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Volume 271, Number 34, Issue of August 23, 1996 pp. 20853-20860
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.

The Ability of the Inhibitory Domain of the POU Family Transcription Factor Oct-2 to Interfere with Promoter Activation by Different Classes of Activation Domains Is Dependent upon the Nature of the Basal Promoter Elements

(Received for publication, November 10, 1995, and in revised form, May 24, 1996)

Yu-Zhen Liu Dagger , Sally J. Dawson Dagger , Thomas Gerster , Erica Friedl par , Gina Pengue '' , Patrick Matthias par , Luigi Lania '' and David S. Latchman Dagger

From the Dagger  Department of Molecular Pathology, University College London Medical School, The Windeyer Building, Cleveland Street, London W1P 6DB, United Kingdom,  Biozentrum der Universität Basel, CH-4056 Basel, Switzerland, par  Friedrich Miescher-Institut, CH-4002 Basel, Switzerland and '' Dipartimento di Genetica, Universita Federico II, 80134 Naples, Italy

The Oct-2 transcription factor contains an inhibitory domain which is able to repress transcription following DNA binding. Here we show that within the neuronally expressed Oct-2.5 form, the inhibitory domain can strongly inhibit activation by transcription factor activation domains which are either composed predominantly of acidic residues or contain the HOB motif, whereas it has a weaker effect or no effect on proline-rich activation domains and on a glutamine-rich domain. In contrast, the isolated inhibitory domain of Oct-2 can efficiently repress all types of activation domains. This effect is observed however, only on TATA box-containing promoters and not on promoters containing an initiator motif. This widespread inhibition of different activation domains and its dependence on the nature of the basal promoter elements indicate that the inhibitory domain is likely to act by contacting a common downstream target of activation domains within the basal transcriptional complex bound at the TATA box rather than quenching specific activation domains by direct interaction. These effects are discussed in terms of the functional role of the inhibitory domain within Oct-2.5 and the mechanism by which it acts.


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