Chromatin profiling reveals regulatory network shifts and a protective role for hepatocyte nuclear factor 4α during colitis

Sanjay Chahar, Vishal Gandhi, Shiyan Yu, Kinjal Desai, Richard Cowper-Sallari, Yona Kim, Ansu O. Perekatt, Namit Kumar, Joshua K. Thackray, Anthony Musolf, Nikhil Kumar, A. Hoffman, Douglas Londono, Berta N. Vazquez, Lourdes Serrano, Hyunjin Shin, Mathieu Lupien, Nan Gao, Michael P. Verzi

Research output: Contribution to journalArticlepeer-review

30 Scopus citations


Transcriptional regulatory mechanisms likely contribute to the etiology of inflammatory bowel disease (IBD), as genetic variants associated with the disease are disproportionately found at regulatory elements. However, the transcription factors regulating colonic inflammation are unclear. To identify these transcription factors, we mapped epigenomic changes in the colonic epithelium upon inflammation. Epigenetic marks at transcriptional regulatory elements responded dynamically to inflammation and indicated a shift in epithelial transcriptional factor networks. Active enhancer chromatin structure at regulatory regions bound by the transcription factor hepatocyte nuclear factor 4α (HNF4A) was reduced during colitis. In agreement, upon an inflammatory stimulus, HNF4A was downregulated and showed a reduced ability to bind chromatin. Genetic variants that confer a predisposition to IBD map to HNF4A binding sites in the human colon cell line CaCo2, suggesting impaired HNF4A binding could underlie genetic susceptibility to IBD. Despite reduced HNF4A binding during inflammation, a temporal knockout model revealed HNF4A still actively protects against inflammatory phenotypes and promotes immune regulatory gene expression in the inflamed colonic epithelium. These findings highlight the potential for HNF4A agonists as IBD therapeutics.

Original languageEnglish (US)
Pages (from-to)3291-3304
Number of pages14
JournalMolecular and cellular biology
Issue number17
StatePublished - 2014

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Cell Biology


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