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Inducible and tissue‐specific cell labeling in Cre‐ER ( T2 ) transgenic Xenopus lines
Investigating cell lineage requires genetic tools that label cells in a temporal and tissue‐specific manner. The bacteriophage‐derived Cre‐ER ( T2 ) /loxP system has been developed as a genetic tool for lineage tracing in many organisms. We recently reported a stable transgenic Xenopus line with a C...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328194/ https://www.ncbi.nlm.nih.gov/pubmed/35581155 http://dx.doi.org/10.1111/dgd.12791 |
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author | Lin, Tzi‐Yang Taniguchi‐Sugiura, Yuka Murawala, Prayag Hermann, Sarah Tanaka, Elly M. |
author_facet | Lin, Tzi‐Yang Taniguchi‐Sugiura, Yuka Murawala, Prayag Hermann, Sarah Tanaka, Elly M. |
author_sort | Lin, Tzi‐Yang |
collection | PubMed |
description | Investigating cell lineage requires genetic tools that label cells in a temporal and tissue‐specific manner. The bacteriophage‐derived Cre‐ER ( T2 ) /loxP system has been developed as a genetic tool for lineage tracing in many organisms. We recently reported a stable transgenic Xenopus line with a Cre‐ER ( T2 ) /loxP system driven by the mouse Prrx1 (mPrrx1) enhancer to trace limb fibroblasts during the regeneration process (Prrx1:CreER line). Here we describe the detailed technological development and characterization of such line. Transgenic lines carrying a CAG promoter‐driven Cre‐ER ( T2 ) /loxP system showed conditional labeling of muscle, epidermal, and interstitial cells in both the tadpole tail and the froglet leg upon 4‐hydroxytamoxifen (4OHT) treatment. We further improved the labeling efficiency in the Prrx1:CreER lines from 12.0% to 32.9% using the optimized 4OHT treatment regime. Careful histological examination showed that Prrx1:CreER lines also sparsely labeled cells in the brain, spinal cord, head dermis, and fibroblasts in the tail. This work provides the first demonstration of conditional, tissue‐specific cell labeling with the Cre‐ER ( T2 ) /loxP system in stable transgenic Xenopus lines. |
format | Online Article Text |
id | pubmed-9328194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93281942022-07-30 Inducible and tissue‐specific cell labeling in Cre‐ER ( T2 ) transgenic Xenopus lines Lin, Tzi‐Yang Taniguchi‐Sugiura, Yuka Murawala, Prayag Hermann, Sarah Tanaka, Elly M. Dev Growth Differ Methods Investigating cell lineage requires genetic tools that label cells in a temporal and tissue‐specific manner. The bacteriophage‐derived Cre‐ER ( T2 ) /loxP system has been developed as a genetic tool for lineage tracing in many organisms. We recently reported a stable transgenic Xenopus line with a Cre‐ER ( T2 ) /loxP system driven by the mouse Prrx1 (mPrrx1) enhancer to trace limb fibroblasts during the regeneration process (Prrx1:CreER line). Here we describe the detailed technological development and characterization of such line. Transgenic lines carrying a CAG promoter‐driven Cre‐ER ( T2 ) /loxP system showed conditional labeling of muscle, epidermal, and interstitial cells in both the tadpole tail and the froglet leg upon 4‐hydroxytamoxifen (4OHT) treatment. We further improved the labeling efficiency in the Prrx1:CreER lines from 12.0% to 32.9% using the optimized 4OHT treatment regime. Careful histological examination showed that Prrx1:CreER lines also sparsely labeled cells in the brain, spinal cord, head dermis, and fibroblasts in the tail. This work provides the first demonstration of conditional, tissue‐specific cell labeling with the Cre‐ER ( T2 ) /loxP system in stable transgenic Xenopus lines. John Wiley and Sons Inc. 2022-06-05 2022-06 /pmc/articles/PMC9328194/ /pubmed/35581155 http://dx.doi.org/10.1111/dgd.12791 Text en © 2022 The Authors. Development, Growth & Differentiation published by John Wiley & Sons Australia, Ltd on behalf of Japanese Society of Developmental Biologists. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Methods Lin, Tzi‐Yang Taniguchi‐Sugiura, Yuka Murawala, Prayag Hermann, Sarah Tanaka, Elly M. Inducible and tissue‐specific cell labeling in Cre‐ER ( T2 ) transgenic Xenopus lines |
title | Inducible and tissue‐specific cell labeling in
Cre‐ER
(
T2
)
transgenic Xenopus lines |
title_full | Inducible and tissue‐specific cell labeling in
Cre‐ER
(
T2
)
transgenic Xenopus lines |
title_fullStr | Inducible and tissue‐specific cell labeling in
Cre‐ER
(
T2
)
transgenic Xenopus lines |
title_full_unstemmed | Inducible and tissue‐specific cell labeling in
Cre‐ER
(
T2
)
transgenic Xenopus lines |
title_short | Inducible and tissue‐specific cell labeling in
Cre‐ER
(
T2
)
transgenic Xenopus lines |
title_sort | inducible and tissue‐specific cell labeling in
cre‐er
(
t2
)
transgenic xenopus lines |
topic | Methods |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328194/ https://www.ncbi.nlm.nih.gov/pubmed/35581155 http://dx.doi.org/10.1111/dgd.12791 |
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