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Gene silencing using micro-RNA designed hairpins.

机译:使用微RNA设计的发夹进行基因沉默。

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摘要

During RNA interference (RNAi), long dsRNA is processed to approximately 21 nt duplexes, short interfering RNAs (siRNAs), which silence genes through a mRNA degradation pathway. Small temporal RNAs (stRNAs) and micro-RNAs (miRNAs) are approximately 21 nt RNAs that are processed from endogenously encoded hairpin-structured precursors, and function to silence genes via translational repression. Here we report that synthetic hairpin RNAs that mimic siRNAs and miRNA precursor molecules can target a gene for silencing, and the mechanism of silencing appears to be through mRNA degradation and not translational repression. The sequence and structural configuration of these RNAs are important, and even slight modification in structure can affect the silencing activity of the hairpins. Furthermore, these RNAs are active when expressed by DNA vectors containing polymerase III promoters, opening the possibility for new approaches in stable RNAi-based loss of function studies.
机译:在RNA干扰(RNAi)期间,长dsRNA被加工成大约21 nt的双链体,即短干扰RNA(siRNA),通过mRNA降解途径使基因沉默。小型临时RNA(stRNA)和微小RNA(miRNA)约为21 nt RNA,它们是由内源编码的发夹结构前体加工而成的,可通过翻译抑制沉默基因。在这里我们报道,模仿siRNA和miRNA前体分子的合成发夹RNA可以靶向沉默基因,而沉默的机制似乎是通过mRNA降解而不是翻译抑制。这些RNA的序列和结构构型很重要,即使结构上的微小修饰也会影响发夹的沉默活性。此外,这些RNA在含有聚合酶III启动子的DNA载体表达时具有活性,为基于RNAi的稳定功能丧失研究中的新方法开辟了可能性。

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