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内源性微小RNA调控可抑制造血谱系中的转基因表达并实现稳定的基因转移。

Endogenous microRNA regulation suppresses transgene expression in hematopoietic lineages and enables stable gene transfer.

作者信息

Brown Brian D, Venneri Mary Anna, Zingale Anna, Sergi Sergi Lucia, Naldini Luigi

机构信息

San Raffaele Telethon Institute for Gene Therapy (HSR-TIGET), via Olgettina 58, 20132 Milano, Italy.

出版信息

Nat Med. 2006 May;12(5):585-91. doi: 10.1038/nm1398. Epub 2006 Apr 23.

Abstract

MicroRNAs (miRNAs) are small noncoding RNAs that regulate gene expression by repressing translation of target cellular transcripts. Increasing evidence indicates that miRNAs have distinct expression profiles and play crucial roles in numerous cellular processes, although the extent of miRNA regulation is not well known. By challenging mice with lentiviral vectors encoding target sequences of endogenous miRNAs, we show the efficiency of miRNAs in sharply segregating gene expression among different tissues. Transgene expression from vectors incorporating target sequences for mir-142-3p was effectively suppressed in intravascular and extravascular hematopoietic lineages, whereas expression was maintained in nonhematopoietic cells. This expression profile, which could not be attained until now, enabled stable gene transfer in immunocompetent mice, thus overcoming a major hurdle to successful gene therapy. Our results provide novel in situ evidence of miRNA regulation and demonstrate a new paradigm in vector design with applications for genetic engineering and therapeutic gene transfer.

摘要

微小RNA(miRNA)是一类小的非编码RNA,通过抑制靶细胞转录本的翻译来调控基因表达。越来越多的证据表明,miRNA具有独特的表达谱,并在众多细胞过程中发挥关键作用,尽管miRNA调控的程度尚不清楚。通过用编码内源性miRNA靶序列的慢病毒载体感染小鼠,我们展示了miRNA在不同组织中显著区分基因表达的效率。整合了mir-142-3p靶序列的载体的转基因表达在血管内和血管外造血谱系中被有效抑制,而在非造血细胞中表达得以维持。这种迄今为止无法实现的表达谱,使得在免疫健全的小鼠中实现稳定的基因转移成为可能,从而克服了成功进行基因治疗的一个主要障碍。我们的结果提供了miRNA调控的新的原位证据,并展示了一种载体设计的新范式,可应用于基因工程和治疗性基因转移。

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