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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7539917 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
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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