p73 has been identified as a structural and functional homolog of the tumor suppressor p53. The transcriptional coactivator Yes-associated protein (YAP) has been demonstrated to interact with and to enhance p73-dependent apoptosis in response to DNA damage. Here, we show the existence of a proapoptotic autoregulatory feedback loop between p73, YAP, and the promyelocytic leukemia (PML) tumor suppressor gene. We demonstrate that PML is a direct transcriptional target of p73/YAP, and we show that PML transcriptional activation by p73/YAP is under the negative control of the proto-oncogenic Akt/PKB kinase. Importantly, we find that PML and YAP physically interact through their PVPVY and WW domains, respectively, causing PML-mediated sumoylation and stabilization of YAP. Hence, we determine a mechanistic pathway in response to DNA damage that could have relevant implications for the treatment of human cancer.

PML, YAP, and p73 are components of a proapoptotic autoregulatory feedback loop.

PANDOLFI DE RINALDIS, Pier Paolo;
2008-01-01

Abstract

p73 has been identified as a structural and functional homolog of the tumor suppressor p53. The transcriptional coactivator Yes-associated protein (YAP) has been demonstrated to interact with and to enhance p73-dependent apoptosis in response to DNA damage. Here, we show the existence of a proapoptotic autoregulatory feedback loop between p73, YAP, and the promyelocytic leukemia (PML) tumor suppressor gene. We demonstrate that PML is a direct transcriptional target of p73/YAP, and we show that PML transcriptional activation by p73/YAP is under the negative control of the proto-oncogenic Akt/PKB kinase. Importantly, we find that PML and YAP physically interact through their PVPVY and WW domains, respectively, causing PML-mediated sumoylation and stabilization of YAP. Hence, we determine a mechanistic pathway in response to DNA damage that could have relevant implications for the treatment of human cancer.
2008
32
803
814
http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6WSR-4V719BV-B-2&_cdi=7053&_user=7240410&_orig=search&_coverDate=12%2F26%2F2008&_sk=999679993&view=c&wchp=dGLzVlz-zSkWz&md5=9e1f74111cbbafb90b7dc64612bc38e4&ie=/sdarticle.pdf
CELLCYCLE; Adaptor Proteins; Signal Transducing; Animals; Apoptosis; Cell Line; Cisplatin; DNA-Binding Proteins; Feedback; Biochemical; Gene Expression Regulation; Neoplastic; Humans; Lactates; Mice; Models; Biological; Nuclear Proteins; Oligonucleotide Array Sequence Analysis; Phenols; Phosphoproteins; Proteasome Endopeptidase Complex; Protein Binding; Protein Processing; Post-Translational; Protein Stability; Regulatory Sequences; Nucleic Acid; Small Ubiquitin-Related Modifier Proteins; Transcription Factors; Transcription; Genetic; Transcriptional Activation; Tumor Suppressor Proteins; Ubiquitin
E. Lapi;S. D. Agostino;S. Donzelli;H. Gal;E. Domany;G. Rechavi;P. P. Pandolfi;D. Givol;S. Strano;X. Lu;G. Blandino
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/62356
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