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Investigating Engineered Ribonucleoprotein Particles to Improve Oral RNAi Delivery in Crop Insect Pests

机译:研究工程核糖核蛋白颗粒以改善农作物害虫的口服RNAi传递

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摘要

Genetically modified (GM) crops producing double-stranded RNAs (dsRNAs) are being investigated largely as an RNA interference (RNAi)-based resistance strategy against crop insect pests. However, limitations of this strategy include the sensitivity of dsRNA to insect gut nucleases and its poor insect cell membrane penetration. Working with the insect pest cotton boll weevil (Anthonomus grandis), we showed that the chimeric protein PTD-DRBD (peptide transduction domain—dsRNA binding domain) combined with dsRNA forms a ribonucleoprotein particle (RNP) that improves the effectiveness of the RNAi mechanism in the insect. The RNP slows down nuclease activity, probably by masking the dsRNA. Furthermore, PTD-mediated internalization in insect gut cells is achieved within minutes after plasma membrane contact, limiting the exposure time of the RNPs to gut nucleases. Therefore, the RNP provides an approximately 2-fold increase in the efficiency of insect gene silencing upon oral delivery when compared to naked dsRNA. Taken together, these data demonstrate the role of engineered RNPs in improving dsRNA stability and cellular entry, representing a path toward the design of enhanced RNAi strategies in GM plants against crop insect pests.
机译:正在广泛研究生产双链RNA(dsRNA)的转基因(GM)作物,作为基于RNA干扰(RNAi)的对农作物害虫的抗性策略。但是,该策略的局限性包括dsRNA对昆虫肠道核酸酶的敏感性及其对昆虫细胞膜的不良渗透。与昆虫棉铃象鼻虫(Anthonomus grandis)一起工作,我们发现嵌合蛋白PTD-DRBD(肽转导域-dsRNA结合域)与dsRNA结合形成了核糖核蛋白颗粒(RNP),可提高RNAi机制的有效性。昆虫。 RNP可能通过掩盖dsRNA减慢了核酸酶的活性。此外,昆虫肠细胞中PTD介导的内在化是在质膜接触后的数分钟内实现的,从而限制了RNP暴露于肠核酸酶的时间。因此,与裸dsRNA相比,RNP口服递送时昆虫基因沉默的效率提高了约2倍。综上所述,这些数据证明了工程化的RNP在改善dsRNA稳定性和细胞进入方面的作用,代表了设计转基因植物中针对作物害虫的增强RNAi策略的途径。

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