Pluripotency governed by Sox2 via regulation of Oct3/4 expression in mouse embryonic stem cells

被引:889
作者
Masui, Shinji
Nakatake, Yuhki
Toyooka, Yayoi
Shimosato, Daisuke
Yagi, Rika
Takahashi, Kazue
Okochi, Hitoshi
Okuda, Akihiko
Matoba, Ryo
Sharov, Alexei A.
Ko, Minoru S. H.
Niwa, Hitoshi
机构
[1] RIKEN, Ctr Dev Biol, Lab Pluripotent Cell Studies, Chuo Ku, Kobe, Hyogo 6500047, Japan
[2] CREST, Japan Sci & Technol Agcy, Kawaguchi, Saitama 3320012, Japan
[3] Int Med Ctr Japan, Div Mol Biol & Cell Engn, Dept Regenerat Med, Res Inst,Shinjuku Ku, Tokyo 1628655, Japan
[4] Kobe Univ, Lab Dev & Regenerat Med, Grad Sch Med, Chuo Ku, Kobe, Hyogo 6500017, Japan
[5] Saitama Med Univ, Div Dev Biol, Res Ctr Genom Med, Hidaka, Saitama 3501241, Japan
[6] NIA, NIH, Dev Genom & Aging Sect, Genet Lab, Baltimore, MD 21224 USA
关键词
D O I
10.1038/ncb1589
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The pluripotency of embryonic stem (ES) cells is thought to be maintained by a few key transcription factors, including Oct3/4 and Sox2. The function of Oct3/4 in ES cells has been extensively characterized, but that of Sox2 has yet to be determined. Sox2 can act synergistically with Oct3/4 in vitro to activate Oct-Sox enhancers, which regulate the expression of pluripotent stem cell-specific genes, including Nanog, Oct3/4 and Sox2 itself. These findings suggest that Sox2 is required by ES cells for its Oct-Sox enhancer activity. Using inducible Sox2-null mouse ES cells, we show that Sox2 is dispensable for the activation of these Oct-Sox enhancers. In contrast, we demonstrate that Sox2 is necessary for regulating multiple transcription factors that affect Oct3/4 expression and that the forced expression of Oct3/4 rescues the pluripotency of Sox2-null ES cells. These results indicate that the essential function of Sox2 is to stabilize ES cells in a pluripotent state by maintaining the requisite level of Oct3/4 expression.
引用
收藏
页码:625 / U26
页数:15
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