Nanog and transcriptional networks in embryonic stem cell pluripotency

被引:0
|
作者
Guangjin Pan
James A Thomson
机构
[1] The Wisconsin National Primate Research Center,The Department of Anatomy
[2] University of Wisconsin-Madison,undefined
[3] The Genome Center of Wisconsin,undefined
[4] WiCell Research Institute,undefined
[5] PO Box 7365,undefined
[6] University of Wisconsin-Madison Medical School,undefined
来源
Cell Research | 2007年 / 17卷
关键词
Nanog; embryonic stem cell pluripotency; transcription factor;
D O I
暂无
中图分类号
学科分类号
摘要
Several extrinsic signals such as LIF, BMP and Wnt can support the self-renewal and pluripotency of embryonic stem (ES) cells through regulating the “pluripotent genes.” A unique homeobox transcription factor, Nanog, is one of the key downstream effectors of these signals. Elevated level of Nanog can maintain the mouse ES cell self-renewal independent of LIF and enable human ES cell growth without feeder cells. In addition to the external signal pathways, intrinsic transcription factors such as FoxD3, P53 and Oct4 are also involved in regulating the expression of Nanog. Functionally, Nanog works together with other key pluripotent factors such as Oct4 and Sox2 to control a set of target genes that have important functions in ES cell pluripotency. These key factors form a regulatory network to support or limit each other's expression level, which maintains the properties of ES cells.
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页码:42 / 49
页数:7
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