Metabolism and Epigenetics

被引:141
作者
Janke, Ryan [1 ]
Dodson, Anne E.
Rine, Jasper
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
来源
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, VOL 31 | 2015年 / 31卷
关键词
chromatin modification; methylation; acetylation; S-adenosyl methionine; folate; oncometabolite; ACETYL-ADP-RIBOSE; NAD(+) SALVAGE PATHWAY; LIFE-SPAN EXTENSION; DNA METHYLATION; ASCORBIC-ACID; HISTONE DEMETHYLATION; DEPENDENT HISTONE; ONCOMETABOLITE; 2-HYDROXYGLUTARATE; SACCHAROMYCES-CEREVISIAE; REPROGRAMMING FACTORS;
D O I
10.1146/annurev-cellbio-100814-125544
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epigenetic mechanisms by which cells inherit information are, to a large extent, enabled by DNA methylation and posttranslational modifications of histone proteins. These modifications operate both to influence the structure of chromatin per se and to serve as recognition elements for proteins with motifs dedicated to binding particular modifications. Each of these modifications results from an enzyme that consumes one of several important metabolites during catalysis. Likewise, the removal of these marks often results in the consumption of a different metabolite. Therefore, these so-called epigenetic marks have the capacity to integrate the expression state of chromatin with the metabolic state of the cell. This review focuses on the central roles played by acetyl-CoA. S-adenosyl methionine, NAD+, and a growing list of other acvl-CoA derivatives in epigenetic processes. We also review how metabolites that accumulate as a result of oncogenic mutations are thought to subvert the epigenetic program.
引用
收藏
页码:473 / 496
页数:24
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