Longer 19-base pair short interfering RNA duplexes rather than shorter duplexes trigger RNA interference.

Malgorzata Sierant, Julia Kazmierczak-Baranska, Alina Paduszynska, Milena Sobczak, Aleksandra Pietkiewicz, Barbara Nawrot
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引用次数: 7

Abstract

Short interfering RNAs (siRNAs) are valuable reagents for sequence-specific inhibition of gene expression via the RNA interference (RNAi) pathway. Recently, it was suggested that 16-bp siRNAs are effective RNAi triggers and superior to "classical" 19-bp siRNAs. This contradiction with generally accepted knowledge prompted us to reinvestigate this issue. Here, in a series of experiments performed with siRNA duplexes of various lengths (from 19 to 15 bp) designed to silence either overexpressed enhanced green fluorescent protein or endogenously expressed CDK9, we demonstrate that 19-bp siRNAs are more active silencers than shorter corresponding duplexes. The discrepancy between our results and those questioned appears to be due to different modes of shortening the duplex (either at the 3'-end or at the 5'-end, with respect to polarity of the guide strand). Importantly, duplexes with intact 5'-ends but shortened at their 3'-ends retain target site specificity, whereas those shortened at the 5'-end are complementary to different target sites located upstream.

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较长的19碱基对短干扰RNA双链而不是较短的双链触发RNA干扰。
短干扰RNA (sirna)是通过RNA干扰(RNAi)途径对基因表达进行序列特异性抑制的重要试剂。最近,有人认为16bp sirna是有效的RNAi触发器,并且优于“经典”的19bp sirna。这种与常识的矛盾促使我们重新研究这个问题。在一系列实验中,我们使用不同长度的siRNA双链(从19到15 bp)来沉默过表达的增强型绿色荧光蛋白或内源性表达的CDK9,我们证明19-bp的siRNA比相应的短双链更有活性。我们的结果与那些被质疑的结果之间的差异似乎是由于缩短双链的不同模式(在3'端或5'端,相对于导链的极性)。重要的是,具有完整5'端但在其3'端缩短的双链保留了靶点特异性,而在5'端缩短的双链与位于上游的不同靶点互补。
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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来源期刊
Oligonucleotides
Oligonucleotides 生物-生化与分子生物学
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