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Orphan Nuclear Receptor GCNF Is Required for the Repression of Pluripotency Genes during Retinoic Acid-Induced Embryonic Stem Cell Differentiation

机译:维甲酸诱导胚胎干细胞分化过程中多能性基因的抑制需要孤儿核受体GCNF。

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摘要

Embryonic stem (ES) cell pluripotency and differentiation are controlled by a network of transcription factors and signaling molecules. Transcription factors such as Oct4 and Nanog are required for self-renewal and maintain the undifferentiated state of ES cells. Decreases in the expression of these factors indicate the initiation of differentiation of ES cells. Inactivation of the gene encoding the orphan nuclear receptor GCNF showed that it plays an important role in the repression of Oct4 expression in somatic cells during early embryonic development. GCNF−/− ES cells were isolated to study the function of GCNF in the down-regulation of pluripotency genes during differentiation. Loss of repression of ES cell marker genes Oct4, Nanog, Sox2, FGF4, and Stella was observed upon treatment of GCNF−/− ES cells with retinoic acid. The loss of repression of pluripotency genes is either a direct or indirect consequence of loss of GCNF. Both the Oct4 and Nanog genes are direct targets of GCNF repression during ES cell differentiation and early mouse embryonic development. In contrast Sox2 and FGF4 are indirectly regulated by GCNF through Oct4. These findings establish a central role for GCNF in the repression of pluripotency gene expression during retinoic acid-induced ES cell differentiation.
机译:胚胎干(ES)细胞的多能性和分化受转录因子和信号分子网络的控制。自我更新和维持ES细胞未分化状态需要转录因子(例如Oct4和Nanog)。这些因子表达的降低表明ES细胞分化的开始。编码孤儿核受体GCNF的基因失活表明,它在早期胚胎发育过程中在抑制体细胞中Oct4表达中起重要作用。分离GCNF -/- ES细胞,研究GCNF在分化过程中多能性基因下调中的功能。用视黄酸处理GCNF -/- ES细胞后,观察到ES细胞标记基因Oct4,Nanog,Sox2,FGF4和Stella的阻遏丧失。多能性基因抑制的丧失是GCNF丧失的直接或间接后果。 Oct4和Nanog基因都是ES细胞分化和早期小鼠胚胎发育过程中GCNF抑制的直接靶标。相反,Soc2和FGF4通过Oct4受到GCNF的间接调控。这些发现建立了视黄酸诱导的ES细胞分化过程中GCNF在多能性基因表达抑制中的核心作用。

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