The impact of metabolism on DNA methylation

被引:219
作者
Ulrey, CL
Liu, L
Andrews, LG
Tollefsbol, TO
机构
[1] Univ Alabama Birmingham, Dept Biol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Ctr Aging, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Ctr Comprehens Canc, Birmingham, AL 35294 USA
关键词
D O I
10.1093/hmg/ddi100
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
Methylation of genomic cytosines is one of the best characterized epigenetic mechanisms, and investigation of its relationship with other biochemical pathways represents a critical stage in the elucidation of biological information processing. The field also has immense potential for the development of medical treatments for any number of conditions ranging from aging to neurological disorders. The DNA methylation status of genes is responsible for many heritable traits and varies more or less independently of the genetic code. This variation is often a result of cellular environmental factors including metabolism. A key metabolite in this regard is homocysteine. Knowledge of homocysteine metabolism continues to be amassed, yet the part played by aberrant DNA methylation in homocysteine-related pathologies is often, at best, conjectural. In this analysis, we will review recent insights and attempt to speculate meaningfully concerning the dynamics of the methionine cycle in relation to DNA methylation and disease.
引用
收藏
页码:R139 / R147
页数:9
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