一种不含内源性miRNA前体序列的人工miRNA的新表达系统。

Atsushi Shibata, Akiko Iwaki, Yasuyuki Fukumaki
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引用次数: 0

摘要

近年来,人工microRNA (miRNA)介导的RNA干扰(RNAi)系统已成为研究基因功能的有用工具。我们报道了一个人工miRNA前体基序(AMPM),在环和延伸的茎结构中包含几个限制性位点,并在RNA聚合酶II启动子的控制下生成了一个基于载体的AMPM表达系统。位于选择标记基因的内含子或外显子的AMPM介导了HeLa细胞中报告荧光素酶基因表达的沉默。Northern印迹和集落形成实验表明,AMPM被有效地加工成成熟的miRNA。AMPA系统也在稳定的转染中下调内源性p53和laminA/C蛋白。此外,通过适当的间隔物分隔成簇的AMPM,靶向单个mRNA介导的基因沉默中的不同位点,即使目标序列和AMPM部分互补。这表明簇状AMPMs对高度可变靶点(如人类免疫缺陷病毒1型)具有潜在的治疗效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A novel expression system for artificial miRNAs containing no endogenous miRNA precursor sequences.

Recently, artificial microRNA (miRNA)-mediated RNA interference (RNAi) systems have been developed as useful tools to study gene functions. We report an artificial miRNA precursor motif (AMPM) containing several restriction sites in the loop and in the extended stem structures, and generated a vector-based expression system for AMPM under the control of an RNA polymerase II promoter. The AMPM located in the intron or the exon of the selection marker gene mediated silencing of the reporter luciferase gene expression in HeLa cells. Northern blotting and colony formation assays revealed that the AMPM was efficiently and appropriately processed into mature miRNA. The AMPA system also down-regulated endogenous p53 and laminA/C proteins in stable transfectants. Moreover, clustered AMPMs separated by an appropriate spacer, targeting different sites within a single mRNA mediated gene silencing, even if the sequences of the target and the AMPM were partially complementary. This indicates the potential therapeutic utility of clustered AMPMs for highly-mutable targets, such as human immunodeficiency virus type 1.

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