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Activation of the heterodimeric IκB kinase α (IKKα)-IKKβ complex is directional:: IKKα regulates IKKβ under both basal and stimulated conditions
被引:99
作者:
O'Mahony, A
Lin, X
Geleziunas, R
Greene, WC
机构:
[1] Univ Calif San Francisco, Gladstone Inst Cardiovasc Dis, San Francisco, CA 94141 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94141 USA
[3] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94141 USA
关键词:
D O I:
10.1128/MCB.20.4.1170-1178.2000
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:
Signal-induced nuclear expression of the eukaryotic NF-kappa B transcription factor involves the stimulatory action of select mitogen-activated protein kinase kinase kinases on the I kappa B kinases (IKK alpha and IKK beta) which reside in a macromolecular signaling complex termed the signalsome. While genetic studies indicate that IKK beta is the principal kinase involved in proinflammatory cytokine-induced I kappa B phosphorylation, the function of the equivalently expressed IKK alpha is less clear. Here we demonstrate that assembly of IKK alpha with IKK beta in the heterodimeric signalsome serves two important functions: (i) in unstimulated cells, IKK alpha inhibits the constitutive I kappa B kinase activity of IKK beta; (ii) in activated cells, IKK alpha kinase activity is required for the induction of IKK beta. The introduction of kinase-inactive IKK alpha, activation loop mutants of IKK alpha, or IKK alpha antisense RNA into 293 or HeLa cells blocks NIK (NF-kappa B-inducing kinase)-induced phosphorylation of the IKK beta activation loop occurring in functional signalsomes. In contrast, catalytically inactive mutants of IKK beta do not block NIK-mediated phosphorylation of IKK alpha in these macromolecular signaling complexes. This requirement for kinase-proficient IKK alpha to activate IKK beta in heterodimeric IKK signalsomes is also observed with other NF-kappa B inducers, including tumor necrosis factor alpha, human T-cell leukemia virus type 1 Tax, Cot, and MEKK1. Conversely, the theta isoform of protein kinase C, which also induces NF-kappa B/Rel, directly targets IKK beta for phosphorylation and activation, possibly acting through homodimeric IKK beta complexes. Together, our findings indicate that activation of the heterodimeric IKK complex by a variety of different inducers proceeds in a directional manner and is dependent on the kinase activity of IKK alpha to activate IKK beta.
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页码:1170 / 1178
页数:9
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