• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

少一些聚集,多一些复制:病毒对应激颗粒的操纵。

A little less aggregation a little more replication: Viral manipulation of stress granules.

机构信息

Faculty of Health and Medical Sciences, School of Biosciences and Medicine, University of Surrey, Guildford, Surrey, UK.

出版信息

Wiley Interdiscip Rev RNA. 2023 Jan;14(1):e1741. doi: 10.1002/wrna.1741. Epub 2022 Jun 16.

DOI:10.1002/wrna.1741
PMID:35709333
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10078398/
Abstract

Recent exciting studies have uncovered how membrane-less organelles, also known as biocondensates, are providing cells with rapid response pathways, allowing them to re-organize their cellular contents and adapt to stressful conditions. Their assembly is driven by the phase separation of their RNAs and intrinsically disordered protein components into condensed foci. Among these, stress granules (SGs) are dynamic cytoplasmic biocondensates that form in response to many stresses, including activation of the integrated stress response or viral infections. SGs sit at the crossroads between antiviral signaling and translation because they concentrate signaling proteins and components of the innate immune response, in addition to translation machinery and stalled mRNAs. Consequently, they have been proposed to contribute to antiviral activities, and therefore are targeted by viral countermeasures. Equally, SGs components can be commandeered by viruses for their own efficient replication. Phase separation processes are an important component of the viral life cycle, for example, driving the assembly of replication factories or inclusion bodies. Therefore, in this review, we will outline the recent understanding of this complex interplay and tug of war between viruses, SGs, and their components. This article is categorized under: RNA in Disease and Development > RNA in Disease Translation > Regulation RNA Interactions with Proteins and Other Molecules > RNA-Protein Complexes.

摘要

最近令人兴奋的研究揭示了无膜细胞器(也称为生物凝聚物)如何为细胞提供快速反应途径,使它们能够重新组织细胞内容物并适应应激条件。它们的组装是由其 RNA 和固有无序蛋白成分的相分离驱动的,形成浓缩焦点。其中,应激颗粒 (SGs) 是一种动态的细胞质生物凝聚物,可响应多种应激而形成,包括整合应激反应的激活或病毒感染。SGs 位于抗病毒信号和翻译的十字路口,因为它们浓缩信号蛋白和先天免疫反应的成分,以及翻译机制和停滞的 mRNA。因此,它们被认为有助于抗病毒活性,因此成为病毒对策的目标。同样,SGs 的成分也可以被病毒利用来进行自身的有效复制。相分离过程是病毒生命周期的一个重要组成部分,例如,驱动复制工厂或包含体的组装。因此,在这篇综述中,我们将概述最近对病毒、SGs 及其成分之间这种复杂相互作用和拉锯战的理解。本文属于以下分类:RNA 在疾病与发展 > RNA 在疾病中的翻译 > RNA 与蛋白质和其他分子的相互作用调控 > RNA-蛋白质复合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/4c8cba07921c/WRNA-14-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/4077a652b58b/WRNA-14-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/78d5b5173748/WRNA-14-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/a89b658186c0/WRNA-14-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/4745e5167fc8/WRNA-14-0-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/4c8cba07921c/WRNA-14-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/4077a652b58b/WRNA-14-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/78d5b5173748/WRNA-14-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/a89b658186c0/WRNA-14-0-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/4745e5167fc8/WRNA-14-0-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb63/10078398/4c8cba07921c/WRNA-14-0-g006.jpg

