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NAK is an IκB kinase-activating kinase

Author

Listed:
  • Yuichiro Tojima

    (Department of Geriatric Research National Institute for Longevity Sciences
    Nagoya University Medical School)

  • Atsushi Fujimoto

    (Department of Geriatric Research National Institute for Longevity Sciences)

  • Mireille Delhase

    (Laboratory of Gene Regulation and Signal Transduction, University of California San Diego, School of Medicine)

  • Yi Chen

    (Laboratory of Gene Regulation and Signal Transduction, University of California San Diego, School of Medicine)

  • Shigetsugu Hatakeyama

    (Medical Institue of Bioregulation, Kyusyu University
    CREST of Japan Science and Technology Corporation (JST))

  • Kei-ichi Nakayama

    (Medical Institue of Bioregulation, Kyusyu University
    CREST of Japan Science and Technology Corporation (JST))

  • Yoko Kaneko

    (Department of Geriatric Research National Institute for Longevity Sciences)

  • Yuji Nimura

    (Nagoya University Medical School)

  • Noboru Motoyama

    (Department of Geriatric Research National Institute for Longevity Sciences)

  • Kyoji Ikeda

    (Department of Geriatric Research National Institute for Longevity Sciences)

  • Michael Karin

    (Laboratory of Gene Regulation and Signal Transduction, University of California San Diego, School of Medicine)

  • Makoto Nakanishi

    (Department of Geriatric Research National Institute for Longevity Sciences
    Nagoya City University Medical School)

Abstract

Phosphorylation of IκB by the IκB kinase (IKK) complex is a critical step leading to IκB degradation and activation of transcription factor NF-κB1. The IKK complex contains two catalytic subunits, IKKα and IKKβ, the latter being indispensable for NF-κB activation by pro-inflammatory cytokines2,3,4,5,6,7. Although IKK is activated by phosphorylation of the IKKβ activation loop8, the physiological IKK kinases that mediate responses to extracellular stimuli remain obscure1,9. Here we describe an IKK-related kinase, named NAK (NF-κB-activating kinase), that can activate IKK through direct phosphorylation. NAK induces IκB degradation and NF-κB activity through IKKβ. Endogenous NAK is activated by phorbol ester tumour promoters and growth factors, whereas catalytically inactive NAK specifically inhibits activation of NF-κB by protein kinase C-ε (PKCε). Thus, NAK is an IKK kinase that may mediate IKK and NF-κB activation in response to growth factors that stimulate PKCε activity.

Suggested Citation

  • Yuichiro Tojima & Atsushi Fujimoto & Mireille Delhase & Yi Chen & Shigetsugu Hatakeyama & Kei-ichi Nakayama & Yoko Kaneko & Yuji Nimura & Noboru Motoyama & Kyoji Ikeda & Michael Karin & Makoto Nakanis, 2000. "NAK is an IκB kinase-activating kinase," Nature, Nature, vol. 404(6779), pages 778-782, April.
  • Handle: RePEc:nat:nature:v:404:y:2000:i:6779:d:10.1038_35008109
    DOI: 10.1038/35008109
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