• 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

泛素化在病毒感染过程中 NF-κB 信号转导中的作用。

The Role of Ubiquitination in NF-κB Signaling during Virus Infection.

机构信息

Department of Microbiology and Immunology, Tulane University, New Orleans, LA 70112, USA.

出版信息

Viruses. 2021 Jan 20;13(2):145. doi: 10.3390/v13020145.

DOI:10.3390/v13020145
PMID:33498196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7908985/
Abstract

The nuclear factor κB (NF-κB) family are the master transcription factors that control cell proliferation, apoptosis, the expression of interferons and proinflammatory factors, and viral infection. During viral infection, host innate immune system senses viral products, such as viral nucleic acids, to activate innate defense pathways, including the NF-κB signaling axis, thereby inhibiting viral infection. In these NF-κB signaling pathways, diverse types of ubiquitination have been shown to participate in different steps of the signal cascades. Recent advances find that viruses also modulate the ubiquitination in NF-κB signaling pathways to activate viral gene expression or inhibit host NF-κB activation and inflammation, thereby facilitating viral infection. Understanding the role of ubiquitination in NF-κB signaling during viral infection will advance our knowledge of regulatory mechanisms of NF-κB signaling and pave the avenue for potential antiviral therapeutics. Thus, here we systematically review the ubiquitination in NF-κB signaling, delineate how viruses modulate the NF-κB signaling via ubiquitination and discuss the potential future directions.

摘要

核因子 κB(NF-κB)家族是控制细胞增殖、凋亡、干扰素和促炎因子表达以及病毒感染的主要转录因子。在病毒感染过程中,宿主固有免疫系统感知病毒产物,如病毒核酸,激活固有防御途径,包括 NF-κB 信号轴,从而抑制病毒感染。在这些 NF-κB 信号通路中,已经证明多种类型的泛素化参与信号级联的不同步骤。最近的研究进展发现,病毒还可以调节 NF-κB 信号通路中的泛素化,以激活病毒基因表达或抑制宿主 NF-κB 激活和炎症,从而促进病毒感染。了解泛素化在病毒感染过程中 NF-κB 信号转导中的作用将增进我们对 NF-κB 信号转导调控机制的认识,并为潜在的抗病毒治疗铺平道路。因此,在这里我们系统地综述了 NF-κB 信号通路中的泛素化,阐述了病毒如何通过泛素化调节 NF-κB 信号,并讨论了潜在的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e3a/7908985/c03335fc24ad/viruses-13-00145-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e3a/7908985/ef87a3c87053/viruses-13-00145-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e3a/7908985/559afd808bbc/viruses-13-00145-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e3a/7908985/c03335fc24ad/viruses-13-00145-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e3a/7908985/ef87a3c87053/viruses-13-00145-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e3a/7908985/559afd808bbc/viruses-13-00145-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e3a/7908985/c03335fc24ad/viruses-13-00145-g003.jpg

