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Regulation of mammalian 3D genome organization and histone H3K9 dimethylation by H3K9 methyltransferases
Histone H3 lysine 9 dimethylation (H3K9me2) is a highly conserved silencing epigenetic mark. Chromatin marked with H3K9me2 forms large domains in mammalian cells and overlaps well with lamina-associated domains and the B compartment defined by Hi-C. However, the role of H3K9me2 in 3-dimensional (3D)...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119675/ https://www.ncbi.nlm.nih.gov/pubmed/33986449 http://dx.doi.org/10.1038/s42003-021-02089-y |
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author | Fukuda, Kei Shimura, Chikako Miura, Hisashi Tanigawa, Akie Suzuki, Takehiro Dohmae, Naoshi Hiratani, Ichiro Shinkai, Yoichi |
author_facet | Fukuda, Kei Shimura, Chikako Miura, Hisashi Tanigawa, Akie Suzuki, Takehiro Dohmae, Naoshi Hiratani, Ichiro Shinkai, Yoichi |
author_sort | Fukuda, Kei |
collection | PubMed |
description | Histone H3 lysine 9 dimethylation (H3K9me2) is a highly conserved silencing epigenetic mark. Chromatin marked with H3K9me2 forms large domains in mammalian cells and overlaps well with lamina-associated domains and the B compartment defined by Hi-C. However, the role of H3K9me2 in 3-dimensional (3D) genome organization remains unclear. Here, we investigated genome-wide H3K9me2 distribution, transcriptome, and 3D genome organization in mouse embryonic stem cells following the inhibition or depletion of H3K9 methyltransferases (MTases): G9a, GLP, SETDB1, SUV39H1, and SUV39H2. We show that H3K9me2 is regulated by all five MTases; however, H3K9me2 and transcription in the A and B compartments are regulated by different MTases. H3K9me2 in the A compartments is primarily regulated by G9a/GLP and SETDB1, while H3K9me2 in the B compartments is regulated by all five MTases. Furthermore, decreased H3K9me2 correlates with changes to more active compartmental state that accompanied transcriptional activation. Thus, H3K9me2 contributes to inactive compartment setting. |
format | Online Article Text |
id | pubmed-8119675 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81196752021-05-17 Regulation of mammalian 3D genome organization and histone H3K9 dimethylation by H3K9 methyltransferases Fukuda, Kei Shimura, Chikako Miura, Hisashi Tanigawa, Akie Suzuki, Takehiro Dohmae, Naoshi Hiratani, Ichiro Shinkai, Yoichi Commun Biol Article Histone H3 lysine 9 dimethylation (H3K9me2) is a highly conserved silencing epigenetic mark. Chromatin marked with H3K9me2 forms large domains in mammalian cells and overlaps well with lamina-associated domains and the B compartment defined by Hi-C. However, the role of H3K9me2 in 3-dimensional (3D) genome organization remains unclear. Here, we investigated genome-wide H3K9me2 distribution, transcriptome, and 3D genome organization in mouse embryonic stem cells following the inhibition or depletion of H3K9 methyltransferases (MTases): G9a, GLP, SETDB1, SUV39H1, and SUV39H2. We show that H3K9me2 is regulated by all five MTases; however, H3K9me2 and transcription in the A and B compartments are regulated by different MTases. H3K9me2 in the A compartments is primarily regulated by G9a/GLP and SETDB1, while H3K9me2 in the B compartments is regulated by all five MTases. Furthermore, decreased H3K9me2 correlates with changes to more active compartmental state that accompanied transcriptional activation. Thus, H3K9me2 contributes to inactive compartment setting. Nature Publishing Group UK 2021-05-13 /pmc/articles/PMC8119675/ /pubmed/33986449 http://dx.doi.org/10.1038/s42003-021-02089-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Fukuda, Kei Shimura, Chikako Miura, Hisashi Tanigawa, Akie Suzuki, Takehiro Dohmae, Naoshi Hiratani, Ichiro Shinkai, Yoichi Regulation of mammalian 3D genome organization and histone H3K9 dimethylation by H3K9 methyltransferases |
title | Regulation of mammalian 3D genome organization and histone H3K9 dimethylation by H3K9 methyltransferases |
title_full | Regulation of mammalian 3D genome organization and histone H3K9 dimethylation by H3K9 methyltransferases |
title_fullStr | Regulation of mammalian 3D genome organization and histone H3K9 dimethylation by H3K9 methyltransferases |
title_full_unstemmed | Regulation of mammalian 3D genome organization and histone H3K9 dimethylation by H3K9 methyltransferases |
title_short | Regulation of mammalian 3D genome organization and histone H3K9 dimethylation by H3K9 methyltransferases |
title_sort | regulation of mammalian 3d genome organization and histone h3k9 dimethylation by h3k9 methyltransferases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119675/ https://www.ncbi.nlm.nih.gov/pubmed/33986449 http://dx.doi.org/10.1038/s42003-021-02089-y |
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