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Antisense Transcription across Nucleotide Repeat Expansions in Neurodegenerative and Neuromuscular Diseases: Progress and Mysteries

机译:对神经变性和神经肌肉疾病中核苷酸重复扩展的反义转录:进展和奥秘

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摘要

Unstable repeat expansions and insertions cause more than 30 neurodegenerative and neuromuscular diseases. Remarkably, bidirectional transcription of repeat expansions has been identified in at least 14 of these diseases. More remarkably, a growing number of studies has been showing that both sense and antisense repeat RNAs are able to dysregulate important cellular pathways, contributing together to the observed clinical phenotype. Notably, antisense repeat RNAs from spinocerebellar ataxia type 7, myotonic dystrophy type 1, Huntington’s disease and frontotemporal dementia/amyotrophic lateral sclerosis associated genes have been implicated in transcriptional regulation of sense gene expression, acting either at a transcriptional or posttranscriptional level. The recent evidence that antisense repeat RNAs could modulate gene expression broadens our understanding of the pathogenic pathways and adds more complexity to the development of therapeutic strategies for these disorders. In this review, we cover the amazing progress made in the understanding of the pathogenic mechanisms associated with repeat expansion neurodegenerative and neuromuscular diseases with a focus on the impact of antisense repeat transcription in the development of efficient therapies.
机译:不稳定的重复扩展和插入导致30多种神经变性和神经肌肉疾病。值得注意的是,在这些疾病中至少有14个重复扩展的双向转录已经确定。更值得注意的是,越来越多的研究已经表明,感觉和反义重复RNA能够能够消除重要的细胞途径,促进观察到的临床表型。值得注意的是,来自旋转细胞稳定性的反义重复RNA型7型,肌肌营养不良型1,亨廷顿的疾病和胎儿痴呆/肌萎缩侧乳糖中毒相关基因涉及意识基因表达的转录调节,在转录或后术语水平上作用。最近的证据表明反义重复RNA可以调节基因表达,扩大我们对致病途径的理解,并增加了这些疾病的治疗策略的发展更复杂。在本综述中,我们涵盖了理解与重复膨胀神经变性和神经肌肉疾病相关的致病机制,以重点关注反义重复转录在高效疗法发展中的影响。

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