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Genetic aberrations in iPSCs are introduced by a transient G1/S cell cycle checkpoint deficiency
A number of point mutations have been identified in reprogrammed pluripotent stem cells such as iPSCs and ntESCs. The molecular basis for these mutations has remained elusive however, which is a considerable impediment to their potential medical application. Here we report a specific stage at which...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954237/ https://www.ncbi.nlm.nih.gov/pubmed/31924765 http://dx.doi.org/10.1038/s41467-019-13830-x |
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author | Araki, Ryoko Hoki, Yuko Suga, Tomo Obara, Chizuka Sunayama, Misato Imadome, Kaori Fujita, Mayumi Kamimura, Satoshi Nakamura, Miki Wakayama, Sayaka Nagy, Andras Wakayama, Teruhiko Abe, Masumi |
author_facet | Araki, Ryoko Hoki, Yuko Suga, Tomo Obara, Chizuka Sunayama, Misato Imadome, Kaori Fujita, Mayumi Kamimura, Satoshi Nakamura, Miki Wakayama, Sayaka Nagy, Andras Wakayama, Teruhiko Abe, Masumi |
author_sort | Araki, Ryoko |
collection | PubMed |
description | A number of point mutations have been identified in reprogrammed pluripotent stem cells such as iPSCs and ntESCs. The molecular basis for these mutations has remained elusive however, which is a considerable impediment to their potential medical application. Here we report a specific stage at which iPSC generation is not reduced in response to ionizing radiation, i.e. radio-resistance. Quite intriguingly, a G1/S cell cycle checkpoint deficiency occurs in a transient fashion at the initial stage of the genome reprogramming process. These cancer-like phenomena, i.e. a cell cycle checkpoint deficiency resulting in the accumulation of point mutations, suggest a common developmental pathway between iPSC generation and tumorigenesis. This notion is supported by the identification of specific cancer mutational signatures in these cells. We describe efficient generation of human integration-free iPSCs using erythroblast cells, which have only a small number of point mutations and INDELs, none of which are in coding regions. |
format | Online Article Text |
id | pubmed-6954237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69542372020-01-13 Genetic aberrations in iPSCs are introduced by a transient G1/S cell cycle checkpoint deficiency Araki, Ryoko Hoki, Yuko Suga, Tomo Obara, Chizuka Sunayama, Misato Imadome, Kaori Fujita, Mayumi Kamimura, Satoshi Nakamura, Miki Wakayama, Sayaka Nagy, Andras Wakayama, Teruhiko Abe, Masumi Nat Commun Article A number of point mutations have been identified in reprogrammed pluripotent stem cells such as iPSCs and ntESCs. The molecular basis for these mutations has remained elusive however, which is a considerable impediment to their potential medical application. Here we report a specific stage at which iPSC generation is not reduced in response to ionizing radiation, i.e. radio-resistance. Quite intriguingly, a G1/S cell cycle checkpoint deficiency occurs in a transient fashion at the initial stage of the genome reprogramming process. These cancer-like phenomena, i.e. a cell cycle checkpoint deficiency resulting in the accumulation of point mutations, suggest a common developmental pathway between iPSC generation and tumorigenesis. This notion is supported by the identification of specific cancer mutational signatures in these cells. We describe efficient generation of human integration-free iPSCs using erythroblast cells, which have only a small number of point mutations and INDELs, none of which are in coding regions. Nature Publishing Group UK 2020-01-10 /pmc/articles/PMC6954237/ /pubmed/31924765 http://dx.doi.org/10.1038/s41467-019-13830-x 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 Araki, Ryoko Hoki, Yuko Suga, Tomo Obara, Chizuka Sunayama, Misato Imadome, Kaori Fujita, Mayumi Kamimura, Satoshi Nakamura, Miki Wakayama, Sayaka Nagy, Andras Wakayama, Teruhiko Abe, Masumi Genetic aberrations in iPSCs are introduced by a transient G1/S cell cycle checkpoint deficiency |
title | Genetic aberrations in iPSCs are introduced by a transient G1/S cell cycle checkpoint deficiency |
title_full | Genetic aberrations in iPSCs are introduced by a transient G1/S cell cycle checkpoint deficiency |
title_fullStr | Genetic aberrations in iPSCs are introduced by a transient G1/S cell cycle checkpoint deficiency |
title_full_unstemmed | Genetic aberrations in iPSCs are introduced by a transient G1/S cell cycle checkpoint deficiency |
title_short | Genetic aberrations in iPSCs are introduced by a transient G1/S cell cycle checkpoint deficiency |
title_sort | genetic aberrations in ipscs are introduced by a transient g1/s cell cycle checkpoint deficiency |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6954237/ https://www.ncbi.nlm.nih.gov/pubmed/31924765 http://dx.doi.org/10.1038/s41467-019-13830-x |
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