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Interaction of the primordial germ cell-specific protein C2EIP with PTCH2 directs differentiation of embryonic stem cells via HH signaling activation

机译:原始生殖细胞特异性蛋白C2EIP与PTCH2的相互作用通过HH信号激活指导胚胎干细胞的分化

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摘要

Although many marker genes for germ cell differentiation have been identified, genes that specifically regulate primordial germ cell (PGC) generation are more difficult to determine. In the current study, we confirmed that C2EIP is a PGC marker gene that regulates differentiation by influencing the expression of pluripotency-associated genes such as Oct4 and Sox2. Knockout of C2EIP during embryonic development reduced PGC generation efficiency 1.5-fold, whereas C2EIP overexpression nearly doubled the generation efficiency both in vitro and in vivo. C2EIP encodes a cytoplasmic protein that interacted with PTCH2 at the intracellular membrane, promoted PTCH2 ubiquitination, activated the Hedgehog (HH) signaling pathway via competitive inhibition of the GPCR-like protein SMO, and positively regulated PGC generation. Activation and expression of C2EIP are regulated by the transcription factor STAT1, histone acetylation, and promoter methylation. Our data suggest that C2EIP is a novel, specific indicator of PGC generation whose gene product regulates embryonic stem cell differentiation by activating the HH signaling pathway via PTCH2 modification.
机译:尽管已鉴定出许多用于生殖细胞分化的标记基因,但更难以确定特异性调节原始生殖细胞(PGC)生成的基因。在当前的研究中,我们证实C2EIP是一个PGC标记基因,可通过影响多能性相关基因(例如Oct4和Sox2)的表达来调节分化。在胚胎发育过程中敲除C2EIP可使PGC的产生效率降低1.5倍,而C2EIP的过表达在体内和体外的产生效率几乎增加了一倍。 C2EIP编码一种胞质蛋白,该蛋白与胞内膜上的PTCH2相互作用,促进PTCH2泛素化,通过竞争性抑制GPCR样蛋白SMO激活Hedgehog(HH)信号通路,并积极调节PGC的产生。 C2EIP的激活和表达受转录因子STAT1,组蛋白乙酰化和启动子甲基化的调节。我们的数据表明,C2EIP是PGC生成的一种新型,特异性指示剂,其基因产物通过通过PTCH2修饰激活HH信号通路来调节胚胎干细胞的分化。

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