Essential function of Gli2 and Gli3 in the formation of lung, trachea and oesophagus

Nat Genet. 1998 Sep;20(1):54-7. doi: 10.1038/1711.

Abstract

Foregut malformations (oesophageal atresia, tracheo-oesophageal fistula, lung anomalies and congenital stenosis of the oesophagus and trachea) are relatively common anomalies occurring in 1 in 2,000-5,000 live births, although their aetiology is poorly understood. The secreted glycoprotein Sonic hedgehog (Shh) has been suggested to act as an endodermal signal that controls hindgut patterning and lung growth. In mice, three zinc-finger transcription factors, Gli1, Gli2 and Gli3, have been implicated in the transduction of Shh signal. We report here that mutant mice lacking Gli2 function exhibit foregut defects, including stenosis of the oesophagus and trachea, as well as hypoplasia and lobulation defects of the lung. A reduction of 50% in the gene dosage of Gli3 in a Gli2-/- background resulted in oesophageal atresia with tracheo-oesophageal fistula and a severe lung phenotype. Mutant mice lacking both Gli2 and Gli3 function did not form oesophagus, trachea and lung. These results indicate that Gli2 and Gli3 possess specific and overlapping functions in Shh signalling during foregut development, and suggest that mutations in GLI genes may be involved in human foregut malformations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • DNA-Binding Proteins / physiology*
  • Epithelial Cells / metabolism
  • Esophagus / abnormalities
  • Esophagus / embryology*
  • Esophagus / metabolism
  • Gene Expression Regulation, Developmental
  • Hedgehog Proteins
  • Immunohistochemistry
  • In Situ Hybridization
  • Kruppel-Like Transcription Factors
  • Lung / abnormalities
  • Lung / embryology*
  • Lung / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mesoderm / metabolism
  • Mice
  • Mice, Knockout
  • Nerve Tissue Proteins*
  • Oncogene Proteins / genetics
  • Oncogene Proteins / metabolism
  • Patched Receptors
  • Proteins / genetics
  • Proteins / metabolism
  • Receptors, Cell Surface
  • Repressor Proteins*
  • Trachea / abnormalities
  • Trachea / embryology*
  • Trachea / metabolism
  • Trans-Activators*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription Factors / physiology*
  • Xenopus Proteins*
  • Zinc Finger Protein GLI1
  • Zinc Finger Protein Gli2
  • Zinc Finger Protein Gli3

Substances

  • DNA-Binding Proteins
  • GLI3 protein, Xenopus
  • GLI3 protein, human
  • Gli2 protein, mouse
  • Gli3 protein, mouse
  • Hedgehog Proteins
  • Kruppel-Like Transcription Factors
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Oncogene Proteins
  • Patched Receptors
  • Proteins
  • Receptors, Cell Surface
  • Repressor Proteins
  • SHH protein, human
  • Trans-Activators
  • Transcription Factors
  • Xenopus Proteins
  • Zinc Finger Protein GLI1
  • Zinc Finger Protein Gli2
  • Zinc Finger Protein Gli3