• 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

细菌效应蛋白通过劫持宿主泛素途径进行的时间和空间调节。

Bacterial effector-involved temporal and spatial regulation by hijack of the host ubiquitin pathway.

机构信息

Research Institute for Microbial Diseases, Osaka University Suita, Japan.

出版信息

Front Microbiol. 2011 Jul 4;2:145. doi: 10.3389/fmicb.2011.00145. eCollection 2011.

DOI:10.3389/fmicb.2011.00145
PMID:21772836
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3131150/
Abstract

Ubiquitination is one of the most conserved post-translational modifications of proteins, and is involved in essential eukaryotic cellular processes. These include protein degradation, transcriptional regulation, cell-cycle progression, and signaling. Microbial pathogens have evolved sophisticated systems to hijack host cellular functions for their own benefit. Central to these systems are protein transport machineries; many pathogenic bacteria inject "effector proteins" to modulate host cellular processes including the ubiquitin pathway. Numerous bacterial pathogens have been found to modulate the host ubiquitin system in various ways. In this review, we focus on three examples of temporal and spatial regulation of bacterial effectors, which are mediated by the host ubiquitin system. Subversion of the host ubiquitin system must be a widespread strategy among pathogenic bacteria to accomplish successful infection.

摘要

泛素化是蛋白质最保守的翻译后修饰之一,参与真核细胞的基本过程。这些过程包括蛋白质降解、转录调控、细胞周期进展和信号转导。微生物病原体已经进化出复杂的系统来劫持宿主细胞的功能为己所用。这些系统的核心是蛋白质运输机械;许多致病菌注射“效应蛋白”来调节宿主细胞过程,包括泛素途径。已经发现许多细菌病原体以各种方式调节宿主的泛素系统。在这篇综述中,我们重点介绍了三个细菌效应子的时间和空间调节的例子,这些调节是由宿主泛素系统介导的。宿主泛素系统的颠覆必须是致病菌完成成功感染的广泛策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4208/3131150/e0a15de7a03d/fmicb-02-00145-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4208/3131150/3bb38df7a7ab/fmicb-02-00145-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4208/3131150/7e3c20be4fbd/fmicb-02-00145-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4208/3131150/e0a15de7a03d/fmicb-02-00145-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4208/3131150/3bb38df7a7ab/fmicb-02-00145-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4208/3131150/7e3c20be4fbd/fmicb-02-00145-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4208/3131150/e0a15de7a03d/fmicb-02-00145-g003.jpg

相似文献

1
Bacterial effector-involved temporal and spatial regulation by hijack of the host ubiquitin pathway.细菌效应蛋白通过劫持宿主泛素途径进行的时间和空间调节。
Front Microbiol. 2011 Jul 4;2:145. doi: 10.3389/fmicb.2011.00145. eCollection 2011.
2
Exploitation of eukaryotic ubiquitin signaling pathways by effectors translocated by bacterial type III and type IV secretion systems.细菌III型和IV型分泌系统转运效应蛋白对真核泛素信号通路的利用。
PLoS Pathog. 2007 Jan;3(1):e3. doi: 10.1371/journal.ppat.0030003.
3
Hijacking the host proteasome for the temporal degradation of bacterial effectors.劫持宿主蛋白酶体以实现细菌效应蛋白的适时降解。
Methods Mol Biol. 2014;1197:141-52. doi: 10.1007/978-1-4939-1261-2_8.
4
Diversity of bacterial manipulation of the host ubiquitin pathways.宿主泛素途径中细菌操纵的多样性。
Cell Microbiol. 2015 Jan;17(1):26-34. doi: 10.1111/cmi.12384. Epub 2014 Nov 22.
5
Modification of the host ubiquitome by bacterial enzymes.细菌酶对宿主泛素组的修饰。
Microbiol Res. 2020 May;235:126429. doi: 10.1016/j.micres.2020.126429. Epub 2020 Feb 11.
6
Hijacking of the Host Ubiquitin Network by .宿主泛素网络的劫持。
Front Cell Infect Microbiol. 2017 Dec 5;7:487. doi: 10.3389/fcimb.2017.00487. eCollection 2017.
7
Legionella metaeffector exploits host proteasome to temporally regulate cognate effector.军团菌效应物利用宿主蛋白酶体来暂时调节同源效应物。
PLoS Pathog. 2010 Dec 2;6(12):e1001216. doi: 10.1371/journal.ppat.1001216.
8
Bacterial effectors and their functions in the ubiquitin-proteasome system: insight from the modes of substrate recognition.细菌效应蛋白及其在泛素-蛋白酶体系统中的功能:基于底物识别模式的见解
Cells. 2014 Aug 18;3(3):848-64. doi: 10.3390/cells3030848.
9
Exploitation of the Host Ubiquitin System: Means by .对宿主泛素系统的利用:通过……的方式
Front Microbiol. 2021 Dec 22;12:790442. doi: 10.3389/fmicb.2021.790442. eCollection 2021.
10
Revisiting Bacterial Ubiquitin Ligase Effectors: Weapons for Host Exploitation.重新审视细菌泛素连接酶效应物:宿主利用的武器。
Int J Mol Sci. 2018 Nov 13;19(11):3576. doi: 10.3390/ijms19113576.

