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A directional strategy for monitoring Cre-mediated recombination at the cellular level in the mouse

Nature Biotechnology volume 21, pages 562565 (2003) | Download Citation

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Abstract

Functional redundancies, compensatory mechanisms, and lethal phenotypes often prevent the full analysis of gene functions through generation of germline null mutations in the mouse1. The use of site-specific recombinases, such as Cre, which catalyzes recombination between loxP sites2, has allowed the engineering of mice harboring targeted somatic mutations, which are both temporally controlled and cell-type restricted1,3. Many Cre-expressing mouse lines exist, but only a few transgenic lines are available that harbor a reporter gene whose expression is dependent on a Cre-mediated event3. Moreover, their use to monitor gene ablation at the level of individual cells is often limited, as in some tissues the reporter gene may be silenced1, be affected by position-effect variegation4, or reside in a chromatin configuration inaccessible for recombination5. Thus, one cannot validly extrapolate from the expression of a reporter transgene to an identical ablation pattern for the conditional allele of a given gene. By combining the ability of Cre recombinase to invert or excise a DNA fragment, depending on the orientation of the flanking loxP sites6, and the availability of both wild-type (WT) and mutant loxP sites7, we designed a Cre-dependent genetic switch (FLEx switch) through which the expression of a given gene is turned off, while the expression of another one is concomitantly turned on. We demonstrate the efficiency and reliability of this switch to readily detect, in the mouse, at the single cell level, Cre-mediated gene ablation. We discuss how this strategy can be used to generate genetic modifications in a conditional manner.

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Acknowledgements

We thank B. Féret, G. Kimmich, and E. Blondelle for technical assistance, J.M. Garnier, A. Dierich, and M. Mark for their active contribution to this work, and G. Richards for critical reading of the manuscript. We also thank M. Li for K14-Cre mice and J.F. Nicolas for the lacZ gene. This work was supported by funds from the Centre National de la Recherche Scientifique (CNRS), the Institut National de la Santé et de la Recherche Médicale (INSERM), the Université Louis Pasteur (ULP), the Hôpital Universitaire de Strasbourg, the Collège de France, and the Association pour la Recherche sur le Cancer (ARC). F.S. was supported by a Marie Curie Fellowship from the European Community and C.C. by the Institut National de la Recherche Agronomique (INRA).

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    • Frank Schnütgen

    Present address: Molekulare Hämatologie, Theodor Stern Kai 7, Klinikum der Universität Frankfurt, 60590 Frankfurt am Main, Germany.

Affiliations

  1. Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, Collège de France, BP10142, 67404 Illkirch Ce dex, CU de Strasbourg, France.

    • Frank Schnütgen
    • , Nathalie Doerflinger
    • , Cécile Calléja
    • , Olivia Wendling
    • , Pierre Chambon
    •  & Norbert B. Ghyselinck

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The authors declare no competing financial interests.

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Correspondence to Norbert B. Ghyselinck.

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DOI

https://doi.org/10.1038/nbt811

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