相似文献

1
A little less aggregation a little more replication: Viral manipulation of stress granules.少一些聚集,多一些复制:病毒对应激颗粒的操纵。
Wiley Interdiscip Rev RNA. 2023 Jan;14(1):e1741. doi: 10.1002/wrna.1741. Epub 2022 Jun 16.
2
Stress granule components G3BP1 and G3BP2 play a proviral role early in Chikungunya virus replication.应激颗粒成分G3BP1和G3BP2在基孔肯雅病毒复制早期发挥病毒前体作用。
J Virol. 2015 Apr;89(8):4457-69. doi: 10.1128/JVI.03612-14. Epub 2015 Feb 4.
3
Novel stress granule-like structures are induced via a paracrine mechanism during viral infection.新型应激颗粒样结构通过病毒感染中的旁分泌机制诱导产生。
J Cell Sci. 2022 Feb 15;135(4). doi: 10.1242/jcs.259194. Epub 2022 Feb 24.
4
Mouse Norovirus Infection Arrests Host Cell Translation Uncoupled from the Stress Granule-PKR-eIF2α Axis.鼠诺如病毒感染阻断宿主细胞翻译,与应激颗粒-PKR-eIF2α 轴无关。
mBio. 2019 Jun 18;10(3):e00960-19. doi: 10.1128/mBio.00960-19.
5
Rabies Virus Infection Induces the Formation of Stress Granules Closely Connected to the Viral Factories.狂犬病病毒感染诱导形成与病毒工厂紧密相连的应激颗粒。
PLoS Pathog. 2016 Oct 17;12(10):e1005942. doi: 10.1371/journal.ppat.1005942. eCollection 2016 Oct.
6
Defining the Role of Stress Granules in Innate Immune Suppression by the Herpes Simplex Virus 1 Endoribonuclease VHS.定义单纯疱疹病毒 1 内切核糖核酸酶 VHS 在先天免疫抑制中的应激颗粒作用。
J Virol. 2018 Jul 17;92(15). doi: 10.1128/JVI.00829-18. Print 2018 Aug 1.
7
Feline Calicivirus Infection Disrupts Assembly of Cytoplasmic Stress Granules and Induces G3BP1 Cleavage.猫杯状病毒感染破坏细胞质应激颗粒的组装并诱导G3BP1裂解。
J Virol. 2016 Jun 24;90(14):6489-6501. doi: 10.1128/JVI.00647-16. Print 2016 Jul 15.
8
Zika Virus Subverts Stress Granules To Promote and Restrict Viral Gene Expression.寨卡病毒颠覆应激颗粒以促进和限制病毒基因表达。
J Virol. 2019 May 29;93(12). doi: 10.1128/JVI.00520-19. Print 2019 Jun 15.
9
TDRD3 is an antiviral restriction factor that promotes IFN signaling with G3BP1.TDRD3 是一种抗病毒限制因子,它与 G3BP1 一起促进 IFN 信号转导。
PLoS Pathog. 2022 Jan 27;18(1):e1010249. doi: 10.1371/journal.ppat.1010249. eCollection 2022 Jan.
10
Inhibition of anti-viral stress granule formation by coronavirus endoribonuclease nsp15 ensures efficient virus replication.冠状病毒内切核糖核酸酶 nsp15 抑制抗病毒应激颗粒形成以确保病毒高效复制。
PLoS Pathog. 2021 Feb 26;17(2):e1008690. doi: 10.1371/journal.ppat.1008690. eCollection 2021 Feb.

引用本文的文献

1
Uukuniemi virus infection causes a pervasive remodelling of the RNA-binding proteome in tick cells.乌库涅米病毒感染导致蜱细胞中RNA结合蛋白质组的广泛重塑。
PLoS Pathog. 2025 Aug 4;21(8):e1013393. doi: 10.1371/journal.ppat.1013393. eCollection 2025 Aug.
2
Multi-Faceted Roles of Stress Granules in Viral Infection.应激颗粒在病毒感染中的多方面作用
Microorganisms. 2025 Jun 20;13(7):1434. doi: 10.3390/microorganisms13071434.
3
Stress granules and cell death: crosstalk and potential therapeutic strategies in infectious diseases.

