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Protein phosphatase 2Cα inhibits the human stress‐responsive p38 and JNK MAPK pathways
Author(s) -
Takekawa Mutsuhiro,
Maeda Tatsuya,
Saito Haruo
Publication year - 1998
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/17.16.4744
Subject(s) - mapk/erk pathway , biology , phosphatase , p38 mitogen activated protein kinases , protein kinase a , microbiology and biotechnology , phosphorylation , kinase , dual specificity phosphatase , map kinase kinase kinase , signal transduction , mitogen activated protein kinase kinase , dusp6 , mitogen activated protein kinase , c raf , protein phosphatase 1 , protein phosphatase 2
MAPK (mitogen‐activated protein kinase) cascades are common eukaryotic signaling modules that consist of a MAPK, a MAPK kinase (MAPKK) and a MAPKK kinase (MAPKKK). Because phosphorylation is essential for the activation of both MAPKKs and MAPKs, protein phosphatases are likely to be important regulators of signaling through MAPK cascades. To identify protein phosphatases that negatively regulate the stress‐responsive p38 and JNK MAPK cascades, we screened human cDNA libraries for genes that down‐regulated the yeast HOG1 MAPK pathway, which shares similarities with the p38 and JNK pathways, using a hyperactivating yeast mutant. In this screen, the human protein phosphatase type 2Cα (PP2Cα) was found to negatively regulate the HOG1 pathway in yeast. Moreover, when expressed in mammalian cells, PP2Cα inhibited the activation of the p38 and JNK cascades induced by environmental stresses. Both in vivo and in vitro observations indicated that PP2Cα dephosphorylated and inactivated MAPKKs (MKK6 and SEK1) and a MAPK (p38) in the stress‐responsive MAPK cascades. Furthermore, a direct interaction of PP2Cα and p38 was demonstrated by a co‐immunoprecipitation assay. This interaction was observed only when cells were stimulated with stresses or when a catalytically inactive PP2Cα mutant was used, suggesting that only the phosphorylated form of p38 interacts with PP2Cα.