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网格蛋白介导的内吞作用以及两种类Sid-1跨膜蛋白在科罗拉多马铃薯甲虫中肠双链RNA摄取中的作用。

The involvement of clathrin-mediated endocytosis and two Sid-1-like transmembrane proteins in double-stranded RNA uptake in the Colorado potato beetle midgut.

作者信息

Cappelle K, de Oliveira C F R, Van Eynde B, Christiaens O, Smagghe G

机构信息

Department of Crop Protection, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.

Department of Biochemistry, Institute of Biology, University of Campinas, Campinas, Sao Paulo, Brazil.

出版信息

Insect Mol Biol. 2016 Jun;25(3):315-23. doi: 10.1111/imb.12222. Epub 2016 Mar 9.

Abstract

RNA interference (RNAi) is a powerful tool in entomology and shows promise as a crop protection strategy, but variability in its efficiency across different insect species limits its applicability. For oral uptake of the double-stranded RNA (dsRNA), the RNAi trigger, two different mechanisms are known: systemic RNA interference deficient-1 (Sid-1) transmembrane channel-mediated uptake and clathrin-mediated endocytosis. So far, a wide range of experiments has been conducted, confirming the involvement of one of the pathways in dsRNA uptake, but never both pathways in the same species. We investigated the role of both pathways in dsRNA uptake in the Colorado potato beetle, Leptinotarsa decemlineata, known to have an efficient RNAi response. Through RNAi-of-RNAi experiments, we demonstrated the contribution of two different sid-1-like (sil) genes, silA and silC, and clathrin heavy chain and the 16kDa subunit of the vacuolar H(+) ATPase (vha16), elements of the endocytic pathway, to the RNAi response. Furthermore, the sid-1-like genes were examined through phylogenetic and hydrophobicity analysis. This article reports for the first time on the involvement of two pathways in dsRNA uptake in an insect species and stresses the importance of evaluating both pathways through a well-devised reporter system in any future experiments on cellular dsRNA uptake.

摘要

RNA干扰(RNAi)是昆虫学中的一种强大工具,有望成为一种作物保护策略,但其在不同昆虫物种中的效率差异限制了其适用性。对于双链RNA(dsRNA)这种RNAi触发因子的口服摄取,已知有两种不同机制:系统性RNA干扰缺陷-1(Sid-1)跨膜通道介导的摄取和网格蛋白介导的内吞作用。到目前为止,已经进行了大量实验,证实了其中一种途径参与dsRNA摄取,但从未在同一物种中证实两种途径都参与。我们研究了这两种途径在科罗拉多马铃薯甲虫(Leptinotarsa decemlineata)dsRNA摄取中的作用,该甲虫已知具有高效的RNAi反应。通过RNAi的RNAi实验,我们证明了两个不同的类Sid-1(sil)基因silA和silC、网格蛋白重链以及液泡H(+)ATP酶(vha16)的16kDa亚基(内吞途径的元件)对RNAi反应的贡献。此外,通过系统发育和疏水性分析对类Sid-1基因进行了研究。本文首次报道了两种途径参与昆虫物种dsRNA摄取的情况,并强调在未来任何关于细胞dsRNA摄取的实验中,通过精心设计的报告系统评估这两种途径的重要性。

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