Core transcriptional regulatory circuitry in human embryonic stem cells

被引:3578
作者
Boyer, LA
Lee, TI
Cole, MF
Johnstone, SE
Levine, SS
Zucker, JR
Guenther, MG
Kumar, RM
Murray, HL
Jenner, RG
Gifford, DK
Melton, DA
Jaenisch, R
Young, RA
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02139 USA
[3] Harvard Univ, Howard Hughes Med Inst, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
[4] MIT, CSAIL, Cambridge, MA 02139 USA
[5] MIT, Broad Inst, Cambridge, MA 02139 USA
[6] Harvard Univ, Broad Inst, Cambridge, MA 02139 USA
关键词
D O I
10.1016/j.cell.2005.08.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transcription factors OCT4, SOX2, and NANOG have essential roles in early development and are required for the propagation of undifferentiated embryonic stem (ES) cells in culture. To gain insights into transcriptional regulation of human ES cells, we have identified OCT4, SOX2, and NANOG target genes using genome-scale location analysis. We found, surprisingly, that OCT4, SOX2, and NANOG co-occupy a substantial portion of their target genes. These target genes frequently encode transcription factors, many of which are developmentally important homeodomain proteins. Our data also indicate that OCT4, SOX2, and NANOG collaborate to form regulatory circuitry consisting of autoregulatory and feedforward loops. These results provide new insights into the transcriptional regulation of stem cells and reveal how OCT4, SOX2, and NANOG contribute to pluripotency and self-renewal.
引用
收藏
页码:947 / 956
页数:10
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