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Identification of NAP1, a regulatory subunit of IκB kinase-related kinases that potentiates NF-κB signaling
被引:144
作者:
Fujita, F
Taniguchi, Y
Kato, T
Narita, Y
Furuya, A
Ogawa, T
Sakurai, H
Joh, T
Itoh, M
Delhase, M
Karin, M
Nakanishi, M
机构:
[1] Nagoya City Univ, Dept Biochem & Cell Biol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[2] Nagoya City Univ, Dept Med, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[3] Nagoya City Univ, Grad Sch Med, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[4] Kyowa Hakko Kogyo Co Ltd, Tokyo Res Labs, Machida, Tokyo 1948533, Japan
[5] Toyama Med & Pharmaceut Univ, Inst Nat Med, Dept Pathogen Biochem, Sugitani, Toyama 9300194, Japan
[6] Univ Calif San Diego, Sch Med, Dept Pharmacol, Lab Gene Regulat & Signal Transduct, La Jolla, CA 92093 USA
关键词:
D O I:
10.1128/MCB.23.21.7780-7793.2003
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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 IKKepsilon (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.
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页码:7780 / 7793
页数:14
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