Histone oxidation as a new mechanism of metabolic control over gene expression

被引:6
作者
Gantner, Benjamin N. [1 ]
Palma, Flavio R. [2 ]
Kayzuka, Cezar [2 ,3 ,4 ]
Lacchini, Riccardo [4 ]
Foltz, Daniel R. [5 ]
Backman, Vadim [5 ,6 ]
Kelleher, Neil [5 ,7 ]
Shilatifard, Ali
Bonini, Marcelo G. [2 ,5 ]
机构
[1] Med Coll Wisconsin, Dept Med, Div Endocrinol, Milwaukee, WI USA
[2] Northwestern Univ, Feinberg Sch Med, Div Hematol Oncol, Chicago, IL 60611 USA
[3] Univ Sao Paulo, Ribeirao Preto Med Sch, Dept Pharmacol, Sao Paulo, Brazil
[4] Univ Sao Paulo, Ribeirao Preto Coll Nursing, Dept Psychiat Nursing & Human Sci, Sao Paulo, Brazil
[5] Northwestern Univ, Feinberg Sch Med, Dept Biochem & Mol Genet, Chicago, IL 60611 USA
[6] Northwestern Univ, Mormick Sch Engn, Dept Bioengn, Chicago, IL USA
[7] Northwestern Univ, Chem Life Proc Inst, Chicago, IL USA
基金
巴西圣保罗研究基金会;
关键词
STRESS; GLUTATHIONYLATION; QUANTIFICATION; ACTIVATION; NITRATION; INTERPLAY; RADICALS; CELLS; CYCLE; ROS;
D O I
10.1016/j.tig.2024.05.012
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The emergence of aerobic respiration created unprecedented bioenergetic advantages, while imposing the need to protect critical genetic information from reactive byproducts of oxidative metabolism (i.e., reactive oxygen species, ROS). The evolution of histone proteins fulfilled the need to shield DNA from these potentially damaging toxins, while providing the means to compact and structure massive eukaryotic genomes. To date, several metabolism-linked histone post-translational modifications (PTMs) have been shown to regulate chromatin structure and gene expression. However, whether and how PTMs enacted by metabolically produced ROS regulate adaptive chromatin remodeling remain relatively unexplored. Here, we review novel mechanistic insights into the interactions of ROS with histones and their consequences for the control of gene expression regulation, cellular plasticity, and behavior.
引用
收藏
页码:739 / 746
页数:8
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