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Rosa26 docking sites for investigating genetic circuit silencing in stem cells
Approaches in mammalian synthetic biology have transformed how cells can be programmed to have reliable and predictable behavior, however, the majority of mammalian synthetic biology has been accomplished using immortalized cell lines that are easy to grow and easy to transfect. Genetic circuits tha...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644442/ https://www.ncbi.nlm.nih.gov/pubmed/33195816 http://dx.doi.org/10.1093/synbio/ysaa014 |
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author | Fitzgerald, Michael Livingston, Mark Gibbs, Chelsea Deans, Tara L |
author_facet | Fitzgerald, Michael Livingston, Mark Gibbs, Chelsea Deans, Tara L |
author_sort | Fitzgerald, Michael |
collection | PubMed |
description | Approaches in mammalian synthetic biology have transformed how cells can be programmed to have reliable and predictable behavior, however, the majority of mammalian synthetic biology has been accomplished using immortalized cell lines that are easy to grow and easy to transfect. Genetic circuits that integrate into the genome of these immortalized cell lines remain functional for many generations, often for the lifetime of the cells, yet when genetic circuits are integrated into the genome of stem cells gene silencing is observed within a few generations. To investigate the reactivation of silenced genetic circuits in stem cells, the Rosa26 locus of mouse pluripotent stem cells was modified to contain docking sites for site-specific integration of genetic circuits. We show that the silencing of genetic circuits can be reversed with the addition of sodium butyrate, a histone deacetylase inhibitor. These findings demonstrate an approach to reactivate the function of genetic circuits in pluripotent stem cells to ensure robust function over many generations. Altogether, this work introduces an approach to overcome the silencing of genetic circuits in pluripotent stem cells that may enable the use of genetic circuits in pluripotent stem cells for long-term function. |
format | Online Article Text |
id | pubmed-7644442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76444422020-11-12 Rosa26 docking sites for investigating genetic circuit silencing in stem cells Fitzgerald, Michael Livingston, Mark Gibbs, Chelsea Deans, Tara L Synth Biol (Oxf) Research Article Approaches in mammalian synthetic biology have transformed how cells can be programmed to have reliable and predictable behavior, however, the majority of mammalian synthetic biology has been accomplished using immortalized cell lines that are easy to grow and easy to transfect. Genetic circuits that integrate into the genome of these immortalized cell lines remain functional for many generations, often for the lifetime of the cells, yet when genetic circuits are integrated into the genome of stem cells gene silencing is observed within a few generations. To investigate the reactivation of silenced genetic circuits in stem cells, the Rosa26 locus of mouse pluripotent stem cells was modified to contain docking sites for site-specific integration of genetic circuits. We show that the silencing of genetic circuits can be reversed with the addition of sodium butyrate, a histone deacetylase inhibitor. These findings demonstrate an approach to reactivate the function of genetic circuits in pluripotent stem cells to ensure robust function over many generations. Altogether, this work introduces an approach to overcome the silencing of genetic circuits in pluripotent stem cells that may enable the use of genetic circuits in pluripotent stem cells for long-term function. Oxford University Press 2020-08-19 /pmc/articles/PMC7644442/ /pubmed/33195816 http://dx.doi.org/10.1093/synbio/ysaa014 Text en © The Author(s) 2020. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Fitzgerald, Michael Livingston, Mark Gibbs, Chelsea Deans, Tara L Rosa26 docking sites for investigating genetic circuit silencing in stem cells |
title | Rosa26 docking sites for investigating genetic circuit silencing in stem cells |
title_full | Rosa26 docking sites for investigating genetic circuit silencing in stem cells |
title_fullStr | Rosa26 docking sites for investigating genetic circuit silencing in stem cells |
title_full_unstemmed | Rosa26 docking sites for investigating genetic circuit silencing in stem cells |
title_short | Rosa26 docking sites for investigating genetic circuit silencing in stem cells |
title_sort | rosa26 docking sites for investigating genetic circuit silencing in stem cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7644442/ https://www.ncbi.nlm.nih.gov/pubmed/33195816 http://dx.doi.org/10.1093/synbio/ysaa014 |
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