相似文献

1
The Role of Ubiquitination in NF-κB Signaling during Virus Infection.泛素化在病毒感染过程中 NF-κB 信号转导中的作用。
Viruses. 2021 Jan 20;13(2):145. doi: 10.3390/v13020145.
2
Regulation of NF-κB by ubiquitination.泛素化调节 NF-κB。
Curr Opin Immunol. 2013 Feb;25(1):4-12. doi: 10.1016/j.coi.2012.12.005. Epub 2013 Jan 8.
3
Hepatitis B e Antigen Inhibits NF-κB Activity by Interrupting K63-Linked Ubiquitination of NEMO.乙型肝炎 e 抗原通过中断 NEMO 的 K63 链接泛素化来抑制 NF-κB 活性。
J Virol. 2019 Jan 4;93(2). doi: 10.1128/JVI.00667-18. Print 2019 Jan 15.
4
The ORF61 Protein Encoded by Simian Varicella Virus and Varicella-Zoster Virus Inhibits NF-κB Signaling by Interfering with IκBα Degradation.猴水痘病毒和水痘-带状疱疹病毒编码的ORF61蛋白通过干扰IκBα降解来抑制NF-κB信号通路。
J Virol. 2015 Sep;89(17):8687-700. doi: 10.1128/JVI.01149-15. Epub 2015 Jun 17.
5
The role of nuclear factor κB in the interferon response.核因子 κB 在干扰素反应中的作用。
J Interferon Cytokine Res. 2011 Jul;31(7):553-9. doi: 10.1089/jir.2011.0028. Epub 2011 Jun 1.
6
Manipulation of Non-canonical NF-κB Signaling by Non-oncogenic Viruses.非致癌性病毒对非典型 NF-κB 信号的调控。
Arch Immunol Ther Exp (Warsz). 2019 Feb;67(1):41-48. doi: 10.1007/s00005-018-0522-x. Epub 2018 Sep 8.
7
Porcine Reproductive and Respiratory Syndrome Virus nsp1α Inhibits NF-κB Activation by Targeting the Linear Ubiquitin Chain Assembly Complex.猪繁殖与呼吸综合征病毒nsp1α通过靶向线性泛素链组装复合体抑制NF-κB激活。
J Virol. 2017 Jan 18;91(3). doi: 10.1128/JVI.01911-16. Print 2017 Feb 1.
8
Phosphorylation meets ubiquitination: the control of NF-[kappa]B activity.磷酸化与泛素化相遇:NF-κB活性的调控
Annu Rev Immunol. 2000;18:621-63. doi: 10.1146/annurev.immunol.18.1.621.
9
SAMHD1 suppresses innate immune responses to viral infections and inflammatory stimuli by inhibiting the NF-κB and interferon pathways.SAMHD1 通过抑制 NF-κB 和干扰素途径来抑制病毒感染和炎症刺激的先天免疫反应。
Proc Natl Acad Sci U S A. 2018 Apr 17;115(16):E3798-E3807. doi: 10.1073/pnas.1801213115. Epub 2018 Apr 2.
10
Viral hijacking of the host ubiquitin system to evade interferon responses.病毒劫持宿主泛素系统以逃避干扰素反应。
Curr Opin Microbiol. 2010 Aug;13(4):517-23. doi: 10.1016/j.mib.2010.05.012. Epub 2010 Jun 17.

引用本文的文献

1
RACK1 promotes NF-κB pathway activation and glioma cell proliferation by inhibiting RPS2 ubiquitination.RACK1通过抑制RPS2泛素化促进NF-κB信号通路激活和胶质瘤细胞增殖。
Mol Biol Rep. 2025 Jun 16;52(1):600. doi: 10.1007/s11033-025-10691-0.
2
Human Structural Homologues of SARS-CoV-2 PL as Anti-Targets: A Strategic Panel Analysis.作为抗靶点的新型冠状病毒2型木瓜蛋白酶样蛋白酶的人类结构同源物:一项策略性小组分析
MicroPubl Biol. 2025 Apr 14;2025. doi: 10.17912/micropub.biology.001418. eCollection 2025.
3
BEV 2C protein inhibits the NF-κB signalling pathway to promote viral replication by targeting IKBKB and p65.

