Quantitative control of noise in mammalian gene expression by dynamic histone regulation

Fluctuation ('noise') in gene expression is critical for mammalian cellular processes. Numerous mechanisms contribute to its origins, yet the mechanisms behind large fluctuations that are induced by single transcriptional activators remain elusive. Here, we probed putative mechanisms by st...

Full description

Bibliographic Details
Main Authors: Deng Tan, Rui Chen, Yuejian Mo, Shu Gu, Jiao Ma, Wei Xu, Xibin Lu, Huiyu He, Fan Jiang, Weimin Fan, Yili Wang, Xi Chen, Wei Huang
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-08-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/65654
id doaj-5700c6aaedfb44b7ae44370c952718a2
record_format Article
spelling doaj-5700c6aaedfb44b7ae44370c952718a22021-08-13T10:08:31ZengeLife Sciences Publications LtdeLife2050-084X2021-08-011010.7554/eLife.65654Quantitative control of noise in mammalian gene expression by dynamic histone regulationDeng Tan0Rui Chen1Yuejian Mo2Shu Gu3Jiao Ma4Wei Xu5Xibin Lu6Huiyu He7Fan Jiang8Weimin Fan9Yili Wang10Xi Chen11https://orcid.org/0000-0003-2648-3146Wei Huang12https://orcid.org/0000-0002-6755-5807School of Life Sciences, Southern University of Science and Technology, Shenzhen, China; Department of Chemistry, The Hong Kong University of Science and Technology, Kowloon, Hong Kong, ChinaSchool of Life Sciences, Southern University of Science and Technology, Shenzhen, ChinaSchool of Life Sciences, Southern University of Science and Technology, Shenzhen, ChinaSchool of Life Sciences, Southern University of Science and Technology, Shenzhen, ChinaSchool of Life Sciences, Southern University of Science and Technology, Shenzhen, ChinaShenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen, ChinaCore Research Facilities, Southern University of Science and Technology, Shenzhen, ChinaSchool of Life Sciences, Southern University of Science and Technology, Shenzhen, ChinaDepartment of Biomedical Engineering, Southern University of Science and Technology, Shenzhen, ChinaSchool of Life Sciences, Southern University of Science and Technology, Shenzhen, ChinaCore Research Facilities, Southern University of Science and Technology, Shenzhen, ChinaShenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen, ChinaSchool of Life Sciences, Southern University of Science and Technology, Shenzhen, ChinaFluctuation ('noise') in gene expression is critical for mammalian cellular processes. Numerous mechanisms contribute to its origins, yet the mechanisms behind large fluctuations that are induced by single transcriptional activators remain elusive. Here, we probed putative mechanisms by studying the dynamic regulation of transcriptional activator binding, histone regulator inhibitors, chromatin accessibility, and levels of mRNAs and proteins in single cells. Using a light-induced expression system, we showed that the transcriptional activator could form an interplay with dual functional co-activator/histone acetyltransferases CBP/p300. This interplay resulted in substantial heterogeneity in H3K27ac, chromatin accessibility, and transcription. Simultaneous attenuation of CBP/p300 and HDAC4/5 reduced heterogeneity in the expression of endogenous genes, suggesting that this mechanism is universal. We further found that the noise was reduced by pulse-wide modulation of transcriptional activator binding possibly as a result of alternating the epigenetic states. Our findings suggest a mechanism for the modulation of noise in synthetic and endogenous gene expression systems.https://elifesciences.org/articles/65654epigenetic bistabilitygene expression noisehistone modificationtranscriptional activatorsynthetic circuitoscillation
collection DOAJ
language English
format Article
sources DOAJ
author Deng Tan
Rui Chen
Yuejian Mo
Shu Gu
Jiao Ma
Wei Xu
Xibin Lu
Huiyu He
Fan Jiang
Weimin Fan
Yili Wang
Xi Chen
Wei Huang
spellingShingle Deng Tan
Rui Chen
Yuejian Mo
Shu Gu
Jiao Ma
Wei Xu
Xibin Lu
Huiyu He
Fan Jiang
Weimin Fan
Yili Wang
Xi Chen
Wei Huang
Quantitative control of noise in mammalian gene expression by dynamic histone regulation
eLife
epigenetic bistability
gene expression noise
histone modification
transcriptional activator
synthetic circuit
oscillation
author_facet Deng Tan
Rui Chen
Yuejian Mo
Shu Gu
Jiao Ma
Wei Xu
Xibin Lu
Huiyu He
Fan Jiang
Weimin Fan
Yili Wang
Xi Chen
Wei Huang
author_sort Deng Tan
title Quantitative control of noise in mammalian gene expression by dynamic histone regulation
title_short Quantitative control of noise in mammalian gene expression by dynamic histone regulation
title_full Quantitative control of noise in mammalian gene expression by dynamic histone regulation
title_fullStr Quantitative control of noise in mammalian gene expression by dynamic histone regulation
title_full_unstemmed Quantitative control of noise in mammalian gene expression by dynamic histone regulation
title_sort quantitative control of noise in mammalian gene expression by dynamic histone regulation
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2021-08-01
description Fluctuation ('noise') in gene expression is critical for mammalian cellular processes. Numerous mechanisms contribute to its origins, yet the mechanisms behind large fluctuations that are induced by single transcriptional activators remain elusive. Here, we probed putative mechanisms by studying the dynamic regulation of transcriptional activator binding, histone regulator inhibitors, chromatin accessibility, and levels of mRNAs and proteins in single cells. Using a light-induced expression system, we showed that the transcriptional activator could form an interplay with dual functional co-activator/histone acetyltransferases CBP/p300. This interplay resulted in substantial heterogeneity in H3K27ac, chromatin accessibility, and transcription. Simultaneous attenuation of CBP/p300 and HDAC4/5 reduced heterogeneity in the expression of endogenous genes, suggesting that this mechanism is universal. We further found that the noise was reduced by pulse-wide modulation of transcriptional activator binding possibly as a result of alternating the epigenetic states. Our findings suggest a mechanism for the modulation of noise in synthetic and endogenous gene expression systems.
topic epigenetic bistability
gene expression noise
histone modification
transcriptional activator
synthetic circuit
oscillation
url https://elifesciences.org/articles/65654
work_keys_str_mv AT dengtan quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT ruichen quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT yuejianmo quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT shugu quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT jiaoma quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT weixu quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT xibinlu quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT huiyuhe quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT fanjiang quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT weiminfan quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT yiliwang quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT xichen quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
AT weihuang quantitativecontrolofnoiseinmammaliangeneexpressionbydynamichistoneregulation
_version_ 1721208529123016704