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The role of arginine methylation in the DNA damage response
被引:73
|作者:
Auclair, Yannick
Richard, Stephane
[1
]
机构:
[1] McGill Univ, Dept Oncol, Sir Mortimer B Davis Jewish Gen Hosp, Terry Fox Mol Oncol Grp, Montreal, PQ H3T 1E2, Canada
来源:
关键词:
PRMTs;
DNA damage;
Arginine methylation;
Cancer;
DOUBLE-STRAND BREAKS;
FLAP ENDONUCLEASE-1 ACTIVITY;
DEPENDENT NUCLEAR-DYNAMICS;
PROTEIN-KINASE-C;
CELL-CYCLE;
POLYMERASE-BETA;
MRE11;
COMPLEX;
POSTTRANSLATIONAL MODIFICATIONS;
HOMOLOGOUS RECOMBINATION;
SYMMETRIC DIMETHYLATION;
D O I:
10.1016/j.dnarep.2013.04.006
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Post-translational modifications are well-known modulators of DNA damage signaling and epigenetic gene expression. Protein arginine methylation is a covalent modification that results in the addition of methyl groups to the nitrogen atoms of the arginine side chains and is catalyzed by a family of protein arginine methyltransferases (PRMTs). In the past, arginine methylation was mainly observed on abundant proteins such as RNA-binding proteins and histones, but recent advances have revealed a plethora of arginine methylated proteins implicated in a variety of cellular processes including RNA metabolism, epigenetic regulation and DNA repair pathways. Herein, we discuss these recent advances, focusing on the role of PRMTs in DNA damage signaling and its importance for maintaining genomic stability. (C) 2013 Elsevier B.V. All rights reserved.
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页码:459 / 465
页数:7
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