本文引用的文献

1
Molecular bases for HOIPINs-mediated inhibition of LUBAC and innate immune responses.HOIPINs 介导的 LUBAC 抑制和固有免疫反应的分子基础。
Commun Biol. 2020 Apr 3;3(1):163. doi: 10.1038/s42003-020-0882-8.
2
Cellular functions and molecular mechanisms of non-lysine ubiquitination.非赖氨酸泛素化的细胞功能和分子机制。
Open Biol. 2019 Sep 27;9(9):190147. doi: 10.1098/rsob.190147. Epub 2019 Sep 18.
3
Non-proteolytic ubiquitination of OTULIN regulates NF-κB signaling pathway.OTULIN 的非蛋白水解泛素化调节 NF-κB 信号通路。
BEV 2C蛋白通过靶向IKBKB和p65抑制NF-κB信号通路以促进病毒复制。
Vet Res. 2025 Feb 16;56(1):42. doi: 10.1186/s13567-025-01453-8.
4
BK Polyomavirus and acute kidney injury in transplant recipients: signaling pathways and molecular mechanisms.BK多瘤病毒与移植受者的急性肾损伤:信号通路与分子机制
Virol J. 2025 Jan 4;22(1):2. doi: 10.1186/s12985-024-02620-7.
5
Understanding Post-Translational Modifications in Porcine Reproductive and Respiratory Syndrome Virus Infection.了解猪繁殖与呼吸综合征病毒感染中的翻译后修饰
Vet Sci. 2024 Dec 16;11(12):654. doi: 10.3390/vetsci11120654.
6
Linear ubiquitination mediates coronavirus NSP14-induced NF-κB activation.线性泛素化介导冠状病毒 NSP14 诱导的 NF-κB 激活。
Cell Commun Signal. 2024 Nov 30;22(1):573. doi: 10.1186/s12964-024-01949-4.
7
Mechanistic Role of TRIM26 in Viral Infection and Host Defense.TRIM26 在病毒感染和宿主防御中的作用机制。
Genes (Basel). 2024 Nov 15;15(11):1476. doi: 10.3390/genes15111476.
8
IP-10 acts early in CV-A16 infection to induce BBB destruction and promote virus entry into the CNS by increasing TNF-α expression.IP-10 在 CV-A16 感染早期发挥作用,通过增加 TNF-α 的表达诱导 BBB 破坏,并促进病毒进入中枢神经系统。
Front Immunol. 2024 Nov 4;15:1374447. doi: 10.3389/fimmu.2024.1374447. eCollection 2024.
9
Mandarin fish von Hippel-Lindau protein regulates the NF-κB signaling pathway via interaction with IκB to promote fish ranavirus replication.喉鳜鱼希佩尔-林道蛋白通过与 IκB 相互作用调节 NF-κB 信号通路,从而促进鱼类弹状病毒的复制。
Zool Res. 2024 Sep 18;45(5):990-1000. doi: 10.24272/j.issn.2095-8137.2023.392.
10
Ubiquitination and deubiquitination in cancer: from mechanisms to novel therapeutic approaches.泛素化和去泛素化在癌症中的作用:从机制到新的治疗方法。
Mol Cancer. 2024 Jul 25;23(1):148. doi: 10.1186/s12943-024-02046-3.
J Mol Cell Biol. 2020 Apr 24;12(3):163-175. doi: 10.1093/jmcb/mjz081.
4
Tripartite motif proteins: an emerging antiviral protein family.三聚体基序蛋白:一个新兴的抗病毒蛋白家族。
Future Virol. 2019 Feb;14(2):107-122. doi: 10.2217/fvl-2018-0161. Epub 2019 Jan 21.
5
RIPLET, and not TRIM25, is required for endogenous RIG-I-dependent antiviral responses.RIPLET 而非 TRIM25 是内源性 RIG-I 依赖性抗病毒反应所必需的。
Immunol Cell Biol. 2019 Oct;97(9):840-852. doi: 10.1111/imcb.12284. Epub 2019 Aug 19.
6
RNF34 functions in immunity and selective mitophagy by targeting MAVS for autophagic degradation.RNF34 通过靶向 MAVS 进行自噬降解在免疫和选择性线粒体自噬中发挥作用。
EMBO J. 2019 Jul 15;38(14):e100978. doi: 10.15252/embj.2018100978. Epub 2019 Jun 17.
7
Ubiquitin-Dependent and -Independent Roles of E3 Ligase RIPLET in Innate Immunity.RIPLET 在天然免疫中的泛素依赖性和非依赖性 E3 连接酶作用。
Cell. 2019 May 16;177(5):1187-1200.e16. doi: 10.1016/j.cell.2019.03.017. Epub 2019 Apr 18.
8
The Otubain YOD1 Suppresses Aggregation and Activation of the Signaling Adaptor MAVS through Lys63-Linked Deubiquitination.Otubain YOD1 通过赖氨酸 63 连接的去泛素化抑制信号接头 MAVS 的聚集和激活。
J Immunol. 2019 May 15;202(10):2957-2970. doi: 10.4049/jimmunol.1800656. Epub 2019 Apr 5.
9
Induction of OTUD4 by viral infection promotes antiviral responses through deubiquitinating and stabilizing MAVS.病毒感染诱导 OTUD4 通过去泛素化和稳定 MAVS 促进抗病毒反应。
Cell Res. 2019 Jan;29(1):67-79. doi: 10.1038/s41422-018-0107-6. Epub 2018 Nov 8.
10
Hepatitis B e Antigen Inhibits NF-κB Activity by Interrupting K63-Linked Ubiquitination of NEMO.乙型肝炎 e 抗原通过中断 NEMO 的 K63 链接泛素化来抑制 NF-κB 活性。
J Virol. 2019 Jan 4;93(2). doi: 10.1128/JVI.00667-18. Print 2019 Jan 15.