• 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

细胞信号转导和人类疾病中的非蛋白水解泛素化作用。

Non-proteolytic ubiquitylation in cellular signaling and human disease.

机构信息

Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France.

Centre National de la Recherche Scientifique (CNRS), UMR 7104, Strasbourg, France.

出版信息

Commun Biol. 2022 Feb 8;5(1):114. doi: 10.1038/s42003-022-03060-1.

DOI:10.1038/s42003-022-03060-1
PMID:35136173
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8826416/
Abstract

Ubiquitylation is one of the most common post-translational modifications (PTMs) of proteins that frequently targets substrates for proteasomal degradation. However it can also result in non-proteolytic events which play important functions in cellular processes such as intracellular signaling, membrane trafficking, DNA repair and cell cycle. Emerging evidence demonstrates that dysfunction of non-proteolytic ubiquitylation is associated with the development of multiple human diseases. In this review, we summarize the current knowledge and the latest concepts on how non-proteolytic ubiquitylation pathways are involved in cellular signaling and in disease-mediating processes. Our review, may advance our understanding of the non-degradative ubiquitylation process.

摘要

泛素化是蛋白质最常见的翻译后修饰(PTMs)之一,它经常将底物靶向蛋白酶体降解。然而,它也可以导致非蛋白水解事件,这些事件在细胞过程中发挥着重要的功能,如细胞内信号转导、膜运输、DNA 修复和细胞周期。新出现的证据表明,非蛋白水解泛素化的功能障碍与多种人类疾病的发展有关。在这篇综述中,我们总结了目前关于非蛋白水解泛素化途径如何参与细胞信号转导和疾病介导过程的知识和最新概念。我们的综述可能会增进我们对非降解泛素化过程的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/d30380b9250d/42003_2022_3060_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/a436717d257d/42003_2022_3060_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/789c6e3241ac/42003_2022_3060_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/70ee7abf3f33/42003_2022_3060_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/91ea216360c7/42003_2022_3060_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/d30380b9250d/42003_2022_3060_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/a436717d257d/42003_2022_3060_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/789c6e3241ac/42003_2022_3060_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/70ee7abf3f33/42003_2022_3060_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/91ea216360c7/42003_2022_3060_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd4b/8826416/d30380b9250d/42003_2022_3060_Fig5_HTML.jpg

相似文献

1
Non-proteolytic ubiquitylation in cellular signaling and human disease.细胞信号转导和人类疾病中的非蛋白水解泛素化作用。
Commun Biol. 2022 Feb 8;5(1):114. doi: 10.1038/s42003-022-03060-1.
2
DNA damage-induced ubiquitylation of proteasome controls its proteolytic activity.DNA损伤诱导的蛋白酶体泛素化调控其蛋白水解活性。
Oncotarget. 2013 Sep;4(9):1338-48. doi: 10.18632/oncotarget.1060.
3
A proteome-wide, quantitative survey of in vivo ubiquitylation sites reveals widespread regulatory roles.一种基于蛋白质组的、定量的体内泛素化位点调查揭示了广泛的调节作用。
Mol Cell Proteomics. 2011 Oct;10(10):M111.013284. doi: 10.1074/mcp.M111.013284. Epub 2011 Sep 1.
4
Ubiquitylation of ABA Receptors and Protein Phosphatase 2C Coreceptors to Modulate ABA Signaling and Stress Response.泛素化 ABA 受体和蛋白磷酸酶 2C 共受体以调节 ABA 信号和应激响应。
Int J Mol Sci. 2021 Jul 1;22(13):7103. doi: 10.3390/ijms22137103.
5
The Emerging Role of Non-traditional Ubiquitination in Oncogenic Pathways.非传统泛素化在致癌途径中的新兴作用
J Biol Chem. 2017 Mar 3;292(9):3543-3551. doi: 10.1074/jbc.R116.755694. Epub 2017 Feb 1.
6
RNF8-independent Lys63 poly-ubiquitylation prevents genomic instability in response to replication-associated DNA damage.不依赖RNF8的赖氨酸63多聚泛素化可防止因复制相关DNA损伤而导致的基因组不稳定。
PLoS One. 2014 Feb 28;9(2):e89997. doi: 10.1371/journal.pone.0089997. eCollection 2014.
7
Timing of DNA lesion recognition: Ubiquitin signaling in the NER pathway.DNA损伤识别的时机:核苷酸切除修复途径中的泛素信号传导
Cell Cycle. 2017 Jan 17;16(2):163-171. doi: 10.1080/15384101.2016.1261227. Epub 2016 Dec 8.
8
[Histone ubiquitylation and its roles in DNA damage response].[组蛋白泛素化及其在DNA损伤应答中的作用]
Yi Chuan. 2019 Jan 20;41(1):29-40. doi: 10.16288/j.yczz.18-112.
9
The ubiquitin codes in cellular stress responses.泛素码在细胞应激反应中的作用。
Protein Cell. 2024 Feb 29;15(3):157-190. doi: 10.1093/procel/pwad045.
10
Disorders of ubiquitylation: unchained inflammation.泛素化紊乱:脱链的炎症。
Nat Rev Rheumatol. 2022 Aug;18(8):435-447. doi: 10.1038/s41584-022-00778-4. Epub 2022 May 6.

