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SPIN reveals genome-wide landscape of nuclear compartmentalization
We report SPIN, an integrative computational method to reveal genome-wide intranuclear chromosome positioning and nuclear compartmentalization relative to multiple nuclear structures, which are pivotal for modulating genome function. As a proof-of-principle, we use SPIN to integrate nuclear compartm...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809771/ https://www.ncbi.nlm.nih.gov/pubmed/33446254 http://dx.doi.org/10.1186/s13059-020-02253-3 |
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author | Wang, Yuchuan Zhang, Yang Zhang, Ruochi van Schaik, Tom Zhang, Liguo Sasaki, Takayo Peric-Hupkes, Daniel Chen, Yu Gilbert, David M. van Steensel, Bas Belmont, Andrew S. Ma, Jian |
author_facet | Wang, Yuchuan Zhang, Yang Zhang, Ruochi van Schaik, Tom Zhang, Liguo Sasaki, Takayo Peric-Hupkes, Daniel Chen, Yu Gilbert, David M. van Steensel, Bas Belmont, Andrew S. Ma, Jian |
author_sort | Wang, Yuchuan |
collection | PubMed |
description | We report SPIN, an integrative computational method to reveal genome-wide intranuclear chromosome positioning and nuclear compartmentalization relative to multiple nuclear structures, which are pivotal for modulating genome function. As a proof-of-principle, we use SPIN to integrate nuclear compartment mapping (TSA-seq and DamID) and chromatin interaction data (Hi-C) from K562 cells to identify 10 spatial compartmentalization states genome-wide relative to nuclear speckles, lamina, and putative associations with nucleoli. These SPIN states show novel patterns of genome spatial organization and their relation to other 3D genome features and genome function (transcription and replication timing). SPIN provides critical insights into nuclear spatial and functional compartmentalization. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s13059-020-02253-3). |
format | Online Article Text |
id | pubmed-7809771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78097712021-01-18 SPIN reveals genome-wide landscape of nuclear compartmentalization Wang, Yuchuan Zhang, Yang Zhang, Ruochi van Schaik, Tom Zhang, Liguo Sasaki, Takayo Peric-Hupkes, Daniel Chen, Yu Gilbert, David M. van Steensel, Bas Belmont, Andrew S. Ma, Jian Genome Biol Method We report SPIN, an integrative computational method to reveal genome-wide intranuclear chromosome positioning and nuclear compartmentalization relative to multiple nuclear structures, which are pivotal for modulating genome function. As a proof-of-principle, we use SPIN to integrate nuclear compartment mapping (TSA-seq and DamID) and chromatin interaction data (Hi-C) from K562 cells to identify 10 spatial compartmentalization states genome-wide relative to nuclear speckles, lamina, and putative associations with nucleoli. These SPIN states show novel patterns of genome spatial organization and their relation to other 3D genome features and genome function (transcription and replication timing). SPIN provides critical insights into nuclear spatial and functional compartmentalization. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at (10.1186/s13059-020-02253-3). BioMed Central 2021-01-14 /pmc/articles/PMC7809771/ /pubmed/33446254 http://dx.doi.org/10.1186/s13059-020-02253-3 Text en © The Author(s) 2021 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 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/. The Creative Commons Public Domain Dedication waiver (http://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 | Method Wang, Yuchuan Zhang, Yang Zhang, Ruochi van Schaik, Tom Zhang, Liguo Sasaki, Takayo Peric-Hupkes, Daniel Chen, Yu Gilbert, David M. van Steensel, Bas Belmont, Andrew S. Ma, Jian SPIN reveals genome-wide landscape of nuclear compartmentalization |
title | SPIN reveals genome-wide landscape of nuclear compartmentalization |
title_full | SPIN reveals genome-wide landscape of nuclear compartmentalization |
title_fullStr | SPIN reveals genome-wide landscape of nuclear compartmentalization |
title_full_unstemmed | SPIN reveals genome-wide landscape of nuclear compartmentalization |
title_short | SPIN reveals genome-wide landscape of nuclear compartmentalization |
title_sort | spin reveals genome-wide landscape of nuclear compartmentalization |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809771/ https://www.ncbi.nlm.nih.gov/pubmed/33446254 http://dx.doi.org/10.1186/s13059-020-02253-3 |
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