Efficient gene activation in mammalian cells by using recombinant adenovirus expressing site-specific Cre recombinase (original) (raw)

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Laboaory of Molecular Genetics University of Tokyo

4-6-1 Shirokanedi, Minato-ku, Tokyo 108, Japan

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Laboaory of Molecular Genetics University of Tokyo

4-6-1 Shirokanedi, Minato-ku, Tokyo 108, Japan

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1

Laboaory of Molecular Genetics University of Tokyo

4-6-1 Shirokanedi, Minato-ku, Tokyo 108, Japan

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1

Laboaory of Molecular Genetics University of Tokyo

4-6-1 Shirokanedi, Minato-ku, Tokyo 108, Japan

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Laboaory of Molecular Genetics University of Tokyo

4-6-1 Shirokanedi, Minato-ku, Tokyo 108, Japan

3

Discovery Research Laboratories III, Sumitomo Pharmaceuticals Research Center

3-1-98 Kasugade-naka, Konohana-ku, Osaka 554, Japan

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Discovery Research Laboratories III, Sumitomo Pharmaceuticals Research Center

3-1-98 Kasugade-naka, Konohana-ku, Osaka 554, Japan

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Deparment of Virology, institute of Medical Science, University of Tokyo

4-6-1 Shirokanedai, Minato-ku, Tokyo 108, Japan

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Laboaory of Molecular Genetics University of Tokyo

4-6-1 Shirokanedi, Minato-ku, Tokyo 108, Japan

* To whom correspondence should be addressed

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Published:

11 October 1995

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Yumi Kanegae, Gwang Lee, Yumi Sato, Mieko Tanaka, Michio Nakal, Toshiyuki Sakaki, Sumio Sugano, Izumu Saito, Efficient gene activation in mammalian cells by using recombinant adenovirus expressing site-specific Cre recombinase, Nucleic Acids Research, Volume 23, Issue 19, 11 October 1995, Pages 3816–3821, https://doi.org/10.1093/nar/23.19.3816
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Abstract

A recombinant adenovirus (Ad) expressing Cre recombinase derived from bacteriophage P1 was constructed. To assay the Cre activity in mammalian colls, another recombinant Ad bearing an on/off-switching reporter unit, where a LacZ -expression unit can be activated by the Cre-mediated exclsionai deletion of an interposed stuffer DNA, was also constructed. Co-infection experiments together with the Cre-expressing and the reporter recombinant Ads showed that the Cre-mediated switching of gene expression was detected in nearly 100% of cultured CV1, HeLa and Jurkat cells. These results suggest that the recombinant Ad efficiently expressed functional Cre and offers a basis for estabilshing a powerful on/off switching strategy of gene expression incultured mammalian cells and presumably in transgenic animals. The method is also applicable to construction of recombinant Ad bearing a gene the expression of which is deleterious to propagation of recombinant Ad.

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