オバラ チズカ
Obara Chizuka
小原 千寿香 所属 東邦大学 理学部 生物学科 職種 博士研究員 |
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論文種別 | 原著 |
言語種別 | 英語 |
査読の有無 | 査読あり |
表題 | Genetic aberrations in iPSCs are introduced by a transient G1/S cell cycle checkpoint deficiency. |
掲載誌名 | 正式名:Nature communications |
掲載区分 | 国外 |
巻・号・頁 | 11(1),pp.197-197 |
著者・共著者 | Ryoko Araki,Yuko Hoki,Tomo Suga,Chizuka Obara,Misato Sunayama,Kaori Imadome,Mayumi Fujita,Satoshi Kamimura,Miki Nakamura,Sayaka Wakayama,Andras Nagy,Teruhiko Wakayama,Masumi Abe |
発行年月 | 2020/01/10 |
概要 | 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. |
DOI | 10.1038/s41467-019-13830-x |
PMID | 31924765 |
PermalinkURL | https://www.nature.com/articles/s41467-019-13830-x#citeas |