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胚胎干细胞多能性中的Nanog与转录网络

Nanog and transcriptional networks in embryonic stem cell pluripotency.

作者信息

Pan Guangjin, Thomson James A

机构信息

The Wisconsin National Primate Research Center, University of Wisconsin-Madison, 1220 Capitol Court, Madison, WI 53715-1299, USA.

出版信息

Cell Res. 2007 Jan;17(1):42-9. doi: 10.1038/sj.cr.7310125.

Abstract

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.

摘要

几种外在信号,如白血病抑制因子(LIF)、骨形态发生蛋白(BMP)和Wnt,可以通过调节“多能基因”来支持胚胎干细胞(ES细胞)的自我更新和多能性。一种独特的同源盒转录因子Nanog是这些信号的关键下游效应器之一。Nanog水平的升高可以维持小鼠ES细胞的自我更新而不依赖LIF,并使人ES细胞在没有饲养层细胞的情况下生长。除了外部信号通路外,内在转录因子如FoxD3、P53和Oct4也参与调节Nanog的表达。在功能上,Nanog与其他关键的多能因子如Oct4和Sox2共同作用,控制一组在ES细胞多能性中具有重要功能的靶基因。这些关键因子形成一个调控网络,相互支持或限制彼此的表达水平,从而维持ES细胞的特性。

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