1
IRUS Total
Downloads
  Altmetric

BET inhibition disrupts transcription but retains enhancer-promoter contact

File Description SizeFormat 
BET inhibition disrupts transcription but retains enhancer-promoter contact.pdfPublished version3 MBAdobe PDFView/Open
Title: BET inhibition disrupts transcription but retains enhancer-promoter contact
Authors: Crump, NT
Ballabio, E
Godfrey, L
Thorne, R
Repapi, E
Kerry, J
Tapia, M
Hua, P
Lagerholm, C
Filippakopoulos, P
Davies, JOJ
Milne, TA
Item Type: Journal Article
Abstract: Enhancers are DNA sequences that enable complex temporal and tissue-specific regulation of genes in higher eukaryotes. Although it is not entirely clear how enhancer-promoter interactions can increase gene expression, this proximity has been observed in multiple systems at multiple loci and is thought to be essential for the maintenance of gene expression. Bromodomain and Extra-Terminal domain (BET) and Mediator proteins have been shown capable of forming phase condensates and are thought to be essential for super-enhancer function. Here, we show that targeting of cells with inhibitors of BET proteins or pharmacological degradation of BET protein Bromodomain-containing protein 4 (BRD4) has a strong impact on transcription but very little impact on enhancer-promoter interactions. Dissolving phase condensates reduces BRD4 and Mediator binding at enhancers and can also strongly affect gene transcription, without disrupting enhancer-promoter interactions. These results suggest that activation of transcription and maintenance of enhancer-promoter interactions are separable events. Our findings further indicate that enhancer-promoter interactions are not dependent on high levels of BRD4 and Mediator, and are likely maintained by a complex set of factors including additional activator complexes and, at some sites, CTCF and cohesin.
Issue Date: 11-Jan-2021
Date of Acceptance: 1-Dec-2020
URI: http://hdl.handle.net/10044/1/107855
DOI: 10.1038/s41467-020-20400-z
ISSN: 2041-1723
Publisher: Nature Portfolio
Journal / Book Title: Nature Communications
Volume: 12
Copyright Statement: © The Author(s) 2021 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/.
Publication Status: Published
Article Number: 223
Online Publication Date: 2021-01-11
Appears in Collections:Department of Immunology and Inflammation



This item is licensed under a Creative Commons License Creative Commons