IKK-1 and IKK-2: cytokine-activated IkappaB kinases essential for NF-kappaB activation.

Journal:

Science 1997 Oct

Authors:

Mercurio F, Zhu H, Murray BW, Shevchenko A, Bennett BL, Li J, Young DB, Barbosa M, Mann M, Manning A, Rao A

Abstract

Activation of the transcription factor nuclear factor kappa B (NF-kappaB) is controlled by sequential phosphorylation, ubiquitination, and degradation of its inhibitory subunit IkappaB. A large multiprotein complex, the IkappaB kinase (IKK) signalsome, was purified from HeLa cells and found to contain a cytokine-inducible IkappaB kinase activity that phosphorylates IkappaB-alpha and IkappaB-beta. Two components of the IKK signalsome, IKK-1 and IKK-2, were identified as closely related protein se
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rine kinases containing leucine zipper and helix-loop-helix protein interaction motifs. Mutant versions of IKK-2 had pronounced effects on RelA nuclear translocation and NF-kappaB-dependent reporter activity, consistent with a critical role for the IKK kinases in the NF-kappaB signaling pathway.[less]

Mesh Headings:

Cell Cycle Proteins, Cloning, Molecular, Dual Specificity Phosphatase 1, Enzyme Activation, HeLa Cells, Helix-Loop-Helix Motifs, Humans, I-kappa B Kinase, Immediate-Early Proteins, Leucine Zippers, Molecular Sequence Data, NF-kappa B, Phosphoprotein Phosphatases, Phosphorylation, Protein Phosphatase 1, Protein Tyrosine Phosphatases, Protein-Serine-Threonine Kinases, Sequence Homology, Amino Acid, Substrate Specificity