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A platform for rapid generation of single and multiplexed reporters in human iPSC lines

Induced pluripotent stem cells (iPSC) are important tools for drug discovery assays and toxicology screens. In this manuscript, we design high efficiency TALEN and ZFN to target two safe harbor sites on chromosome 13 and 19 in a widely available and well-characterized integration-free iPSC line. We...

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Autores principales: Pei, Ying, Sierra, Guadalupe, Sivapatham, Renuka, Swistowski, Andrzej, Rao, Mahendra S., Zeng, Xianmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361878/
https://www.ncbi.nlm.nih.gov/pubmed/25777362
http://dx.doi.org/10.1038/srep09205
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author Pei, Ying
Sierra, Guadalupe
Sivapatham, Renuka
Swistowski, Andrzej
Rao, Mahendra S.
Zeng, Xianmin
author_facet Pei, Ying
Sierra, Guadalupe
Sivapatham, Renuka
Swistowski, Andrzej
Rao, Mahendra S.
Zeng, Xianmin
author_sort Pei, Ying
collection PubMed
description Induced pluripotent stem cells (iPSC) are important tools for drug discovery assays and toxicology screens. In this manuscript, we design high efficiency TALEN and ZFN to target two safe harbor sites on chromosome 13 and 19 in a widely available and well-characterized integration-free iPSC line. We show that these sites can be targeted in multiple iPSC lines to generate reporter systems while retaining pluripotent characteristics. We extend this concept to making lineage reporters using a C-terminal targeting strategy to endogenous genes that express in a lineage-specific fashion. Furthermore, we demonstrate that we can develop a master cell line strategy and then use a Cre-recombinase induced cassette exchange strategy to rapidly exchange reporter cassettes to develop new reporter lines in the same isogenic background at high efficiency. Equally important we show that this recombination strategy allows targeting at progenitor cell stages, further increasing the utility of the platform system. The results in concert provide a novel platform for rapidly developing custom single or dual reporter systems for screening assays.
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spelling pubmed-43618782015-03-19 A platform for rapid generation of single and multiplexed reporters in human iPSC lines Pei, Ying Sierra, Guadalupe Sivapatham, Renuka Swistowski, Andrzej Rao, Mahendra S. Zeng, Xianmin Sci Rep Article Induced pluripotent stem cells (iPSC) are important tools for drug discovery assays and toxicology screens. In this manuscript, we design high efficiency TALEN and ZFN to target two safe harbor sites on chromosome 13 and 19 in a widely available and well-characterized integration-free iPSC line. We show that these sites can be targeted in multiple iPSC lines to generate reporter systems while retaining pluripotent characteristics. We extend this concept to making lineage reporters using a C-terminal targeting strategy to endogenous genes that express in a lineage-specific fashion. Furthermore, we demonstrate that we can develop a master cell line strategy and then use a Cre-recombinase induced cassette exchange strategy to rapidly exchange reporter cassettes to develop new reporter lines in the same isogenic background at high efficiency. Equally important we show that this recombination strategy allows targeting at progenitor cell stages, further increasing the utility of the platform system. The results in concert provide a novel platform for rapidly developing custom single or dual reporter systems for screening assays. Nature Publishing Group 2015-03-17 /pmc/articles/PMC4361878/ /pubmed/25777362 http://dx.doi.org/10.1038/srep09205 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Pei, Ying
Sierra, Guadalupe
Sivapatham, Renuka
Swistowski, Andrzej
Rao, Mahendra S.
Zeng, Xianmin
A platform for rapid generation of single and multiplexed reporters in human iPSC lines
title A platform for rapid generation of single and multiplexed reporters in human iPSC lines
title_full A platform for rapid generation of single and multiplexed reporters in human iPSC lines
title_fullStr A platform for rapid generation of single and multiplexed reporters in human iPSC lines
title_full_unstemmed A platform for rapid generation of single and multiplexed reporters in human iPSC lines
title_short A platform for rapid generation of single and multiplexed reporters in human iPSC lines
title_sort platform for rapid generation of single and multiplexed reporters in human ipsc lines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4361878/
https://www.ncbi.nlm.nih.gov/pubmed/25777362
http://dx.doi.org/10.1038/srep09205
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