• 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

病毒对宿主泛素系统的接管。

Viral takeover of the host ubiquitin system.

机构信息

Vaccine and Gene Therapy Institute, Oregon Health & Science University Beaverton, OR, USA.

出版信息

Front Microbiol. 2011 Jul 28;2:161. doi: 10.3389/fmicb.2011.00161. eCollection 2011.

DOI:10.3389/fmicb.2011.00161
PMID:21847386
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3147166/
Abstract

Like the other more well-characterized post-translational modifications (phosphorylation, methylation, acetylation, acylation, etc.), the attachment of the 76 amino acid ubiquitin (Ub) protein to substrates has been shown to govern countless cellular processes. As obligate intracellular parasites, viruses have evolved the capability to commandeer many host processes in order to maximize their own survival, whether it be to increase viral production or to ensure the long-term survival of latently infected host cells. The first evidence that viruses could usurp the Ub system came from the DNA tumor viruses and Adenoviruses, each of which use Ub to dysregulate the host cell cycle (Scheffner et al., 1990; Querido et al., 2001). Today, the list of viruses that utilize Ub includes members from almost every viral class, encompassing both RNA and DNA viruses. Among these, there are examples of Ub usage at every stage of the viral life cycle, involving both ubiquitination and de-ubiquitination. In addition to viruses that merely modify the host Ub system, many of the large DNA viruses encode their own Ub modifying machinery. In this review, we highlight the latest discoveries regarding the myriad ways that viruses utilize Ub to their advantage.

摘要

与其他更为典型的翻译后修饰(如磷酸化、甲基化、乙酰化、酰化等)一样,76 个氨基酸的泛素(Ub)蛋白与底物的连接已被证明可以控制无数的细胞过程。作为专性细胞内寄生虫,病毒已经进化出了操纵许多宿主过程的能力,以最大限度地提高自身的生存能力,无论是增加病毒产量还是确保潜伏感染宿主细胞的长期存活。病毒可以篡夺 Ub 系统的第一个证据来自于 DNA 肿瘤病毒和腺病毒,它们都利用 Ub 来扰乱宿主细胞周期(Scheffner 等人,1990;Querido 等人,2001)。如今,利用 Ub 的病毒包括几乎所有病毒类别的成员,包括 RNA 和 DNA 病毒。在这些病毒中,有 Ub 在病毒生命周期的各个阶段使用的例子,包括泛素化和去泛素化。除了仅仅修饰宿主 Ub 系统的病毒外,许多大型 DNA 病毒还编码自己的 Ub 修饰机制。在这篇综述中,我们强调了关于病毒利用 Ub 获得优势的最新发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b027/3147166/26f0c16596cf/fmicb-02-00161-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b027/3147166/26f0c16596cf/fmicb-02-00161-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b027/3147166/26f0c16596cf/fmicb-02-00161-g001.jpg

相似文献

1
Viral takeover of the host ubiquitin system.病毒对宿主泛素系统的接管。
Front Microbiol. 2011 Jul 28;2:161. doi: 10.3389/fmicb.2011.00161. eCollection 2011.
2
Viral Mimicry to Usurp Ubiquitin and SUMO Host Pathways.病毒模仿以篡夺泛素和类泛素化修饰宿主途径
Viruses. 2015 Aug 28;7(9):4854-72. doi: 10.3390/v7092849.
3
The ubiquitin-conjugating system: multiple roles in viral replication and infection.泛素连接系统:在病毒复制和感染中的多种作用。
Cells. 2014 May 6;3(2):386-417. doi: 10.3390/cells3020386.
4
Regulating the Regulators: Recent Revelations in the Control of E3 Ubiquitin Ligases.调控调节因子:E3泛素连接酶控制方面的最新发现
J Biol Chem. 2015 Aug 28;290(35):21244-51. doi: 10.1074/jbc.R115.675165. Epub 2015 Jul 17.
5
Plant Virus Infection and the Ubiquitin Proteasome Machinery: Arms Race along the Endoplasmic Reticulum.植物病毒感染与泛素蛋白酶体机制:在内质网上的军备竞赛
Viruses. 2016 Nov 19;8(11):314. doi: 10.3390/v8110314.
6
The ubiquitin-proteasome system in positive-strand RNA virus infection.正链 RNA 病毒感染中的泛素-蛋白酶体系统。
Rev Med Virol. 2013 Mar;23(2):85-96. doi: 10.1002/rmv.1725. Epub 2012 Jul 11.
7
Mapping the interactome of HPV E6 and E7 oncoproteins with the ubiquitin-proteasome system.描绘 HPV E6 和 E7 癌蛋白与泛素-蛋白酶体系统的相互作用组。
FEBS J. 2017 Oct;284(19):3171-3201. doi: 10.1111/febs.14193. Epub 2017 Aug 29.
8
Antigen presentation and the ubiquitin-proteasome system in host-pathogen interactions.宿主-病原体相互作用中的抗原呈递与泛素-蛋白酶体系统
Adv Immunol. 2006;92:225-305. doi: 10.1016/S0065-2776(06)92006-9.
9
Lysine-specific post-translational modifications of proteins in the life cycle of viruses.病毒生命周期中蛋白质的赖氨酸特异性翻译后修饰。
Cell Cycle. 2019 Sep;18(17):1995-2005. doi: 10.1080/15384101.2019.1639305. Epub 2019 Jul 10.
10
Functional Interaction Between the ESCRT-I Component TSG101 and the HSV-1 Tegument Ubiquitin Specific Protease.内体分选转运复合体-I组分TSG101与单纯疱疹病毒1型被膜泛素特异性蛋白酶之间的功能相互作用
J Cell Physiol. 2015 Aug;230(8):1794-806. doi: 10.1002/jcp.24890.

