Literature DB >> 28043171

The story of protein arginine methylation: characterization, regulation, and function.

Chao Peng1,2, Catherine Cl Wong1,2.   

Abstract

INTRODUCTION: Arginine methylation is an important post-translational modification (PTM) in cells, which is catalyzed by a group of protein arginine methyltransferases (PRMTs). It plays significant roles in diverse cellular processes and various diseases. Misregulation and aberrant expression of PRMTs can provide potential biomarkers and therapeutic targets for drug discovery. Areas covered: Herein, we review the arginine methylation literature and summarize the methodologies for the characterization of this modification, as well as describe the recent insights into arginine methyltransferases and their biological functions in diseases. Expert commentary: Benefits from the enzyme-based large-scale screening approach, the novel affinity enrichment strategies, arginine methylated protein family is the focus of attention. Although a number of arginine methyltransferases and related substrates are identified, the catalytic mechanism of different types of PRMTs remains unclear and few related demethylases are characterized. Novel functional studies continuously reveal the importance of this modification in the cell cycle and diseases. A deeper understanding of arginine methylated proteins, modification sites, and their mechanisms of regulation is needed to explore their role in life processes, especially their relationship with diseases, thus accelerating the generation of potent, selective, cell-penetrant drug candidates.

Entities:  

Keywords:  PRMT; Protein arginine methylation; S-adenosylmethionine; post-translational modification; sDMA&aDMA; tandem mass spectrometry

Mesh:

Substances:

Year:  2017        PMID: 28043171     DOI: 10.1080/14789450.2017.1275573

Source DB:  PubMed          Journal:  Expert Rev Proteomics        ISSN: 1478-9450            Impact factor:   3.940


  16 in total

Review 1.  PRMT7 as a unique member of the protein arginine methyltransferase family: A review.

Authors:  Kanishk Jain; Steven G Clarke
Journal:  Arch Biochem Biophys       Date:  2019-02-22       Impact factor: 4.013

Review 2.  DNA damage response and repair pathway modulation by non-histone protein methylation: implications in neurodegeneration.

Authors:  Madhusoodanan Urulangodi; Abhishek Mohanty
Journal:  J Cell Commun Signal       Date:  2019-11-20       Impact factor: 5.782

3.  Intricate Effects of α-Amino and Lysine Modifications on Arginine Methylation of the N-Terminal Tail of Histone H4.

Authors:  Melody D Fulton; Jing Zhang; Maomao He; Meng-Chiao Ho; Y George Zheng
Journal:  Biochemistry       Date:  2017-07-07       Impact factor: 3.162

4.  Purification and Identification of Natural Inhibitors of Protein Arginine Methyltransferases from Plants.

Authors:  Zhengxin Wang; Ling Xiong; Quanbo Xiong
Journal:  Mol Cell Biol       Date:  2022-03-21       Impact factor: 5.069

5.  Whole-body arginine dimethylation is associated with all-cause mortality in adult renal transplant recipients.

Authors:  Adrian Post; Alexander Bollenbach; Stephan J L Bakker; Dimitrios Tsikas
Journal:  Amino Acids       Date:  2021-03-02       Impact factor: 3.520

Review 6.  Protein arginine methylation: an emerging regulator of the cell cycle.

Authors:  Anita E Raposo; Sabine C Piller
Journal:  Cell Div       Date:  2018-03-20       Impact factor: 5.130

7.  PRMT5 Is Required for Bovine Leukemia Virus Infection In Vivo and Regulates BLV Gene Expression, Syncytium Formation, and Glycosylation In Vitro.

Authors:  Wlaa Assi; Tomoya Hirose; Satoshi Wada; Ryosuke Matsuura; Shin-Nosuke Takeshima; Yoko Aida
Journal:  Viruses       Date:  2020-06-16       Impact factor: 5.048

8.  Arginine methylation of APE1 promotes its mitochondrial translocation to protect cells from oxidative damage.

Authors:  Yilan Zhang; Qi Zhang; LuLu Li; Dan Mu; Ke Hua; Shusheng Ci; Lei Shen; Li Zheng; Binghui Shen; Zhigang Guo
Journal:  Free Radic Biol Med       Date:  2020-07-15       Impact factor: 7.376

Review 9.  Urinary Dimethylamine (DMA) and Its Precursor Asymmetric Dimethylarginine (ADMA) in Clinical Medicine, in the Context of Nitric Oxide (NO) and Beyond.

Authors:  Dimitrios Tsikas
Journal:  J Clin Med       Date:  2020-06-12       Impact factor: 4.241

10.  Proteome-wide identification of arginine methylation in colorectal cancer tissues from patients.

Authors:  Yongchul Lim; Ju Yeon Lee; Su Jin Ha; Suyeun Yu; Jung Kyong Shin; Hee Cheol Kim
Journal:  Proteome Sci       Date:  2020-05-19       Impact factor: 2.480

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