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Originally published In Press as doi:10.1074/jbc.M207567200 on December 17, 2002
J. Biol. Chem., Vol. 278, Issue 16, 13696-13705, April 18, 2003
The Co-activator p300 Associates Physically with and Can
Mediate the Action of the Distal Enhancer of the FGF-4
Gene*
Tamara
Nowling §,
Cory
Bernadt ¶,
Lance
Johnson ¶,
Michelle
Desler , and
Angie
Rizzino ¶
From the Eppley Institute for Research in Cancer and
Allied Diseases and the ¶ Department of Pathology and
Microbiology, University of Nebraska Medical Center, Omaha, Nebraska
68198
Distal enhancers commonly regulate gene
expression. However, the mechanisms of transcriptional mediation by
distal enhancers remain largely unknown. To better understand distal
enhancer-mediated transcription, we examined the regulation of the
FGF-4 gene. The FGF-4 gene is regulated during
early development by a powerful distal enhancer located downstream of
the promoter in exon 3. Sox-2 and Oct-3 bind to the enhancer and are
required for the activation of the FGF-4 gene. Previously,
we implicated the co-activator p300 as a mediator of Sox-2/Oct-3
synergistic activation of a heterologous promoter, suggesting that p300
may play a role in mediating enhancer activation of the
FGF-4 gene. In this study, we provide both functional and
physical evidence that p300 plays an important role in the action of
the FGF-4 enhancer. Specifically, we show that E1a, but not
a mutant form of E1a that is unable to bind p300, inhibits enhancer
activation of the FGF-4 promoter. We also demonstrate that
Gal4/p300 fusion proteins can stimulate the FGF-4
promoter when bound to the FGF-4 enhancer.
Additionally, we present evidence that p300 mediation of the
FGF-4 enhancer requires acetyltransferase activity.
Importantly, we also show that Sox-2 and p300 are physically associated
with the endogenous FGF-4 enhancer but weakly associated
with the endogenous FGF-4 promoter. These results are
consistent with a model of transitory interaction between the distal
enhancer and the FGF-4 promoter. Our results also suggest
that intragenic distal enhancers may use mechanisms that differ from
extragenic distal enhancers.
*
This work was supported in part by NCI, National Institutes
of Health Grant CA 74771. Core facilities of the University of Nebraska
Medical Center, Eppley Cancer Institute used in the course of this work
were supported in part by NCI Laboratory Cancer Research Center Support
Grant CA 36727.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.
§
Supported in part by NCI, National Institutes of Health Training
Grant CA 00476.
To whom correspondence should be addressed: Eppley Inst. for
Research in Cancer and Allied Diseases, University of Nebraska Medical
Center, 986805 Nebraska Medical Center, Omaha, NE 68198-6805. Tel.:
402-559-6338; Fax: 402-559-4651; E-mail: arizzino@unmc.edu.
Copyright © 2003 by The American Society for Biochemistry and Molecular Biology, Inc.

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