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TAD cliques predict key features of chromatin organization

BACKGROUND: Mechanisms underlying genome 3D organization and domain formation in the mammalian nucleus are not completely understood. Multiple processes such as transcriptional compartmentalization, DNA loop extrusion and interactions with the nuclear lamina dynamically act on chromatin at multiple...

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Autores principales: Liyakat Ali, Tharvesh M., Brunet, Annaël, Collas, Philippe, Paulsen, Jonas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8254932/
https://www.ncbi.nlm.nih.gov/pubmed/34217222
http://dx.doi.org/10.1186/s12864-021-07815-8
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author Liyakat Ali, Tharvesh M.
Brunet, Annaël
Collas, Philippe
Paulsen, Jonas
author_facet Liyakat Ali, Tharvesh M.
Brunet, Annaël
Collas, Philippe
Paulsen, Jonas
author_sort Liyakat Ali, Tharvesh M.
collection PubMed
description BACKGROUND: Mechanisms underlying genome 3D organization and domain formation in the mammalian nucleus are not completely understood. Multiple processes such as transcriptional compartmentalization, DNA loop extrusion and interactions with the nuclear lamina dynamically act on chromatin at multiple levels. Here, we explore long-range interaction patterns between topologically associated domains (TADs) in several cell types. RESULTS: We find that TAD long-range interactions are connected to many key features of chromatin organization, including open and closed compartments, compaction and loop extrusion processes. Domains that form large TAD cliques tend to be repressive across cell types, when comparing gene expression, LINE/SINE repeat content and chromatin subcompartments. Further, TADs in large cliques are larger in genomic size, less dense and depleted of convergent CTCF motifs, in contrast to smaller and denser TADs formed by a loop extrusion process. CONCLUSIONS: Our results shed light on the organizational principles that govern repressive and active domains in the human genome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07815-8.
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spelling pubmed-82549322021-07-06 TAD cliques predict key features of chromatin organization Liyakat Ali, Tharvesh M. Brunet, Annaël Collas, Philippe Paulsen, Jonas BMC Genomics Research Article BACKGROUND: Mechanisms underlying genome 3D organization and domain formation in the mammalian nucleus are not completely understood. Multiple processes such as transcriptional compartmentalization, DNA loop extrusion and interactions with the nuclear lamina dynamically act on chromatin at multiple levels. Here, we explore long-range interaction patterns between topologically associated domains (TADs) in several cell types. RESULTS: We find that TAD long-range interactions are connected to many key features of chromatin organization, including open and closed compartments, compaction and loop extrusion processes. Domains that form large TAD cliques tend to be repressive across cell types, when comparing gene expression, LINE/SINE repeat content and chromatin subcompartments. Further, TADs in large cliques are larger in genomic size, less dense and depleted of convergent CTCF motifs, in contrast to smaller and denser TADs formed by a loop extrusion process. CONCLUSIONS: Our results shed light on the organizational principles that govern repressive and active domains in the human genome. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07815-8. BioMed Central 2021-07-03 /pmc/articles/PMC8254932/ /pubmed/34217222 http://dx.doi.org/10.1186/s12864-021-07815-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Liyakat Ali, Tharvesh M.
Brunet, Annaël
Collas, Philippe
Paulsen, Jonas
TAD cliques predict key features of chromatin organization
title TAD cliques predict key features of chromatin organization
title_full TAD cliques predict key features of chromatin organization
title_fullStr TAD cliques predict key features of chromatin organization
title_full_unstemmed TAD cliques predict key features of chromatin organization
title_short TAD cliques predict key features of chromatin organization
title_sort tad cliques predict key features of chromatin organization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8254932/
https://www.ncbi.nlm.nih.gov/pubmed/34217222
http://dx.doi.org/10.1186/s12864-021-07815-8
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