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Transcriptional activity of TAp63 promoter is regulated by c‐jun
Author(s) -
Yao JengYuan,
Pao ChiaChu,
Chen JanKan
Publication year - 2010
Publication title -
journal of cellular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.529
H-Index - 174
eISSN - 1097-4652
pISSN - 0021-9541
DOI - 10.1002/jcp.22300
Subject(s) - transactivation , promoter , gene knockdown , transcription factor , biology , carcinogenesis , cell growth , gene , microbiology and biotechnology , transcription (linguistics) , cell , gene expression , cancer research , genetics , linguistics , philosophy
The transcription factor p63 belongs to the p53 protein family and plays an important role in epithelial development. Recent studies showed that p63 is over‐expressed in some human squamous cell carcinomas of the head and neck, suggesting a role in carcinogenesis. The p63 gene contains two promoters and alternative promoter usage generates two groups of proteins with (TAp63) or without (ΔNp63) the transactivation domain. Although the roles of TAp63 in epithelial development have been described in numerous recent studies, the regulation of its expression has not been elucidated. In this study, we showed that the transcriptional activity of the TAp63 promoter and TAp63 protein level were both up‐regulated by an increased c‐jun activity in Hep3B human hepatocellular carcinoma cell. Moreover, the elevated TAp63 expression was coincided with an increased binding of c‐jun to the TAp63 promoter. Point mutation of the sp1 binding site within the TAp63 promoter region attenuated the effect of c‐jun on TAp63 expression. Knockdown of TAp63 expression by shRNA led to increased proliferation of Hep3B cell compared to that of the mock cell, suggesting a growth suppressive effect of TAp63. J. Cell. Physiol. 225: 898–904, 2010. © 2010 Wiley‐Liss, Inc.