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Large scale RNAi screen in Tribolium reveals novel target genes for pest control and the proteasome as prime target

机译:Tribolium中的大规模RNAi筛选揭示了用于害虫控制的新靶标基因和蛋白酶体为主要靶标

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Insect pest control is challenged by insecticide resistance and negative impact on ecology and health. One promising pest specific alternative is the generation of transgenic plants, which express double stranded RNAs targeting essential genes of a pest species. Upon feeding, the dsRNA induces gene silencing in the pest resulting in its death. However, the identification of efficient RNAi target genes remains a major challenge as genomic tools and breeding capacity is limited in most pest insects impeding whole-animal-high-throughput-screening. We use the red flour beetle Tribolium castaneum as a screening platform in order to identify the most efficient RNAi target genes. From about 5,000 randomly screened genes of the iBeetle RNAi screen we identify 11 novel and highly efficient RNAi targets. Our data allowed us to determine GO term combinations that are predictive for efficient RNAi target genes with proteasomal genes being most predictive. Finally, we show that RNAi target genes do not appear to act synergistically and that protein sequence conservation does not correlate with the number of potential off target sites. Our results will aid the identification of RNAi target genes in many pest species by providing a manageable number of excellent candidate genes to be tested and the proteasome as prime target. Further, the identified GO term combinations will help to identify efficient target genes from organ specific transcriptomes. Our off target analysis is relevant for the sequence selection used in transgenic plants.
机译:杀虫剂的抗药性及其对生态和健康的负面影响挑战着害虫的防治。一种有希望的有害生物特异性替代物是产生转基因植物,其表达靶向有害生物物种必需基因的双链RNA。进食后,dsRNA在有害生物中诱导基因沉默,导致其死亡。但是,有效的RNAi靶基因的鉴定仍然是一个主要挑战,因为基因组学工具和繁殖能力在大多数害虫中都受到限制,阻碍了对全动物高通量筛选。我们使用红色面粉甲虫Tribolium castaneum作为筛选平台,以鉴定最有效的RNAi靶基因。从iBeetle RNAi筛选的约5,000个随机筛选的基因中,我们鉴定出11个新颖且高效的RNAi靶标。我们的数据使我们能够确定可预测有效RNAi靶基因的GO术语组合,而蛋白酶体基因则最可预测。最后,我们表明,RNAi靶基因似乎没有协同作用,并且蛋白质序列保守性与潜在的靶位点数量无关。我们的结果将通过提供可管理数量的待测优秀候选基因和蛋白酶体作为主要靶标,来帮助鉴定许多有害生物中的RNAi靶标基因。此外,所鉴定的GO术语组合将有助于从器官特异性转录组中鉴定有效的靶基因。我们的脱靶分析与转基因植物中使用的序列选择有关。

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