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Short non-coding RNA biology and neurodegenerative disorders: novel disease targets and therapeutics

机译:短的非编码RNA生物学和神经退行性疾病:新的疾病靶点和治疗方法

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摘要

Genomic studies in model organisms and in humans have shown that complexity in biological systems arises not from the absolute number of genes, but from the differential use of combinations of genetic programmes and the myriad ways in which these are regulated spatially and temporally during development, senescence and in disease. Nowhere is this lesson in biological complexity likely to be more apparent than in the human nervous system. Increasingly, the role of genomic non-protein coding small regulatory RNAs, in particular the microRNAs (miRNAs), in regulating cellular pathways controlling fundamental functions in the nervous system and in neurodegenerative disease is being appreciated. Not only might dysregulated expression of miRNAs serve as potential disease biomarkers but increasingly such short regulatory RNAs are being implicated directly in the pathogenesis of complex, sporadic neurodegenerative disease. Moreover, the targeting and exploitation of short RNA silencing pathways, commonly known as RNA interference, and the development of related tools, offers novel therapeutic approaches to target upstream disease components with the promise of providing future disease modifying therapies for neurodegenerative disorders.
机译:在模型生物和人类中进行的基因组研究表明,生物系统的复杂性不是由基因的绝对数量引起的,而是由遗传程序组合的不同使用以及在发育,衰老过程中时空调控这些遗传程序的无数种方式引起的。和疾病。在生物复杂性方面的这一课比在人的神经系统中更明显。人们越来越认识到基因组非蛋白编码的小调节RNA,特别是微RNA(miRNA)在调节控制神经系统和神经退行性疾病基本功能的细胞途径中的作用。 miRNA的表达失调不仅可能成为潜在的疾病生物标志物,而且越来越短的调控RNA越来越直接地牵涉到复杂的散发性神经退行性疾病的发病机理中。此外,短RNA沉默途径的靶向和开发,通常被称为RNA干扰,以及相关工具的开发,提供了靶向上游疾病成分的新颖治疗方法,有望为神经退行性疾病提供未来的疾病改良疗法。

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