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PMID: 16079158 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Puckered, a Drosophila MAPK phosphatase, ensures cell viability by antagonizing JNK-induced apoptosis.

Development (Cambridge, England) ·Vol. 132 ·No. 17 ·2005-09-00 ·Pages 3935-46

McEwen DG, Peifer M

Abstract

MAPK phosphatases (MKPs) are important negative regulators of MAPKs in vivo, but ascertaining the role of specific MKPs is hindered by functional redundancy in vertebrates. Thus, we characterized MKP function by examining the function of Puckered (Puc), the sole Drosophila Jun N-terminal kinase (JNK)-specific MKP, during embryonic and imaginal disc development. We demonstrate that Puc is a key anti-apoptotic factor that prevents apoptosis in epithelial cells by restraining basal JNK signaling. Furthermore, we demonstrate that JNK signaling plays an important role in gamma-irradiation-induced apoptosis, and examine how JNK signaling fits into the circuitry regulating this process. Radiation upregulates both JNK activity and puc expression in a p53-dependent manner, and apoptosis induced by loss of Puc can be suppressed by p53 inactivation. JNK signaling acts upstream of both Reaper and effector caspases. Finally, we demonstrate that JNK signaling directs normal developmentally regulated apoptotic events. However, if cell death is prevented, JNK activation can trigger tissue overgrowth. Thus, MKPs are key regulators of the delicate balance between proliferation, differentiation and apoptosis during development.

MeSH Terms
Animals Apoptosis/radiation effects Cell Survival Drosophila Proteins/genetics,metabolism Drosophila melanogaster/cytology,embryology,enzymology,growth & development Gene Expression Regulation, Developmental/radiation effects JNK Mitogen-Activated Protein Kinases/antagonists & inhibitors,genetics,metabolism MAP Kinase Signaling System Phosphoprotein Phosphatases/genetics,metabolism Tumor Suppressor Protein p53/genetics,metabolism
Chemicals
Drosophila Proteins Tumor Suppressor Protein p53 rpr protein, Drosophila JNK Mitogen-Activated Protein Kinases puc protein, Drosophila Phosphoprotein Phosphatases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
McEwen Donald G
Lineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA. mcewen@uthscsa.edu
Peifer Mark
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
2005-09-00
Epub
2005-00-03
Pages
3935-46
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NIGMS NIH HHS · 1F32GM19824 · United States
NIGMS NIH HHS · GM47857 · United States
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