Regulation of apoptosis signal-regulating kinase 1 by protein phosphatase 2Cε

Jun Ichi Saito, Shinnosuke Toriumi, Kenjiro Awano, Hidenori Ichijo, Keiichi Sasaki, Takayasu Kobayashi, Shinri Tamura

研究成果: Article査読

35 被引用数 (Scopus)


ASK1 (apoptosis signal-regulating kinase 1), a MKKK (mitogen-activated protein kinase kinase kinase), is activated in response to cytotoxic stresses, such as H2O2 and TNFα (tumour necrosis factor α). ASK1 induction initiates a signalling cascade leading to apoptosis. After exposure of cells to H2O2, ASK1 is transiently activated by autophosphorylation at Thr845. The protein then associates with PP5 (protein serine/threonine phosphatase 5), which inactivates ASK1 by dephosphorylation of Thr845. Although this feedback regulation mechanism has been elucidated, it remains unclear how ASK1 is maintained in the dephosphorylated state under non-stressed conditions. In the present study, we have examined the possible role of PP2Cε (protein phosphatase 2Cε), a member of PP2C family, in the regulation of ASK1 signalling. Following expression in HEK-293 cells (human embryonic kidney cells), wild-type PP2Cε inhibited ASK1-induced activation of an AP-1 (activator protein 1) reporter gene. Conversely, a dominant-negative PP2Cε mutant enhanced AP-1 activity. Exogenous PP2Cε associated with exogenous ASK1 in HEK-293 cells under non-stressed conditions, inactivating ASK1 by decreasing Thr845 phosphorylation. The association of endogenous PP2Cε and ASK1 was also observed in mouse brain extracts. PP2Cε directly dephosphorylated ASK1 at Thr845 in vitro. In contrast with PP5, PP2Cε transiently dissociated from ASK 1 within cells upon H 2O2 treatment. These results suggest that PP2Cε maintains ASK1 in an inactive state by dephosphorylation in quiescent cells, supporting the possibility that PP2Cε and PP5 play different roles in H2O2-induced regulation of ASK1 activity.

ジャーナルBiochemical Journal
出版ステータスPublished - 2007 8 1

ASJC Scopus subject areas

  • 生化学
  • 分子生物学
  • 細胞生物学


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