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Spatial density of open chromatin: an effective metric for the functional characterization of topologically associated domains
Topologically associated domains (TADs) are spatial and functional units of metazoan chromatin structure. Interpretation of the interplay between regulatory factors and chromatin structure within TADs is crucial to understand the spatial and temporal regulation of gene expression. However, a computa...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138881/ https://www.ncbi.nlm.nih.gov/pubmed/32987404 http://dx.doi.org/10.1093/bib/bbaa210 |
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author | Jiang, Shuai Li, Hao Hong, Hao Du, Guifang Huang, Xin Sun, Yu Wang, Junting Tao, Huan Xu, Kang Li, Cheng Chen, Yang Chen, Hebing Bo, Xiaochen |
author_facet | Jiang, Shuai Li, Hao Hong, Hao Du, Guifang Huang, Xin Sun, Yu Wang, Junting Tao, Huan Xu, Kang Li, Cheng Chen, Yang Chen, Hebing Bo, Xiaochen |
author_sort | Jiang, Shuai |
collection | PubMed |
description | Topologically associated domains (TADs) are spatial and functional units of metazoan chromatin structure. Interpretation of the interplay between regulatory factors and chromatin structure within TADs is crucial to understand the spatial and temporal regulation of gene expression. However, a computational metric for the sensitive characterization of TAD regulatory landscape is lacking. Here, we present the spatial density of open chromatin (SDOC) metric as a quantitative measurement of intra-TAD chromatin state and structure. SDOC sensitively reflects epigenetic properties and gene transcriptional activity in TADs. During mouse T-cell development, we found that TADs with decreased SDOC are enriched in repressed developmental genes, and the joint effect of SDOC-decreasing and TAD clustering corresponds to the highest level of gene repression. In addition, we revealed a pervasive preference for TADs with similar SDOC to interact with each other, which may reflect the principle of chromatin organization. |
format | Online Article Text |
id | pubmed-8138881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81388812021-05-25 Spatial density of open chromatin: an effective metric for the functional characterization of topologically associated domains Jiang, Shuai Li, Hao Hong, Hao Du, Guifang Huang, Xin Sun, Yu Wang, Junting Tao, Huan Xu, Kang Li, Cheng Chen, Yang Chen, Hebing Bo, Xiaochen Brief Bioinform Problem Solving Protocol Topologically associated domains (TADs) are spatial and functional units of metazoan chromatin structure. Interpretation of the interplay between regulatory factors and chromatin structure within TADs is crucial to understand the spatial and temporal regulation of gene expression. However, a computational metric for the sensitive characterization of TAD regulatory landscape is lacking. Here, we present the spatial density of open chromatin (SDOC) metric as a quantitative measurement of intra-TAD chromatin state and structure. SDOC sensitively reflects epigenetic properties and gene transcriptional activity in TADs. During mouse T-cell development, we found that TADs with decreased SDOC are enriched in repressed developmental genes, and the joint effect of SDOC-decreasing and TAD clustering corresponds to the highest level of gene repression. In addition, we revealed a pervasive preference for TADs with similar SDOC to interact with each other, which may reflect the principle of chromatin organization. Oxford University Press 2020-09-28 /pmc/articles/PMC8138881/ /pubmed/32987404 http://dx.doi.org/10.1093/bib/bbaa210 Text en © The Author(s) 2020. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://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 | Problem Solving Protocol Jiang, Shuai Li, Hao Hong, Hao Du, Guifang Huang, Xin Sun, Yu Wang, Junting Tao, Huan Xu, Kang Li, Cheng Chen, Yang Chen, Hebing Bo, Xiaochen Spatial density of open chromatin: an effective metric for the functional characterization of topologically associated domains |
title | Spatial density of open chromatin: an effective metric for the functional characterization of topologically associated domains |
title_full | Spatial density of open chromatin: an effective metric for the functional characterization of topologically associated domains |
title_fullStr | Spatial density of open chromatin: an effective metric for the functional characterization of topologically associated domains |
title_full_unstemmed | Spatial density of open chromatin: an effective metric for the functional characterization of topologically associated domains |
title_short | Spatial density of open chromatin: an effective metric for the functional characterization of topologically associated domains |
title_sort | spatial density of open chromatin: an effective metric for the functional characterization of topologically associated domains |
topic | Problem Solving Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8138881/ https://www.ncbi.nlm.nih.gov/pubmed/32987404 http://dx.doi.org/10.1093/bib/bbaa210 |
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