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Disruption of epidermal specific gene expression and delayed skin development in AP-2 gamma mutant mice
Authors:Guttormsen Jillian  Koster Maranke I  Stevens John R  Roop Dennis R  Williams Trevor  Winger Quinton A
Affiliation:a Department of Animal, Dairy and Veterinary Sciences, Utah State University, Logan, UT, USA
b Mathematics and Statistics, Utah State University, Logan, UT, USA
c Department of Dermatology and Charles C. Gates Regenerative Medicine and Stem Cell Biology Program, University of Colorado Denver, Aurora, CO, USA
d Departments of Craniofacial Biology and Cell and Developmental Biology, University of Colorado Denver, Aurora, CO, USA
Abstract:Summary Sentence: Conditional ablation of AP-2γ 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-2γ is expressed in skin and previous research suggested a pathway where p63 gene induction results in increased expression of AP-2γ, which in turn is responsible for induction of K14. This study uses a conditional gene ablation model to further explore the role of AP-2γ in skin development. Mice deficient for AP-2γ 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-2γ in skin development, and reveal the existence of regulatory factors that can compensate for AP-2γ in its absence.
Keywords:AP-2   Tcfap2c   Skin   Epidermis   Keratinocyte   Filaggrin   Keratin   Differentiation   Embryo development
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