Abstract
ONE of the important regulatory concepts to emerge from studies of eukaryotic gene expression is that RNA polymerase II promo-ters and their upstream activators are composed of functional mod-ules whose synergistic action regulates the transcriptional activity of a nearby gene1-3. Biochemical analysis of synergy by ZEBRA, a non-acidic activator of the Epstein-Barr virus (EBV) lytic cycle4, showed that the synergistic transcriptional effect of promoter sites and activation modules correlates with assembly of the TFIID: TFIIA (DA) complex in DNase I footprinting and gel shift assays. The activator-dependent DA complex differs from a basal DA complex by its ability to bind TFIIB stably in an interaction regulated by TATA-binding protein-associated factors (TAFs). TFIIB enhances the degree of synergism by increasing complex stability. Similar findings were made with the acidic activator GAL4-VP16. Our data suggest a unifying mechanism for gene t To whom correspondence should be addressed. 254 activation and synergy by acidic and non-acidic activators, and indicate that synergy is manifested at the earliest stage of preinitia-tion complex assembly.
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Chi, T., Lieberman, P., Ellwood, K. et al. A general mechanism for transcriptional synergy by eukaryotic activators. Nature 377, 254–257 (1995). https://doi.org/10.1038/377254a0
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DOI: https://doi.org/10.1038/377254a0
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