Interferon induction by siRNAs and ssRNAs synthesized by phage polymerase

被引:311
作者
Kim, DH
Longo, M
Han, Y
Lundberg, P
Cantin, E
Rossi, JJ
机构
[1] City Hope Natl Med Ctr, Div Mol Biol, Duarte, CA 91010 USA
[2] City Hope Natl Med Ctr, Div Virol, Duarte, CA 91010 USA
[3] City Hope Natl Med Ctr, Grad Sch Biol Sci, Duarte, CA 91010 USA
[4] City Hope Natl Med Ctr, Beckman Res Inst, Duarte, CA 91010 USA
关键词
D O I
10.1038/nbt940
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Small interfering RNAs (siRNA) are potent reagents for directed post-transcriptional gene silencing 1 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 and in a variety of cell lines. Surprisingly, we also found very potent induction of interferon and 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.
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页码:321 / 325
页数:5
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