Compartmentalized phosphorylation of IAP by protein kinase A regulates cytoprotection

Mol Cell. 2007 Jul 6;27(1):17-28. doi: 10.1016/j.molcel.2007.06.004.

Abstract

Cell death pathways are likely regulated in specialized subcellular microdomains, but how this occurs is not understood. Here, we show that cyclic AMP-dependent protein kinase A (PKA) phosphorylates the inhibitor of apoptosis (IAP) protein survivin on Ser20 in the cytosol, but not in mitochondria. This phosphorylation event disrupts the binding interface between survivin and its antiapoptotic cofactor, XIAP. Conversely, mitochondrial survivin or a non-PKA phosphorylatable survivin mutant binds XIAP avidly, enhances XIAP stability, synergistically inhibits apoptosis, and accelerates tumor growth, in vivo. Therefore, differential phosphorylation of survivin by PKA in subcellular microdomains regulates tumor cell apoptosis via its interaction with XIAP.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Apoptosis
  • Cell Compartmentation*
  • Cell Line, Tumor
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • Cytoprotection*
  • Humans
  • Inhibitor of Apoptosis Proteins / chemistry
  • Inhibitor of Apoptosis Proteins / metabolism*
  • Mice
  • Microtubule-Associated Proteins / chemistry
  • Microtubule-Associated Proteins / metabolism*
  • Mitochondria / metabolism
  • Neoplasms / pathology
  • Phosphorylation
  • Protein Structure, Secondary
  • Serine / metabolism
  • Transplantation, Heterologous
  • X-Linked Inhibitor of Apoptosis Protein / metabolism

Substances

  • Inhibitor of Apoptosis Proteins
  • Microtubule-Associated Proteins
  • X-Linked Inhibitor of Apoptosis Protein
  • Serine
  • Cyclic AMP-Dependent Protein Kinases