Id2 Determines Intestinal Identity through Repression of the Foregut Transcription Factor Irx5

Mol Cell Biol. 2018 Apr 16;38(9):e00250-17. doi: 10.1128/MCB.00250-17. Print 2018 May 1.

Abstract

The cellular components and function of the gastrointestinal epithelium exhibit distinct characteristics depending on the region, e.g., stomach or intestine. How these region-specific epithelial characteristics are generated during development remains poorly understood. Here, we report on the involvement of the helix-loop-helix inhibitor Id2 in establishing the specific characteristics of the intestinal epithelium. Id2-/- mice developed tumors in the small intestine. Histological analysis indicated that the intestinal tumors were derived from gastric metaplasia formed in the small intestine during development. Heterotopic Id2 expression in developing gastric epithelium induced a fate change to intestinal epithelium. Gene expression analysis revealed that foregut-enriched genes encoding Irx3 and Irx5 were highly induced in the midgut of Id2-/- embryos, and transgenic mice expressing Irx5 in the midgut endoderm developed tumors recapitulating the characteristics of Id2-/- mice. Altogether, our results demonstrate that Id2 plays a crucial role in the development of regional specificity in the gastrointestinal epithelium.

Keywords: Id2; Irx transcription factor; cancer; cell differentiation; cell fate specification; endoderm; gastric mucosa; intestinal development; intestinal epithelium; tumorigenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Gene Expression Regulation / genetics
  • Homeodomain Proteins / genetics
  • Homeodomain Proteins / metabolism*
  • Homeodomain Proteins / physiology
  • Inhibitor of Differentiation Protein 2 / metabolism*
  • Inhibitor of Differentiation Protein 2 / physiology*
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / physiology
  • Intestine, Small / physiology
  • Intestines / physiology
  • Metaplasia
  • Mice
  • Mice, 129 Strain
  • Protein Domains
  • Stomach
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcription Factors / physiology

Substances

  • Homeodomain Proteins
  • Idb2 protein, mouse
  • Inhibitor of Differentiation Protein 2
  • Irx3 protein, mouse
  • Irx5 protein, mouse
  • Transcription Factors