引用本文的文献

1
The emerging roles of ubiquitin-like modifications in regulating HIV replication and host defense.类泛素修饰在调控HIV复制和宿主防御中的新作用。
Front Cell Infect Microbiol. 2025 Jun 11;15:1593445. doi: 10.3389/fcimb.2025.1593445. eCollection 2025.
2
Impaired K48-polyubiquitination downmodulates mouse norovirus propagation.K48-多聚泛素化受损会下调小鼠诺如病毒的增殖。
Front Cell Infect Microbiol. 2025 May 6;15:1530166. doi: 10.3389/fcimb.2025.1530166. eCollection 2025.
3
Clinical implications of activation of the LIMD1-VHL-HIF1α pathway during head-&-neck squamous cell carcinoma development.

本文引用的文献

1
A pre-immediate-early role for tegument ICP0 in the proteasome-dependent entry of herpes simplex virus.ICP0 衣壳蛋白在疱疹病毒蛋白酶体依赖性进入中的即刻早期前作用。
J Virol. 2011 Jun;85(12):5910-8. doi: 10.1128/JVI.00267-11. Epub 2011 Apr 6.
2
Host protein Ku70 binds and protects HIV-1 integrase from proteasomal degradation and is required for HIV replication.宿主蛋白 Ku70 结合并保护 HIV-1 整合酶免受蛋白酶体降解,这对于 HIV 复制是必需的。
J Biol Chem. 2011 May 20;286(20):17722-35. doi: 10.1074/jbc.M110.184739. Epub 2011 Mar 29.
3
Epstein-Barr virus nuclear antigen 3C facilitates G1-S transition by stabilizing and enhancing the function of cyclin D1.
头颈部鳞状细胞癌发展过程中 LIMD1-VHL-HIF1α 通路的激活的临床意义。
Indian J Med Res. 2024 May;159(5):479-493. doi: 10.25259/ijmr_1262_22.
4
Fibrillar Alpha-Synuclein Alters the Intracellular Chaperone Levels within Hours of Its Internalization.纤维状α-突触核蛋白在其内化数小时内改变细胞内伴侣蛋白水平。
ACS Omega. 2024 Apr 4;9(15):17185-17194. doi: 10.1021/acsomega.3c10036. eCollection 2024 Apr 16.
5
Genetically Encoded Crosslinking Enables Identification of Multivalent Ubiquitin-Deubiquitylating Enzyme Interactions.基因编码交联技术可用于鉴定多价泛素-去泛素化酶相互作用。
Chembiochem. 2023 Aug 1;24(15):e202300305. doi: 10.1002/cbic.202300305. Epub 2023 Jul 7.
6
Prediction of human protein interactome of dengue virus non-structural protein 5 (NS5) and its downstream immunological implications.登革病毒非结构蛋白5(NS5)的人类蛋白质相互作用组预测及其下游免疫学意义。
3 Biotech. 2023 Jun;13(6):180. doi: 10.1007/s13205-023-03569-0. Epub 2023 May 12.
7
Finding shortest and nearly shortest path nodes in large substantially incomplete networks by hyperbolic mapping.通过双曲映射找到大型极不完整网络中的最短和次短路径节点。
Nat Commun. 2023 Jan 17;14(1):186. doi: 10.1038/s41467-022-35181-w.
8
