Abstract

The c-Jun N-terminal kinase (JNK) signaling pathway plays a crucial role in cellular responses stimulated by stress-inducing agents and proinflammatory cytokines. The group I germinal center kinase family members selectively activate the JNK pathway. In this study, we have isolated a mouse cDNA encoding a protein kinase homologous to Nck-interacting kinase (NIK), a member of the group I germinal center kinase family. This protein kinase is expressed during the late stages of embryogenesis, but not in adult tissues, and thus named NESK (NIK-like embryo-specific kinase). NESK selectively activated the JNK pathway when overexpressed in HEK 293 cells but did not stimulate the p38 kinase or extracellular signal-regulated kinase (ERK) pathways. NESK-induced JNK activation was inhibited by the dominant negative mutants of MEKK1 and MKK4. Tumor necrosis factor (TNF)-alpha or TNF receptor-associated factor 2 (TRAF2) stimulated the NESK activity. Furthermore, the dominant negative NESK mutant inhibited the JNK activation induced by TNF-alpha or TRAF2. These results suggest that NESK, a novel activator of the JNK pathway, functions in coupling TRAF2 to the MEKK1 --> MKK4 --> JNK kinase cascade during the late stages of mammalian embryogenesis.

Highlights

  • The germinal center kinase (GCK)1 family is a subfamily of the Ste20 family of protein kinases [1]

  • These results suggest that NESK, a novel activator of the Jun N-terminal kinase (JNK) pathway, functions in coupling TNF receptor-associated factor 2 (TRAF2) to the MEKK1 3 MKK4 3 JNK kinase cascade during the late stages of mammalian embryogenesis

  • JNKs are activated through threonine and tyrosine phosphorylations by mitogen-activated protein kinase kinases such as MKK4 and MKK7, which are in turn phosphorylated and activated by mitogen-activated protein kinase kinase kinase, including MEKK1, mixed lineage kinase 2, and mixed lineage kinase 3 [18]

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Summary

Introduction

The germinal center kinase (GCK)1 family is a subfamily of the Ste20 family of protein kinases [1]. These results suggest that NESK, a novel activator of the JNK pathway, functions in coupling TRAF2 to the MEKK1 3 MKK4 3 JNK kinase cascade during the late stages of mammalian embryogenesis. We demonstrate in this report that NESK, like other group I GCK family members, can selectively activate the JNK pathway when overexpressed in HEK 293 cells.

Results
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