利用microRNA调控基因工程。

Tissue antigens Pub Date : 2012-11-01 DOI:10.1111/tan.12002
B Gentner, L Naldini
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引用次数: 36

摘要

RNA干扰(RNAi)是科学上具有里程碑意义的发现。一个典型的应用是通过将小干扰RNA (siRNA)传递到细胞中触发互补mRNA的降解来降低内源性基因的表达。然而,RNAi也可以反过来利用:利用内源性microrna (miRNA)的巨大多样性,外源引入的标记有人工miRNA靶序列的基因的表达可以根据给定miRNA的活性进行负调控,这些miRNA可以是组织特异性的,谱系特异性的,激活特异性的或分化阶段特异性的。这极大地扩展了基因转移载体的调控潜力,并将有利于基础科学和治疗应用。本文简要介绍了利用miRNA调控的技术基础,然后讨论了miRNA调控载体/病毒在基础研究、基因和病毒治疗中的具体应用。
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Exploiting microRNA regulation for genetic engineering.

RNA interference (RNAi) has been a landmark discovery in science. A typical application is to knock down the expression of endogenous genes by delivering small interfering RNA (siRNA) into cells triggering the degradation of complementary mRNA. However, RNAi can also be exploited the other way round: making use of the huge diversity of endogenous microRNAs (miRNA), the expression of exogenously introduced genes tagged with artificial miRNA target sequences can be negatively regulated according to the activity of a given miRNA which can be tissue-, lineage-, activation- or differentiation stage specific. This has significantly expanded the regulatory potential of gene transfer vectors and will benefit both basic science and therapeutic applications. This review briefly introduces the reader to the technical basis for exploiting miRNA regulation, followed by a discussion of specific applications for miRNA-regulated vectors/viruses in basic research, gene- and virotherapy.

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来源期刊
Tissue antigens
Tissue antigens 医学-病理学
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审稿时长
6 months
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