ZNF750 Is a p63 Target Gene that Induces KLF4 to Drive Terminal Epidermal Differentiation

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• 作者：George  ; L. Sen³ ; Lisa  ; D. Boxer² ; Dan  ; E. Webster² ; Rose  ; T. Bussat² ; Kun Qu² ; Brian  ; J. Zarnegar² ; Danielle Johnston² ; Zurab Siprashvili² ; Paul  ; A. Khavari¹ ; ² ; ^{khavari@stanford.edu}
• 刊名：Developmental Cell
• 出版年：2012
• 出版时间：13 March, 2012
• 年：2012
• 卷：22
• 期：3
• 页码：669-677
• 全文大小：1021 K

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Summary

Disrupted epidermal differentiation characterizes numerous diseases that impact >25 % of the population. In a search for dominant mediators of differentiation, we defined a requirement for ZNF750 in terminal epidermal differentiation. ZNF750 controlled genes mutated in numerous human skin diseases, including FLG, LOR, LCE3B, ALOXE3, and SPINK5. ZNF750 induced progenitor differentiation via an evolutionarily conserved C2H2 zinc finger motif. The epidermal master regulator, p63, bound the ZNF750 promoter and was necessary for its induction. ZNF750 restored differentiation to p63-deficient tissue, suggesting that it acts downstream of p63. A search for functionally important ZNF750 targets via analysis of ZNF750-regulated genes identified KLF4, a transcription factor that activates late epidermal differentiation. ZNF750 binds to KLF4 at multiple sites flanking the transcriptional start site and controls its expression. ZNF750 thus directly links?a tissue-specifying factor, p63, to an effector of terminal differentiation, KLF4, and represents a potential future target for disorders of this process.