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Principles of 3D compartmentalization of the human genome

Chromatin is organized in the nucleus via CTCF loops and compartmental domains. Here, we compare different cell types to identify distinct paradigms of compartmental domain formation in human tissues. We identify and quantify compartmental forces correlated with histone modifications characteristic...

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Autores principales: Nichols, Michael H., Corces, Victor G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265014/
https://www.ncbi.nlm.nih.gov/pubmed/34192544
http://dx.doi.org/10.1016/j.celrep.2021.109330
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author Nichols, Michael H.
Corces, Victor G.
author_facet Nichols, Michael H.
Corces, Victor G.
author_sort Nichols, Michael H.
collection PubMed
description Chromatin is organized in the nucleus via CTCF loops and compartmental domains. Here, we compare different cell types to identify distinct paradigms of compartmental domain formation in human tissues. We identify and quantify compartmental forces correlated with histone modifications characteristic of transcriptional activity and previously underappreciated roles for distinct compartmental domains correlated with the presence of H3K27me3 and H3K9me3, respectively. We present a computer simulation model capable of predicting compartmental organization based on the biochemical characteristics of independent chromatin features. Using this model, we show that the underlying forces responsible for compartmental domain formation in human cells are conserved and that the diverse compartmentalization patterns seen across cell types are due to differences in chromatin features. We extend these findings to Drosophila to suggest that the same principles are at work beyond humans. These results offer mechanistic insights into the fundamental forces driving the 3D organization of the genome.
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spelling pubmed-82650142021-07-08 Principles of 3D compartmentalization of the human genome Nichols, Michael H. Corces, Victor G. Cell Rep Article Chromatin is organized in the nucleus via CTCF loops and compartmental domains. Here, we compare different cell types to identify distinct paradigms of compartmental domain formation in human tissues. We identify and quantify compartmental forces correlated with histone modifications characteristic of transcriptional activity and previously underappreciated roles for distinct compartmental domains correlated with the presence of H3K27me3 and H3K9me3, respectively. We present a computer simulation model capable of predicting compartmental organization based on the biochemical characteristics of independent chromatin features. Using this model, we show that the underlying forces responsible for compartmental domain formation in human cells are conserved and that the diverse compartmentalization patterns seen across cell types are due to differences in chromatin features. We extend these findings to Drosophila to suggest that the same principles are at work beyond humans. These results offer mechanistic insights into the fundamental forces driving the 3D organization of the genome. 2021-06-29 /pmc/articles/PMC8265014/ /pubmed/34192544 http://dx.doi.org/10.1016/j.celrep.2021.109330 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Article
Nichols, Michael H.
Corces, Victor G.
Principles of 3D compartmentalization of the human genome
title Principles of 3D compartmentalization of the human genome
title_full Principles of 3D compartmentalization of the human genome
title_fullStr Principles of 3D compartmentalization of the human genome
title_full_unstemmed Principles of 3D compartmentalization of the human genome
title_short Principles of 3D compartmentalization of the human genome
title_sort principles of 3d compartmentalization of the human genome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8265014/
https://www.ncbi.nlm.nih.gov/pubmed/34192544
http://dx.doi.org/10.1016/j.celrep.2021.109330
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