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

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 de...

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Autores principales: van de Moosdijk, Anoeska Agatha Alida, van de Grift, Yorick Bernardus Cornelis, de Man, Saskia Madelon Ada, Zeeman, Amber Lisanne, van Amerongen, Renée
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539917/
https://www.ncbi.nlm.nih.gov/pubmed/32643876
http://dx.doi.org/10.1002/dvg.23387
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author van de Moosdijk, Anoeska Agatha Alida
van de Grift, Yorick Bernardus Cornelis
de Man, Saskia Madelon Ada
Zeeman, Amber Lisanne
van Amerongen, Renée
author_facet van de Moosdijk, Anoeska Agatha Alida
van de Grift, Yorick Bernardus Cornelis
de Man, Saskia Madelon Ada
Zeeman, Amber Lisanne
van Amerongen, Renée
author_sort van de Moosdijk, Anoeska Agatha Alida
collection PubMed
description 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 Axin2 (P2A‐rtTA3‐T2A‐3xNLS‐SGFP2) strain labels WNT/CTNNB1 responsive 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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spelling pubmed-75399172020-10-09 A novel Axin2 knock‐in mouse model for visualization and lineage tracing of WNT/CTNNB1 responsive cells van de Moosdijk, Anoeska Agatha Alida van de Grift, Yorick Bernardus Cornelis de Man, Saskia Madelon Ada Zeeman, Amber Lisanne van Amerongen, Renée Genesis Technology Reports 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 Axin2 (P2A‐rtTA3‐T2A‐3xNLS‐SGFP2) strain labels WNT/CTNNB1 responsive 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. John Wiley & Sons, Inc. 2020-07-09 2020-09 /pmc/articles/PMC7539917/ /pubmed/32643876 http://dx.doi.org/10.1002/dvg.23387 Text en © 2020 The Authors. Genesis published by Wiley Periodicals LLC This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technology Reports
van de Moosdijk, Anoeska Agatha Alida
van de Grift, Yorick Bernardus Cornelis
de Man, Saskia Madelon Ada
Zeeman, Amber Lisanne
van Amerongen, Renée
A novel Axin2 knock‐in mouse model for visualization and lineage tracing of WNT/CTNNB1 responsive cells
title A novel Axin2 knock‐in mouse model for visualization and lineage tracing of WNT/CTNNB1 responsive cells
title_full A novel Axin2 knock‐in mouse model for visualization and lineage tracing of WNT/CTNNB1 responsive cells
title_fullStr A novel Axin2 knock‐in mouse model for visualization and lineage tracing of WNT/CTNNB1 responsive cells
title_full_unstemmed A novel Axin2 knock‐in mouse model for visualization and lineage tracing of WNT/CTNNB1 responsive cells
title_short A novel Axin2 knock‐in mouse model for visualization and lineage tracing of WNT/CTNNB1 responsive cells
title_sort novel axin2 knock‐in mouse model for visualization and lineage tracing of wnt/ctnnb1 responsive cells
topic Technology Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7539917/
https://www.ncbi.nlm.nih.gov/pubmed/32643876
http://dx.doi.org/10.1002/dvg.23387
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