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Disruption of ATRX-RNA interactions uncovers roles in ATRX localization and PRC2 function
Heterochromatin in the eukaryotic genome is rigorously controlled by the concerted action of protein factors and RNAs. Here, we investigate the RNA binding function of ATRX, a chromatin remodeler with roles in silencing of repetitive regions of the genome and in recruitment of the polycomb repressiv...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203109/ https://www.ncbi.nlm.nih.gov/pubmed/32376827 http://dx.doi.org/10.1038/s41467-020-15902-9 |
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author | Ren, Wenqing Medeiros, Nicole Warneford-Thomson, Robert Wulfridge, Phillip Yan, Qingqing Bian, Joyce Sidoli, Simone Garcia, Benjamin A. Skordalakes, Emmanuel Joyce, Eric Bonasio, Roberto Sarma, Kavitha |
author_facet | Ren, Wenqing Medeiros, Nicole Warneford-Thomson, Robert Wulfridge, Phillip Yan, Qingqing Bian, Joyce Sidoli, Simone Garcia, Benjamin A. Skordalakes, Emmanuel Joyce, Eric Bonasio, Roberto Sarma, Kavitha |
author_sort | Ren, Wenqing |
collection | PubMed |
description | Heterochromatin in the eukaryotic genome is rigorously controlled by the concerted action of protein factors and RNAs. Here, we investigate the RNA binding function of ATRX, a chromatin remodeler with roles in silencing of repetitive regions of the genome and in recruitment of the polycomb repressive complex 2 (PRC2). We identify ATRX RNA binding regions (RBRs) and discover that the major ATRX RBR lies within the N-terminal region of the protein, distinct from its PHD and helicase domains. Deletion of this ATRX RBR (ATRXΔRBR) compromises ATRX interactions with RNAs in vitro and in vivo and alters its chromatin binding properties. Genome-wide studies reveal that loss of RNA interactions results in a redistribution of ATRX on chromatin. Finally, our studies identify a role for ATRX-RNA interactions in regulating PRC2 localization to a subset of polycomb target genes. |
format | Online Article Text |
id | pubmed-7203109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72031092020-05-13 Disruption of ATRX-RNA interactions uncovers roles in ATRX localization and PRC2 function Ren, Wenqing Medeiros, Nicole Warneford-Thomson, Robert Wulfridge, Phillip Yan, Qingqing Bian, Joyce Sidoli, Simone Garcia, Benjamin A. Skordalakes, Emmanuel Joyce, Eric Bonasio, Roberto Sarma, Kavitha Nat Commun Article Heterochromatin in the eukaryotic genome is rigorously controlled by the concerted action of protein factors and RNAs. Here, we investigate the RNA binding function of ATRX, a chromatin remodeler with roles in silencing of repetitive regions of the genome and in recruitment of the polycomb repressive complex 2 (PRC2). We identify ATRX RNA binding regions (RBRs) and discover that the major ATRX RBR lies within the N-terminal region of the protein, distinct from its PHD and helicase domains. Deletion of this ATRX RBR (ATRXΔRBR) compromises ATRX interactions with RNAs in vitro and in vivo and alters its chromatin binding properties. Genome-wide studies reveal that loss of RNA interactions results in a redistribution of ATRX on chromatin. Finally, our studies identify a role for ATRX-RNA interactions in regulating PRC2 localization to a subset of polycomb target genes. Nature Publishing Group UK 2020-05-06 /pmc/articles/PMC7203109/ /pubmed/32376827 http://dx.doi.org/10.1038/s41467-020-15902-9 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Ren, Wenqing Medeiros, Nicole Warneford-Thomson, Robert Wulfridge, Phillip Yan, Qingqing Bian, Joyce Sidoli, Simone Garcia, Benjamin A. Skordalakes, Emmanuel Joyce, Eric Bonasio, Roberto Sarma, Kavitha Disruption of ATRX-RNA interactions uncovers roles in ATRX localization and PRC2 function |
title | Disruption of ATRX-RNA interactions uncovers roles in ATRX localization and PRC2 function |
title_full | Disruption of ATRX-RNA interactions uncovers roles in ATRX localization and PRC2 function |
title_fullStr | Disruption of ATRX-RNA interactions uncovers roles in ATRX localization and PRC2 function |
title_full_unstemmed | Disruption of ATRX-RNA interactions uncovers roles in ATRX localization and PRC2 function |
title_short | Disruption of ATRX-RNA interactions uncovers roles in ATRX localization and PRC2 function |
title_sort | disruption of atrx-rna interactions uncovers roles in atrx localization and prc2 function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203109/ https://www.ncbi.nlm.nih.gov/pubmed/32376827 http://dx.doi.org/10.1038/s41467-020-15902-9 |
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