Epromoters function as a hub to recruit key transcription factors required for the inflammatory response

Nat Commun. 2021 Nov 18;12(1):6660. doi: 10.1038/s41467-021-26861-0.

Abstract

Gene expression is controlled by the involvement of gene-proximal (promoters) and distal (enhancers) regulatory elements. Our previous results demonstrated that a subset of gene promoters, termed Epromoters, work as bona fide enhancers and regulate distal gene expression. Here, we hypothesized that Epromoters play a key role in the coordination of rapid gene induction during the inflammatory response. Using a high-throughput reporter assay we explored the function of Epromoters in response to type I interferon. We find that clusters of IFNa-induced genes are frequently associated with Epromoters and that these regulatory elements preferentially recruit the STAT1/2 and IRF transcription factors and distally regulate the activation of interferon-response genes. Consistently, we identified and validated the involvement of Epromoter-containing clusters in the regulation of LPS-stimulated macrophages. Our findings suggest that Epromoters function as a local hub recruiting the key TFs required for coordinated regulation of gene clusters during the inflammatory response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Enhancer Elements, Genetic / drug effects
  • Enhancer Elements, Genetic / physiology*
  • Gene Expression Regulation
  • HeLa Cells
  • Humans
  • Inflammation / genetics*
  • Inflammation / metabolism
  • Interferon Regulatory Factors / metabolism*
  • Interferon Type I / metabolism
  • Interferon-alpha / pharmacology
  • K562 Cells
  • Lipopolysaccharides / pharmacology
  • Macrophages / drug effects
  • Mice
  • Multigene Family / drug effects
  • Multigene Family / genetics
  • Promoter Regions, Genetic / drug effects
  • Promoter Regions, Genetic / physiology*
  • STAT1 Transcription Factor / metabolism
  • STAT2 Transcription Factor / metabolism

Substances

  • Interferon Regulatory Factors
  • Interferon Type I
  • Interferon-alpha
  • Lipopolysaccharides
  • STAT1 Transcription Factor
  • STAT2 Transcription Factor