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鉴定和描述美洲棉铃虫多角体病毒 LEF5 的核仁定位信号。

Identification and Characterization of the Nucleolar Localization Signal of Autographa californica Multiple Nucleopolyhedrovirus LEF5.

机构信息

State Key Laboratory of Rice Biology, China National Rice Research Institute, Hangzhou, China.

Department of Molecular and Cellular Biology, University of Guelph, Guelph, Ontario, Canada.

出版信息

J Virol. 2020 Jan 31;94(4). doi: 10.1128/JVI.01891-19.

Abstract

Autographa californica multiple nucleopolyhedrovirus (AcMNPV) late expression factor 5 (LEF5) is highly conserved in all sequenced baculovirus genomes and plays an important role in production of infectious viral progeny. In this study, nucleolar localization of AcMNPV LEF5 was characterized. Through transcriptome analysis, we identified two putative nucleolar proteins, nucleostemin (SfNS) and fibrillarin (SfFBL), from Sf9 cells. Immunofluorescence analysis demonstrated that SfNS and SfFBL were localized to the nucleolus. AcMNPV infection resulted in reorganization of the nucleoli of infected cells. Colocalization of LEF5 and SfNS showed that AcMNPV LEF5 was localized to the nucleolus in Sf9 cells. Bioinformatic analysis revealed that basic amino acids of LEF5 are enriched at residues 184 to 213 and may contain a nucleolar localization signal (NoLS). Green fluorescent protein (GFP) fused to NoLS of AcMNPV LEF5 localized to the nucleoli of transfected cells. Multiple-point mutation analysis demonstrated that amino acid residues 197 to 204 are important for nucleolar localization of LEF5. To identify whether the NoLS in AcMNPV LEF5 is important for production of viral progeny, a -null AcMNPV bacmid was constructed; several NoLS-mutated LEF5 proteins were reinserted into the -null AcMNPV bacmid with a GFP reporter. The constructs containing point mutations at residues 185 to 189 or 197 to 204 in AcMNPV LEF5 resulted in reduction in production of infectious viral progeny and occlusion body yield in bacmid-transfected cells. Together, these data suggested that AcMNPV LEF5 contains an NoLS, which is important for nucleolar localization of LEF5, progeny production, and occlusion body production. Many viruses, including human and plant viruses, target nucleolar functions as part of their infection strategy. However, nucleolar localization for baculovirus proteins has not yet been characterized. In this study, two nucleolar proteins, SfNS and SfFBL, were identified in Sf9 cells. Our results showed that Autographa californica multiple nucleopolyhedrovirus (AcMNPV) infection resulted in redistribution of the nucleoli of infected cells. We demonstrated that AcMNPV late expression factor 5 (LEF5) could localize to the nucleolus and contains a nucleolar localization signal (NoLS), which is important for nucleolar localization of AcMNPV LEF5 and for production of viral progeny and yield of occlusion bodies.

摘要

棉铃虫多核型多角体病毒(AcMNPV)晚期表达因子 5(LEF5)在所有已测序的杆状病毒基因组中高度保守,在产生感染性病毒后代方面发挥重要作用。在本研究中,我们对 AcMNPV LEF5 的核仁定位进行了表征。通过转录组分析,我们从 Sf9 细胞中鉴定出两种假定的核仁蛋白,核仁干细胞(SfNS)和核仁纤维蛋白(SfFBL)。免疫荧光分析表明,SfNS 和 SfFBL 定位于核仁。AcMNPV 感染导致感染细胞的核仁重新分布。LEF5 和 SfNS 的共定位表明,AcMNPV LEF5 在 Sf9 细胞中定位于核仁。生物信息学分析表明,LEF5 的碱性氨基酸在残基 184 到 213 处富集,可能含有核仁定位信号(NoLS)。绿色荧光蛋白(GFP)融合到 AcMNPV LEF5 的 NoLS 后定位于转染细胞的核仁。多点突变分析表明,残基 197 到 204 对于 LEF5 的核仁定位很重要。为了确定 AcMNPV LEF5 中的 NoLS 是否对病毒后代的产生很重要,构建了一个缺失 -null AcMNPV 杆状病毒载体制粒;将含有 GFP 报告基因的几个 NoLS 突变的 LEF5 蛋白重新插入到 -null AcMNPV 杆状病毒载体制粒中。在 AcMNPV LEF5 中残基 185 到 189 或 197 到 204 的点突变导致感染细胞中产生的感染性病毒后代和包含体产量减少。总之,这些数据表明 AcMNPV LEF5 含有一个 NoLS,该信号对于 LEF5 的核仁定位、后代产生和包含体产生很重要。许多病毒,包括人类和植物病毒,将核仁功能作为其感染策略的一部分。然而,杆状病毒蛋白的核仁定位尚未得到表征。在本研究中,在 Sf9 细胞中鉴定出两种核仁蛋白,SfNS 和 SfFBL。我们的结果表明,棉铃虫多核型多角体病毒(AcMNPV)感染导致感染细胞的核仁重新分布。我们证明,AcMNPV 晚期表达因子 5(LEF5)可以定位于核仁并含有核仁定位信号(NoLS),该信号对于 AcMNPV LEF5 的核仁定位以及病毒后代的产生和包含体产量很重要。

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