GATA-4:FOG interactions regulate gastric epithelial development in the mouse

Dev Dyn. 2005 Oct;234(2):355-62. doi: 10.1002/dvdy.20552.

Abstract

Transcription factor GATA-4 is a key participant in cytodifferentiation of the mouse hindstomach. Here we show that GATA-4 cooperates with a Friend-of-GATA (FOG) cofactor to direct gene expression in this segment of gut. Immunohistochemical staining revealed that GATA-4 and FOG-1 are co-expressed in hindstomach epithelial cells from embryonic days (E) 11.5 to 18.5. The other member of the mammalian FOG family, FOG-2, was not detected in gastric epithelium. To show that GATA-4:FOG interactions influence stomach development, we analyzed Gata4(ki/ki) mice, which express a mutant GATA-4 that cannot bind FOG cofactors. Sonic Hedgehog, an endoderm-derived signaling molecule normally down-regulated in the distal stomach, was over-expressed in hindstomach epithelium of E11.5 Gata4(ki/ki) mice, and there was a concomitant decrease in fibroblast growth factor-10 in adjacent mesenchyme. We conclude that functional interaction between GATA-4 and a member of the FOG family, presumably FOG-1, is required for proper epithelial-mesenchymal signaling in the developing stomach.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Down-Regulation
  • Endothelium / metabolism
  • Endothelium, Vascular / metabolism
  • Epithelium / embryology*
  • Epithelium / metabolism
  • Fibroblast Growth Factor 10 / genetics
  • Fibroblast Growth Factor 10 / physiology
  • GATA4 Transcription Factor / metabolism
  • GATA4 Transcription Factor / physiology*
  • Gene Expression Regulation, Developmental*
  • Hedgehog Proteins
  • Immunohistochemistry
  • In Situ Hybridization
  • Mesoderm / metabolism*
  • Mice
  • Mice, Transgenic
  • Mutation
  • Nuclear Proteins / genetics
  • Nuclear Proteins / physiology*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Stomach / embryology*
  • Time Factors
  • Trans-Activators / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription Factors / physiology*
  • Transcription, Genetic
  • Transcriptional Activation

Substances

  • FGF10 protein, human
  • Fibroblast Growth Factor 10
  • GATA4 Transcription Factor
  • Hedgehog Proteins
  • Nuclear Proteins
  • SHH protein, human
  • Trans-Activators
  • Transcription Factors
  • Zfpm1 protein, mouse