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Functional regulation of FoxO1 in neural stem cell differentiation

机译:FoxO1在神经干细胞分化中的功能调节

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摘要

Forkhead transcription factor family O (FoxO) maintains adult stem cell reserves by supporting their long-term proliferative potential. MicroRNAs (miRs) regulate neuronal stem/progenitor cell (NSPC) proliferation and differentiation during neural development by controlling the expression of a specific set of target genes. In the neurogenic subventricular zone, FoxO1 is specifically expressed in NSPCs and is no longer detected during the transition to neuroblast stage, forming an inverse correlation with miR-9 expression. The 3′-untranslated region of FoxO1 contains a conserved target sequence of miR-9 and FoxO1 expression is coordinated in concert with miR-9 during neuronal differentiation. Our study demonstrates that FoxO1 contributes to NSPC fate decision through its cooperation with the Notch signaling pathway.
机译:叉头转录因子家族O(FoxO)通过支持其长期增殖潜力来维持成人干细胞储备。 MicroRNA(miR)通过控制一组特定的靶基因的表达来调节神经发育过程中神经元干/祖细胞(NSPC)的增殖和分化。在神经源性脑室下区,FoxO1在NSPCs中特异性表达,在过渡到成神经细胞阶段期间不再被检测到,与miR-9表达呈反相关。 FoxO1的3'-非翻译区包含一个保守的miR-9靶序列,在神经元分化过程中FoxO1的表达与miR-9协调。我们的研究表明,FoxO1通过与Notch信号通路的合作为NSPC的命运决定做出了贡献。

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