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首页> 外文期刊>Molecular Neurobiology >MicroRNA-338 Attenuates Cortical Neuronal Outgrowth by Modulating the Expression of Axon Guidance Genes
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MicroRNA-338 Attenuates Cortical Neuronal Outgrowth by Modulating the Expression of Axon Guidance Genes

机译:MicroRNA-338通过调节轴突引导基因的表达来衰减皮质神经元产量

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摘要

MicroRNAs (miRs) are small non-coding RNAs that confer robustness to gene networks through post-transcriptional gene regulation. Previously, we identified miR-338 as a modulator of axonal outgrowth in sympathetic neurons. In the current study, we examined the role of miR-338 in the development of cortical neurons and uncovered its downstream mRNA targets. Long-term inhibition of miR-338 during neuronal differentiation resulted in reduced dendritic complexity and altered dendritic spine morphology. Furthermore, monitoring axon outgrowth in cortical cells revealed that miR-338 overexpression decreased, whereas inhibition of miR-338 increased axonal length. To identify gene targets mediating the observed phenotype, we inhibited miR-338 in cortical neurons and performed whole-transcriptome analysis. Pathway analysis revealed that miR-338 modulates a subset of transcripts involved in the axonal guidance machinery by means of direct and indirect gene targeting. Collectively, our results implicate miR-338 as a novel regulator of cortical neuronal maturation by fine-tuning the expression of gene networks governing cortical outgrowth.
机译:MicroRNA(MIRS)是小型非编码RNA,通过转录后基因调控赋予基因网络的鲁棒性。以前,我们将MIR-338识别为交感神经元轴突上的轴突过度的调节剂。在目前的研究中,我们检查了MIR-338在皮质神经元的发育中的作用,并发现了其下游mRNA靶标。神经细分期间miR-338的长期抑制导致树枝状复杂性降低和树突脊柱形态改变。此外,在皮质细胞中监测轴突外生长显示,MIR-338过表达降低,而MIR-338的抑制增加了轴突长度。为了鉴定介导观察到的表型的基因靶,我们抑制皮质神经元中的miR-338并进行了全转录组分析。途径分析显示,MiR-338通过直接和间接基因靶向调节伴随轴突引导机械中涉及的转录物的子集。通过微调治疗皮质遗传的基因网络的表达,集体,我们的结果通过微调基因网络的表达来暗示MiR-338作为皮质神经元成熟的新调节因子。

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