Journal article

Cyclic-AMP-dependent protein kinase A regulates apoptosis by stabilizing the BH3-only protein Bim

D Moujalled, R Weston, H Anderton, R Ninnis, P Goel, A Coley, DC Huang, L Wu, A Strasser, H Puthalakath

EMBO Reports | WILEY | Published : 2011

Abstract

The proapoptotic Bcl2 homology domain 3(BH3)-only protein Bim is controlled by stringent post-translational regulation, predominantly through alterations in phosphorylation status. To identify new kinases involved in its regulation, we carried out a yeast two-hybrid screen using a non-spliceable variant of the predominant isoform-BimEL-as the bait and identified the regulatory subunit of cyclic-AMP-dependent protein kinase A-PRKAR1A-as an interacting partner. We also show that protein kinase A (PKA) is a BimEL isoform-specific kinase that promotes its stabilization. Inhibition of PKA or mutation of the PKA phosphorylation site within BimEL resulted in its accelerated proteasome-dependent deg..

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Grants

Awarded by National Health and Medical Research Council


Funding Acknowledgements

We thank L. O'Connor, N. Hoogenraad and D. L. Vaux for helpful discussion; L. A. O'Reilly, P. Bouillet, D. Chau, J. Silke and P. Ekert for reagents and cell lines and I. Wertz for the beta TrCP1 construct. H. P. is supported by Australian Research Council Future Fellowship and National Health and Medical Research Council project grant (487311). A. S. is supported by the Leukemia and Lymphoma Society (7413) and the National Health and Medical Research Council (461221, 461299). D. M. is supported by a La Trobe Postgraduate Award and Cooperative Research Centre for Biomarker Translation.