Complementation cloning of NEMO, a component of the IκB kinase complex essential for NF-κB activation

被引:926
作者
Yamaoka, S
Courtois, G
Bessia, C
Whiteside, ST
Weil, R
Agou, F
Kirk, HE
Kay, RJ
Israël, A
机构
[1] Inst Pasteur, Unite Biol Mol Express Gen, CNRS, URA 1773, F-75724 Paris 15, France
[2] Inst Pasteur, Unite Regulat Enzymat Act Cellulaires, CNRS, URA 1773, F-75724 Paris, France
[3] British Columbia Canc Agcy, Terry Fox Lab, Vancouver, BC V5Z 4E6, Canada
[4] Kyoto Univ, Inst Virus Res, Sakyo Ku, Kyoto 606, Japan
基金
英国医学研究理事会;
关键词
D O I
10.1016/S0092-8674(00)81466-X
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
We have characterized a flat cellular variant of HTLV-1 Tax-transformed rat fibroblasts, 5R, which is unresponsive to all tested NF-kappa B activating stimuli, and we report here its genetic complementation. The recovered full-length cDNA encodes a 48 kDa protein, NEMO (NF-kappa B Essential MOdulator), which contains a putative leucine zipper motif. This protein is absent from 5R cells, is part of the high molecular weight I kappa B kinase complex, and is required for its formation. In vitro, NEMO can homodimerize and directly interacts with IKK-2. The NEMO cDNA was also able to complement another NF-kappa B-unresponsive cell line, 1.3E2, in which the protein is also absent, allowing us to demonstrate that this factor is required not only for Tax but also for LPS, PMA, and IL-1 stimulation of NF-kappa B activity.
引用
收藏
页码:1231 / 1240
页数:10
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