Your browser doesn't support javascript.
loading
Nuclear role of I kappa B Kinase-gamma/NF-kappa B essential modulator (IKK gamma/NEMO) in NF-kappa B-dependent gene expression.
Verma, Udit N; Yamamoto, Yumi; Prajapati, Shashi; Gaynor, Richard B.
Affiliation
  • Verma UN; Division of Hematology-Oncology, Department of Medicine, University of Texas Southwestern Medical Center, Dallas, Texas 75390-8594, USA.
J Biol Chem ; 279(5): 3509-15, 2004 Jan 30.
Article in En | MEDLINE | ID: mdl-14597638
The I kappa B kinase (IKK) complex, which is composed of the two kinases IKK alpha and IKK beta and the regulatory subunit IKK gamma/nuclear factor-kappa B (NF-kappa B) essential modulator (NEMO), is important in the cytokine-induced activation of the NF-kappa B pathway. In addition to modulation of IKK activity, the NF-kappa B pathway is also regulated by other processes, including the nucleocytoplasmic shuttling of various components of this pathway and the post-translational modification of factors bound to NF-kappa B-dependent promoters. In this study, we explored the role of the nucleocytoplasmic shuttling of components of the IKK complex in the regulation of the NF-kappa B pathway. IKK gamma/NEMO was demonstrated to shuttle between the cytoplasm and the nucleus and to interact with the nuclear coactivator cAMP-responsive element-binding protein-binding protein (CBP). Using both in vitro and in vivo analysis, we demonstrated that IKK gamma/NEMO competed with p65 and IKK alpha for binding to the N terminus of CBP, inhibiting CBP-dependent transcriptional activation. These results indicate that, in addition to the key role of IKK gamma/NEMO in regulating cytokine-induced IKK activity, its ability to shuttle between the cytoplasm and the nucleus and to bind to CBP can lead to transcriptional repression of the NF-kappa B pathway.
Subject(s)
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Cell Nucleus / Protein Serine-Threonine Kinases Limits: Humans Language: En Journal: J Biol Chem Year: 2004 Document type: Article Affiliation country: United States Country of publication: United States
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Cell Nucleus / Protein Serine-Threonine Kinases Limits: Humans Language: En Journal: J Biol Chem Year: 2004 Document type: Article Affiliation country: United States Country of publication: United States