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Genetic ablation of Dicer in adult forebrain neurons results in abnormal tau hyperphosphorylation and neurodegeneration.成年大脑神经元中 Dicer 的基因缺失导致异常的 tau 过度磷酸化和神经退行性变。
Hum Mol Genet. 2010 Oct 15;19(20):3959-69. doi: 10.1093/hmg/ddq311. Epub 2010 Jul 21.
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Large-scale expression analysis reveals distinct microRNA profiles at different stages of human neurodevelopment.大规模表达分析揭示了人类神经发育不同阶段的独特 microRNA 图谱。
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miR-7 and miR-214 are specifically expressed during neuroblastoma differentiation, cortical development and embryonic stem cells differentiation, and control neurite outgrowth in vitro.miR-7 和 miR-214 在神经母细胞瘤分化、皮质发育和胚胎干细胞分化过程中特异性表达,并在体外控制神经突生长。
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MicroRNA-mediated control of oligodendrocyte differentiation.微小 RNA 介导的少突胶质细胞分化调控。
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Dicer1 and miR-219 Are required for normal oligodendrocyte differentiation and myelination.Dicer1 和 miR-219 对于正常少突胶质细胞分化和髓鞘形成是必需的。
Neuron. 2010 Mar 11;65(5):597-611. doi: 10.1016/j.neuron.2010.01.027.
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MicroRNA let-7b regulates neural stem cell proliferation and differentiation by targeting nuclear receptor TLX signaling.miRNA let-7b 通过靶向核受体 TLX 信号调控神经干细胞的增殖和分化。
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BMPR1a and BMPR1b signaling exert opposing effects on gliosis after spinal cord injury.BMPR1a 和 BMPR1b 信号在脊髓损伤后对神经胶质增生发挥相反的作用。
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中枢神经系统创伤和退行性疾病中的 microRNA。

MicroRNA in central nervous system trauma and degenerative disorders.

机构信息

Spinal Cord and Brain Injury Research Group, Stark Neurosciences Research Institute and Department of Neurological Surgery, Indiana University School of Medicine, Indianapolis, Indiana. 46202, USA.

出版信息

Physiol Genomics. 2011 May 1;43(10):571-80. doi: 10.1152/physiolgenomics.00168.2010. Epub 2011 Mar 8.

DOI:10.1152/physiolgenomics.00168.2010
PMID:21385946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3110891/
Abstract

MicroRNAs (miRNAs) are a novel class of small noncoding RNAs that negatively regulate gene expression at the posttranscriptional level by binding to the 3'-untranslated region of target mRNAs leading to their translational inhibition or sometimes degradation. MiRNAs are predicted to control the activity of at least 20-30% of human protein-coding genes. Recent studies have demonstrated that miRNAs are highly expressed in the central nervous system (CNS) including the brain and spinal cord. Although we are currently in the initial stages of understanding how this novel class of gene regulators is involved in neurological biological functions, a growing body of exciting evidence suggests that miRNAs are important regulators of diverse biological processes such as cell differentiation, growth, proliferation, and apoptosis. Moreover, miRNAs are key modulators of both CNS development and plasticity. Some miRNAs have been implicated in several neurological disorders such as traumatic CNS injuries and neurodegenerative diseases. Recently, several studies suggested the possibility of miRNA involvement in neurodegeneration. Identifying the roles of miRNAs and their target genes and signaling pathways in neurological disorders will be critical for future research. miRNAs may represent a new layer of regulators for neurobiology and a novel class of therapeutic targets for neurological diseases.

摘要

微小 RNA(miRNA)是一类新型的小非编码 RNA,通过与靶 mRNA 的 3'非翻译区结合,在转录后水平负调控基因表达,导致其翻译抑制或有时降解。miRNA 预计可以控制至少 20-30%的人类蛋白编码基因的活性。最近的研究表明,miRNA 在中枢神经系统(CNS)中高度表达,包括大脑和脊髓。虽然我们目前正处于理解这一新类基因调控因子如何参与神经生物学功能的初始阶段,但越来越多令人兴奋的证据表明,miRNA 是细胞分化、生长、增殖和凋亡等多种生物学过程的重要调控因子。此外,miRNA 是中枢神经系统发育和可塑性的关键调节剂。一些 miRNA 已被牵连到几种神经疾病中,如创伤性中枢神经系统损伤和神经退行性疾病。最近,一些研究表明 miRNA 可能参与神经退行性变。确定 miRNA 及其靶基因和信号通路在神经疾病中的作用,将是未来研究的关键。miRNA 可能代表神经生物学的一个新的调控层,也是神经疾病的一类新的治疗靶点。