Risk predisposition for Crohn disease: a "ménage à trois" combining IRGM allele, miRNA and xenophagy

Autophagy. 2011 Jul;7(7):786-7. doi: 10.4161/auto.7.7.15595. Epub 2011 Jul 1.

Abstract

Susceptibility to Crohn disease (CD), an inflammatory bowel disease, is influenced by common variants at many loci like the exonic synonymous IRGM SNP (rs10065172, NM_001145805.1, c.313C>T). We recently showed that miR-196 is overexpressed in the inflammatory intestinal epithelia of individuals with CD and downregulates the IRGM protective (c.313C) but not the risk-associated (c.313T) allele. Eventually, loss of: IRGM/miRNA regulation compromises xenophagy. These results highlight a critical "ménage à trois" in risk susceptibility combining IRGM allele, miRNA and xenophagy.

MeSH terms

  • Alleles*
  • Autophagy / genetics*
  • Crohn Disease / genetics*
  • GTP-Binding Proteins / genetics*
  • Gene Expression Regulation
  • Genetic Predisposition to Disease*
  • Humans
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Models, Biological
  • Risk Factors

Substances

  • MicroRNAs
  • GTP-Binding Proteins
  • IRGM protein, human