首页> 外文期刊>African Journal of Biotechnology >Short hairpin RNA expression for enhancing the resistance of Bombyx mori (Bm) to nucleopolyhedrovirus in vitro and in vivo
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Short hairpin RNA expression for enhancing the resistance of Bombyx mori (Bm) to nucleopolyhedrovirus in vitro and in vivo

机译:短发夹RNA表达可增强家蚕在体外和体内对核多角体病毒的抗性

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摘要

A new paradigm of RNAi technology has been studied for enhancing the resistance to virus in plants and animals. Previous studies have shown that the Bombyx mori (Bm) U6 promoter based shRNA is an effective tool for inducing RNAi in Bombyx mori cell line. However, widespread knockdown and induction of phenotypes in Bm larvae have not been fully demonstrated. In this study, we examined Bm U6 promoter based shRNA expression for suppressing Bm nucleopolyhedrovirus (NPV) in the Bm cell line and silkworm larvae. We measured the relative expression level of replication genes of BmNPV in hemolymph of silkworm larvae and BmN cells transfected with recombinant targeting shRNA by quantitative real time polymerase chain reaction (PCR). These results indicated that the recombinant shRNA expression system was a useful tool for resistance to BmNPV in vivo and in vitro. The approach opens the door of RNAi technology as a wide range of strategies that offer a technically simpler, cheaper, and quicker gene-knockdown by recombinant shRNA for future genetics in silkworm Bm and other related species.
机译:已经研究了一种新的RNAi技术范式,用于增强动植物对病毒的抗性。先前的研究表明,基于家蚕(Bm)U6启动子的shRNA是在家蚕细胞系中诱导RNAi的有效工具。但是,尚未完全证明Bm幼虫广泛的敲除和表型的诱导。在这项研究中,我们检查了基于Bm U6启动子的shRNA表达,以抑制Bm细胞系和家蚕幼虫中的Bm核多角体病毒(NPV)。通过定量实时聚合酶链反应(PCR),我们测量了BmNPV复制基因在家蚕幼虫血淋巴和以重组靶向shRNA转染的BmN细胞中的相对表达水平。这些结果表明,重组shRNA表达系统是体内和体外抗BmNPV的有用工具。该方法为RNAi技术的广泛应用打开了大门,这些策略为重组Bm和其他相关物种的未来遗传学提供了技术上更简单,更便宜,更快的重组shRNA基因敲除技术。

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