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RNA polymerase II and PARP1 shape enhancer-promoter contacts [preprint]

Barshad, Gilad
Lewis, James J.
Chivu, Alexandra G.
Abuhashem, Abderhman
Krietenstein, Nils
Rice, Edward J.
Rando, Oliver J.
Hadjantonakis, Anna-Katerina
Danko, Charles G.
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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.

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RNA polymerase II and PARP1 shape enhancer-promoter contacts Gilad Barshad, James J. Lewis, Alexandra G. Chivu, Abderhman Abuhashem, Nils Krietenstein, Edward J. Rice, Oliver J. Rando, Anna-Katerina Hadjantonakis, Charles G. Danko bioRxiv 2022.07.07.499190; doi: https://doi.org/10.1101/2022.07.07.499190

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10.1101/2022.07.07.499190
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This article is a preprint. Preprints are preliminary reports of work that have not been certified by peer review.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.Attribution 4.0 International