Author
Listed:
- Nicolas Léveillé
(The Netherlands Cancer Institute)
- Carlos A. Melo
(The Netherlands Cancer Institute
Doctoral Programme in Biomedicine and Experimental Biology, Centre for Neuroscience and Cell Biology, Coimbra University)
- Koos Rooijers
(The Netherlands Cancer Institute)
- Angel Díaz-Lagares
(Cancer Epigenetics and Biology Program (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Catalonia 08908, Spain)
- Sonia A. Melo
(University of Texas MD Anderson Cancer Center)
- Gozde Korkmaz
(The Netherlands Cancer Institute)
- Rui Lopes
(The Netherlands Cancer Institute)
- Farhad Akbari Moqadam
(Erasmus University Medical Center, Erasmus MC)
- Ana R. Maia
(The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands)
- Patrick J. Wijchers
(Hubrecht Institute-KNAW, University Medical Centre Utrecht)
- Geert Geeven
(Hubrecht Institute-KNAW, University Medical Centre Utrecht)
- Monique L. den Boer
(Erasmus University Medical Center, Erasmus MC)
- Raghu Kalluri
(University of Texas MD Anderson Cancer Center)
- Wouter de Laat
(Hubrecht Institute-KNAW, University Medical Centre Utrecht)
- Manel Esteller
(Cancer Epigenetics and Biology Program (PEBC), Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Catalonia 08908, Spain
School of Medicine, University of Barcelona, Barcelona, Catalonia 08036, Spain
Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Catalonia 08010, Spain)
- Reuven Agami
(The Netherlands Cancer Institute
Erasmus MC, Rotterdam University, 3000 CA Rotterdam)
Abstract
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.
Suggested Citation
Nicolas Léveillé & Carlos A. Melo & Koos Rooijers & Angel Díaz-Lagares & Sonia A. Melo & Gozde Korkmaz & Rui Lopes & Farhad Akbari Moqadam & Ana R. Maia & Patrick J. Wijchers & Geert Geeven & Monique , 2015.
"Genome-wide profiling of p53-regulated enhancer RNAs uncovers a subset of enhancers controlled by a lncRNA,"
Nature Communications, Nature, vol. 6(1), pages 1-12, May.
Handle:
RePEc:nat:natcom:v:6:y:2015:i:1:d:10.1038_ncomms7520
DOI: 10.1038/ncomms7520
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