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ARID1A spatially partitions interphase chromosomes

ARID1A, a subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) chromatin-remodeling complex, localizes to both promoters and enhancers to influence transcription. However, the role of ARID1A in higher-order spatial chromosome partitioning and genome organization is unknown. Here, we show that ARI...

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Autores principales: Wu, Shuai, Fatkhutdinov, Nail, Rosin, Leah, Luppino, Jennifer M., Iwasaki, Osamu, Tanizawa, Hideki, Tang, Hsin-Yao, Kossenkov, Andrew V., Gardini, Alessandro, Noma, Ken-ichi, Speicher, David W., Joyce, Eric F., Zhang, Rugang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531001/
https://www.ncbi.nlm.nih.gov/pubmed/31131328
http://dx.doi.org/10.1126/sciadv.aaw5294
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author Wu, Shuai
Fatkhutdinov, Nail
Rosin, Leah
Luppino, Jennifer M.
Iwasaki, Osamu
Tanizawa, Hideki
Tang, Hsin-Yao
Kossenkov, Andrew V.
Gardini, Alessandro
Noma, Ken-ichi
Speicher, David W.
Joyce, Eric F.
Zhang, Rugang
author_facet Wu, Shuai
Fatkhutdinov, Nail
Rosin, Leah
Luppino, Jennifer M.
Iwasaki, Osamu
Tanizawa, Hideki
Tang, Hsin-Yao
Kossenkov, Andrew V.
Gardini, Alessandro
Noma, Ken-ichi
Speicher, David W.
Joyce, Eric F.
Zhang, Rugang
author_sort Wu, Shuai
collection PubMed
description ARID1A, a subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) chromatin-remodeling complex, localizes to both promoters and enhancers to influence transcription. However, the role of ARID1A in higher-order spatial chromosome partitioning and genome organization is unknown. Here, we show that ARID1A spatially partitions interphase chromosomes and regulates higher-order genome organization. The SWI/SNF complex interacts with condensin II, and they display significant colocalizations at enhancers. ARID1A knockout drives the redistribution of condensin II preferentially at enhancers, which positively correlates with changes in transcription. ARID1A and condensin II contribute to transcriptionally inactive B-compartment formation, while ARID1A weakens the border strength of topologically associated domains. Condensin II redistribution induced by ARID1A knockout positively correlates with chromosome sizes, which negatively correlates with interchromosomal interactions. ARID1A loss increases the trans interactions of small chromosomes, which was validated by three-dimensional interphase chromosome painting. These results demonstrate that ARID1A is important for large-scale genome folding and spatially partitions interphase chromosomes.
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spelling pubmed-65310012019-05-26 ARID1A spatially partitions interphase chromosomes Wu, Shuai Fatkhutdinov, Nail Rosin, Leah Luppino, Jennifer M. Iwasaki, Osamu Tanizawa, Hideki Tang, Hsin-Yao Kossenkov, Andrew V. Gardini, Alessandro Noma, Ken-ichi Speicher, David W. Joyce, Eric F. Zhang, Rugang Sci Adv Research Articles ARID1A, a subunit of the SWItch/Sucrose Non-Fermentable (SWI/SNF) chromatin-remodeling complex, localizes to both promoters and enhancers to influence transcription. However, the role of ARID1A in higher-order spatial chromosome partitioning and genome organization is unknown. Here, we show that ARID1A spatially partitions interphase chromosomes and regulates higher-order genome organization. The SWI/SNF complex interacts with condensin II, and they display significant colocalizations at enhancers. ARID1A knockout drives the redistribution of condensin II preferentially at enhancers, which positively correlates with changes in transcription. ARID1A and condensin II contribute to transcriptionally inactive B-compartment formation, while ARID1A weakens the border strength of topologically associated domains. Condensin II redistribution induced by ARID1A knockout positively correlates with chromosome sizes, which negatively correlates with interchromosomal interactions. ARID1A loss increases the trans interactions of small chromosomes, which was validated by three-dimensional interphase chromosome painting. These results demonstrate that ARID1A is important for large-scale genome folding and spatially partitions interphase chromosomes. American Association for the Advancement of Science 2019-05-22 /pmc/articles/PMC6531001/ /pubmed/31131328 http://dx.doi.org/10.1126/sciadv.aaw5294 Text en Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Wu, Shuai
Fatkhutdinov, Nail
Rosin, Leah
Luppino, Jennifer M.
Iwasaki, Osamu
Tanizawa, Hideki
Tang, Hsin-Yao
Kossenkov, Andrew V.
Gardini, Alessandro
Noma, Ken-ichi
Speicher, David W.
Joyce, Eric F.
Zhang, Rugang
ARID1A spatially partitions interphase chromosomes
title ARID1A spatially partitions interphase chromosomes
title_full ARID1A spatially partitions interphase chromosomes
title_fullStr ARID1A spatially partitions interphase chromosomes
title_full_unstemmed ARID1A spatially partitions interphase chromosomes
title_short ARID1A spatially partitions interphase chromosomes
title_sort arid1a spatially partitions interphase chromosomes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6531001/
https://www.ncbi.nlm.nih.gov/pubmed/31131328
http://dx.doi.org/10.1126/sciadv.aaw5294
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