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Originally published In Press as doi:10.1074/jbc.M200629200 on March 21, 2002
J. Biol. Chem., Vol. 277, Issue 22, 19847-19854, May 31, 2002
The Viral Transactivator E1A Regulates the
Mouse Mammary Tumor Virus Promoter in an Isoform- and
Chromatin-specific Manner*
Edlyn
Soeth ,
Denise B.
Thurber, and
Catharine L.
Smith§
From the Signal Transduction Group, Laboratory of Receptor Biology
and Gene Expression, Center for Cancer Research, NCI, National
Institutes of Health, Bethesda, Maryland 20892
Proteins encoded by the adenovirus E1A gene
regulate both cellular and viral genes to mediate effects on cell
cycle, differentiation, and cell growth control. We have identified the
mouse mammary tumor virus (MMTV) promoter as a target of E1A action and
investigated the role nucleoprotein structure plays in its response to
E1A. Both 12 and 13 S forms target the MMTV promoter when it has a disorganized and accessible chromatin configuration. However, whereas
the 13 S form is stimulatory, the 12 S form is repressive. When the
MMTV promoter adopts an organized and repressed chromatin structure, it
is targeted only by the 13 S form, which stimulates it. Although
evidence indicates that E1A interacts with the SWI/SNF remodeling
complex, E1A had no effect on chromatin remodeling at the MMTV promoter
in organized chromatin. Analysis of E1A mutants showed that stimulation
of the MMTV promoter is mediated solely through conserved region
3 and does not require interaction with Rb, p300/CBP-associated
factor, or CBP/p300. Imaging analysis showed that E1A
colocalizes with MMTV sequences in vivo, suggesting that it
functions directly at the promoter. These results indicate that E1A
stimulates the MMTV promoter in a fashion independent of chromatin
conformation and through a direct mechanism involving interaction with
the basal transcription machinery.
*
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 by a fellowship from the Deutsche
Forschungsgemeinschaft. Present address: Molecular Oncology, Dept. of
General Surgery and Thoracic Surgery, Christian-Albrechts-University, 24105 Kiel, Germany.
§
To whom correspondence and reprint requests should be
addressed: National Institutes of Health, Laboratory of Receptor
Biology and Gene Expression, Bldg. 41 Rm. B608, 41 Library Dr. MSC
5055, Bethesda, MD 20892-5055. Tel.: 301-496-7538; Fax: 301-496-4951; E-mail: smithcat@exchange.nih.gov.
Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 2002 by the American Society for Biochemistry and Molecular Biology.
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