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Temporal Control of Retroviral Transgene Expression in Newborn Cells in the Adult Brain
Neural stem/progenitor cells (NSPCs) generate new neurons throughout life in distinct areas of the adult mammalian brain. Besides classical transgenesis-based approaches, retrovirus-mediated genetic manipulation is frequently used to study mechanisms that regulate neurogenesis in the nervous system....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757750/ https://www.ncbi.nlm.nih.gov/pubmed/24052947 http://dx.doi.org/10.1016/j.stemcr.2013.06.003 |
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author | Braun, Simon M.G. Machado, Raquel A.C. Jessberger, Sebastian |
author_facet | Braun, Simon M.G. Machado, Raquel A.C. Jessberger, Sebastian |
author_sort | Braun, Simon M.G. |
collection | PubMed |
description | Neural stem/progenitor cells (NSPCs) generate new neurons throughout life in distinct areas of the adult mammalian brain. Besides classical transgenesis-based approaches, retrovirus-mediated genetic manipulation is frequently used to study mechanisms that regulate neurogenesis in the nervous system. Here, we show that fusion of a tamoxifen-regulatable estrogen receptor (ER(T2)) motif to transcription factors (i.e., ASCL1 and NEUROD1) enables temporal control of transgene expression in adult mouse NSPCs in vitro and in vivo. Thus, the approach described here represents a versatile strategy for regulating gene expression to study gene function in dividing cells and their progeny. |
format | Online Article Text |
id | pubmed-3757750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-37577502013-09-17 Temporal Control of Retroviral Transgene Expression in Newborn Cells in the Adult Brain Braun, Simon M.G. Machado, Raquel A.C. Jessberger, Sebastian Stem Cell Reports Report Neural stem/progenitor cells (NSPCs) generate new neurons throughout life in distinct areas of the adult mammalian brain. Besides classical transgenesis-based approaches, retrovirus-mediated genetic manipulation is frequently used to study mechanisms that regulate neurogenesis in the nervous system. Here, we show that fusion of a tamoxifen-regulatable estrogen receptor (ER(T2)) motif to transcription factors (i.e., ASCL1 and NEUROD1) enables temporal control of transgene expression in adult mouse NSPCs in vitro and in vivo. Thus, the approach described here represents a versatile strategy for regulating gene expression to study gene function in dividing cells and their progeny. Elsevier 2013-07-11 /pmc/articles/PMC3757750/ /pubmed/24052947 http://dx.doi.org/10.1016/j.stemcr.2013.06.003 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Report Braun, Simon M.G. Machado, Raquel A.C. Jessberger, Sebastian Temporal Control of Retroviral Transgene Expression in Newborn Cells in the Adult Brain |
title | Temporal Control of Retroviral Transgene Expression in Newborn Cells in the Adult Brain |
title_full | Temporal Control of Retroviral Transgene Expression in Newborn Cells in the Adult Brain |
title_fullStr | Temporal Control of Retroviral Transgene Expression in Newborn Cells in the Adult Brain |
title_full_unstemmed | Temporal Control of Retroviral Transgene Expression in Newborn Cells in the Adult Brain |
title_short | Temporal Control of Retroviral Transgene Expression in Newborn Cells in the Adult Brain |
title_sort | temporal control of retroviral transgene expression in newborn cells in the adult brain |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3757750/ https://www.ncbi.nlm.nih.gov/pubmed/24052947 http://dx.doi.org/10.1016/j.stemcr.2013.06.003 |
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