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Journal of Virology, February 1999, p. 1254-1261, Vol. 73, No. 2
Virology Department, Paul-Ehrlich-Institut,
D-63225 Langen, Germany
Received 20 July 1998/Accepted 15 October 1998
The human endogenous retrovirus HTDV/HERV-K, which resides in
moderate copy numbers in the human genome, is expressed in a cell-type-specific manner, predominantly in teratocarcinoma cells. We
have analyzed the regulatory potential of the 5' enhancer of the HERV-K
long terminal repeat. Protein extracts of HERV-K-expressing teratocarcinoma cell lines (GH and Tera2) and nonexpressing HeLa and
HepG2 cells form different protein complexes on the enhancer sequence
as detected by electrophoretic mobility shift assays (EMSA). Using
competition EMSAs, DNase I footprinting, and supershift experiments, we
localized the binding site of these complexes to a 20-bp sequence
within the enhancer and showed that the transcription factor YY1 is one
component of the HERV-K enhancer complex. Replacement of the YY1
binding site with unrelated sequences reduced expression of the
luciferase gene as a reporter in transient-transfection assays.
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Expression of the Human Endogenous Retrovirus HTDV/HERV-K Is
Enhanced by Cellular Transcription Factor YY1
*
Corresponding author. Mailing address: Virology
Department, Paul-Ehrlich-Institut, Paul-Ehrlich-Strasse 51-59, D-63225
Langen, Germany. Phone: 49-6103-77-2000. Fax: 49-6103-77-1252. E-mail: loejo{at}pei.de.
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