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Mol. Cell. Biol., 10 1995, 5492-5498, Vol 15, No. 10
A TenHarmsel and MD Biggin
Previous studies indicated that repression by eve involves cooperative DNA
binding and leads to the formation of a DNA loop which encompasses the DNA
sequences normally bound by the RNA polymerase II general transcription
factors. To test the general principle of whether bending of a basal
promoter sequence can contribute directly to repression of transcription, a
minicircle template of 245 bp was used. In a purified transcription system,
transcription from the minicircular DNA is greatly reduced compared with
that from the identical DNA fragment in linear form. Transcription is also
reduced when the minicircle contains a single-stranded nick, indicating
that transcription is reduced because of DNA bending, rather than any
constraint on supercoiling. We show that the reduced transcription from the
minicircle in these experiments is not due to a reduced rate of elongation
by RNA polymerase II. Rather, repression occurs, at least in part, because
binding of the general transcription factor TFIID to the minicircle is
strongly inhibited compared with binding to the linear DNA. We suggest that
bending DNA may be a mechanism by which eukaryotic transcription may be
regulated, by modulating the activity of the general transcription factors.
Copyright © 1995, American Society for Microbiology
Bending DNA can repress a eukaryotic basal promoter and inhibit TFIID binding
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520-8114, USA.
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