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雌激素相关受体β与八聚体结合转录因子4相互作用,正向调控Nanog基因的表达。

Estrogen-related receptor beta interacts with Oct4 to positively regulate Nanog gene expression.

作者信息

van den Berg Debbie L C, Zhang Wensheng, Yates Adam, Engelen Erik, Takacs Katalin, Bezstarosti Karel, Demmers Jeroen, Chambers Ian, Poot Raymond A

机构信息

Department of Cell Biology, Erasmus MC, Dr. Molewaterplein 50, 3015GE Rotterdam, The Netherlands.

出版信息

Mol Cell Biol. 2008 Oct;28(19):5986-95. doi: 10.1128/MCB.00301-08. Epub 2008 Jul 28.

Abstract

Embryonic stem (ES) cell self-renewal is regulated by transcription factors, including Oct4, Sox2, and Nanog. A number of additional transcriptional regulators of ES cell self-renewal have recently been identified, including the orphan nuclear receptor estrogen-related receptor beta (Esrrb). However, the mode of action of Esrrb in ES cells is unknown. Here, using an Oct4 affinity screen, we identify Esrrb as an Oct4 partner protein. Esrrb can interact with Oct4 independently of DNA. Esrrb is recruited near the Oct-Sox element in the Nanog proximal promoter, where it positively regulates Nanog expression. Esrrb recruitment to the Nanog promoter requires both the presence of Oct4 and a degenerate estrogen-related receptor DNA element. Consistent with its role in Nanog regulation, expression of the Esrrb protein within the Oct4-positive ES cell population is mosaic and correlates with the mosaic expression of the Nanog protein. Together with previous reports that Nanog may regulate Esrrb gene expression, our results suggest that Esrrb and Nanog act as part of a feedback regulatory circuit that modulates the fluctuating self-renewal capacity of ES cell populations.

摘要

胚胎干细胞(ES细胞)的自我更新受转录因子调控,包括Oct4、Sox2和Nanog。最近还鉴定出了一些ES细胞自我更新的其他转录调节因子,包括孤儿核受体雌激素相关受体β(Esrrb)。然而,Esrrb在ES细胞中的作用模式尚不清楚。在此,我们通过Oct4亲和筛选,将Esrrb鉴定为Oct4的伙伴蛋白。Esrrb可独立于DNA与Oct4相互作用。Esrrb被招募到Nanog近端启动子中的Oct-Sox元件附近,在那里它正向调节Nanog的表达。Esrrb被招募到Nanog启动子需要Oct4的存在以及一个简并的雌激素相关受体DNA元件。与其在Nanog调节中的作用一致,Esrrb蛋白在Oct4阳性ES细胞群体中的表达是镶嵌式的,并且与Nanog蛋白的镶嵌式表达相关。结合之前关于Nanog可能调节Esrrb基因表达的报道,我们的结果表明,Esrrb和Nanog作为反馈调节回路的一部分发挥作用,该回路调节ES细胞群体波动的自我更新能力。

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