THE ADENOVIRUS E1A REPRESSION DOMAIN DISRUPTS THE INTERACTION BETWEENTHE TATA-BINDING PROTEIN AND THE TATA BOX IN A MANNER REVERSIBLE BY TFIIB

The human adenovirus E1A 243 amino acid oncoprotein possesses a transc ription repression function that appears to be linked with its ability to induce cell cycle progression and to inhibit cell differentiation. The molecular mechanism of E1A repression has been poorly understood. Recently, we reported that the TATA binding protein (TBP) is a cellul ar target of E1A repression, Here we demonstrate that the interaction between TBP and the E1A repression domain is direct and specific, The TBP binding domain within E1A 243R maps to E1A N-terminal residues sim ilar to 1 to 35 and is distinct from the TBP binding domain within con served region 3 unique to the E1A 289R transactivator. An E1A protein fragment consisting of only the EIA N-terminal 80 amino acids (E1A 1-8 0) and containing the E1A repression function was found to block the i nteraction between TBP and the TATA box element as shown by gel mobili ty and DNase protection analysis. Interestingly, a preformed TBP-TATA box promoter complex can be dissociated by E1A 1-80. Further, TFIIB ca n prevent E1A disruption of TBP-TATA box interaction. TFIIB, like TBP, can overcome EIA repression of transcription in vitro. The ability of the E1A repression domain to block TBP interaction with the TATA box and the ability of TFIIB to reverse E1A disruption of the TBP-TATA box complex implies a mechanism for E1A repression distinct from those of known cellular repressors that target TBP.