• Title of article

    PH Domain-Only Protein PHLDA3 Is a p53-Regulated Repressor of Akt

  • Author/Authors

    Tatsuya Kawase، نويسنده , , Rieko Ohki، نويسنده , , Tatsuhiro Shibata، نويسنده , , Shuichi Tsutsumi، نويسنده , , Naoko Kamimura، نويسنده , , Johji Inazawa، نويسنده , , Tsutomu Ohta، نويسنده , , Hitoshi Ichikawa، نويسنده , , Hiroyuki Aburatani، نويسنده , , Fumio Tashiro، نويسنده , , Yoichi Taya، نويسنده ,

  • Issue Information
    هفته نامه با شماره پیاپی سال 2009
  • Pages
    16
  • From page
    535
  • To page
    550
  • Abstract
    p53 and Akt are critical players regulating tumorigenesis with opposite effects: whereas p53 transactivates target genes to exert its function as a tumor suppressor, Akt phosphorylates its substrates and transduces downstream survival signals. In addition, p53 and Akt negatively regulate each other to balance survival and death signals within a cell. We now identify PHLDA3 as a p53 target gene that encodes a PH domain-only protein. We find that PHLDA3 competes with the PH domain of Akt for binding of membrane lipids, thereby inhibiting Akt translocation to the cellular membrane and activation. Ablation of endogenous PHLDA3 results in enhanced Akt activity and decrease of p53-dependent apoptosis. We also demonstrate the suppression of anchorage-independent cell growth by PHLDA3. Loss of the PHLDA3 genomic locus was frequently observed in primary lung cancers, suggesting a role of PHLDA3 in tumor suppression. Our results reveal a new mode of coordination between the p53 and Akt pathways.
  • Journal title
    CELL
  • Serial Year
    2009
  • Journal title
    CELL
  • Record number

    1019622