Utilize este identificador para referenciar este registo: https://hdl.handle.net/10316/109239
Título: Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA
Autor: 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 
Data: 27-Mar-2015
Editora: Springer Nature
Projeto: SFRH/BD/33472/2008 
SFRH/BD/74476/2010; POPH/FSE) 
Human Frontiers Program to S.A.M 
Netherlands Organization for Scientific Research (‘NWO’ Vidi grant) to M.L.dB. 
F.A.M., ‘Sara Borrell’ postdoctoral contract (CD12/00738) from the ISCIII at the Spanish Ministry of Economy and Competitiveness to A.D.L., European Research Council (ERC) Advanced Grant EPINORC (# 268626) to M.E. 
European Research Council (ERC) Advanced Grant EnhReg to R.A. 
Título da revista, periódico, livro ou evento: Nature Communications
Volume: 6
Número: 1
Resumo: 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.
URI: https://hdl.handle.net/10316/109239
ISSN: 2041-1723
DOI: 10.1038/ncomms7520
Direitos: openAccess
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