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A novel Axin2 knock-in mouse model for visualization and lineage tracing of WNT/CTNNB1 responsive cells

Anoeska Agatha Alida van de Moosdijk, Yorick Bernardus Cornelis van de Grift, Saskia Madelon Ada de Man, Amber Lisanne Zeeman, View ORCID ProfileRenée van Amerongen
doi: https://doi.org/10.1101/2020.04.03.024182
Anoeska Agatha Alida van de Moosdijk
1Section of Molecular Cytology, Swammerdam Institute for Life Science, University of Amsterdam, Postbus 1212, 1000 BE, Amsterdam, the Netherlands
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Yorick Bernardus Cornelis van de Grift
1Section of Molecular Cytology, Swammerdam Institute for Life Science, University of Amsterdam, Postbus 1212, 1000 BE, Amsterdam, the Netherlands
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Saskia Madelon Ada de Man
1Section of Molecular Cytology, Swammerdam Institute for Life Science, University of Amsterdam, Postbus 1212, 1000 BE, Amsterdam, the Netherlands
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Amber Lisanne Zeeman
1Section of Molecular Cytology, Swammerdam Institute for Life Science, University of Amsterdam, Postbus 1212, 1000 BE, Amsterdam, the Netherlands
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Renée van Amerongen
1Section of Molecular Cytology, Swammerdam Institute for Life Science, University of Amsterdam, Postbus 1212, 1000 BE, Amsterdam, the Netherlands
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  • ORCID record for Renée van Amerongen
  • For correspondence: r.vanamerongen@uva.nl
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Abstract

Wnt signal transduction controls tissue morphogenesis, maintenance and regeneration in all multicellular animals. In mammals, the WNT/CTNNB1 (Wnt/β-catenin) pathway controls cell proliferation and cell fate decisions before and after birth. It plays a critical role at multiple stages of embryonic development, but also governs stem cell maintenance and homeostasis in adult tissues. However, it remains challenging to monitor endogenous WNT/CTNNB1 signaling dynamics in vivo. Here we report the generation and characterization of a new knock-in mouse strain that doubles as a fluorescent reporter and lineage tracing driver for WNT/CTNNB1 responsive cells. We introduced a multi-cistronic targeting cassette at the 3’ end of the universal WNT/CTNNB1 target gene Axin2. The resulting knock-in allele expresses a bright fluorescent reporter (3xNLS-SGFP2) and a doxycycline-inducible driver for lineage tracing (rtTA3). We show that the Axin2P2A-rtTA3-T2A-3xNLS-SGFP2 strain labels WNT/CTNNB1 cells at multiple anatomical sites during different stages of embryonic and postnatal development. It faithfully reports the subtle and dynamic changes in physiological WNT/CTNNB1 signaling activity that occur in vivo. We expect this mouse strain to be a useful resource for biologists who want to track and trace the location and developmental fate of WNT/CTNNB1 responsive stem cells in different contexts.

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  • http://shorturl.at/ilqIO

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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A novel Axin2 knock-in mouse model for visualization and lineage tracing of WNT/CTNNB1 responsive cells
Anoeska Agatha Alida van de Moosdijk, Yorick Bernardus Cornelis van de Grift, Saskia Madelon Ada de Man, Amber Lisanne Zeeman, Renée van Amerongen
bioRxiv 2020.04.03.024182; doi: https://doi.org/10.1101/2020.04.03.024182
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A novel Axin2 knock-in mouse model for visualization and lineage tracing of WNT/CTNNB1 responsive cells
Anoeska Agatha Alida van de Moosdijk, Yorick Bernardus Cornelis van de Grift, Saskia Madelon Ada de Man, Amber Lisanne Zeeman, Renée van Amerongen
bioRxiv 2020.04.03.024182; doi: https://doi.org/10.1101/2020.04.03.024182

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