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蟋蟀麻痹病毒抑制因子可抑制由果蝇AGO2蛋白介导的微小RNA沉默。

The cricket paralysis virus suppressor inhibits microRNA silencing mediated by the Drosophila Argonaute-2 protein.

作者信息

Besnard-Guérin Corinne, Jacquier Caroline, Pidoux Josette, Deddouche Safia, Antoniewski Christophe

机构信息

Drosophila Genetics and Epigenetics, Institut de Biologie Paris Seine, CNRS UMR7622 & Université Pierre et Marie Curie, 9 quai Saint-Bernard, F75005, Paris, France.

出版信息

PLoS One. 2015 Mar 20;10(3):e0120205. doi: 10.1371/journal.pone.0120205. eCollection 2015.

DOI:10.1371/journal.pone.0120205
PMID:25793377
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4368812/
Abstract

Small RNAs are potent regulators of gene expression. They also act in defense pathways against invading nucleic acids such as transposable elements or viruses. To counteract these defenses, viruses have evolved viral suppressors of RNA silencing (VSRs). Plant viruses encoded VSRs interfere with siRNAs or miRNAs by targeting common mediators of these two pathways. In contrast, VSRs identified in insect viruses to date only interfere with the siRNA pathway whose effector Argonaute protein is Argonaute-2 (Ago-2). Although a majority of Drosophila miRNAs exerts their silencing activity through their loading into the Argonaute-1 protein, recent studies highlighted that a fraction of miRNAs can be loaded into Ago-2, thus acting as siRNAs. In light of these recent findings, we re-examined the role of insect VSRs on Ago-2-mediated miRNA silencing in Drosophila melanogaster. Using specific reporter systems in cultured Schneider-2 cells and transgenic flies, we showed here that the Cricket Paralysis virus VSR CrPV1-A but not the Flock House virus B2 VSR abolishes silencing by miRNAs loaded into the Ago-2 protein. Thus, our results provide the first evidence that insect VSR have the potential to directly interfere with the miRNA silencing pathway.

摘要

小RNA是基因表达的有效调节因子。它们也在针对转座元件或病毒等入侵核酸的防御途径中发挥作用。为了对抗这些防御机制,病毒进化出了RNA沉默病毒抑制因子(VSRs)。植物病毒编码的VSRs通过靶向这两条途径的共同介质来干扰小干扰RNA(siRNAs)或微小RNA(miRNAs)。相比之下,迄今为止在昆虫病毒中鉴定出的VSRs仅干扰效应蛋白为AGO2(AGO-2)的siRNA途径。尽管大多数果蝇miRNA通过加载到AGO1蛋白中发挥其沉默活性,但最近的研究强调,一部分miRNA可以加载到AGO2中,从而作为siRNA发挥作用。鉴于这些最新发现,我们重新审视了昆虫VSRs在黑腹果蝇中对AGO2介导的miRNA沉默的作用。利用培养的施耐德2细胞和转基因果蝇中的特定报告系统,我们在此表明,蟋蟀麻痹病毒VSR CrPV1-A而非鸡瘟病毒B2 VSR消除了加载到AGO2蛋白中的miRNA的沉默作用。因此,我们的结果提供了首个证据,证明昆虫VSR有直接干扰miRNA沉默途径的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac1/4368812/4b7d2b9c3fc0/pone.0120205.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac1/4368812/e76d21fdee30/pone.0120205.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac1/4368812/71177c872725/pone.0120205.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac1/4368812/76aaff6d1c09/pone.0120205.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac1/4368812/4b7d2b9c3fc0/pone.0120205.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac1/4368812/e76d21fdee30/pone.0120205.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac1/4368812/71177c872725/pone.0120205.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac1/4368812/76aaff6d1c09/pone.0120205.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac1/4368812/4b7d2b9c3fc0/pone.0120205.g004.jpg

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