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Korean Society for Biochemistry and Molecular Biology (생화학분자생물학회)
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Disruption of ATP binding destabilizes NPM/B23 and inhibits anti-apoptotic function

  • Choi, Joung-Woo (Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine) ;
  • Lee, Sang-Bae (Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine) ;
  • Ahn, Jee-Yin (Department of Molecular Cell Biology, Sungkyunkwan University School of Medicine) ;
  • Lee, Kyung-Hoon (Department of Anatomy, Sungkyunkwan University School of Medicine)
  • Published : 2008.12.31
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Abstract

Nucleophosmin/B23, a major nucleolar phosphoprotein, is overexpressed in actively proliferating cells. In this study, we demonstrate that B23 exclusively localizes in the nucleolus, whereas ATP depletion results in the redistribution of B23 throughout the whole nucleus and destabilizes B23 via caspase-3 mediated cleavage. Interestingly, ATP binding precedes PI(3,4,5)P3 binding at lysine 263 and ATP binding mutants fail to restore the anti-apoptotic functions of B23 in PC12 cells. Thus, the ATP-B23 interaction is required for the stability of the B23 protein and regulates cell survival, confining B23 within the nucleolus in PC12 cells.

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References

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