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Identification of an Activator of the Microtubule‐Associated Protein 2 Kinases ERK1 and ERK2 in PC12 Cells Stimulated with Nerve Growth Factor or Bradykinin
Author(s) -
Ahn Natalie G.,
Robbins David J.,
Haycock John W.,
Seger Rony,
Cobb Melanie H.,
Krebs Edwin G.
Publication year - 1992
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.1992.tb08885.x
Subject(s) - activator (genetics) , kinase , bradykinin , nerve growth factor , microtubule , mitogen activated protein kinase , microbiology and biotechnology , mapk/erk pathway , identification (biology) , neuroscience , chemistry , biology , biochemistry , gene , receptor , botany
Treatment of PC12 pheochromocytoma cells with nerve growth factor (NGF) or bradykinin leads to the activation of extracellular signal‐regulated kinases ERK1 and ERK2, two isozymes of microtubule‐associated protein 2 (MAP) kinase that are present in numerous cell lines and regulated by diverse extracellular signals. The activation of MAP kinase is associated with its phosphorylation on tyro‐sine and threonine residues, both of which are required for activity. In the present studies, we have identified a factor in extracts of PC12 cells treated with NGF or bradykinin, named MAP kinase activator, that, when reconstituted with inactive MAP kinase from untreated cells, dramatically increased MAP kinase activity. Activation of MAP kinase in vitro by this factor required MgATP and was associated with the phosphorylation of a 42‐ (ERK1) and 44‐kDa (ERK2) polypeptide. Incorporation of 32 P into ERK1 and ERK2 occurred primarily on tyrosine and threonine residues and was associated with a single tryptic peptide, which is identical to one whose phosphorylation is increased by treatment of intact PC12 cells with NGF. Thus, the MAP kinase activator identified in PC12 cells is likely to be a physiologically important intermediate in the signaling pathways activated by NGF and bradykinin. Moreover, stimulation of the activator by NGF and bradykinin suggests that tyrosine kinase receptors and guanine nucleotide‐binding protein‐coupled receptors are both capable of regulating these pathways.