Systems Bioinformatics Reveals Possible Relationship between COVID-19 and the Development of Neurological Diseases and Neuropsychiatric Disorders.系统生物信息学揭示了 COVID-19 与神经系统疾病和神经精神障碍发展之间的可能关系。
Viruses. 2022 Oct 16;14(10):2270. doi: 10.3390/v14102270.
9
African Swine Fever Virus pI215L Inhibits Type I Interferon Signaling by Targeting Interferon Regulatory Factor 9 for Autophagic Degradation.非洲猪瘟病毒 pI215L 通过靶向干扰素调节因子 9 进行自噬降解来抑制 I 型干扰素信号通路。
J Virol. 2022 Sep 14;96(17):e0094422. doi: 10.1128/jvi.00944-22. Epub 2022 Aug 16.
10
Disrupting the HDAC6-ubiquitin interaction impairs infection by influenza and Zika virus and cellular stress pathways.阻断 HDAC6-泛素相互作用可损害流感和寨卡病毒感染及细胞应激途径。
Cell Rep. 2022 Apr 26;39(4):110736. doi: 10.1016/j.celrep.2022.110736.
EB 病毒核抗原 3C 通过稳定和增强细胞周期蛋白 D1 的功能促进 G1-S 期转换。
PLoS Pathog. 2011 Feb 10;7(2):e1001275. doi: 10.1371/journal.ppat.1001275.
4
N-terminal hemagglutinin tag renders lysine-deficient APOBEC3G resistant to HIV-1 Vif-induced degradation by reduced polyubiquitination.N 端血凝素标签使赖氨酸缺陷型 APOBEC3G 对 HIV-1 Vif 诱导的降解具有抗性,这是通过降低多泛素化实现的。
J Virol. 2011 May;85(9):4510-9. doi: 10.1128/JVI.01925-10. Epub 2011 Feb 23.
5
Ubiquitinated proteome: ready for global?泛素化蛋白质组:准备好全球化了吗?
Mol Cell Proteomics. 2011 May;10(5):R110.006882. doi: 10.1074/mcp.R110.006882. Epub 2011 Feb 21.
6
Hepatitis B virus x protein in the pathogenesis of hepatitis B virus-induced hepatocellular carcinoma.乙型肝炎病毒 X 蛋白在乙型肝炎病毒诱导的肝细胞癌发病机制中的作用。
J Gastroenterol Hepatol. 2011 Jan;26 Suppl 1:144-52. doi: 10.1111/j.1440-1746.2010.06546.x.
7
Ubiquitin-regulated nuclear-cytoplasmic trafficking of the Nipah virus matrix protein is important for viral budding.泛素调控的尼帕病毒基质蛋白的核质转运对病毒出芽是重要的。
PLoS Pathog. 2010 Nov 11;6(11):e1001186. doi: 10.1371/journal.ppat.1001186.
8
The E4orf6/E1B55K E3 ubiquitin ligase complexes of human adenoviruses exhibit heterogeneity in composition and substrate specificity.人腺病毒 E4orf6/E1B55K E3 泛素连接酶复合物在组成和底物特异性上表现出异质性。
J Virol. 2011 Jan;85(2):765-75. doi: 10.1128/JVI.01890-10. Epub 2010 Nov 10.
9
Serine-threonine ubiquitination mediates downregulation of BST-2/tetherin and relief of restricted virion release by HIV-1 Vpu.丝氨酸-苏氨酸泛素化介导 BST-2/ tetherin 的下调和 HIV-1 Vpu 缓解病毒粒子释放的限制。
J Virol. 2011 Jan;85(1):51-63. doi: 10.1128/JVI.01795-10. Epub 2010 Oct 27.
10
Ancient origin of animal U-box ubiquitin ligases.动物 U-box 泛素连接酶的古老起源。
BMC Evol Biol. 2010 Oct 27;10:331. doi: 10.1186/1471-2148-10-331.