NFκB Signaling Is Induced by the Oncoprotein Tio through Direct Interaction with TRAF6

• Published in: The Journal of biological chemistry 2006-03, Vol.281 (13), p.8565-8572
• Main Authors: Heinemann, Stefanie, Biesinger, Brigitte, Fleckenstein, Bernhard, Albrecht, Jens-Christian
• Format: Article
• Language: English
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M510891200

The transcription factor NFκB is a major regulator of genes involved in inflammation and oncogenesis. NFκB is induced upon stimulation of cellular receptors coupled to different intracellular signaling molecules. Further downstream, TRAF6 links at least two receptor pathways to take control of IκB, the administrator of NFκB activity. Here we report on a strong NFκB activation by Tio, a unique herpesviral oncoprotein promoting transformation of human T cells in a Src-kinase-dependent manner. NFκB induction by Tio is independent of Src-kinase interaction and tyrosine phosphorylation of Tio. Mutation of a glutamic acid-rich motif at the N terminus of Tio, corresponding to a TRAF6 consensus binding motif, completely abrogated NFκB activation. Cotransfection of a dominant negative TRAF6 construct led to a decrease in NFκB activation. Furthermore, we provide evidence that TRAF6 directly binds to the Tio oncoprotein. Identification of TRAF6 as the direct target of Tio describes a novel mechanism for the constitutive activation of NFκB through an oncoprotein.