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Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions

The occurrence of repetitive genomic changes that provide a selective growth advantage in pluripotent stem cells is of concern for their clinical application. However, the effect of different culture conditions on the underlying mutation rate is unknown. Here we show that the mutation rate in two hu...

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Autores principales: Thompson, Oliver, von Meyenn, Ferdinand, Hewitt, Zoe, Alexander, John, Wood, Andrew, Weightman, Richard, Gregory, Sian, Krueger, Felix, Andrews, Simon, Barbaric, Ivana, Gokhale, Paul J., Moore, Harry D., Reik, Wolf, Milo, Marta, Nik-Zainal, Serena, Yusa, Kosuke, Andrews, Peter W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089967/
https://www.ncbi.nlm.nih.gov/pubmed/32251294
http://dx.doi.org/10.1038/s41467-020-15271-3
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author Thompson, Oliver
von Meyenn, Ferdinand
Hewitt, Zoe
Alexander, John
Wood, Andrew
Weightman, Richard
Gregory, Sian
Krueger, Felix
Andrews, Simon
Barbaric, Ivana
Gokhale, Paul J.
Moore, Harry D.
Reik, Wolf
Milo, Marta
Nik-Zainal, Serena
Yusa, Kosuke
Andrews, Peter W.
author_facet Thompson, Oliver
von Meyenn, Ferdinand
Hewitt, Zoe
Alexander, John
Wood, Andrew
Weightman, Richard
Gregory, Sian
Krueger, Felix
Andrews, Simon
Barbaric, Ivana
Gokhale, Paul J.
Moore, Harry D.
Reik, Wolf
Milo, Marta
Nik-Zainal, Serena
Yusa, Kosuke
Andrews, Peter W.
author_sort Thompson, Oliver
collection PubMed
description The occurrence of repetitive genomic changes that provide a selective growth advantage in pluripotent stem cells is of concern for their clinical application. However, the effect of different culture conditions on the underlying mutation rate is unknown. Here we show that the mutation rate in two human embryonic stem cell lines derived and banked for clinical application is low and not substantially affected by culture with Rho Kinase inhibitor, commonly used in their routine maintenance. However, the mutation rate is reduced by >50% in cells cultured under 5% oxygen, when we also found alterations in imprint methylation and reversible DNA hypomethylation. Mutations are evenly distributed across the chromosomes, except for a slight increase on the X-chromosome, and an elevation in intergenic regions suggesting that chromatin structure may affect mutation rate. Overall the results suggest that pluripotent stem cells are not subject to unusually high rates of genetic or epigenetic alterations.
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spelling pubmed-70899672020-03-26 Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions Thompson, Oliver von Meyenn, Ferdinand Hewitt, Zoe Alexander, John Wood, Andrew Weightman, Richard Gregory, Sian Krueger, Felix Andrews, Simon Barbaric, Ivana Gokhale, Paul J. Moore, Harry D. Reik, Wolf Milo, Marta Nik-Zainal, Serena Yusa, Kosuke Andrews, Peter W. Nat Commun Article The occurrence of repetitive genomic changes that provide a selective growth advantage in pluripotent stem cells is of concern for their clinical application. However, the effect of different culture conditions on the underlying mutation rate is unknown. Here we show that the mutation rate in two human embryonic stem cell lines derived and banked for clinical application is low and not substantially affected by culture with Rho Kinase inhibitor, commonly used in their routine maintenance. However, the mutation rate is reduced by >50% in cells cultured under 5% oxygen, when we also found alterations in imprint methylation and reversible DNA hypomethylation. Mutations are evenly distributed across the chromosomes, except for a slight increase on the X-chromosome, and an elevation in intergenic regions suggesting that chromatin structure may affect mutation rate. Overall the results suggest that pluripotent stem cells are not subject to unusually high rates of genetic or epigenetic alterations. Nature Publishing Group UK 2020-03-23 /pmc/articles/PMC7089967/ /pubmed/32251294 http://dx.doi.org/10.1038/s41467-020-15271-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Thompson, Oliver
von Meyenn, Ferdinand
Hewitt, Zoe
Alexander, John
Wood, Andrew
Weightman, Richard
Gregory, Sian
Krueger, Felix
Andrews, Simon
Barbaric, Ivana
Gokhale, Paul J.
Moore, Harry D.
Reik, Wolf
Milo, Marta
Nik-Zainal, Serena
Yusa, Kosuke
Andrews, Peter W.
Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions
title Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions
title_full Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions
title_fullStr Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions
title_full_unstemmed Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions
title_short Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions
title_sort low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7089967/
https://www.ncbi.nlm.nih.gov/pubmed/32251294
http://dx.doi.org/10.1038/s41467-020-15271-3
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