All three IκB isoforms and most Rel family members are stably associated with the IκB kinase 1/2 complex

• Published in: European journal of biochemistry Vol. 259; no. 1‐2; pp. 253 - 261
• Main Authors: Heilker, Ralf, Freuler, Felix, Pulfer, Ruth, Di Padova, Franco, Eder, Jörg
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Science Ltd 01.01.1999
• Subjects: casein kinase II; I^KB protein; Ik B; Ik B kinase; kinase±substrate complex; NF‐κ B; S6 kinase; tumor necrosis factor-^a
• ISSN: 0014-2956; 1432-1033
• DOI: 10.1046/j.1432-1327.1999.00028.x

Nuclear factor kappa B (NF‐κB) is an important transcription factor for the genes of many pro‐inflammatory proteins and is strongly activated by the cytokines interleukin‐1 and tumor necrosis factor (TNF)α under various pathological conditions. In nonstimulated cells, NF‐κB is present in the cytosol where it is complexed to its inhibitor IκB. Activation of NF‐κB depends on the signal‐induced phosphorylation of IκB by specific IκB kinases which initiates the inhibitor's conjugation to ubiquitin and subsequent degradation by the proteasome. We used both TNF‐stimulated and okadaic‐acid‐stimulated HeLa cells to purify three biochemically distinct kinase activities targeting one or both of the two serines (S32 and S36) in IκBα which induce its rapid degradation upon cytokine stimulation. All three activities correspond to known IκB kinases: the mitogen‐activated 90 kDa ribosomal S6 kinase (p90rsk1), the IκB kinase 1/2 complex (IKK1/2) and casein kinase II (CK II). However, we found that only one of the activities, namely the IKK1/2 complex, exists as a pre‐assembled kinase–substrate complex in which the IKKs are directly or indirectly associated with several NF‐κB‐related and IκB‐related proteins: RelA, RelB, cRel, p100, p105, IκBα, IκBβ and IκBε. The existence of stable kinase–substrate complexes, the presence of all three known IκB isoforms in these complexes and our observation that the IKK complex is capable of phosphorylating IκBα‐, IκBβ‐ and IκBε‐derived peptides at the respective degradation‐relevant serines suggests that the IKK complex exerts a broad regulatory role for the activation of different NF‐κB species.  In contrast to previous studies, which locate CK II phosphorylation sites exclusively to the C‐terminal PEST sequence of IκBα, we observed efficient phosphorylation of serine 32 in IκBα by the purified endogenous CK II complex. Therefore, both p90rsk1 and CK II have the same preference for phosphorylating only one of the two serines which are relevant for inducible degradation.