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NF45与NF90/NF110协同调节胚胎干细胞的多能性与分化。

NF45 and NF90/NF110 coordinately regulate ESC pluripotency and differentiation.

作者信息

Ye Julia, Jin Hu, Pankov Aleksandr, Song Jun S, Blelloch Robert

机构信息

The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, Center for Reproductive Sciences, University of California, San Francisco, San Francisco, California 94143, USA.

Department of Urology, University of California, San Francisco, San Francisco, California 94143, USA.

出版信息

RNA. 2017 Aug;23(8):1270-1284. doi: 10.1261/rna.061499.117. Epub 2017 May 9.

Abstract

While years of investigation have elucidated many aspects of embryonic stem cell (ESC) regulation, the contributions of post-transcriptional and translational mechanisms to the pluripotency network remain largely unexplored. In particular, little is known in ESCs about the function of RNA binding proteins (RBPs), the protein agents of post-transcriptional regulation. We performed an unbiased RNAi screen of RBPs in an ESC differentiation assay and identified two related genes, and , whose knockdown promoted differentiation to an epiblast-like state. Characterization of KO, KO, and KO ESCs showed that loss of NF45 or NF90 + NF110 impaired ESC proliferation and led to dysregulated differentiation down embryonic lineages. Additionally, we found that NF45 and NF90/NF110 physically interact and influence the expression of each other at different levels of regulation. Globally across the transcriptome, KO ESCs and + KO ESCs show similar expression changes. Moreover, NF90 + NF110 RNA immunoprecipitation (RIP)-seq in ESCs suggested that NF90/NF110 directly regulate proliferation, differentiation, and RNA-processing genes. Our data support a model in which NF45, NF90, and NF110 operate in feedback loops that enable them, through both overlapping and independent targets, to help balance the push and pull of pluripotency and differentiation cues.

摘要

尽管多年的研究已经阐明了胚胎干细胞(ESC)调控的许多方面,但转录后和翻译机制对多能性网络的贡献在很大程度上仍未得到探索。特别是,在胚胎干细胞中,对于RNA结合蛋白(RBPs)的功能知之甚少,RNA结合蛋白是转录后调控的蛋白因子。我们在胚胎干细胞分化试验中对RNA结合蛋白进行了无偏向性RNA干扰筛选,并鉴定出两个相关基因,其敲低促进了向类外胚层状态的分化。对NF45基因敲除、NF90+NF110基因敲除和NF90基因敲除的胚胎干细胞的表征表明,NF45或NF90+NF110的缺失损害了胚胎干细胞的增殖,并导致沿胚胎谱系的分化失调。此外,我们发现NF45和NF90/NF110在物理上相互作用,并在不同的调控水平上相互影响表达。在整个转录组中,NF45基因敲除的胚胎干细胞和NF90+NF110基因敲除的胚胎干细胞显示出相似的表达变化。此外,胚胎干细胞中的NF90+NF110 RNA免疫沉淀(RIP)-测序表明,NF90/NF直接调控增殖、分化和RNA加工基因。我们的数据支持了一个模型,其中NF45、NF90和NF110在反馈回路中发挥作用,通过重叠和独立的靶标,帮助平衡多能性和分化信号的推拉。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46a6/5513071/cebbcd024b89/1270f01.jpg

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