Analysis of CREB mutants in Tax complex formation and trans-activation

• Published in: AIDS research and human retroviruses Vol. 16; no. 16; p. 1597
• Main Authors: Mick, J E, Colgin, M A, Brauweiler, A, Nyborg, J K
• Format: Journal Article
• Language: English
• Published: United States 01.11.2000
• Subjects: CREB-Binding Protein; Cyclic AMP Response Element-Binding Protein - genetics; Cyclic AMP Response Element-Binding Protein - metabolism; Gene Deletion; Gene Products, tax - genetics; Gene Products, tax - metabolism; Human T-lymphotropic virus 1 - genetics; Human T-lymphotropic virus 1 - metabolism; Humans; Nuclear Proteins - metabolism; Trans-Activators - metabolism; Transcriptional Activation; Transfection; Tumor Cells, Cultured
• ISSN: 0889-2229; 1931-8405
• DOI: 10.1089/08892220050193010

The human T cell leukemia virus type 1 (HTLV-1) oncoprotein Tax interacts with cellular transcription factors to facilitate viral replication in infected cells. Tax binds to the cellular transcription factor CREB and the cellular coactivator protein CBP to form a stable nucleoprotein complex on the viral enhancer elements. The formation of this complex is believed to promote strong Tax-dependent transcriptional activation of viral gene expression. In this study, we characterize a series of internal CREB deletion mutants with respect to Tax and CBP recruitment and transcriptional activation. We find that, although several of these mutants are unable to support ternary complex formation with Tax and the viral CRE DNA, they are fully competent for cooperation with Tax in CBP recruitment. Unexpectedly, CREB proteins that carry deletions in a carboxyterminal region of the KID domain, while competent for ternary and quaternary complex formation, were defective for Tax trans-activation in vivo. These studies suggest that CREB may serve more than just a "scaffolding" role in Tax trans-activation, cooperating directly with Tax (and CBP) to mediate strong transcriptional activation of the provirus.