引用本文的文献

1
A comprehensive two-hybrid analysis to explore the effector-effector interactome.一项探索效应器-效应器相互作用组的全面双杂交分析。
mSystems. 2024 Dec 17;9(12):e0100424. doi: 10.1128/msystems.01004-24. Epub 2024 Nov 11.
2
Microbial genotoxin-elicited host DNA mutations related to mitochondrial dysfunction, a momentous contributor for colorectal carcinogenesis.微生物遗传毒素引发的与线粒体功能障碍相关的宿主 DNA 突变,是结直肠癌发生的一个重要因素。
mSystems. 2024 Sep 17;9(9):e0088724. doi: 10.1128/msystems.00887-24. Epub 2024 Aug 27.
3
The emerging role and therapeutic implications of bacterial and parasitic deubiquitinating enzymes.

本文引用的文献

1
Exploitation of Host Polyubiquitination Machinery through Molecular Mimicry by Eukaryotic-Like Bacterial F-Box Effectors.真核样细菌F-Box效应蛋白通过分子模拟对宿主多聚泛素化机制的利用
Front Microbiol. 2010 Nov 11;1:122. doi: 10.3389/fmicb.2010.00122. eCollection 2010.
2
Comprehensive identification of protein substrates of the Dot/Icm type IV transporter of Legionella pneumophila.全面鉴定肺炎军团菌 Dot/Icm 型 IV 转运器的蛋白底物。
PLoS One. 2011 Mar 9;6(3):e17638. doi: 10.1371/journal.pone.0017638.
3
Legionella metaeffector exploits host proteasome to temporally regulate cognate effector.
细菌和寄生虫去泛素化酶的新兴作用和治疗意义。
Front Immunol. 2023 Nov 22;14:1303072. doi: 10.3389/fimmu.2023.1303072. eCollection 2023.
4
Structural basis for the toxicity of Legionella pneumophila effector SidH.军团菌效应蛋白 SidH 毒性的结构基础
Nat Commun. 2023 Nov 3;14(1):7068. doi: 10.1038/s41467-023-42683-8.
5
Structural Basis of Ubiquitin Recognition by a Bacterial Ovarian Tumor Deubiquitinase LotA.细菌性卵巢肿瘤去泛素化酶 LotA 识别泛素的结构基础。
J Bacteriol. 2022 Jan 18;204(1):e0037621. doi: 10.1128/JB.00376-21. Epub 2021 Oct 11.
6
Divergence of Legionella Effectors Reversing Conventional and Unconventional Ubiquitination.嗜肺军团菌效应蛋白在逆转传统和非传统泛素化方面的差异
Front Cell Infect Microbiol. 2020 Aug 21;10:448. doi: 10.3389/fcimb.2020.00448. eCollection 2020.
7
Chloroplasts at the Crossroad of Photosynthesis, Pathogen Infection and Plant Defense.叶绿体在光合作用、病原体感染和植物防御中的作用。
Int J Mol Sci. 2018 Dec 5;19(12):3900. doi: 10.3390/ijms19123900.
8
Legionella pneumophila-Derived Outer Membrane Vesicles Promote Bacterial Replication in Macrophages.嗜肺军团菌衍生的外膜囊泡促进巨噬细胞中的细菌复制。
PLoS Pathog. 2016 Apr 22;12(4):e1005592. doi: 10.1371/journal.ppat.1005592. eCollection 2016 Apr.
