TGFbeta2 knockout mice have multiple developmental defects that are non-overlapping with other TGFbeta knockout phenotypes

Development. 1997 Jul;124(13):2659-70. doi: 10.1242/dev.124.13.2659.

Abstract

The growth and differentiation factor transforming growth factor-beta2 (TGFbeta2) is thought to play important roles in multiple developmental processes. Targeted disruption of the TGFbeta2 gene was undertaken to determine its essential role in vivo. TGFbeta2-null mice exhibit perinatal mortality and a wide range of developmental defects for a single gene disruption. These include cardiac, lung, craniofacial, limb, spinal column, eye, inner ear and urogenital defects. The developmental processes most commonly involved in the affected tissues include epithelial-mesenchymal interactions, cell growth, extracellular matrix production and tissue remodeling. In addition, many affected tissues have neural crest-derived components and simulate neural crest deficiencies. There is no phenotypic overlap with TGFbeta1- and TGFbeta3-null mice indicating numerous non-compensated functions between the TGFbeta isoforms.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Animals
  • Bone and Bones / abnormalities
  • Cleft Palate / genetics
  • Craniofacial Abnormalities / genetics
  • Cyanosis / congenital
  • Ear, Inner / abnormalities
  • Embryonic Induction / genetics
  • Epithelium / embryology
  • Eye Abnormalities
  • Genes, Homeobox
  • Heart Defects, Congenital / genetics
  • Mesoderm
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Phenotype
  • Transforming Growth Factor beta / classification
  • Transforming Growth Factor beta / genetics*
  • Tretinoin / metabolism
  • Urogenital Abnormalities

Substances

  • Transforming Growth Factor beta
  • Tretinoin