[HTML][HTML] Compartmentalized phosphorylation of IAP by protein kinase A regulates cytoprotection

T Dohi, F Xia, DC Altieri - Molecular cell, 2007 - cell.com
T Dohi, F Xia, DC Altieri
Molecular cell, 2007cell.com
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 …
Summary
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.
cell.com