The PP2A-Associated Protein α4 Is an Essential Inhibitor of Apoptosis

Author:

Kong Mei12345,Fox Casey J.12345,Mu James12345,Solt Laura12345,Xu Anne12345,Cinalli Ryan M.12345,Birnbaum Morris J.12345,Lindsten Tullia12345,Thompson Craig B.12345

Affiliation:

1. Abramson Family Cancer Research Institute, University of Pennsylvania, Philadelphia, PA 19104, USA.

2. Howard Hughes Medical Institute, University of Pennsylvania, Philadelphia, PA 19104, USA.

3. Department of Cancer Biology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

4. Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

5. Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

Abstract

Despite evidence that protein kinases are regulators of apoptosis, a specific role for phosphatases in regulating cell survival has not been established. Here we show that α4, a noncatalytic subunit of protein phosphatase 2A (PP2A), is required to repress apoptosis in murine cells. α4 is a nonredundant regulator of the dephosphorylation of the transcription factors c-Jun and p53. As a result of α 4 deletion, multiple proapoptotic genes were transcribed. Either inhibition of new protein synthesis or Bcl-x L overexpression suppressed apoptosis initiated by α 4 deletion. Thus, mammalian cell viability depends on repression of transcription-initiated apoptosis mediated by a component of PP2A.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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