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Mechanisms and Inhibitors of Histone Arginine Methylation.
- Source :
-
Chemical record (New York, N.Y.) [Chem Rec] 2018 Dec; Vol. 18 (12), pp. 1792-1807. Date of Electronic Publication: 2018 Sep 19. - Publication Year :
- 2018
-
Abstract
- Histone methylation plays an important regulatory role in chromatin restructuring and RNA transcription. Arginine methylation that is enzymatically catalyzed by the family of protein arginine methyltransferases (PRMTs) can either activate or repress gene expression depending on cellular contexts. Given the strong correlation of PRMTs with pathophysiology, great interest is seen in understanding molecular mechanisms of PRMTs in diseases and in developing potent PRMT inhibitors. Herein, we reviewed key research advances in the study of biochemical mechanisms of PRMT catalysis and their relevance to cell biology. We highlighted how a random binary, ordered ternary kinetic model for PRMT1 catalysis reconciles the literature reports and endorses a distributive mechanism that the enzyme active site utilizes for multiple turnovers of arginine methylation. We discussed the impacts of histone arginine methylation and its biochemical interplays with other key epigenetic marks. Challenges in developing small-molecule PRMT inhibitors were also discussed.<br /> (© 2018 The Chemical Society of Japan & Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)
- Subjects :
- Animals
Enzyme Inhibitors chemistry
Enzyme Inhibitors metabolism
Histones antagonists & inhibitors
Humans
Methylation
Protein Isoforms antagonists & inhibitors
Protein Isoforms metabolism
Protein Processing, Post-Translational
Protein-Arginine N-Methyltransferases antagonists & inhibitors
Protein-Arginine N-Methyltransferases metabolism
S-Adenosylmethionine chemistry
S-Adenosylmethionine metabolism
Arginine metabolism
Histones metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1528-0691
- Volume :
- 18
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Chemical record (New York, N.Y.)
- Publication Type :
- Academic Journal
- Accession number :
- 30230223
- Full Text :
- https://doi.org/10.1002/tcr.201800082