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ASSAY and Drug Development Technologies
Recombinant Baculoviruses Used to Study Estrogen Receptor Function in Human Osteosarcoma Cells

To cite this article:
William C. Clay, J. Patrick Condreay, Linda B. Moore, Susan L. Weaver, Michael A. Watson, Thomas A. Kost, Jennifer J. Lorenz. ASSAY and Drug Development Technologies. December 2003, 1(6): 801-810. doi:10.1089/154065803772613435.

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William C. Clay
Department of Gene Expression and Protein Biochemistry, GlaxoSmithKline Discovery Research, Research Triangle Park, NC
J. Patrick Condreay
Department of Gene Expression and Protein Biochemistry, GlaxoSmithKline Discovery Research, Research Triangle Park, NC
Linda B. Moore
Department of Systems Research and Protein Biochemistry, GlaxoSmithKline Discovery Research, Research Triangle Park, NC
Susan L. Weaver
Department of Systems Research and Protein Biochemistry, GlaxoSmithKline Discovery Research, Research Triangle Park, NC
Michael A. Watson
Department of High Throughput Biology and Protein Biochemistry, GlaxoSmithKline Discovery Research, Research Triangle Park, NC
Thomas A. Kost
Department of Gene Expression and Protein Biochemistry, GlaxoSmithKline Discovery Research, Research Triangle Park, NC
Jennifer J. Lorenz
Department of Gene Expression and Protein Biochemistry, GlaxoSmithKline Discovery Research, Research Triangle Park, NC

We report that modified baculoviruses, termed BacMam viruses, can efficiently deliver multiple genes into mammalian cells to generate a heterologous transcription factor/reporter gene system. Using human estrogen receptor (ER) as a model nuclear receptor, we demonstrate how this approach can be successfully applied to assay development in Saos-2 human osteosarcoma cells. BacMam viruses containing full-length cDNAs were constructed for both human ER subtypes, ERα and ERβ, and a third BacMam virus containing an ER-responsive reporter gene cassette. Using these viruses, we found that BacMam-ER expression/reporter constructs could be used to profile the effects of the agonist 17β-estradiol and the partial agonist raloxifene in human Saos-2 cells. A comparison of assay data obtained with the BacMam-based system with that using standard DNA transfections demonstrates that the two systems are functionally equivalent, giving comparable EC50 and IC50 values for estrogen and estrogen plus raloxifene treatments, respectively. Our results indicate that BacMam-mediated gene transfer offers a novel and efficient method for delivery of nuclear receptors and associated genes for mammalian cell-based assay development.

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