Back to Search Start Over

Mechanisms and Inhibitors of Histone Arginine Methylation.

Authors :
Fulton MD
Brown T
Zheng YG
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.)

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