Impact of aging on DNA methylation

被引:336
作者
Richardson, B
机构
[1] Univ Michigan, Dept Med, Ann Arbor, MI 48109 USA
[2] Ann Arbor VA Hosp, Ann Arbor, MI 48105 USA
关键词
DNA methylation; aging; autoimmunity; cancer; chromatin structure;
D O I
10.1016/S1568-1637(03)00010-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The biochemistry of aging is complex, with biologically significant changes occurring in proteins, lipids and nucleic acids. One of these changes is in the methylation of DNA. DNA methylation is a mechanism modifying gene expression. The methylation of sequences in or near regulatory elements can suppress gene expression through effects on DNA binding proteins and chromatin structure. Both increases and decreases in methylation occur with aging, depending on the tissue and the gene. These changes can have pathologic consequences, contributing to the development of malignancies and autoimmunity with aging, and possibly to other disorders as well. Thus, while aging can impact on DNA methylation, the changes in DNA methylation can also impact on aging. This review summarizes current evidence for changes in the methylation status of specific genes with aging, their impact on diseases that develop with aging, and mechanisms that may contribute to the altered DNA methylation patterns. As this field is still developing, it is anticipated that new knowledge will continue to accumulate rapidly. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:245 / 261
页数:17
相关论文
共 90 条
[1]   Modulation of chromatin structure regulates cytokine gene expression during T cell differentiation [J].
Agarwal, S ;
Rao, A .
IMMUNITY, 1998, 9 (06) :765-775
[2]   Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 [J].
Amir, RE ;
Van den Veyver, IB ;
Wan, M ;
Tran, CQ ;
Francke, U ;
Zoghbi, HY .
NATURE GENETICS, 1999, 23 (02) :185-188
[3]   NUMBER OF CPG ISLANDS AND GENES IN HUMAN AND MOUSE [J].
ANTEQUERA, F ;
BIRD, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11995-11999
[4]  
ANTEQUERA F, 1993, DNA METHYLATION MOL, P169
[5]   Dnmt3a and Dnmt3b are transcriptional repressors that exhibit unique localization properties to heterochromatin [J].
Bachman, KE ;
Rountree, MR ;
Baylin, SB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (34) :32282-32287
[6]   Epigenetic regulation of an IAP retrotransposon in the aging mouse: progressive demethylation and de-silencing of the element by its repetitive induction [J].
Barbot, W ;
Dupressoir, A ;
Lazar, V ;
Heidmann, T .
NUCLEIC ACIDS RESEARCH, 2002, 30 (11) :2365-2373
[7]   Mechanisms underlying epigenetically mediated gene silencing in cancer [J].
Baylin, SB .
SEMINARS IN CANCER BIOLOGY, 2002, 12 (05) :331-337
[8]   CLONING AND SEQUENCING OF A CDNA-ENCODING DNA METHYLTRANSFERASE OF MOUSE CELLS - THE CARBOXYL-TERMINAL DOMAIN OF THE MAMMALIAN ENZYMES IS RELATED TO BACTERIAL RESTRICTION METHYLTRANSFERASES [J].
BESTOR, T ;
LAUDANO, A ;
MATTALIANO, R ;
INGRAM, V .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 203 (04) :971-983
[9]   A mammalian protein with specific demethylase activity for mCpG DNA [J].
Bhattacharya, SK ;
Ramchandani, S ;
Cervoni, N ;
Szyf, M .
NATURE, 1999, 397 (6720) :579-583
[10]   THE ESSENTIALS OF DNA METHYLATION [J].
BIRD, A .
CELL, 1992, 70 (01) :5-8