Yamamoto Y, Yin M J, Gaynor R B
Division of Hematology-Oncology, Department of Medicine, Harold Simmons Cancer Center, University of Texas Southwestern Medical Center, Dallas, Texas 75235-8594, USA.
Mol Cell Biol. 2000 May;20(10):3655-66. doi: 10.1128/MCB.20.10.3655-3666.2000.
Two related kinases, IkappaB kinase alpha (IKKalpha) and IKKbeta, phosphorylate the IkappaB proteins, leading to their degradation and the subsequent activation of gene expression by NF-kappaB. IKKbeta has a much higher level of kinase activity for the IkappaB proteins than does IKKalpha and is more critical than IKKalpha in modulating tumor necrosis factor alpha activation of the NF-kappaB pathway. These results indicate an important role for IKKbeta in activating the NF-kappaB pathway but leave open the question of the role of IKKalpha in regulating this pathway. In the current study, we demonstrate that IKKalpha directly phosphorylates IKKbeta. Moreover, IKKalpha either directly or indirectly enhances IKKbeta kinase activity for IkappaBalpha. Finally, transfection studies to analyze NF-kappaB-directed gene expression suggest that IKKalpha is upstream of IKKbeta in activating the NF-kappaB pathway. These results indicate that IKKalpha, in addition to its previously described ability to phosphorylate IkappaBalpha, can increase the ability of IKKbeta to phosphorylate IkappaBalpha.
两种相关激酶,即IκB激酶α(IKKα)和IKKβ,可使IκB蛋白磷酸化,导致其降解以及随后由核因子κB(NF-κB)激活基因表达。IKKβ对IκB蛋白的激酶活性水平比IKKα高得多,并且在调节NF-κB途径的肿瘤坏死因子α激活方面比IKKα更关键。这些结果表明IKKβ在激活NF-κB途径中起重要作用,但IKKα在调节该途径中的作用问题仍未解决。在当前研究中,我们证明IKKα直接使IKKβ磷酸化。此外,IKKα直接或间接增强IKKβ对IκBα的激酶活性。最后,用于分析NF-κB指导的基因表达的转染研究表明,在激活NF-κB途径中IKKα位于IKKβ的上游。这些结果表明,IKKα除了其先前描述的使IκBα磷酸化的能力外,还可以增强IKKβ使IκBα磷酸化的能力。