Abstract

NF-κB plays an important role in oncogenesis. Recently, we have demonstrated that loss of p53 function enhances DNA binding and transcriptional activities of NF-κB via IKKα and IKKβ, and that glycolysis, activated by NF-κB, has an integral role in oncogene-induced cell transformation. Here, we show that ectopically expressed p53 induces acetylation and phosphorylation at Ser 536 of p65, an NF-κB component, and enhances DNA-binding activity of NF-κB. However, activated p53 suppresses transcriptional activity of NF-κB. Under non-stimulating conditions, p65 formed a complex with IKKα and IKKβ. Activated p53 bound to p65 on DNA and disrupted binding of p65 to IKKβ. Moreover, histone H3 kinase activity, which requires transcriptional activation of NF-κB, was diminished by p53. Thus, activated p53 may suppress transcriptional activity of NF-κB through inhibition of IKK and histone H3 kinase on DNA, suggesting a novel p53-mediated suppression system for tumorigenesis.

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