HTLV-I tax protein binds to MEKK1 to stimulate IκB kinase activity and NF-κB activation

被引:230
|
作者
Yin, MJ
Christerson, LB
Yamamoto, Y
Kwak, YT
Xu, SC
Mercurio, F
Barbosa, M
Cobb, MH
Gaynor, RB [1 ]
机构
[1] Univ Texas, SW Med Ctr, Dept Med, Div Hematol Oncol,Harold Simmons Canc Ctr, Dallas, TX 75235 USA
[2] Univ Texas, SW Med Ctr, Dept Pharmacol, Harold Simmons Canc Ctr,Div Hematol Oncol, Dallas, TX 75235 USA
[3] Signal Pharmaceut Inc, San Diego, CA 92121 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0092-8674(00)81447-6
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
NF-kappa B, a key regulator of the cellular inflammatory and immune response, is activated by the HTLV-I transforming and transactivating protein Tax. We show that Tax binds to the amino terminus of the protein kinase MEKK1, a component of an I kappa B kinase complex, and stimulates MEKK1 kinase activity. Tax expression increases the activity of I kappa B kinase 8 (IKK beta) to enhance phosphorylation of serine residues in I kappa B alpha that lead to its degradation. Dominant negative mutants of both IKK beta and MEKK1 prevent Tax activation of the NF-kappa B pathway. Furthermore, recombinant MEKK1 stimulates IKK beta phosphorylation of I kappa B alpha. Thus, Tax-mediated increases in NF-kappa B nuclear translocation result from direct interactions of Tax and MEKK1 leading to enhanced IKK beta phosphorylation of I kappa B alpha.
引用
收藏
页码:875 / 884
页数:10
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