| Literature DB >> 28475875 |
Rasmus Siersbæk1, Jesper Grud Skat Madsen1, Biola Maria Javierre2, Ronni Nielsen1, Emilie Kristine Bagge1, Jonathan Cairns2, Steven William Wingett3, Sofie Traynor1, Mikhail Spivakov2, Peter Fraser4, Susanne Mandrup5.
Abstract
Interactions between transcriptional promoters and their distal regulatory elements play an important role in transcriptional regulation; however, the extent to which these interactions are subject to rapid modulations in response to signals is unknown. Here, we use promoter capture Hi-C to demonstrate a rapid reorganization of promoter-anchored chromatin loops within 4 hr after inducing differentiation of 3T3-L1 preadipocytes. The establishment of new promoter-enhancer loops is tightly coupled to activation of poised (histone H3 lysine 4 mono- and dimethylated) enhancers, as evidenced by the acquisition of histone H3 lysine 27 acetylation and the binding of MED1, SMC1, and P300 proteins to these regions, as well as to activation of target genes. Intriguingly, formation of loops connecting activated enhancers and promoters is also associated with extensive recruitment of corepressors such as NCoR and HDACs, indicating that this class of coregulators may play a previously unrecognized role during enhancer activation.Entities:
Keywords: ChIP-seq; adipocyte differentiation; chromatin looping; corepressors; poised enhancers; promoter capture Hi-C; single nucleotide variance; super-enhancers; topologically associating domains; transcriptional regulation
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Year: 2017 PMID: 28475875 DOI: 10.1016/j.molcel.2017.04.010
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970