| Literature DB >> 33397184 |
Jiasheng Chen1, Yingchuan Peng1,2, Hainan Zhang1, Kangxu Wang1,3, Chunqing Zhao1, Guanheng Zhu4, Subba Reddy Palli4, Zhaojun Han1.
Abstract
RNAi is a potent technique for the knockdown of target genes. However, its potential off-target effects limit the widespread applications in both reverse genetic analysis and genetic manipulation. Previous efforts have uncovered rules underlying specificity of siRNA-based silencing, which has broad applications in humans, but the basis for specificity of dsRNAs, which are better suited for use as insecticides, is poorly understood. Here, we investigated the rules governing dsRNA specificity. Mutational analyses showed that dsRNAs with >80% sequence identity with target genes triggered RNAi efficiently. dsRNAs with ≥16 bp segments of perfectly matched sequence or >26 bp segments of almost perfectly matched sequence with one or two mismatches scarcely distributed (single mismatches inserted between ≥5 bp matching segments or mismatched couplets inserted between ≥8 bp matching segments) also able to trigger RNAi. Using these parameters to predict off-target risk, dsRNAs can be designed to optimize specificity and efficiency, paving the way to the widespread, rational application of RNAi in pest control.Entities:
Keywords: RNA interference; RNAi efficiency; dsRNA specificity; off-target effect; risk assessment; sequence identity
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Year: 2021 PMID: 33397184 PMCID: PMC8583100 DOI: 10.1080/15476286.2020.1868680
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652