Disruption of epidermal specific gene expression and delayed skin development in AP-2 gamma mutant mice

Dev Biol. 2008 May 1;317(1):187-95. doi: 10.1016/j.ydbio.2008.02.017. Epub 2008 Feb 21.

Abstract

Summary Sentence: Conditional ablation of AP-2 gamma results in a delay in skin development and abnormal expression of p63, K14, K1, filaggrin, repetin and secreted Ly6/Plaur domain containing 1, key genes required for epidermal development and differentiation. The development of the epidermis, a stratified squamous epithelium, is dependent on the regulated differentiation of keratinocytes. Differentiation begins with the initiation of stratification, a process tightly controlled through proper gene expression. AP-2 gamma is expressed in skin and previous research suggested a pathway where p63 gene induction results in increased expression of AP-2 gamma, which in turn is responsible for induction of K14. This study uses a conditional gene ablation model to further explore the role of AP-2 gamma in skin development. Mice deficient for AP-2 gamma exhibited delayed expression of p63, K14, and K1, key genes required for development and differentiation of the epidermis. In addition, microarray analysis of E16.5 skin revealed delayed expression of additional late epidermal differentiation genes: filaggrin, repetin and secreted Ly6/Plaur domain containing 1, in mutant mice. The genetic delay in skin development was further confirmed by a functional delay in the formation of an epidermal barrier. These results document an important role for AP-2 gamma in skin development, and reveal the existence of regulatory factors that can compensate for AP-2 gamma in its absence.

Publication types

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

MeSH terms

  • Animals
  • Embryo, Mammalian / metabolism
  • Epidermal Cells
  • Epidermis / embryology*
  • Epidermis / metabolism
  • Female
  • Filaggrin Proteins
  • Genes, Lethal
  • Intermediate Filament Proteins / genetics
  • Keratinocytes / cytology
  • Keratinocytes / metabolism
  • Male
  • Mice
  • Mutation
  • Transcription Factor AP-2 / genetics*
  • Transcription Factor AP-2 / metabolism*

Substances

  • Filaggrin Proteins
  • Intermediate Filament Proteins
  • Tfap2c protein, mouse
  • Transcription Factor AP-2