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 alpha4, a noncatalytic subunit of protein phosphatase 2A (PP2A), is required to repress apoptosis in murine cells. alpha4 is a nonredundant regulator of the dephosphorylation of the transcription factors c-Jun and p53. As a result of alpha4 deletion, multiple proapoptotic genes were transcribed. Either inhibition of new protein synthesis or Bcl-xL overexpression suppressed apoptosis initiated by alpha4 deletion. Thus, mammalian cell viability depends on repression of transcription-initiated apoptosis mediated by a component of PP2A.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Adaptor Proteins, Signal Transducing
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Adipocytes / cytology
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Animals
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Apoptosis*
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Cell Differentiation
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Cell Line
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Cell Survival
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Cells, Cultured
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Cycloheximide / pharmacology
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Gene Deletion
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Gene Expression Profiling
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Intercellular Signaling Peptides and Proteins
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Liver / cytology
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Liver / metabolism
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Mice
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Mice, Transgenic
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Molecular Chaperones
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Oligonucleotide Array Sequence Analysis
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PPAR gamma / metabolism
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Phosphoprotein Phosphatases / metabolism*
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Phosphoproteins / metabolism*
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Phosphorylation
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Protein Phosphatase 2
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Protein Synthesis Inhibitors / pharmacology
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Proto-Oncogene Proteins c-bcl-2 / metabolism
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Proto-Oncogene Proteins c-jun / metabolism
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Transcription, Genetic
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Tumor Suppressor Protein p53 / metabolism
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bcl-X Protein
Substances
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Adaptor Proteins, Signal Transducing
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Bcl2l1 protein, mouse
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Igbp1 protein, mouse
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Intercellular Signaling Peptides and Proteins
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Molecular Chaperones
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PPAR gamma
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Phosphoproteins
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Protein Synthesis Inhibitors
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Proto-Oncogene Proteins c-bcl-2
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Proto-Oncogene Proteins c-jun
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Tumor Suppressor Protein p53
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bcl-X Protein
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Cycloheximide
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Phosphoprotein Phosphatases
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Protein Phosphatase 2