Oxidative post-translational modifications in histones

被引:16
|
作者
Luis Garcia-Gimenez, Jose
Roma-Mateo, Carlos
Pallardo, Federico V.
机构
[1] Center for Biomedical Network Research on Rare Diseases (CIBERER), Institute of Health Carlos III, Valencia
[2] INCLIVA Biomedical Research Institute, Valencia
[3] Department of Physiology, School of Medicine and Dentistry, Universitat de València (UV), Valencia
关键词
ESCHERICHIA-COLI; NUCLEAR GLUTATHIONE; COMMON FEATURES; CELL-CYCLE; IN-VIVO; CHROMATIN; STRESS; MECHANISMS; NITRATION; TYROSINE;
D O I
10.1002/biof.1532
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epigenetic regulation is attracting much attention because it explains many of the effects that the external environment induces in organisms. Changes in the cellular redox status and even more specifically in its nuclear redox compartment is one of these examples. Redox changes can induce modulation of the epigenetic regulation in cells. Here we present a few cases where reactive oxygen or nitrogen species induces epigenetic marks in histones. Posttranslational modification of these proteins like histone nitrosylation, carbonylation, or glutathionylation together with other mechanisms not reviewed here are the cornerstones of redox-related epigenetic regulation. We currently face a new field of research with potential important consequences for the treatment of many pathologies.
引用
收藏
页码:641 / 650
页数:10
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