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Pericentromeric heterochromatin is hierarchically organized and spatially contacts H3K9me2 islands in euchromatin
Membraneless pericentromeric heterochromatin (PCH) domains play vital roles in chromosome dynamics and genome stability. However, our current understanding of 3D genome organization does not include PCH domains because of technical challenges associated with repetitive sequences enriched in PCH geno...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147806/ https://www.ncbi.nlm.nih.gov/pubmed/32203508 http://dx.doi.org/10.1371/journal.pgen.1008673 |
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author | Lee, Yuh Chwen G. Ogiyama, Yuki Martins, Nuno M. C. Beliveau, Brian J. Acevedo, David Wu, C.-ting Cavalli, Giacomo Karpen, Gary H. |
author_facet | Lee, Yuh Chwen G. Ogiyama, Yuki Martins, Nuno M. C. Beliveau, Brian J. Acevedo, David Wu, C.-ting Cavalli, Giacomo Karpen, Gary H. |
author_sort | Lee, Yuh Chwen G. |
collection | PubMed |
description | Membraneless pericentromeric heterochromatin (PCH) domains play vital roles in chromosome dynamics and genome stability. However, our current understanding of 3D genome organization does not include PCH domains because of technical challenges associated with repetitive sequences enriched in PCH genomic regions. We investigated the 3D architecture of Drosophila melanogaster PCH domains and their spatial associations with the euchromatic genome by developing a novel analysis method that incorporates genome-wide Hi-C reads originating from PCH DNA. Combined with cytogenetic analysis, we reveal a hierarchical organization of the PCH domains into distinct “territories.” Strikingly, H3K9me2-enriched regions embedded in the euchromatic genome show prevalent 3D interactions with the PCH domain. These spatial contacts require H3K9me2 enrichment, are likely mediated by liquid-liquid phase separation, and may influence organismal fitness. Our findings have important implications for how PCH architecture influences the function and evolution of both repetitive heterochromatin and the gene-rich euchromatin. |
format | Online Article Text |
id | pubmed-7147806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-71478062020-04-16 Pericentromeric heterochromatin is hierarchically organized and spatially contacts H3K9me2 islands in euchromatin Lee, Yuh Chwen G. Ogiyama, Yuki Martins, Nuno M. C. Beliveau, Brian J. Acevedo, David Wu, C.-ting Cavalli, Giacomo Karpen, Gary H. PLoS Genet Research Article Membraneless pericentromeric heterochromatin (PCH) domains play vital roles in chromosome dynamics and genome stability. However, our current understanding of 3D genome organization does not include PCH domains because of technical challenges associated with repetitive sequences enriched in PCH genomic regions. We investigated the 3D architecture of Drosophila melanogaster PCH domains and their spatial associations with the euchromatic genome by developing a novel analysis method that incorporates genome-wide Hi-C reads originating from PCH DNA. Combined with cytogenetic analysis, we reveal a hierarchical organization of the PCH domains into distinct “territories.” Strikingly, H3K9me2-enriched regions embedded in the euchromatic genome show prevalent 3D interactions with the PCH domain. These spatial contacts require H3K9me2 enrichment, are likely mediated by liquid-liquid phase separation, and may influence organismal fitness. Our findings have important implications for how PCH architecture influences the function and evolution of both repetitive heterochromatin and the gene-rich euchromatin. Public Library of Science 2020-03-23 /pmc/articles/PMC7147806/ /pubmed/32203508 http://dx.doi.org/10.1371/journal.pgen.1008673 Text en © 2020 Lee et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lee, Yuh Chwen G. Ogiyama, Yuki Martins, Nuno M. C. Beliveau, Brian J. Acevedo, David Wu, C.-ting Cavalli, Giacomo Karpen, Gary H. Pericentromeric heterochromatin is hierarchically organized and spatially contacts H3K9me2 islands in euchromatin |
title | Pericentromeric heterochromatin is hierarchically organized and spatially contacts H3K9me2 islands in euchromatin |
title_full | Pericentromeric heterochromatin is hierarchically organized and spatially contacts H3K9me2 islands in euchromatin |
title_fullStr | Pericentromeric heterochromatin is hierarchically organized and spatially contacts H3K9me2 islands in euchromatin |
title_full_unstemmed | Pericentromeric heterochromatin is hierarchically organized and spatially contacts H3K9me2 islands in euchromatin |
title_short | Pericentromeric heterochromatin is hierarchically organized and spatially contacts H3K9me2 islands in euchromatin |
title_sort | pericentromeric heterochromatin is hierarchically organized and spatially contacts h3k9me2 islands in euchromatin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147806/ https://www.ncbi.nlm.nih.gov/pubmed/32203508 http://dx.doi.org/10.1371/journal.pgen.1008673 |
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