Identification of NAP1, a regulatory subunit of IkappaB kinase-related kinases that potentiates NF-kappaB signaling

  • Mol Cell Biol. 2003 Nov;23(21):7780-93. doi: 10.1128/MCB.23.21.7780-7793.2003.
Fumitaka Fujita  1 ,  Yuko Taniguchi ,  Takashi Kato ,  Yasuko Narita ,  Akiko Furuya ,  Tatsuhiro Ogawa ,  Hiroaki Sakurai ,  Takashi Joh ,  Makoto Itoh ,  Mireille Delhase ,  Michael Karin ,  Makoto Nakanishi
Affiliations
  • 1. Department of Biochemistry and Cell Biology, Graduate School of Medicine, Nagoya City University, Mizuho-ku, Nagoya 467-8601, Japan.
Abstract

The IkappaB kinase (IKK)-related kinase NAK (also known as TBK or T2K) contributes to the activation of NF-kappaB-dependent gene expression. Here we identify NAP1 (for NAK-associated protein 1), a protein that interacts with NAK and its relative IKK epsilon (also known as IKKi). NAP1 activates NAK and facilitates its oligomerization. Interestingly, the NAK-NAP1 complex itself effectively phosphorylated serine 536 of the p65/RelA subunit of NF-kappaB, and this activity was stimulated by tumor necrosis factor Alpha (TNF-alpha). Overexpression of NAP1 specifically enhanced cytokine induction of an NF-kappaB-dependent, but not an AP-1-dependent, reporter. Depletion of NAP1 reduced NF-kappaB-dependent reporter gene expression and sensitized cells to TNF-alpha-induced Apoptosis. These results define NAP1 as an activator of IKK-related Kinases and suggest that the NAK-NAP1 complex may protect cells from TNF-alpha-induced Apoptosis by promoting NF-kappaB activation.