
IκB kinase all zipped up | Nature
- Select a language for the TTS:
- UK English Female
- UK English Male
- US English Female
- US English Male
- Australian Female
- Australian Male
- Language selected: (auto detect) - EN
Play all audios:

Access through your institution Buy or subscribe Even before the first member of the NF-κB family was cloned, it was recognized that the association of IκB with NF-κB is controlled by
phosphorylation, and thus the search for the protein kinase responsible began. On page 548of this issue3, DiDonato_et al_. report the purification and cloning of a cytokine-responsive IκB
kinase which might put an end to this long and frustrating search. In 1990, Ghosh and Baltimore4 demonstrated that treatment of a partially purified NF-κB/IκB complex by certain kinases
could induce dissociation of the complex and activation of NF-κB DNA-binding activity. Cloning5 of the complementary DNA encoding IκBα, one of the three forms of IκB now known, then
stimulated an intense burst of research which to some extent clarified the signalling events. In response to extracellular stimuli, the IκBα molecule becomes phosphorylated by a
serine-specific kinase at positions 32 and 36. This phosphorylation in turn induces polyubiquitination of the molecule, which targets it for rapid degradation (and not for dissociation from
NF-κB, as originally postulated)2. This is a preview of subscription content, access via your institution ACCESS OPTIONS Access through your institution Subscribe to this journal Receive 51
print issues and online access $199.00 per year only $3.90 per issue Learn more Buy this article * Purchase on SpringerLink * Instant access to full article PDF Buy now Prices may be subject
to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our FAQs * Contact customer support REFERENCES *
Sen, R. & Baltimore, D. _Cell_ 47, 921–928 (1986). Google Scholar * Baldwin, A. S. _Annu. Rev. Immunol_. 14, 649–683 (1996). Google Scholar * DiDonato, J. A., Hayakawa, M., Rothwarf,
D. M., Zandi, E. & Karin, M. _Nature_ 388, 548–554 (1997). Article ADS CAS Google Scholar * Ghosh, S. & Baltimore, D. _Nature_ 344, 678–682 (1990). Article ADS CAS Google
Scholar * Haskill, S._et al._ _Cell_ 65, 1281–1289 (1991). Google Scholar * Chen, Z. J., Parent, L. & Maniatis, T. _Cell_ 84, 853–862 (1996). Google Scholar * Lee, F. S., Hagler, J.,
Chen, Z. J. & Maniatis, T. _Cell_ 88, 213–222 (1997). Google Scholar * Connelly, M. A. & Marcu, K. B. _Cell. Mol. Biol. Res._ 41, 537–549 (1995). Google Scholar * Thompson, J. E.,
Phillips, R. J., Erdjument-Bromage, H., Tempst, P. & Ghosh, S. _Cell_ 80, 573–582 (1995). Google Scholar * Choi, K. Y., Satterberg, B., Lyons, D. M. & Elion, E. A. _Cell_ 78,
499–512 (1994). Google Scholar * Schouten, G. J._et al._ _EMBO J._ 16, 3133–3144 (1997). Google Scholar Download references AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Unité de Biologie
Molculaire de l'Expression Gnique, UMR 321 CNRS, Institut Pasteur, 25 rue du Dr Roux, Paris, 75724 Cedex 15, France Alain Israë Authors * Alain Israë View author publications You can
also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Israë, A. IκB kinase all zipped up. _Nature_ 388,
520–521 (1997). https://doi.org/10.1038/41433 Download citation * Issue Date: 07 August 1997 * DOI: https://doi.org/10.1038/41433 SHARE THIS ARTICLE Anyone you share the following link with
will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt
content-sharing initiative