| Literature DB >> 30110629 |
Ryan Raisner1, Samir Kharbanda2, Lingyan Jin1, Edwin Jeng3, Emily Chan4, Mark Merchant4, Peter M Haverty5, Russell Bainer5, Tommy Cheung6, David Arnott6, E Megan Flynn7, F Anthony Romero8, Steven Magnuson9, Karen E Gascoigne10.
Abstract
Acetylation of histone H3 at lysine 27 is a well-defined marker of enhancer activity. However, the functional impact of this modification at enhancers is poorly understood. Here, we use a chemical genetics approach to acutely block the function of the cAMP response element binding protein (CREB) binding protein (CBP)/P300 bromodomain in models of hematological malignancies and describe a consequent loss of H3K27Ac specifically from enhancers, despite the continued presence of CBP/P300 at chromatin. Using this approach to dissect the role of H3K27Ac at enhancers, we identify a critical role for this modification in the production of enhancer RNAs and transcription of enhancer-regulated gene networks.Entities:
Keywords: CBP; H3K27Ac; P300; bromodomain; enhancer; histone acetylation
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Year: 2018 PMID: 30110629 DOI: 10.1016/j.celrep.2018.07.041
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423