本文引用的文献

1
Double-stranded RNA drives SARS-CoV-2 nucleocapsid protein to undergo phase separation at specific temperatures.双链 RNA 促使 SARS-CoV-2 核衣壳蛋白在特定温度下发生液-液相分离。
Nucleic Acids Res. 2022 Aug 12;50(14):8168-8192. doi: 10.1093/nar/gkac596.
2
Minding the message: tactics controlling RNA decay, modification, and translation in virus-infected cells.关注信息:病毒感染细胞中控制 RNA 衰变、修饰和翻译的策略。
Genes Dev. 2022 Feb 1;36(3-4):108-132. doi: 10.1101/gad.349276.121.
3
Novel stress granule-like structures are induced via a paracrine mechanism during viral infection.
应激颗粒与细胞死亡:传染病中的相互作用及潜在治疗策略
Cell Death Dis. 2025 Jul 5;16(1):495. doi: 10.1038/s41419-025-07800-z.
4
Proximity interactome of alphavirus replicase component nsP3 includes proviral host factors eIF4G and AHNAK.甲病毒复制酶组分nsP3的邻近相互作用组包括前病毒宿主因子eIF4G和AHNAK。
PLoS Pathog. 2025 Apr 7;21(4):e1013050. doi: 10.1371/journal.ppat.1013050. eCollection 2025 Apr.
5
Two Birds With One Stone: RNA Virus Strategies to Manipulate G3BP1 and Other Stress Granule Components.一石二鸟:RNA病毒操纵G3BP1及其他应激颗粒成分的策略
Wiley Interdiscip Rev RNA. 2025 Mar-Apr;16(2):e70005. doi: 10.1002/wrna.70005.
6
Nuclear RNA-binding proteins meet cytoplasmic viruses.核RNA结合蛋白与细胞质病毒相遇。
RNA. 2025 Feb 19;31(3):444-451. doi: 10.1261/rna.080313.124.
7
Interactions between epithelial mesenchymal plasticity, barrier dysfunction and innate immune pathways shape the genesis of allergic airway disease.上皮-间质可塑性、屏障功能障碍与固有免疫途径之间的相互作用塑造了过敏性气道疾病的发生发展。
Expert Rev Respir Med. 2025 Jan;19(1):29-41. doi: 10.1080/17476348.2024.2449079. Epub 2025 Jan 6.
8
Virus-modified paraspeckle-like condensates are hubs for viral RNA processing and their formation drives genomic instability.病毒修饰的类核纤层小体凝聚物是病毒 RNA 加工的枢纽,其形成驱动基因组不稳定性。
Nat Commun. 2024 Nov 26;15(1):10240. doi: 10.1038/s41467-024-54592-5.
9
SARS-CoV-2 Nucleocapsid Protein Antagonizes GADD34-Mediated Innate Immune Pathway through Atypical Foci.SARS-CoV-2 核衣壳蛋白通过非典型病灶拮抗 GADD34 介导的先天免疫途径。
Molecules. 2024 Oct 10;29(20):4792. doi: 10.3390/molecules29204792.
10
Stress Granule Core Protein-Derived Peptides Inhibit Assembly of Stress Granules and Improve Sorafenib Sensitivity in Cancer Cells.应激颗粒核心蛋白衍生肽抑制应激颗粒的组装并提高癌细胞对索拉非尼的敏感性。
Molecules. 2024 May 4;29(9):2134. doi: 10.3390/molecules29092134.
新型应激颗粒样结构通过病毒感染中的旁分泌机制诱导产生。
J Cell Sci. 2022 Feb 15;135(4). doi: 10.1242/jcs.259194. Epub 2022 Feb 24.
4
SARS-CoV-2 nucleocapsid protein forms condensates with viral genomic RNA.SARS-CoV-2 核衣壳蛋白与病毒基因组 RNA 形成凝聚物。
PLoS Biol. 2021 Oct 11;19(10):e3001425. doi: 10.1371/journal.pbio.3001425. eCollection 2021 Oct.
5
Plant Stress Granules: Trends and Beyond.植物应激颗粒:趋势与展望
Front Plant Sci. 2021 Aug 9;12:722643. doi: 10.3389/fpls.2021.722643. eCollection 2021.
6
Murine Norovirus Infection Results in Anti-inflammatory Response Downstream of Amino Acid Depletion in Macrophages.鼠诺如病毒感染导致巨噬细胞中氨基酸耗竭下游的抗炎反应。
J Virol. 2021 Sep 27;95(20):e0113421. doi: 10.1128/JVI.01134-21. Epub 2021 Aug 4.
7
A condensate-hardening drug blocks RSV replication in vivo.一种冷凝硬化药物可阻止 RSV 在体内复制。
Nature. 2021 Jul;595(7868):596-599. doi: 10.1038/s41586-021-03703-z. Epub 2021 Jul 7.
8
I(nsp1)ecting SARS-CoV-2-ribosome interactions.鉴定 SARS-CoV-2-核糖体相互作用。
Commun Biol. 2021 Jun 10;4(1):715. doi: 10.1038/s42003-021-02265-0.
9
SARS-CoV-2 nucleocapsid protein impairs stress granule formation to promote viral replication.严重急性呼吸综合征冠状病毒2核衣壳蛋白损害应激颗粒形成以促进病毒复制。
Cell Discov. 2021 May 25;7(1):38. doi: 10.1038/s41421-021-00275-0.
10
Arginine methylation of SARS-Cov-2 nucleocapsid protein regulates RNA binding, its ability to suppress stress granule formation, and viral replication.SARS-CoV-2 核衣壳蛋白的精氨酸甲基化调节 RNA 结合、抑制应激颗粒形成的能力和病毒复制。
J Biol Chem. 2021 Jul;297(1):100821. doi: 10.1016/j.jbc.2021.100821. Epub 2021 May 23.