich Boeger
Linking stochastic fluctuations in chromatin structure and gene expression.
PLoS Biology
author_facet Christopher R Brown
Changhui Mao
Elena Falkovskaia
Melissa S Jurica
Hinrich Boeger
author_sort Christopher R Brown
title Linking stochastic fluctuations in chromatin structure and gene expression.
title_short Linking stochastic fluctuations in chromatin structure and gene expression.
title_full Linking stochastic fluctuations in chromatin structure and gene expression.
title_fullStr Linking stochastic fluctuations in chromatin structure and gene expression.
title_full_unstemmed Linking stochastic fluctuations in chromatin structure and gene expression.
title_sort linking stochastic fluctuations in chromatin structure and gene expression.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2013-01-01
description The number of mRNA and protein molecules expressed from a single gene molecule fluctuates over time. These fluctuations have been attributed, in part, to the random transitioning of promoters between transcriptionally active and inactive states, causing transcription to occur in bursts. However, the molecular basis of transcriptional bursting remains poorly understood. By electron microscopy of single PHO5 gene molecules from yeast, we show that the "activated" promoter assumes alternative nucleosome configurations at steady state, including the maximally repressive, fully nucleosomal, and the maximally non-repressive, nucleosome-free, configuration. We demonstrate that the observed probabilities of promoter nucleosome configurations are obtained from a simple, intrinsically stochastic process of nucleosome assembly, disassembly, and position-specific sliding; and we show that gene expression and promoter nucleosome configuration can be mechanistically coupled, relating promoter nucleosome dynamics and gene expression fluctuations. Together, our findings suggest a structural basis for transcriptional bursting, and offer new insights into the mechanism of transcriptional regulation and the kinetics of promoter nucleosome transitions.
url http://europepmc.org/articles/PMC3735467?pdf=render
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AT elenafalkovskaia linkingstochasticfluctuationsinchromatinstructureandgeneexpression
AT melissasjurica linkingstochasticfluctuationsinchromatinstructureandgeneexpression
AT hinrichboeger linkingstochasticfluctuationsinchromatinstructureandgeneexpression
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