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Complexities in the role of acetylation dynamics in modifying inducible gene activation parameters
High levels of histone acetylation are associated with the regulatory elements of active genes, suggesting a link between acetylation and gene activation. We revisited this model, in the context of EGF-inducible gene expression and found that rather than a simple unifying model, there are two broad...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8682737/ https://www.ncbi.nlm.nih.gov/pubmed/34850951 http://dx.doi.org/10.1093/nar/gkab1176 |
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author | Carrera, Samantha O’Donnell, Amanda Li, Yaoyong Nowicki-Osuch, Karol Yang, Shen-Hsi Baker, Syed Murtuza Spiller, David Sharrocks, Andrew D |
author_facet | Carrera, Samantha O’Donnell, Amanda Li, Yaoyong Nowicki-Osuch, Karol Yang, Shen-Hsi Baker, Syed Murtuza Spiller, David Sharrocks, Andrew D |
author_sort | Carrera, Samantha |
collection | PubMed |
description | High levels of histone acetylation are associated with the regulatory elements of active genes, suggesting a link between acetylation and gene activation. We revisited this model, in the context of EGF-inducible gene expression and found that rather than a simple unifying model, there are two broad classes of genes; one in which high lysine acetylation activity is required for efficient gene activation, and a second group where the opposite occurs and high acetylation activity is inhibitory. We examined the latter class in more detail using EGR2 as a model gene and found that lysine acetylation levels are critical for several activation parameters, including the timing of expression onset, and overall amplitudes of the transcriptional response. In contrast, DUSP1 responds in the canonical manner and its transcriptional activity is promoted by acetylation. Single cell approaches demonstrate heterogenous activation kinetics of a given gene in response to EGF stimulation. Acetylation levels modify these heterogenous patterns and influence both allele activation frequencies and overall expression profile parameters. Our data therefore point to a complex interplay between acetylation equilibria and target gene induction where acetylation level thresholds are an important determinant of transcriptional induction dynamics that are sensed in a gene-specific manner. |
format | Online Article Text |
id | pubmed-8682737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-86827372021-12-20 Complexities in the role of acetylation dynamics in modifying inducible gene activation parameters Carrera, Samantha O’Donnell, Amanda Li, Yaoyong Nowicki-Osuch, Karol Yang, Shen-Hsi Baker, Syed Murtuza Spiller, David Sharrocks, Andrew D Nucleic Acids Res Gene regulation, Chromatin and Epigenetics High levels of histone acetylation are associated with the regulatory elements of active genes, suggesting a link between acetylation and gene activation. We revisited this model, in the context of EGF-inducible gene expression and found that rather than a simple unifying model, there are two broad classes of genes; one in which high lysine acetylation activity is required for efficient gene activation, and a second group where the opposite occurs and high acetylation activity is inhibitory. We examined the latter class in more detail using EGR2 as a model gene and found that lysine acetylation levels are critical for several activation parameters, including the timing of expression onset, and overall amplitudes of the transcriptional response. In contrast, DUSP1 responds in the canonical manner and its transcriptional activity is promoted by acetylation. Single cell approaches demonstrate heterogenous activation kinetics of a given gene in response to EGF stimulation. Acetylation levels modify these heterogenous patterns and influence both allele activation frequencies and overall expression profile parameters. Our data therefore point to a complex interplay between acetylation equilibria and target gene induction where acetylation level thresholds are an important determinant of transcriptional induction dynamics that are sensed in a gene-specific manner. Oxford University Press 2021-12-01 /pmc/articles/PMC8682737/ /pubmed/34850951 http://dx.doi.org/10.1093/nar/gkab1176 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Carrera, Samantha O’Donnell, Amanda Li, Yaoyong Nowicki-Osuch, Karol Yang, Shen-Hsi Baker, Syed Murtuza Spiller, David Sharrocks, Andrew D Complexities in the role of acetylation dynamics in modifying inducible gene activation parameters |
title | Complexities in the role of acetylation dynamics in modifying inducible gene activation parameters |
title_full | Complexities in the role of acetylation dynamics in modifying inducible gene activation parameters |
title_fullStr | Complexities in the role of acetylation dynamics in modifying inducible gene activation parameters |
title_full_unstemmed | Complexities in the role of acetylation dynamics in modifying inducible gene activation parameters |
title_short | Complexities in the role of acetylation dynamics in modifying inducible gene activation parameters |
title_sort | complexities in the role of acetylation dynamics in modifying inducible gene activation parameters |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8682737/ https://www.ncbi.nlm.nih.gov/pubmed/34850951 http://dx.doi.org/10.1093/nar/gkab1176 |
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