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体外和体内的小干扰RNA介导的基因沉默

siRNA-mediated gene silencing in vitro and in vivo.

作者信息

Xia Haibin, Mao Qinwen, Paulson Henry L, Davidson Beverly L

机构信息

Program in Gene Therapy, Department of Internal Medicine, University of Iowa College of Medicine, Iowa City, IA 52242, USA.

出版信息

Nat Biotechnol. 2002 Oct;20(10):1006-10. doi: 10.1038/nbt739. Epub 2002 Sep 16.

Abstract

RNA interference is now established as an important biological strategy for gene silencing, but its application to mammalian cells has been limited by nonspecific inhibitory effects of long dsRNA on translation. Here, we describe a viral-mediated delivery mechanism that results in specific silencing of targeted genes through expression of small interfering RNA (siRNA). We establish proof of principle by markedly diminishing expression of exogenous and endogenous genes in vitro and in vivo in brain and liver, and further apply this strategy to a model system of a major class of neurodegenerative disorders, the polyglutamine diseases, to show reduced polyglutamine aggregation in cells. This viral-mediated strategy should prove generally useful in reducing expression of target genes to model biological processes or to provide therapy for dominant human diseases.

摘要

RNA干扰现已成为一种重要的基因沉默生物学策略,但其在哺乳动物细胞中的应用一直受到长双链RNA对翻译的非特异性抑制作用的限制。在此,我们描述了一种病毒介导的递送机制,该机制通过小干扰RNA(siRNA)的表达导致靶向基因的特异性沉默。我们通过在体外以及脑和肝的体内实验中显著降低外源和内源基因的表达来建立原理证明,并进一步将该策略应用于一大类神经退行性疾病——多聚谷氨酰胺疾病的模型系统,以显示细胞中多聚谷氨酰胺聚集的减少。这种病毒介导的策略在降低靶基因表达以模拟生物学过程或为显性人类疾病提供治疗方面应具有普遍的实用性。

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