Epigenetic Regulation of Cellular Senescence and Aging

被引:93
|
作者
Sidler, Corinne [1 ]
Kovalchuk, Olga [1 ]
Kovalchuk, Igor [1 ]
机构
[1] Univ Lethbridge, Dept Biol Sci, Lethbridge, AB, Canada
来源
FRONTIERS IN GENETICS | 2017年 / 8卷
基金
加拿大自然科学与工程研究理事会;
关键词
aging; cell senescence; epigenetic regulation; DNA methylation; heterochromatin; histone modifications; NUCLEAR LAMINA INTERACTIONS; CEREBRAL-CORTEX NEURONS; DNA-DAMAGE RESPONSE; HUMAN-CELLS; HUMAN FIBROBLASTS; HISTONE H3; LIFE-SPAN; TELOMERE LENGTH; STEM-CELLS; T-CELLS;
D O I
10.3389/fgene.2017.00138
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Aging is characterized by functional decline of diverse organs and an increased risk for several diseases. Therefore, a high interest exists in understanding the molecular mechanisms that stimulate aging at all levels, from cells and tissues to organs and organisms, in order to develop ways to promote healthy aging. While many molecular and biochemical mechanisms are already understood in some detail, the role of changes in epigenetic regulation has only begun to be considered in recent years. The age-dependent global reduction in heterochromatin, along with site-specific changes in the patterns of DNA methylation and modification of histones, have been observed in several aging model systems. However, understanding of the precise role of such changes requires further research. In this review, we will discuss the role of epigenetic regulation in aging and indicate future research directions that will help elucidate the mechanistic details of it.
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收藏
页数:11
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