Identifying Division Symmetry of Mouse Embryonic Stem Cells: Negative Impact of DNA Methyltransferases on Symmetric Self-Renewal

被引:13
作者
Jasnos, Lukasz [1 ]
Aksoy, Fatma Betul [1 ]
Hersi, Hersi Mohamed [1 ]
Wantuch, Slawomir [1 ]
Sawado, Tomoyuki [1 ]
机构
[1] Inst Canc Res, Div Canc Biol, Div Mol Pathol, Haematooncol Res Unit, Sutton SM2 5NG, Surrey, England
关键词
GROUND-STATE PLURIPOTENCY; SINGLY LABELED PROBES; ES CELLS; SIGNALING PATHWAYS; DIFFERENTIATION; GENES; NANOG; IDENTIFICATION; MOLECULES; PROTEINS;
D O I
10.1016/j.stemcr.2013.08.005
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Cell division is a process by which a mother cell divides into genetically identical sister cells, although sister cells often display considerable diversity. In this report, over 350 sister embryonic stem cells (ESCs) were isolated through a microdissection method, and then expression levels of 48 key genes were examined for each sister cell. Our system revealed considerable diversities between sister ESCs at both pluripotent and differentiated states, whereas the similarity between sister ESCs was significantly elevated in a 2i (MEK and GSK3b inhibitors) condition, which is believed to mimic the ground state of pluripotency. DNA methyltransferase 3a/3b were downregulated in 2i-grown ESCs, and the loss of DNA methyltransferases was sufficient to generate nearly identical sister cells. These results suggest that DNA methylation is a major cause of the diversity between sister cells at the pluripotent states, and thus demethylation per se plays an important role in promoting ESC's self-renewal.
引用
收藏
页码:360 / 369
页数:10
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