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[Cancer Research 49, 6318-6323, November 15, 1989]
© 1989 American Association for Cancer Research

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Expression of Human DNA Topoisomerase I in Yeast Cells Lacking Yeast DNA Topoisomerase I: Restoration of Sensitivity of the Cells to the Antitumor Drug Camptothecin1

Mary-Ann Bjornsti2, Piero Benedetti, Gregory A. Viglianti3 and James C. Wang

Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, Massachusetts 02138 [M-A. B., P. B., J. C. W.], and Department of Cancer Biology, Harvard School of Public Health, Boston, Massachusetts 02115 [G. A. V.]

Yeast Saccharomyces cerevisiae strains that are permeable to the antitumor alkaloid camptothecin are killed by the drug if they express DNA topoisomerase I, the cellular target of the drug (J. Nitiss and J. C. Wang, Proc. Natl. Acad. Sci. USA, 85: 7501–7505, 1988). We show that in a yeast strain permeable to camptothecin but lacking DNA topoisomerase I, sensitivity to the drug was restored upon expression of human DNA topoisomerase I from a plasmid-borne human complementary DNA clone. When the human enzyme was expressed from a galactose-inducible, glucose-repressible yeast promoter, PGAL1, sensitivity to camptothecin was observed in the presence of galactose but not in the presence of glucose. Expression of human DNA topoisomerase I in Escherichia coli was also demonstrated by the complementation of a conditional lethal E. coli DNA topoisomerase I mutant. These systems can be used in the study of human DNA topoisomerase I-camptothecin interactions and in the screening of additional therapeutics targeting the enzyme.

1 Supported by USPHS Grant CA47958. P. B. was supported in part by a fellowship from the American-Italian Foundation for Cancer Research (AIFRC 88-102).

2 Present address: Department of Biochemistry and Molecular Biology, Thomas Jefferson University, 1020 Locust Street, Philadelphia, PA 19107.

3 Present address: Program in Molecular Medicine, University of Massachusetts Medical Center, Worcester, MA 01655.

Received 5/18/89. Revised 8/18/89. Accepted 8/22/89.




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Copyright © 1989 by the American Association for Cancer Research.