Volume 44, Issue 1 pp. 34-43
Technology Report
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Spatiotemporal gene control by the Cre-ERT2 system in melanocytes

Ichiro Yajima

Ichiro Yajima

Developmental Genetics of Melanocytes, UMR 146 CNRS-Institut Curie, Centre Universitaire, Orsay, France

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Elodie Belloir

Elodie Belloir

Developmental Genetics of Melanocytes, UMR 146 CNRS-Institut Curie, Centre Universitaire, Orsay, France

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Yveline Bourgeois

Yveline Bourgeois

Developmental Genetics of Melanocytes, UMR 146 CNRS-Institut Curie, Centre Universitaire, Orsay, France

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Mayuko Kumasaka

Mayuko Kumasaka

Developmental Genetics of Melanocytes, UMR 146 CNRS-Institut Curie, Centre Universitaire, Orsay, France

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Véronique Delmas

Véronique Delmas

Developmental Genetics of Melanocytes, UMR 146 CNRS-Institut Curie, Centre Universitaire, Orsay, France

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Lionel Larue

Corresponding Author

Lionel Larue

Developmental Genetics of Melanocytes, UMR 146 CNRS-Institut Curie, Centre Universitaire, Orsay, France

Developmental Genetics of Melanocytes, UMR 146 CNRS-Institut Curie, Bat. 110, Centre Universitaire, 91405, Orsay Cedex, FranceSearch for more papers by this author
First published: 17 January 2006
Citations: 73

Abstract

The organ-specific and temporal control of gene activation/inactivation is a key issue in the understanding of protein function during normal and pathological development and during oncogenesis. We generated transgenic mice bearing a tamoxifen-dependent Cre recombinase (Tyr::Cre-ERT2) gene expressed under the control of a 6.1 kb murine tyrosinase promoter in order to facilitate targeted spatiotemporally controlled somatic recombination in melanoblasts/melanocytes. Cre-ERT2 production was detected in tissues containing melanocytes. After tamoxifen induction at various times during embryogenesis and adulthood in a Cre-responsive reporter mouse strain, genetic recombination was detected in the melanoblasts and melanocytes of the skin. Thus, the Tyr::Cre-ERT2 transgenic mice provides a valuable tool for following this cell lineage and for investigating gene function in melanocyte development and transformation. genesis 44:34–43, 2006. © 2006 Wiley-Liss, Inc.

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