Premium
p53‐inducible Wip1 phosphatase mediates a negative feedback regulation of p38 MAPK‐p53 signaling in response to UV radiation
Author(s) -
Takekawa Mutsuhiro,
Adachi Masaaki,
Nakahata Atsuko,
Nakayama Ichiro,
Itoh Fumio,
Tsukuda Hiroyuki,
Taya Yoichi,
Imai Kohzoh
Publication year - 2000
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1093/emboj/19.23.6517
Subject(s) - biology , phosphatase , p38 mitogen activated protein kinases , mapk/erk pathway , microbiology and biotechnology , signal transduction , negative feedback , phosphorylation , physics , quantum mechanics , voltage
The stress‐responsive p38 MAPK, when activated by genotoxic stresses such as UV radiation, enhances p53 activity by phosphorylation and leads to cell cycle arrest or apoptosis. Here we report that a member of the protein phosphatase type 2C family, Wip1, has a role in down‐regulating p38‐p53 signaling during the recovery phase of the damaged cells. Wip1 was originally identified as a gene whose expression is induced following γ or UV radiation in a p53‐dependent manner. We found that Wip1 is also inducible by other environmental stresses, such as anisomycin, H 2 O 2 and methyl methane sulfonate. UV‐induction of Wip1 requires p38 activity in addition to the wild‐type p53. Wip1 selectively inactivates p38 by specific dephosphorylation of its conserved threonine residue. Furthermore, Wip1 expression attenuates UV‐induced p53 phosphorylation at Ser33 and Ser46, residues previously reported to be phosphorylated by p38. Wip1 expression also suppresses both p53‐mediated transcription and apoptosis in response to UV radiation. These results suggest that p53‐dependent expression of Wip1 mediates a negative feedback regulation of p38‐p53 signaling and contributes to suppression of the UV‐induced apoptosis.