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Error-free and error-prone DNA repair gene expression data through reprogramming and passage in human iPS cells

We recently found that DNA repair-related gene expression could be altered by reprogramming as well as the increased expression of genes that accurately convey genomic information, such as homologous recombination (HR) and mismatch repair (MMR), and the decreased expression of error-prone translesio...

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Autores principales: Yoshimura, Yasuhide, Okuzaki, Daisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016224/
https://www.ncbi.nlm.nih.gov/pubmed/32071995
http://dx.doi.org/10.1016/j.dib.2020.105228
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author Yoshimura, Yasuhide
Okuzaki, Daisuke
author_facet Yoshimura, Yasuhide
Okuzaki, Daisuke
author_sort Yoshimura, Yasuhide
collection PubMed
description We recently found that DNA repair-related gene expression could be altered by reprogramming as well as the increased expression of genes that accurately convey genomic information, such as homologous recombination (HR) and mismatch repair (MMR), and the decreased expression of error-prone translesion synthesis (TLS) polymerase. Here, we confirmed this change in expression in another cell-line and found that such alteration was maintained by overlapping passages as well as OCT3/4 and NANOG. Our findings suggest that changes in the expression of DNA repair-related genes associated with reprogramming and their maintenance can be novel indicators of the quality control of the cells exhibiting pluripotency.
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spelling pubmed-70162242020-02-18 Error-free and error-prone DNA repair gene expression data through reprogramming and passage in human iPS cells Yoshimura, Yasuhide Okuzaki, Daisuke Data Brief Biochemistry, Genetics and Molecular Biology We recently found that DNA repair-related gene expression could be altered by reprogramming as well as the increased expression of genes that accurately convey genomic information, such as homologous recombination (HR) and mismatch repair (MMR), and the decreased expression of error-prone translesion synthesis (TLS) polymerase. Here, we confirmed this change in expression in another cell-line and found that such alteration was maintained by overlapping passages as well as OCT3/4 and NANOG. Our findings suggest that changes in the expression of DNA repair-related genes associated with reprogramming and their maintenance can be novel indicators of the quality control of the cells exhibiting pluripotency. Elsevier 2020-02-06 /pmc/articles/PMC7016224/ /pubmed/32071995 http://dx.doi.org/10.1016/j.dib.2020.105228 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Biochemistry, Genetics and Molecular Biology
Yoshimura, Yasuhide
Okuzaki, Daisuke
Error-free and error-prone DNA repair gene expression data through reprogramming and passage in human iPS cells
title Error-free and error-prone DNA repair gene expression data through reprogramming and passage in human iPS cells
title_full Error-free and error-prone DNA repair gene expression data through reprogramming and passage in human iPS cells
title_fullStr Error-free and error-prone DNA repair gene expression data through reprogramming and passage in human iPS cells
title_full_unstemmed Error-free and error-prone DNA repair gene expression data through reprogramming and passage in human iPS cells
title_short Error-free and error-prone DNA repair gene expression data through reprogramming and passage in human iPS cells
title_sort error-free and error-prone dna repair gene expression data through reprogramming and passage in human ips cells
topic Biochemistry, Genetics and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016224/
https://www.ncbi.nlm.nih.gov/pubmed/32071995
http://dx.doi.org/10.1016/j.dib.2020.105228
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