9
Host Cell-catalyzed S-Palmitoylation Mediates Golgi Targeting of the Legionella Ubiquitin Ligase GobX.宿主细胞催化的S-棕榈酰化介导嗜肺军团菌泛素连接酶GobX靶向高尔基体。
J Biol Chem. 2015 Oct 16;290(42):25766-81. doi: 10.1074/jbc.M115.637397. Epub 2015 Aug 27.
10
Type III chaperones & Co in bacterial plant pathogens: a set of specialized bodyguards mediating effector delivery.III 型分子伴侣及相关因子在植物病原菌中的作用:一类介导效应子传递的专业化“保镖”。
Front Plant Sci. 2013 Nov 22;4:435. doi: 10.3389/fpls.2013.00435.
军团菌效应物利用宿主蛋白酶体来暂时调节同源效应物。
PLoS Pathog. 2010 Dec 2;6(12):e1001216. doi: 10.1371/journal.ppat.1001216.
4
Large-scale identification and translocation of type IV secretion substrates by Coxiella burnetii.贝氏柯克斯体通过 IV 型分泌系统进行大规模底物的识别和转位。
Proc Natl Acad Sci U S A. 2010 Dec 14;107(50):21755-60. doi: 10.1073/pnas.1010485107. Epub 2010 Nov 23.
5
Biochemical and structural studies of a HECT-like ubiquitin ligase from Escherichia coli O157:H7.大肠杆菌 O157:H7 的一种 HECT 样泛素连接酶的生化和结构研究。
J Biol Chem. 2011 Jan 7;286(1):441-9. doi: 10.1074/jbc.M110.167643. Epub 2010 Oct 27.
6
Modulation of host cell function by Legionella pneumophila type IV effectors.军团菌属Ⅳ型效应物对宿主细胞功能的调节。
Annu Rev Cell Dev Biol. 2010;26:261-83. doi: 10.1146/annurev-cellbio-100109-104034.
7
NleG Type 3 effectors from enterohaemorrhagic Escherichia coli are U-Box E3 ubiquitin ligases.肠出血性大肠杆菌 NleG 型 3 效应子是 U-Box E3 泛素连接酶。
PLoS Pathog. 2010 Jun 24;6(6):e1000960. doi: 10.1371/journal.ppat.1000960.
8
Identification of an unconventional E3 binding surface on the UbcH5 ~ Ub conjugate recognized by a pathogenic bacterial E3 ligase.鉴定一种非常规的 UbcH5~Ub 缀合物上的 E3 结合表面,该表面被一种致病细菌的 E3 连接酶所识别。
Proc Natl Acad Sci U S A. 2010 Feb 16;107(7):2848-53. doi: 10.1073/pnas.0914821107. Epub 2010 Feb 1.
9
Hijacking the host ubiquitin pathway: structural strategies of bacterial E3 ubiquitin ligases.劫持宿主泛素途径:细菌 E3 泛素连接酶的结构策略。
Curr Opin Microbiol. 2010 Feb;13(1):41-6. doi: 10.1016/j.mib.2009.11.008. Epub 2009 Dec 28.
10
A bacterial E3 ubiquitin ligase IpaH9.8 targets NEMO/IKKgamma to dampen the host NF-kappaB-mediated inflammatory response.一种细菌 E3 泛素连接酶 IpaH9.8 靶向 NEMO/IKKγ,以抑制宿主 NF-κB 介导的炎症反应。
Nat Cell Biol. 2010 Jan;12(1):66-73; sup pp 1-9. doi: 10.1038/ncb2006. Epub 2009 Dec 13.