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Molecular and Cellular Biology, November 2005, p. 10159-10170, Vol. 25, No. 22
0270-7306/05/$08.00+0     doi:10.1128/MCB.25.22.10159-10170.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Enhanceosome Formation over the Beta Interferon Promoter Underlies a Remote-Control Mechanism Mediated by YY1 and YY2

Martin Klar and Juergen Bode*

German Research Centre for Biotechnology (GBF), 38124 Braunschweig, Germany

Received 29 April 2005/ Returned for modification 30 May 2005/ Accepted 16 August 2005

The expression of beta interferon genes from humans and mice is under the immediate control of a virus-responsive element (VRE) that terminates 110 bp upstream from the transcriptional start site. Whereas a wealth of information is available for the enhanceosome that is formed on the VRE upon the signals generated by viral infection, early observations indicating the existence of other far-upstream control elements have so far remained without a molecular fundament. Guided by a computational analysis of DNA structures, we could locate three as-yet-unknown transcription factor-binding regions at –0.5, –2, and –3 kb. Our present study delineates the interplay of factors YY1 and YY2 as it occurs at the sites at –3 kb and –2 kb (otherwise called HS1 and HS2), consistent with the idea that the novel factor YY2 antagonizes the negative actions exerted by YY1. Differences between the human and murine control regions will be described.

* Corresponding author. Mailing address: German Research Center for Biotechnology, RDIF/Epigenetic Regulation, Mascheroder Weg 1, 38124 Braunschweig, Germany. Phone: 49 (531) 6181-251. Fax: 49 (531) 6181-262. E-mail: jbo{at}gbf.de.

Molecular and Cellular Biology, November 2005, p. 10159-10170, Vol. 25, No. 22
0022-538X/05/$08.00+0     doi:10.1128/MCB.25.22.10159-10170.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.



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