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Functional expression cloning reveals proapoptotic role for protein phosphatase 4

Mourtada-Maarabouni, M; Kirkham, L; Jenkins, B; Rayner, J; Gonda, T J; Starr, R; Trayner, I; Farzaneh, F; Williams, G T

Authors

L Kirkham

B Jenkins

J Rayner

T J Gonda

R Starr

I Trayner

F Farzaneh

G T Williams



Contributors

M. Mourtada-Maarabouni
Other

L. Kirkham
Other

B. Jenkins
Other

J. Rayner
Other

T.J. Gonda
Other

R. Starr
Other

I. Trayner
Other

F. Farzaneh
Other

G.T. Williams
Other

Abstract

Functional expression cloning strategies are highly suitable for the analysis of the molecular control of apoptosis. This approach has two critical advantages. Firstly, it eliminates prior assumptions about the properties of the proteins involved, and, secondly, it selectively targets proteins that are causally involved in apoptosis control and which affect the crucial cellular decision between survival and death. The application of this strategy to the isolation of cDNAs conferring resistance to dexamethasone and γ-irradiation resulted in the isolation of a partial cDNA for the catalytic subunit of protein phosphatase 4 (PP4). Cells transfected with this partial cDNA in an expression vector downregulated PP4 and were resistant to both dexamethasone and UV radiation, as demonstrated by both membrane integrity and colony-forming assays. These observations suggest that PP4 plays an important proapoptotic role in T lymphocytes.

Citation

Mourtada-Maarabouni, M., Kirkham, L., Jenkins, B., Rayner, J., Gonda, T. J., Starr, R., …Williams, G. T. (2003). Functional expression cloning reveals proapoptotic role for protein phosphatase 4. Cell Death and Differentiation, 10, Article 1016–1024. https://doi.org/10.1038/sj.cdd.4401274

Journal Article Type Article
Acceptance Date Apr 15, 2003
Online Publication Date Aug 22, 2003
Publication Date Sep 1, 2003
Deposit Date May 16, 2024
Journal Cell Death and Differentiation
Print ISSN 1350-9047
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 10
Article Number 1016–1024
ISBN 13509047
DOI https://doi.org/10.1038/sj.cdd.4401274
Public URL https://keele-repository.worktribe.com/output/543809
Publisher URL https://www.nature.com/articles/4401274