Nature GeneticsGenomicsPeer-reviewed journal article
RNA polymerase II and PARP1 shape enhancer-promoter contacts
Gilad BarshadiD, James J. LewisiD, Alexandra G. ChivuiD, Abderhman AbuhashemiD, Nils KrietensteiniD, Edward J. Rice, Yitian MaiD, Zhong WangiD, Oliver J. RandoiD, Anna‐Katerina HadjantonakisiD, Charles G. DankoiD
Abstract
How enhancers control target gene expression over long genomic distances remains an important unsolved problem. Here we studied enhancer-promoter contact architecture and communication by integrating data from nucleosome-resolution genomic contact maps, nascent transcription, and perturbations to transcription-associated proteins and thousands of candidate enhancers. Contact frequency between functionally validated enhancer-promoter pairs was most enriched near the +1 and +2 nucleosomes at enhancers and target promoters, indicating that functional enhancer-promoter pairs spend time in close physical proximity. Blocking RNA polymerase II (Pol II) caused major disruptions to enhancer-promoter contacts. Paused Pol II occupancy and the enzymatic activity of poly (ADP-ribose) polymerase 1 (PARP1) stabilized enhancer-promoter contacts. Based on our findings, we propose an updated model that couples transcriptional dynamics and enhancer-promoter communication.
- organism: human
- assay: ChIP-seq
- assay: Hi-C
- research focus: cell-cell communication
- approach: experimental assay
- Citations
- 119
- FWCI
- 10.39
- Field percentile
- top 1%
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