Chromosome contacts in activated T cells identify autoimmune disease candidate genes

Genome Biol. 2017 Sep 4;18(1):165. doi: 10.1186/s13059-017-1285-0.

Abstract

Background: Autoimmune disease-associated variants are preferentially found in regulatory regions in immune cells, particularly CD4+ T cells. Linking such regulatory regions to gene promoters in disease-relevant cell contexts facilitates identification of candidate disease genes.

Results: Within 4 h, activation of CD4+ T cells invokes changes in histone modifications and enhancer RNA transcription that correspond to altered expression of the interacting genes identified by promoter capture Hi-C. By integrating promoter capture Hi-C data with genetic associations for five autoimmune diseases, we prioritised 245 candidate genes with a median distance from peak signal to prioritised gene of 153 kb. Just under half (108/245) prioritised genes related to activation-sensitive interactions. This included IL2RA, where allele-specific expression analyses were consistent with its interaction-mediated regulation, illustrating the utility of the approach.

Conclusions: Our systematic experimental framework offers an alternative approach to candidate causal gene identification for variants with cell state-specific functional effects, with achievable sample sizes.

Keywords: Autoimmune disease; CD4+ T cell activation; CD4+ T cells; Chromatin conformation; Genetics; Genome-wide association studies; Genomics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoimmune Diseases / genetics*
  • Autoimmune Diseases / immunology
  • CD4-Positive T-Lymphocytes / immunology*
  • Chromatin
  • Chromosome Mapping*
  • Enhancer Elements, Genetic
  • Humans
  • Interleukin-2 Receptor alpha Subunit / genetics
  • Lymphocyte Activation / genetics*
  • Promoter Regions, Genetic*
  • Transcriptome

Substances

  • Chromatin
  • IL2RA protein, human
  • Interleukin-2 Receptor alpha Subunit