Pcbp1 constrains Oct4 expression in the context of pluripotency

Evgeny I. Bakhmet, Anna S. Zinovyeva, Andrey A. Kuzmin, Daria V. Smirnova, Mikhail N. Gordeev, Ekaterina E. Petrenko, Nikolay D. Aksenov, Alexey N. Tomilin
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Abstract

Oct4 is a commonly known marker of pluripotent stem cells as well as one of the key factors required for pluripotency induction. Its gene (Pou5f1) is subject to complicated regulation through distal and proximal enhancers. Noteworthy, this protein also plays an important role in primitive endoderm (PrE) specification, though the mechanisms driving its expression during this process are still unknown. Here we show that KH-domain protein Pcbp1 occupies poly(C)-sites of the Pou5f1 enhancers, but Pcbp1 knockout does not affect the Oct4 expression level in ESCs. On the contrary, Pcbp1 is essential for timely Oct4 downregulation upon differentiation signals. Residual Oct4 expression in turn leads to PrE specification, and this phenotype is reminiscent of that in ESCs constitutively expressing Oct4. Overall, our results point to Pcbp1 is a transcriptional regulator of Pou5f1, purported to synchronize Oct4 expression decline with the pluripotency network shutdown during differentiation. Oct4 being outside of this network loss its functions as factor of pluripotency and acts as PrE specifier.
Pcbp1 在多能性背景下制约 Oct4 的表达
Oct4 是众所周知的多能干细胞标记,也是诱导多能性所需的关键因子之一。其基因(Pou5f1)通过远端和近端增强子受到复杂的调控。值得注意的是,该蛋白在原始内胚层(PrE)规格化过程中也发挥着重要作用,但其在这一过程中的表达机制尚不清楚。在这里,我们发现KH-domain蛋白Pcbp1占据了Pou5f1增强子的poly(C)位点,但Pcbp1敲除并不影响ESC中Oct4的表达水平。相反,Pcbp1 对分化信号发生时 Oct4 的及时下调至关重要。剩余的 Oct4 表达反过来又会导致 PrE 分化,这种表型与组成型表达 Oct4 的 ESC 中的表型相似。总之,我们的研究结果表明,Pcbp1 是 Pou5f1 的转录调节因子,据说它能使 Oct4 表达的下降与多能性网络在分化过程中的关闭同步。Oct4处于该网络之外,失去了其作为多能性因子的功能,并充当了PrE规格器的角色。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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