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Abstract

RNA and DNA expression vectors containing genes for chloramphenicol acetyltransferase, luciferase, and β-galactosidase were separately injected into mouse skeletal muscle in vivo. Protein expression was readily detected in all cases, and no special delivery system was required for these effects. The extent of expression from both the RNA and DNA constructs was comparable to that obtained from fibroblasts transfected in vitro under optimal conditions. In situ cytochemical staining for β-galactosidase activity was localized to muscle cells following injection of the β-galactosidase DNA vector. After injection of the DNA luciferase expression vector, luciferase activity was present in the muscle for at least 2 months.

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Science
Volume 247 | Issue 4949
23 March 1990

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Published in print: 23 March 1990

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Authors

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Jon A. Wolff
Departments of Pediatrics and Genetics, Waisman Center, University of Wisconsin, Madison, WI 53706.
Robert W. Malone
Vical Inc., San Diego, CA 92121.
Phillip Williams
Departments of Pediatrics and Genetics, Waisman Center, University of Wisconsin, Madison, WI 53706.
Wang Chong
Departments of Pediatrics and Genetics, Waisman Center, University of Wisconsin, Madison, WI 53706.
Gyula Acsadi
Departments of Pediatrics and Genetics, Waisman Center, University of Wisconsin, Madison, WI 53706.
Agnes Jani
Departments of Pediatrics and Genetics, Waisman Center, University of Wisconsin, Madison, WI 53706.
Philip L. Felgner
Vical Inc., San Diego, CA 92121.

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