引用本文的文献

1
The ubiquitin-proteasome system in circadian regulation.昼夜节律调节中的泛素-蛋白酶体系统。
Front Neurosci. 2025 Aug 26;19:1632905. doi: 10.3389/fnins.2025.1632905. eCollection 2025.
2
Unraveling chain specific ubiquitination in cells using tandem ubiquitin binding entities.利用串联泛素结合实体解析细胞中特定链的泛素化
Sci Rep. 2025 Jul 2;15(1):22961. doi: 10.1038/s41598-025-07242-9.
3
Cullin 3-mediated ubiquitination restricts enterovirus D68 replication and is counteracted by viral protease 3C.Cullin 3介导的泛素化作用限制肠道病毒D68的复制,并被病毒蛋白酶3C所抵消。

本文引用的文献

1
MKRN3 regulates the epigenetic switch of mammalian puberty via ubiquitination of MBD3.MKRN3通过MBD3的泛素化作用调节哺乳动物青春期的表观遗传开关。
Natl Sci Rev. 2020 Mar;7(3):671-685. doi: 10.1093/nsr/nwaa023. Epub 2020 Feb 14.
2
RNF8-mediated regulation of Akt promotes lung cancer cell survival and resistance to DNA damage.RNF8 介导的 Akt 调节促进肺癌细胞存活和抵抗 DNA 损伤。
Cell Rep. 2021 Oct 19;37(3):109854. doi: 10.1016/j.celrep.2021.109854.
3
Deubiquitinase OTUB2 exacerbates the progression of colorectal cancer by promoting PKM2 activity and glycolysis.
J Virol. 2025 Jun 17;99(6):e0035425. doi: 10.1128/jvi.00354-25. Epub 2025 May 21.
4
Rewired glycolysis by DTL accelerates oncometabolite L-lactate generation to promote breast cancer progression.DTL 重编程糖酵解加速致癌代谢物 L-乳酸生成以促进乳腺癌进展。
Front Oncol. 2025 May 5;15:1583752. doi: 10.3389/fonc.2025.1583752. eCollection 2025.
5
Nanoparticle-Mediated Targeted Protein Degradation: An Emerging Therapeutics Technology.纳米颗粒介导的靶向蛋白质降解:一种新兴的治疗技术。
Angew Chem Int Ed Engl. 2025 May 5:e202503958. doi: 10.1002/anie.202503958.
6
Identification of E3 Ubiquitin Ligase Substrates Using Biotin Ligase-Based Proximity Labeling Approaches.使用基于生物素连接酶的邻近标记方法鉴定E3泛素连接酶底物
Biomedicines. 2025 Apr 2;13(4):854. doi: 10.3390/biomedicines13040854.
7
Cullin-RING Ubiquitin Ligases in Neurodevelopment and Neurodevelopmental Disorders.神经发育及神经发育障碍中的Cullin-RING泛素连接酶
Biomedicines. 2025 Mar 28;13(4):810. doi: 10.3390/biomedicines13040810.
8
Proximity-dependent biotinylation reveals an interaction between ubiquitin-specific peptidase 46 and centrosome-related proteins.邻近依赖性生物素化揭示了泛素特异性肽酶46与中心体相关蛋白之间的相互作用。
