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J Biol Chem, Vol. 273, Issue 32, 20463-20472, August 7, 1998
From the Department of Microbiology and Molecular Genetics and the
Markey Center for Molecular Genetics, University of Vermont,
Burlington, Vermont 05405-0068
In the yeast Saccharomyces
cerevisiae, heat shock transcription factor (HSF) binds heat
shock element (HSE) DNA shortly after DNA replication, independently of
its activation by heat shock. To determine if HSF binding occurs before
newly replicated DNA is packaged into nucleosomes, we inserted an HSE
into a DNA segment that normally forms a positioned nucleosome in
vivo. Transcription from constructs designed to create steric
competition between binding of HSF and histone H2A-H2B dimers was
generally poor, suggesting that nucleosome assembly precedes and
inhibits HSF binding. However, one such construct was as
transcriptionally active as a nucleosome-free control. Structural
analyses suggested that ~40 base pairs of DNA, including
the HSE, had unwrapped from the 3' edge of the histone octamer,
allowing HSF to bind; ~100 base pairs remained in
association with the histone octamer, with the same translational and
rotational orientation as was seen for the poorly transcribed
constructs. Modeling studies suggest that the active and inactive
constructs differ from one another in the ease with which the HSE and
flanking sequences can adopt the curvature needed to form a stable
nucleosome. These differences may influence the probability of DNA
unwrapping from already assembled nucleosomes and the subsequent
binding of HSF.
Evidence That Partial Unwrapping of DNA from Nucleosomes
Facilitates the Binding of Heat Shock Factor following DNA
Replication in Yeast
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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