Human embryonic stem cells reveal recurrent genomic instability at 20q11.21

被引:165
作者
Lefort, Nathalie [1 ]
Feyeux, Maxime [1 ]
Bas, Cecile [2 ]
Feraud, Olivier [3 ]
Bennaceur-Griscelli, Annelise [3 ]
Tachdjian, Gerard [2 ]
Peschanski, Marc [1 ]
Perrier, Anselme L. [1 ]
机构
[1] Inst Stem Cell Therapy & Explorat Monogen Dis, AFM, INSERM, UEVE,I STEM,UMR 861, F-91030 Evry, France
[2] Univ Paris 11, Hop Antoine Beclere, INSERM, Serv Biol & Genet Reprod,U782, Clamart, France
[3] Univ Paris 11, Hop Paul Brousse, INSERM, U602, Villejuif, France
关键词
D O I
10.1038/nbt.1509
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
By analyzing five human embryonic stem (hES) cell lines over long-term culture, we identified a recurrent genomic instability in the human genome. An amplification of 2.5-4.6 Mb at 20q11.21, encompassing similar to 23 genes in common, was detected in four cell lines of different origins. This amplification, which has been associated with oncogenic transformation, may provide a selective advantage to hES cells in culture.
引用
收藏
页码:1364 / 1366
页数:3
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