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精氨酸单甲基化和二甲基化的功能动力学

Functional Dynamics of Arginine Mono- and Di-Methylation.

作者信息

Wang Xi'ang, Zhu Bin, Winn Robert, Lu Shanfa, Wang Hengbin

机构信息

Department of Internal Medicine, Division of Hematology, Oncology and Palliative Care, Massey Comprehensive Cancer Center, School of Medicine, Virginia Commonwealth University, Richmond, VI 23298, USA.

State Key Laboratory for Quality Ensurance and Sustainable Use of Dao-di Herbs, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100193, China.

出版信息

Cells. 2025 May 29;14(11):796. doi: 10.3390/cells14110796.

DOI:10.3390/cells14110796
PMID:40497972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12153873/
Abstract

Arginine methylation is a crucial post-translational modification (PTM) that plays a significant role in various biological processes. It occurs in two primary forms: mono-methylation (MMA) and di-methylation (DMA), with the latter further classified into symmetric (SDMA) and asymmetric methylation (ADMA). This review examines the functional implications of these methylation states, current detection methodologies, proteomics-based analytical approaches, and the different impacts of these methylations on protein function. Finally, the role of protein arginine methyltransferases (PRMTs) and their substrate specificity in shaping the arginine methylome are discussed.

摘要

精氨酸甲基化是一种关键的翻译后修饰(PTM),在各种生物学过程中发挥着重要作用。它以两种主要形式出现:单甲基化(MMA)和二甲基化(DMA),后者进一步分为对称二甲基化(SDMA)和不对称甲基化(ADMA)。本综述探讨了这些甲基化状态的功能意义、当前的检测方法、基于蛋白质组学的分析方法,以及这些甲基化对蛋白质功能的不同影响。最后,讨论了蛋白质精氨酸甲基转移酶(PRMTs)的作用及其底物特异性在塑造精氨酸甲基化组中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/b23772418b14/cells-14-00796-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/4cb64f3695ca/cells-14-00796-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/22b35796ee4a/cells-14-00796-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/719d87000edf/cells-14-00796-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/bd0da4cfbc02/cells-14-00796-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/71b9b759eff2/cells-14-00796-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/b23772418b14/cells-14-00796-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/4cb64f3695ca/cells-14-00796-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/22b35796ee4a/cells-14-00796-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/719d87000edf/cells-14-00796-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/bd0da4cfbc02/cells-14-00796-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/71b9b759eff2/cells-14-00796-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad4d/12153873/b23772418b14/cells-14-00796-g006.jpg

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本文引用的文献

1
Biomedical effects of protein arginine methyltransferase inhibitors.蛋白质精氨酸甲基转移酶抑制剂的生物医学效应。
J Biol Chem. 2025 Mar;301(3):108201. doi: 10.1016/j.jbc.2025.108201. Epub 2025 Jan 16.
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Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy.p38α介导的磷酸化和PRMT1介导的精氨酸甲基化在驱动TDP-43蛋白病中的相反作用。
Cell Rep. 2025 Jan 28;44(1):115205. doi: 10.1016/j.celrep.2024.115205. Epub 2025 Jan 14.
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Overview of PRMT1 modulators: Inhibitors and degraders.
PRMT1 调节剂概述:抑制剂和降解剂。
Eur J Med Chem. 2024 Dec 5;279:116887. doi: 10.1016/j.ejmech.2024.116887. Epub 2024 Sep 19.
4
A Chemoenzymatic Method Enables Global Enrichment and Characterization of Protein Arginine Methylation.一种化学酶法实现了蛋白质精氨酸甲基化的全局富集和表征。
Anal Chem. 2024 Sep 10;96(36):14612-14620. doi: 10.1021/acs.analchem.4c03180. Epub 2024 Aug 26.
5
Oligomerization of protein arginine methyltransferase 1 and its effect on methyltransferase activity and substrate specificity.蛋白质精氨酸甲基转移酶 1 的寡聚化及其对甲基转移酶活性和底物特异性的影响。
Protein Sci. 2024 Aug;33(8):e5118. doi: 10.1002/pro.5118.
6
Targeting PRMT9-mediated arginine methylation suppresses cancer stem cell maintenance and elicits cGAS-mediated anticancer immunity.靶向 PRMT9 介导的精氨酸甲基化抑制癌症干细胞维持并引发 cGAS 介导的抗癌免疫。
Nat Cancer. 2024 Apr;5(4):601-624. doi: 10.1038/s43018-024-00736-x. Epub 2024 Feb 27.
7
ETD-Based Proteomic Profiling Improves Arginine Methylation Identification and Reveals Novel PRMT5 Substrates.基于 ETD 的蛋白质组学分析可提高精氨酸甲基化鉴定的准确性,并揭示新的 PRMT5 底物。
J Proteome Res. 2024 Mar 1;23(3):1014-1027. doi: 10.1021/acs.jproteome.3c00724. Epub 2024 Jan 25.
8
Hydrophobic Derivatization Strategy Facilitates Comprehensive Profiling of Protein Methylation.疏水衍生化策略促进蛋白质甲基化的全面分析。
J Proteome Res. 2023 Oct 6;22(10):3275-3281. doi: 10.1021/acs.jproteome.3c00318. Epub 2023 Sep 22.
9
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Proteome-wide Profiling of Asymmetric Dimethylated Arginine in Human Breast Tumors.人类乳腺癌中不对称二甲基精氨酸的蛋白质组学分析。
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