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

被引:132
作者
van den Berg, Debbie L. C. [1 ]
Zhang, Wensheng [2 ]
Yates, Adam [2 ]
Engelen, Erik [1 ]
Takacs, Katalin [3 ]
Bezstarosti, Karel [4 ]
Demmers, Jeroen [4 ]
Chambers, Ian [2 ]
Poot, Raymond A. [1 ]
机构
[1] Erasmus MC, Dept Cell Biol, NL-3015 GE Rotterdam, Netherlands
[2] Univ Edinburgh, Sch Biol Sci, Inst Stem Cell Res, MRC,Ctr Regenerat Med, Edinburgh EH9 3JQ, Midlothian, Scotland
[3] MRC, Ctr Clin Sci, London W12 0NN, England
[4] Erasmus MC, Prote Ctr, NL-3015 GE Rotterdam, Netherlands
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1128/MCB.00301-08
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
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.
引用
收藏
页码:5986 / 5995
页数:10
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