FEBS Open Bio. 2025 Jan;15(1):151-164. doi: 10.1002/2211-5463.13918. Epub 2024 Oct 31.
9
Ubiquitylomics: An Emerging Approach for Profiling Protein Ubiquitylation in Skeletal Muscle.泛素化组学:一种用于分析骨骼肌中蛋白质泛素化的新兴方法。
J Cachexia Sarcopenia Muscle. 2024 Dec;15(6):2281-2294. doi: 10.1002/jcsm.13601. Epub 2024 Sep 16.
10
Bioinformatic Analyses and Integrated Machine Learning to Predict prognosis and therapeutic response Based on E3 Ligase-Related Genes in colon cancer.基于E3泛素连接酶相关基因的生物信息学分析与集成机器学习预测结肠癌的预后和治疗反应
J Cancer. 2024 Aug 19;15(16):5376-5395. doi: 10.7150/jca.98723. eCollection 2024.
去泛素化酶 OTUB2 通过促进 PKM2 活性和糖酵解来加剧结直肠癌的进展。
Oncogene. 2022 Jan;41(1):46-56. doi: 10.1038/s41388-021-02071-2. Epub 2021 Oct 20.
4
SPOP mutation induces replication over-firing by impairing Geminin ubiquitination and triggers replication catastrophe upon ATR inhibition.SPOP 突变通过削弱 Geminin 的泛素化来诱导复制过度激发,并在 ATR 抑制时引发复制灾难。
Nat Commun. 2021 Oct 1;12(1):5779. doi: 10.1038/s41467-021-26049-6.
5
AMBRA1 Promotes TGFβ Signaling via Nonproteolytic Polyubiquitylation of Smad4.AMBRA1 通过 Smad4 的非蛋白水解多泛素化促进 TGFβ 信号转导。
Cancer Res. 2021 Oct 1;81(19):5007-5020. doi: 10.1158/0008-5472.CAN-21-0431. Epub 2021 Aug 6.
6
Cancer metabolism: looking forward.癌症代谢:展望未来。
Nat Rev Cancer. 2021 Oct;21(10):669-680. doi: 10.1038/s41568-021-00378-6. Epub 2021 Jul 16.
7
K29-linked ubiquitin signaling regulates proteotoxic stress response and cell cycle.K29 连接的泛素信号调节蛋白毒性应激反应和细胞周期。
Nat Chem Biol. 2021 Aug;17(8):896-905. doi: 10.1038/s41589-021-00823-5. Epub 2021 Jul 8.
8
An Updated Understanding of the Role of YAP in Driving Oncogenic Responses.对YAP在驱动致癌反应中作用的最新认识。
Cancers (Basel). 2021 Jun 21;13(12):3100. doi: 10.3390/cancers13123100.
9
ATM-phosphorylated SPOP contributes to 53BP1 exclusion from chromatin during DNA replication.ATM 磷酸化的 SPOP 有助于在 DNA 复制过程中使 53BP1 从染色质中排除。
Sci Adv. 2021 Jun 18;7(25). doi: 10.1126/sciadv.abd9208. Print 2021 Jun.
10
OTULIN in NF-κB signaling, cell death, and disease.OTULIN 在 NF-κB 信号转导、细胞死亡和疾病中的作用。
Trends Immunol. 2021 Jul;42(7):590-603. doi: 10.1016/j.it.2021.05.003. Epub 2021 May 29.