Differential regulation of IκB kinase α and β by two upstream kinases, NF-κB-inducing kinase and mitogen-activated protein kinase/ERK kinase kinase-1
0301 basic medicine
DNA, Complementary
Molecular Sequence Data
Gene Transfer Techniques
MAP Kinase Kinase Kinase 1
Protein Serine-Threonine Kinases
Protein-Tyrosine Kinases
Gene Expression Regulation, Enzymologic
Cell Line
I-kappa B Kinase
Enzyme Activation
Mice
03 medical and health sciences
NF-kappaB-Inducing Kinase
Animals
Humans
Amino Acid Sequence
Sequence Alignment
Signal Transduction
DOI:
10.1073/pnas.95.7.3537
Publication Date:
2002-07-26T14:42:40Z
AUTHORS (7)
ABSTRACT
NF-κB is activated by various stimuli including inflammatory cytokines and stresses. A key step in the activation of NF-κB is the phosphorylation of its inhibitors, IκBs, by an IκB kinase (IKK) complex. Recently, two closely related kinases, designated IKKα and IKKβ, have been identified to be the components of the IKK complex that phosphorylate critical serine residues of IκBs for degradation. A previously identified NF-κB-inducing kinase (NIK), which mediates NF-κB activation by TNFα and IL-1, has been demonstrated to activate IKKα. Previous studies showed that mitogen-activated protein kinase/ERK kinase kinase-1 (MEKK1), which constitutes the c-Jun N-terminal kinase/stress-activated protein kinase pathway, also activates NF-κB by an undefined mechanism. Here, we show that overexpression of MEKK1 preferentially stimulates the kinase activity of IKKβ, which resulted in phosphorylation of IκBs. Moreover, a catalytically inactive mutant of IKKβ blocked the MEKK1-induced NF-κB activation. By contrast, overexpression of NIK stimulates kinase activities of both IKKα and IKKβ comparably, suggesting a qualitative difference between NIK- and MEKK1-mediated NF-κB activation pathways. Collectively, these results indicate that NIK and MEKK1 independently activate the IKK complex and that the kinase activities of IKKα and IKKβ are differentially regulated by two upstream kinases, NIK and MEKK1, which are responsive to distinct stimuli.
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