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噬菌体聚合酶合成的小干扰RNA和单链RNA诱导干扰素

Interferon induction by siRNAs and ssRNAs synthesized by phage polymerase.

作者信息

Kim Dong-Ho, Longo Michael, Han Young, Lundberg Patric, Cantin Edouard, Rossi John J

机构信息

Division of Molecular Biology, City of Hope and Beckman Research Institute of the City of Hope, 1450 East Duarte Road, Duarte, California 91010-3011, USA.

出版信息

Nat Biotechnol. 2004 Mar;22(3):321-5. doi: 10.1038/nbt940. Epub 2004 Feb 8.

Abstract

Small interfering RNAs (siRNA) are potent reagents for directed post-transcriptional gene silencing and a major new genetic tool for investigating mammalian cells. When synthetic siRNAs are used for gene silencing, the costs can be substantial because of variations in siRNA efficacies. An alternative to chemically synthesized siRNAs are siRNAs produced by bacteriophage T7 RNA polymerase. We found that siRNAs synthesized from the T7 RNA polymerase system can trigger a potent induction of interferon alpha and beta in a variety of cell lines. Surprisingly, we also found very potent induction of interferon alpha and beta by short single-stranded RNAs (ssRNAs) transcribed with T3, T7 and Sp6 RNA polymerases. Analyses of the potential mediators of this response revealed that the initiating 5' triphosphate is required for interferon induction. We describe here an improved method for T7 siRNA synthesis that alleviates the interferon response while maintaining full efficacy of the siRNAs.

摘要

小干扰RNA(siRNA)是用于定向转录后基因沉默的有效试剂,也是研究哺乳动物细胞的一种重要的新型遗传工具。当使用合成siRNA进行基因沉默时,由于siRNA效力的差异,成本可能很高。化学合成siRNA的替代方法是由噬菌体T7 RNA聚合酶产生的siRNA。我们发现,从T7 RNA聚合酶系统合成的siRNA可在多种细胞系中引发强烈的α和β干扰素诱导。令人惊讶的是,我们还发现,用T3、T7和Sp6 RNA聚合酶转录的短单链RNA(ssRNA)也能非常强烈地诱导α和β干扰素。对这种反应潜在介质的分析表明,起始的5'三磷酸对于干扰素诱导是必需的。我们在此描述一种改进的T7 siRNA合成方法,该方法可减轻干扰素反应,同时保持siRNA的全部效力。

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