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      Functional association between Wwox tumor suppressor protein and p73, a p53 homolog.

      Proceedings of the National Academy of Sciences of the United States of America
      Cell Line, Cell Line, Tumor, DNA-Binding Proteins, genetics, metabolism, Gene Expression Regulation, Genes, Reporter, Genes, Tumor Suppressor, Green Fluorescent Proteins, Humans, Luminescent Proteins, Nuclear Proteins, Phosphorylation, Plasmids, Protein Binding, RNA, Small Interfering, Recombinant Fusion Proteins, Transcription, Genetic, Transcriptional Activation, Transfection, Tumor Suppressor Proteins

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          Abstract

          The WWOX gene is a recently cloned tumor suppressor gene that spans the FRA16D fragile region. Wwox protein contains two WW domains that are generally known to mediate protein-protein interaction. Here we show that Wwox physically interacts via its first WW domain with the p53 homolog, p73. The tyrosine kinase, Src, phosphorylates Wwox at tyrosine 33 in the first WW domain and enhances its binding to p73. Our results further demonstrate that Wwox expression triggers redistribution of nuclear p73 to the cytoplasm and, hence, suppresses its transcriptional activity. In addition, we show that cytoplasmic p73 contributes to the proapoptotic activity of Wwox. Our findings reveal a functional cross-talk between p73 and Wwox tumor suppressor protein.

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