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分析基孔肯雅病毒蛋白表明非结构蛋白 nsP2 和 nsP3 具有 RNA 干扰(RNAi)抑制活性。

Analysis of chikungunya virus proteins reveals that non-structural proteins nsP2 and nsP3 exhibit RNA interference (RNAi) suppressor activity.

机构信息

Insect Resistance Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.

Plant Molecular Biology Group, International Centre for Genetic Engineering and Biotechnology, New Delhi, India.

出版信息

Sci Rep. 2016 Nov 30;6:38065. doi: 10.1038/srep38065.

Abstract

RNAi pathway is an antiviral defence mechanism employed by insects that result in degradation of viral RNA thereby curbing infection. Several viruses including flaviviruses encode viral suppressors of RNAi (VSRs) to counteract the antiviral RNAi pathway. Till date, no VSR has been reported in alphaviruses. The present study was undertaken to evaluate chikungunya virus (CHIKV) proteins for RNAi suppressor activity. We systematically analyzed all nine CHIKV proteins for RNAi suppressor activity using Sf21 RNAi sensor cell line based assay. Two non-structural proteins, namely, nsP2 and nsP3 were found to exhibit RNAi suppressor activity. We further validated the findings in natural hosts, namely in Aedes and in mammalian cell lines and further through EMSA and Agrobacterium infiltration in GFP silenced transgenic tobacco plants. Domains responsible for maximum RNAi suppressor activity were also identified within these proteins. RNA binding motifs in these domains were identified and their participation in RNAi suppression evaluated using site directed mutagenesis. Sequence alignment of these motifs across all species of known alphaviruses revealed conservation of these motifs emphasizing on a similar role of action in other species of alphaviruses as well. Further validation of RNAi suppressor activity of these proteins awaits establishment of specific virus infection models.

摘要

RNAi 途径是昆虫采用的一种抗病毒防御机制,可导致病毒 RNA 降解,从而抑制感染。包括黄病毒在内的几种病毒编码病毒 RNAi 抑制子(VSR)以对抗抗病毒 RNAi 途径。迄今为止,还没有报道过甲病毒中的 VSR。本研究旨在评估基孔肯雅病毒 (CHIKV) 蛋白的 RNAi 抑制活性。我们使用 Sf21 RNAi 传感器细胞系基于测定法系统地分析了所有 9 种 CHIKV 蛋白的 RNAi 抑制活性。发现两种非结构蛋白,即 nsP2 和 nsP3 具有 RNAi 抑制活性。我们进一步在天然宿主(即 Aedes 和哺乳动物细胞系)中验证了这些发现,并通过 EMSA 和 GFP 沉默的转基因烟草植物中的农杆菌浸润进一步验证。还确定了这些蛋白中具有最大 RNAi 抑制活性的区域。使用定点诱变鉴定了这些结构域中的 RNA 结合基序,并评估了它们在 RNAi 抑制中的参与。对这些 motif 在所有已知甲病毒物种中的序列比对揭示了这些 motif 的保守性,强调了它们在其他甲病毒物种中也具有相似的作用。这些蛋白的 RNAi 抑制活性的进一步验证有待于建立特定的病毒感染模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cf7/5128919/ea9f8d53c2a6/srep38065-f1.jpg

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