Takekawa M, Maeda T, Saito H
Dana-Farber Cancer Institute and Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
EMBO J. 1998 Aug 17;17(16):4744-52. doi: 10.1093/emboj/17.16.4744.
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 2Calpha (PP2Calpha) was found to negatively regulate the HOG1 pathway in yeast. Moreover, when expressed in mammalian cells, PP2Calpha inhibited the activation of the p38 and JNK cascades induced by environmental stresses. Both in vivo and in vitro observations indicated that PP2Calpha dephosphorylated and inactivated MAPKKs (MKK6 and SEK1) and a MAPK (p38) in the stress-responsive MAPK cascades. Furthermore, a direct interaction of PP2Calpha 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 PP2Calpha mutant was used, suggesting that only the phosphorylated form of p38 interacts with PP2Calpha.
丝裂原活化蛋白激酶(MAPK)级联反应是常见的真核信号传导模块,由一个MAPK、一个MAPK激酶(MAPKK)和一个MAPKK激酶(MAPKKK)组成。由于磷酸化对于MAPKK和MAPK的激活至关重要,蛋白磷酸酶很可能是通过MAPK级联反应进行信号传导的重要调节因子。为了鉴定对应激反应性p38和JNK MAPK级联反应起负调控作用的蛋白磷酸酶,我们利用一个超激活酵母突变体,在人cDNA文库中筛选下调酵母HOG1 MAPK途径(该途径与p38和JNK途径有相似性)的基因。在这个筛选过程中,发现人2Cα型蛋白磷酸酶(PP2Cα)对酵母中的HOG1途径起负调控作用。此外,当在哺乳动物细胞中表达时,PP2Cα抑制由环境应激诱导的p38和JNK级联反应的激活。体内和体外观察均表明,PP2Cα使应激反应性MAPK级联反应中的MAPKK(MKK6和SEK1)和一个MAPK(p38)去磷酸化并使其失活。此外,通过免疫共沉淀实验证明了PP2Cα与p38之间存在直接相互作用。仅在细胞受到应激刺激时或使用催化失活的PP2Cα突变体时才观察到这种相互作用,这表明只有磷酸化形式的p38与PP2Cα相互作用。