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Originally published In Press as doi:10.1074/jbc.M206786200 on July 26, 2002

J. Biol. Chem., Vol. 277, Issue 41, 38557-38564, October 11, 2002
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The Human Papilloma Virus E7 Oncoprotein Inhibits Transforming Growth Factor-beta Signaling by Blocking Binding of the Smad Complex to Its Target Sequence*

Dug Keun LeeDagger , Byung-Chul KimDagger , Isaac Yi KimDagger , Eun-ah ChoDagger , Daniel J. Satterwhite§, and Seong-Jin KimDagger ||

From the Dagger  Laboratory of Cell Regulation and Carcinogenesis, National Institutes of Health, Bethesda, Maryland 20892 and the § Division of Neonatology, University of Utah, Salt Lake City, Utah 84132

The human papillomavirus (HPV) oncoprotein E7 is implicated in the etiology of cervical cancer associated with infection by HPV. HPV-positive cells develop resistance to TGF-beta growth inhibitory activity through the inhibition of hypophosphorylation of pRb by papillomavirus type 16 E7 oncoprotein. In this study, we examined whether E7, in addition to its well known effects on pRb, might directly target the Smad proteins that mediate TGF-beta signaling. Here, we show that E7 significantly blocks both Smad transcriptional activity and the ability of TGF-beta to inhibit DNA synthesis. We found that E7 interacts constitutively with Smad2, Smad3, and Smad4. Confocal microscopic studies confirm that E7 and Smads co-localize in vivo. Using a canonical Smad DNA binding sequence, we found that E7 blocks Smad3 binding to its target sequence on DNA. These results suggest that suppression of Smad-mediated signaling by E7 may contribute to HPV-associated carcinogenesis.

* 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.

Funded by the Huntsman Cancer Institute.

|| To whom correspondence should be addressed. Tel.: 301-496-8350; Fax: 301-496-8395; E-mail: kims@mail.nih.gov.

Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.
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