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Conserved dual-mode gene regulation programs in higher eukaryotes

Recent genomic data analyses have revealed important underlying logics in eukaryotic gene regulation, such as CpG islands (CGIs)-dependent dual-mode gene regulation. In mammals, genes lacking CGIs at their promoters are generally regulated by interconversion between euchromatin and heterochromatin,...

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Autores principales: Lee, Jun-Yeong, Song, Jawon, LeBlanc, Lucy, Davis, Ian, Kim, Jonghwan, Beck, Samuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969006/
https://www.ncbi.nlm.nih.gov/pubmed/33621342
http://dx.doi.org/10.1093/nar/gkab108
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author Lee, Jun-Yeong
Song, Jawon
LeBlanc, Lucy
Davis, Ian
Kim, Jonghwan
Beck, Samuel
author_facet Lee, Jun-Yeong
Song, Jawon
LeBlanc, Lucy
Davis, Ian
Kim, Jonghwan
Beck, Samuel
author_sort Lee, Jun-Yeong
collection PubMed
description Recent genomic data analyses have revealed important underlying logics in eukaryotic gene regulation, such as CpG islands (CGIs)-dependent dual-mode gene regulation. In mammals, genes lacking CGIs at their promoters are generally regulated by interconversion between euchromatin and heterochromatin, while genes associated with CGIs constitutively remain as euchromatin. Whether a similar mode of gene regulation exists in non-mammalian species has been unknown. Here, through comparative epigenomic analyses, we demonstrate that the dual-mode gene regulation program is common in various eukaryotes, even in the species lacking CGIs. In cases of vertebrates or plants, we find that genes associated with high methylation level promoters are inactivated by forming heterochromatin and expressed in a context-dependent manner. In contrast, the genes with low methylation level promoters are broadly expressed and remain as euchromatin even when repressed by Polycomb proteins. Furthermore, we show that invertebrate animals lacking DNA methylation, such as fruit flies and nematodes, also have divergence in gene types: some genes are regulated by Polycomb proteins, while others are regulated by heterochromatin formation. Altogether, our study establishes gene type divergence and the resulting dual-mode gene regulation as fundamental features shared in a broad range of higher eukaryotic species.
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spelling pubmed-79690062021-03-22 Conserved dual-mode gene regulation programs in higher eukaryotes Lee, Jun-Yeong Song, Jawon LeBlanc, Lucy Davis, Ian Kim, Jonghwan Beck, Samuel Nucleic Acids Res Gene regulation, Chromatin and Epigenetics Recent genomic data analyses have revealed important underlying logics in eukaryotic gene regulation, such as CpG islands (CGIs)-dependent dual-mode gene regulation. In mammals, genes lacking CGIs at their promoters are generally regulated by interconversion between euchromatin and heterochromatin, while genes associated with CGIs constitutively remain as euchromatin. Whether a similar mode of gene regulation exists in non-mammalian species has been unknown. Here, through comparative epigenomic analyses, we demonstrate that the dual-mode gene regulation program is common in various eukaryotes, even in the species lacking CGIs. In cases of vertebrates or plants, we find that genes associated with high methylation level promoters are inactivated by forming heterochromatin and expressed in a context-dependent manner. In contrast, the genes with low methylation level promoters are broadly expressed and remain as euchromatin even when repressed by Polycomb proteins. Furthermore, we show that invertebrate animals lacking DNA methylation, such as fruit flies and nematodes, also have divergence in gene types: some genes are regulated by Polycomb proteins, while others are regulated by heterochromatin formation. Altogether, our study establishes gene type divergence and the resulting dual-mode gene regulation as fundamental features shared in a broad range of higher eukaryotic species. Oxford University Press 2021-02-23 /pmc/articles/PMC7969006/ /pubmed/33621342 http://dx.doi.org/10.1093/nar/gkab108 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Gene regulation, Chromatin and Epigenetics
Lee, Jun-Yeong
Song, Jawon
LeBlanc, Lucy
Davis, Ian
Kim, Jonghwan
Beck, Samuel
Conserved dual-mode gene regulation programs in higher eukaryotes
title Conserved dual-mode gene regulation programs in higher eukaryotes
title_full Conserved dual-mode gene regulation programs in higher eukaryotes
title_fullStr Conserved dual-mode gene regulation programs in higher eukaryotes
title_full_unstemmed Conserved dual-mode gene regulation programs in higher eukaryotes
title_short Conserved dual-mode gene regulation programs in higher eukaryotes
title_sort conserved dual-mode gene regulation programs in higher eukaryotes
topic Gene regulation, Chromatin and Epigenetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969006/
https://www.ncbi.nlm.nih.gov/pubmed/33621342
http://dx.doi.org/10.1093/nar/gkab108
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