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Updated: Jul 13, 2026

Identification of Intracellular Signaling Events Induced in Viable Cells by Interaction with Neighboring Cells Undergoing Apoptotic Cell Death
Published on: December 27, 2016
The PP2A-associated protein alpha4 is an essential inhibitor of apoptosis
Mei Kong1, Casey J Fox, James Mu
1Abramson Family Cancer Research Institute, University of Pennsylvania, 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 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.
Insights
The protein phosphatase 2A (PP2A) subunit alpha4 is crucial for cell survival by repressing apoptosis. Its absence triggers proapoptotic gene transcription, highlighting PP2A
Area of Science:
- Cell biology
- Molecular biology
- Biochemistry
Background:
- Protein kinases are known regulators of apoptosis (programmed cell death).
- The specific role of phosphatases in regulating cell survival remained unclear.
- Protein Phosphatase 2A (PP2A) is a key enzyme involved in various cellular processes.
Purpose of the Study:
- To investigate the role of phosphatases, specifically PP2A, in regulating cell survival.
- To determine if PP2A subunits are involved in controlling apoptosis.
Main Methods:
- Deletion of the alpha4 subunit of PP2A in murine cells.
- Analysis of transcription factors c-Jun and p53 dephosphorylation.
- Gene expression analysis to identify transcribed proapoptotic genes.
- Experiments involving inhibition of protein synthesis and Bcl-xL overexpression.
Main Results:
- The alpha4 subunit of PP2A is essential for repressing apoptosis in murine cells.
- Alpha4 regulates the dephosphorylation of transcription factors c-Jun and p53.
- Alpha4 deletion leads to the transcription of multiple proapoptotic genes.
- Inhibition of protein synthesis or Bcl-xL overexpression counteracted alpha4 deletion-induced apoptosis.
Conclusions:
- Mammalian cell viability is dependent on the repression of transcription-initiated apoptosis.
- A component of PP2A, the alpha4 subunit, plays a critical role in this repression.
- This study establishes a specific role for phosphatases in regulating cell survival.
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