Resumen de Distinct IL‐1α‐responsive enhancers promote acute and coordinated changes in chromatin topology in a hierarchical manner
Sinah‐Sophia Weiterer, Johanna Meier‐Soelch, Theodore Georgomanolis, Athanasia Mizi, Anna Beyerlein, Hendrik Weiser, Lilija Brant, Christin Mayr‐Buro, Liane Jurida, Knut Beuerlein, Helmut Muller, Axel Weber, Ulas Tenekeci, Oliver Dittrich‐Breiholz, Marek Bartkuhn, Andrea Nist, Thorsten Stiewe, Wilfred FJ van IJcken, Tabea Riedlinger, M Lienhard Schmitz, Argyris Papantonis, Michael Kracht
How cytokine‐driven changes in chromatin topology are converted into gene regulatory circuits during inflammation still remains unclear. Here, we show that interleukin (IL)‐1α induces acute and widespread changes in chromatin accessibility via the TAK1 kinase and NF‐κB at regions that are highly enriched for inflammatory disease‐relevant SNPs. Two enhancers in the extended chemokine locus on human chromosome 4 regulate the IL‐1α‐inducible IL8 and CXCL1‐3 genes. Both enhancers engage in dynamic spatial interactions with gene promoters in an IL‐1α/TAK1‐inducible manner. Microdeletions of p65‐binding sites in either of the two enhancers impair NF‐κB recruitment, suppress activation and biallelic transcription of the IL8/CXCL2 genes, and reshuffle higher‐order chromatin interactions as judged by i4C interactome profiles. Notably, these findings support a dominant role of the IL8 “master” enhancer in the regulation of sustained IL‐1α signaling, as well as for IL‐8 and IL‐6 secretion. CRISPR‐guided transactivation of the IL8 locus or cross‐TAD regulation by TNFα‐responsive enhancers in a different model locus supports the existence of complex enhancer hierarchies in response to cytokine stimulation that prime and orchestrate proinflammatory chromatin responses downstream of NF‐κB.
