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Originally published In Press as doi:10.1074/jbc.M204399200 on July 9, 2002
J. Biol. Chem., Vol. 277, Issue 37, 33890-33894, September 13, 2002
Upstream Stimulatory Factor (USF) Is Recruited into a Steroid
Hormone-triggered Regulatory Circuit by the Estrogen-inducible
Transcription Factor EF1*
Naomi B.
Dillner and
Michel M.
Sanders
From the Department of Biochemistry, Molecular Biology, and
Biophysics, University of Minnesota, Minneapolis, Minnesota 55455
In the past decade, investigation into steroid
hormone signaling has focused on the mechanisms of steroid hormone
receptors as they act as signaling molecules and transcription factors
in cells. However, the majority of hormone-responsive genes are not directly regulated by hormone receptors. These genes are termed secondary response genes. To explore the molecular mechanisms by which
the steroid hormone estrogen regulates secondary response genes, the
ovalbumin (Ov) gene was analyzed.
Three protein-protein complexes (Chirp-I, -II, -III), which do not
contain the estrogen receptor, are induced by estrogen to bind to the
5'-flanking region of the Ov gene. The Chirp-III DNA
binding site, which is required for estrogen induction, binds a complex
of proteins that contains the estrogen-inducible transcription factor
EF1. Experiments undertaken to identify proteins complexed with
EF1 led to the elucidation of a novel mechanism of action of
upstream stimulatory factor-1 (USF-1), which involves its tethering to
the Ov gene 5'-flanking region by EF1. Gel mobility
shift assays and co-immunoprecipitation experiments identify USF-1 as a
component of Chirp-III. However, USF-1 is not able to bind to the
Chirp-III site independently. In addition, USF-1 overexpression is able
to induce Ov gene promoter activity in transfection
experiments. USF-1 can also potentiate the induction of the
Ov gene by the transcription factor EF1. Moreover,
mutating the EF1 binding sites in the 5'-flanking region of the
Ov gene abrogates induction of the gene by USF-1. These data begin to establish a molecular mechanism by which
hormone-inducible transcription factors and ubiquitous transcription
factors cooperate to regulate estrogen-induced secondary
response gene expression.
*
This work was supported by Grant R01DK40082 from the
National Institutes of Health (to M. M. S.).The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
To whom correspondence should be addressed: Dept. of Biochemistry,
Molecular Biology, and Biophysics, University of Minnesota, 6-155 Jackson Hall, 321 Church St. SE, Minneapolis, MN 55455. Tel.:
612-624-9637; Fax: 612-625-5476; E-mail: sande001@umn.edu.
Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.

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