Cullen Bryan R
Department of Molecular Genetics and Microbiology, Howard Hughes Medical Institute, Duke University Medical Center, Durham, NC 27710, USA.
Virus Res. 2004 Jun 1;102(1):3-9. doi: 10.1016/j.virusres.2004.01.009.
Small interfering RNA (siRNA) duplexes are generally produced by Dicer cleavage of double-stranded RNAs of frequently exogenous origin and can induce the cleavage and degradation of mRNAs bearing an identical sequence. In contrast, microRNAs (miRNAs) are encoded within the eukaryotic genome as short RNA hairpin structures. While these pre-miRNAs are also processed by Dicer, mature miRNAs appear to function primarily by inhibiting the translation of mRNAs bearing multiple, partially mismatched target sites. Nevertheless, recent data argue that the posttranscriptional regulatory machinery utilized by siRNAs and miRNAs is largely or entirely identical. In this review, I will discuss recent progress in unraveling the RNA processing pathway utilized for the biosynthesis of mature miRNAs and argue that this pathway offers at least three distinct entry points for the functional expression of artificial siRNAs in vertebrate cells. While each of these entry points offers distinct advantages and disadvantages, they all have the potential to induce the effective knock-down of specific genes either in cell culture or in experimental animals.
小干扰RNA(siRNA)双链体通常由Dicer切割常见外源来源的双链RNA产生,并可诱导具有相同序列的mRNA的切割和降解。相比之下,微小RNA(miRNA)在真核基因组中编码为短RNA发夹结构。虽然这些前体miRNA也由Dicer加工,但成熟的miRNA似乎主要通过抑制具有多个部分错配靶位点的mRNA的翻译来发挥作用。然而,最近的数据表明,siRNA和miRNA利用的转录后调控机制在很大程度上或完全相同。在这篇综述中,我将讨论在揭示用于成熟miRNA生物合成的RNA加工途径方面的最新进展,并认为该途径为人工siRNA在脊椎动物细胞中的功能表达提供了至少三个不同的切入点。虽然这些切入点都有各自的优缺点,但它们都有可能在细胞培养或实验动物中诱导特定基因的有效敲低。