List of abbreviations: K, keratin; p63-/-, mouse knockout for p63; p63-/-;TA, p63 knockout mice complemented with TAp63; p63-/-;ΔN, p63 knockout mice complemented with ΔNp63; p63-/-;TA;ΔN, p63 knockout mice complemented with both TAp63 and ΔNp63;IKKα, IkB kinase-α; TA, transactivation domain; ΔN, amino-terminal truncated protein.
AbstractThe epidermis, the outer layer of the skin composed of keratinocytes, is a stratified epithelium that functions as a barrier to protect the organism from dehydration and external insults. The epidermis develops following the action of the transcription factor p63, a member of the p53 family of transcription factors. The Trp63 gene contains two promoters, driving the production of distinct proteins, one with an N-terminal transactivation domain (TAp63) and one without (DeltaNp63), although their relative contribution to epidermal development is not clearly established. Trp63 mutations are involved in the pathogenesis of several human diseases, phenotypically characterized by ectodermal dysplasia. In this review we summarise the current advances that have been made in understanding the role of p63 in epidermal morphogenesis.