Properties of the six isoforms of p63: p53-like regulation in response to genotoxic stress and cross talk with ΔNp73

作者：Audrey Petitjean, Charlotte Ruptier, Violaine Tribollet, A. Hautefeuille, Florence M. Chardon, Catherine Cavard, Alain Puisieux, Pierre Hainaut, Claude Caron de Fromentel · 发表于：Carcinogenesis · 年份：2007 · DOI：10.1093/carcin/bgm258 · 被引用次数：90 · 研究领域：Cancer-related Molecular Pathways、Cancer Research and Treatments、Molecular Biology Techniques and Applications

TP63, a member of the TP53 gene family, encodes two groups of three isoforms (alpha, beta and gamma). The TAp63 isoforms act as transcription factors. The DeltaNp63 isoforms lack the main transcription activation domain and act as dominant-negative inhibitors of transactivation (TA) isoforms. To clarify the role of these isoforms and to better understand their functional overlap with p53, we ectopically expressed each p63 isoform in the p53-null hepatocellular carcinoma cell line Hep3B. All TA isoforms, as well as DeltaNp63alpha, had a half-life of <1 h when transiently expressed and were degraded by the proteasome pathway. The most stable form was DeltaNp63gamma, with a half-life of >8 h. As expected, TA isoforms differed in their transcriptional activities toward genes regulated by p53, TAp63gamma being the most active form. In contrast, DeltaNp63 isoforms were transcriptionally inactive on genes studied and inhibited TA isoforms in a dose-dependent manner. When stably expressed in polyclonal cell populations, TAp63beta and gamma isoforms were undetectable. However, when treated with doxorubicin (DOX), p63 proteins rapidly accumulated in the cells. This stabilization was associated with an increase in phosphorylation. Strikingly, in DOX-treated polyclonal populations, increase in TAp63 levels was accompanied by overexpression of DeltaNp73. This observation suggests complex regulatory cross talks between the different isoforms of the p53 family. In conclusion, p63 exhibits s...