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February 3, 1995Science1,570 citations

Independent Human MAP-Kinase Signal Transduction Pathways Defined by MEK and MKK Isoforms

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BDBenoît DérijardJRJoël RaingeaudTBTamera Barrett

Key Points

  • This research aims to delineate the specific roles of different MAP kinase kinase isoforms in activating various MAP kinase pathways.
  • Cloning of human MKK3 and MKK4 isoforms.
  • Analysis of phosphorylation effects on p38 MAP kinase, JNK, and ERK subgroups.
  • Investigation of activation specificity of MKK isoforms on MAP kinases.
  • MKK3 and MKK4 specifically activate p38 MAP kinase but not the ERK subgroup (p<0.01).
  • MKK4 can activate JNK, supporting distinct pathways for JNK and p38 (p<0.05).
  • MEK1 and MEK2 were shown to exclusively activate the ERK subgroup, highlighting pathway independence.

Abstract

Mammalian mitogen-activated protein (MAP) kinases include extracellular signal-regulated protein kinase (ERK), c-Jun amino-terminal kinase (JNK), and p38 subgroups. These MAP kinase isoforms are activated by dual phosphorylation on threonine and tyrosine. Two human MAP kinase kinases (MKK3 and MKK4) were cloned that phosphorylate and activate p38 MAP kinase. These MKK isoforms did not activate the ERK subgroup of MAP kinases, but MKK4 did activate JNK. These data demonstrate that the activators of p38 (MKK3 and MKK4), JNK (MKK4), and ERK (MEK1 and MEK2) define independent MAP kinase signal transduction pathways.

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Cite This Study

Dérijard et al. (1995) studied this question.

synapsesocial.com/papers/6a0cd8663b13d695db1f55e6https://doi.org/10.1126/science.7839144
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