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Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA
p53 binds enhancers to regulate key target genes. Here, we globally mapped p53-regulated enhancers by looking at enhancer RNA (eRNA) production. Intriguingly, while many p53-induced enhancers contained p53-binding sites, most did not. As long non-coding RNAs (lncRNAs) are prominent regulators of chr...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389233/ https://www.ncbi.nlm.nih.gov/pubmed/25813522 http://dx.doi.org/10.1038/ncomms7520 |
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author | Léveillé, Nicolas Melo, Carlos A. Rooijers, Koos Díaz-Lagares, Angel Melo, Sonia A. Korkmaz, Gozde Lopes, Rui Moqadam, Farhad Akbari Maia, Ana R. Wijchers, Patrick J. Geeven, Geert den Boer, Monique L. Kalluri, Raghu de Laat, Wouter Esteller, Manel Agami, Reuven |
author_facet | Léveillé, Nicolas Melo, Carlos A. Rooijers, Koos Díaz-Lagares, Angel Melo, Sonia A. Korkmaz, Gozde Lopes, Rui Moqadam, Farhad Akbari Maia, Ana R. Wijchers, Patrick J. Geeven, Geert den Boer, Monique L. Kalluri, Raghu de Laat, Wouter Esteller, Manel Agami, Reuven |
author_sort | Léveillé, Nicolas |
collection | PubMed |
description | p53 binds enhancers to regulate key target genes. Here, we globally mapped p53-regulated enhancers by looking at enhancer RNA (eRNA) production. Intriguingly, while many p53-induced enhancers contained p53-binding sites, most did not. As long non-coding RNAs (lncRNAs) are prominent regulators of chromatin dynamics, we hypothesized that p53-induced lncRNAs contribute to the activation of enhancers by p53. Among p53-induced lncRNAs, we identified LED and demonstrate that its suppression attenuates p53 function. Chromatin-binding and eRNA expression analyses show that LED associates with and activates strong enhancers. One prominent target of LED was located at an enhancer region within CDKN1A gene, a potent p53-responsive cell cycle inhibitor. LED knockdown reduces CDKN1A enhancer induction and activity, and cell cycle arrest following p53 activation. Finally, promoter-associated hypermethylation analysis shows silencing of LED in human tumours. Thus, our study identifies a new layer of complexity in the p53 pathway and suggests its dysregulation in cancer. |
format | Online Article Text |
id | pubmed-4389233 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43892332015-04-17 Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA Léveillé, Nicolas Melo, Carlos A. Rooijers, Koos Díaz-Lagares, Angel Melo, Sonia A. Korkmaz, Gozde Lopes, Rui Moqadam, Farhad Akbari Maia, Ana R. Wijchers, Patrick J. Geeven, Geert den Boer, Monique L. Kalluri, Raghu de Laat, Wouter Esteller, Manel Agami, Reuven Nat Commun Article p53 binds enhancers to regulate key target genes. Here, we globally mapped p53-regulated enhancers by looking at enhancer RNA (eRNA) production. Intriguingly, while many p53-induced enhancers contained p53-binding sites, most did not. As long non-coding RNAs (lncRNAs) are prominent regulators of chromatin dynamics, we hypothesized that p53-induced lncRNAs contribute to the activation of enhancers by p53. Among p53-induced lncRNAs, we identified LED and demonstrate that its suppression attenuates p53 function. Chromatin-binding and eRNA expression analyses show that LED associates with and activates strong enhancers. One prominent target of LED was located at an enhancer region within CDKN1A gene, a potent p53-responsive cell cycle inhibitor. LED knockdown reduces CDKN1A enhancer induction and activity, and cell cycle arrest following p53 activation. Finally, promoter-associated hypermethylation analysis shows silencing of LED in human tumours. Thus, our study identifies a new layer of complexity in the p53 pathway and suggests its dysregulation in cancer. Nature Pub. Group 2015-03-27 /pmc/articles/PMC4389233/ /pubmed/25813522 http://dx.doi.org/10.1038/ncomms7520 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Léveillé, Nicolas Melo, Carlos A. Rooijers, Koos Díaz-Lagares, Angel Melo, Sonia A. Korkmaz, Gozde Lopes, Rui Moqadam, Farhad Akbari Maia, Ana R. Wijchers, Patrick J. Geeven, Geert den Boer, Monique L. Kalluri, Raghu de Laat, Wouter Esteller, Manel Agami, Reuven Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA |
title | Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA |
title_full | Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA |
title_fullStr | Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA |
title_full_unstemmed | Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA |
title_short | Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA |
title_sort | genome-wide profiling of p53-regulated enhancer rnas uncovers a subset of enhancers controlled by a lncrna |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4389233/ https://www.ncbi.nlm.nih.gov/pubmed/25813522 http://dx.doi.org/10.1038/ncomms7520 |
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