Frontiers in Genetics (Dec 2020)

Profiling of H3K27Ac Reveals the Influence of Asthma on the Epigenome of the Airway Epithelium

  • Peter McErlean,
  • Peter McErlean,
  • Audrey Kelly,
  • Audrey Kelly,
  • Jaideep Dhariwal,
  • Jaideep Dhariwal,
  • Max Kirtland,
  • Max Kirtland,
  • Julie Watson,
  • Julie Watson,
  • Ismael Ranz,
  • Ismael Ranz,
  • Janet Smith,
  • Alka Saxena,
  • David J. Cousins,
  • David J. Cousins,
  • Antoon Van Oosterhout,
  • Roberto Solari,
  • Roberto Solari,
  • Michael R. Edwards,
  • Michael R. Edwards,
  • Sebastian L. Johnston,
  • Sebastian L. Johnston,
  • Paul Lavender,
  • Paul Lavender

DOI
https://doi.org/10.3389/fgene.2020.585746
Journal volume & issue
Vol. 11

Abstract

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BackgroundAsthma is a chronic airway disease driven by complex genetic–environmental interactions. The role of epigenetic modifications in bronchial epithelial cells (BECs) in asthma is poorly understood.MethodsWe piloted genome-wide profiling of the enhancer-associated histone modification H3K27ac in BECs from people with asthma (n = 4) and healthy controls (n = 3).ResultsWe identified n = 4,321 (FDR < 0.05) regions exhibiting differential H3K27ac enrichment between asthma and health, clustering at genes associated predominately with epithelial processes (EMT). We identified initial evidence of asthma-associated Super-Enhancers encompassing genes encoding transcription factors (TP63) and enzymes regulating lipid metabolism (PTGS1). We integrated published datasets to identify epithelium-specific transcription factors associated with H3K27ac in asthma (TP73) and identify initial relationships between asthma-associated changes in H3K27ac and transcriptional profiles. Finally, we investigated the potential of CRISPR-based approaches to functionally evaluate H3K27ac-asthma landscape in vitro by identifying guide-RNAs capable of targeting acetylation to asthma DERs and inducing gene expression (TLR3).ConclusionOur small pilot study validates genome-wide approaches for deciphering epigenetic mechanisms underlying asthma pathogenesis in the airways.

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