DNA methylation dynamics in health and disease

被引:413
作者
Bergman, Yehudit [1 ]
Cedar, Howard [1 ]
机构
[1] Hebrew Univ Jerusalem, Sch Med, Inst Med Res Israel Canada, Dept Dev Biol & Canc Res, IL-91010 Jerusalem, Israel
关键词
DE-NOVO METHYLATION; CELL-SPECIFIC DEMETHYLATION; CPG ISLAND METHYLATION; ACTIVE DEMETHYLATION; HISTONE H3; EPIGENETIC INHERITANCE; DEVELOPMENTAL PATTERN; CHROMATIN-STRUCTURE; TUMOR-SUPPRESSOR; PATERNAL GENOME;
D O I
10.1038/nsmb.2518
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
DNA methylation is an epigenetic mark that is erased in the early embryo and then reestablished in each individual, through a developmentally regulated program mediated by sequence information and trans-acting factors that direct the de novo DNA methylation and demethylation machinery to its targets in a dynamic manner. Once established, these patterns can be maintained in a stable manner over the lifetime of the organism. Additional changes in methylation that occur during aging and as part of disease processes may also be directed by similar molecular rules using the same complex machinery.
引用
收藏
页码:274 / 281
页数:8
相关论文
共 128 条
[61]   Dynamic changes in the human methylome during differentiation [J].
Laurent, Louise ;
Wong, Eleanor ;
Li, Guoliang ;
Huynh, Tien ;
Tsirigos, Aristotelis ;
Ong, Chin Thing ;
Low, Hwee Meng ;
Sung, Ken Wing Kin ;
Rigoutsos, Isidore ;
Loring, Jeanne ;
Wei, Chia-Lin .
GENOME RESEARCH, 2010, 20 (03) :320-331
[62]   A TARGETING SEQUENCE DIRECTS DNA METHYLTRANSFERASE TO SITES OF DNA-REPLICATION IN MAMMALIAN NUCLEI [J].
LEONHARDT, H ;
PAGE, AW ;
WEIER, HU ;
BESTOR, TH .
CELL, 1992, 71 (05) :865-873
[63]   TARGETED MUTATION OF THE DNA METHYLTRANSFERASE GENE RESULTS IN EMBRYONIC LETHALITY [J].
LI, E ;
BESTOR, TH ;
JAENISCH, R .
CELL, 1992, 69 (06) :915-926
[64]   A Maternal-Zygotic Effect Gene, Zfp57, Maintains Both Maternal and Paternal Imprints [J].
Li, Xiajun ;
Ito, Mitsuteru ;
Zhou, Fen ;
Youngson, Neil ;
Zuo, Xiaopan ;
Leder, Philip ;
Ferguson-Smith, Anne C. .
DEVELOPMENTAL CELL, 2008, 15 (04) :547-557
[65]   Cooperativity between DNA methyltransferases in the maintenance methylation of repetitive elements [J].
Liang, GG ;
Chan, MF ;
Tomigahara, Y ;
Tsai, YC ;
Gonzales, FA ;
Li, E ;
Laird, PW ;
Jones, PA .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (02) :480-491
[66]   B-CELL-SPECIFIC DEMETHYLATION - A NOVEL ROLE FOR THE INTRONIC KAPPA-CHAIN ENHANCER SEQUENCE [J].
LICHTENSTEIN, M ;
KEINI, G ;
CEDAR, H ;
BERGMAN, Y .
CELL, 1994, 76 (05) :913-923
[67]   Identification of genetic elements that autonomously determine DNA methylation states [J].
Lienert, Florian ;
Wirbelauer, Christiane ;
Som, Indrani ;
Dean, Ann ;
Mohn, Fabio ;
Schuebeler, Dirk .
NATURE GENETICS, 2011, 43 (11) :1091-U78
[68]   METHYLATION OF THE HPRT GENE ON THE INACTIVE-X OCCURS AFTER CHROMOSOME INACTIVATION [J].
LOCK, LF ;
TAKAGI, N ;
MARTIN, GR .
CELL, 1987, 48 (01) :39-46
[69]   Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57 [J].
Mackay, Deborah J. G. ;
Callaway, Jonathan L. A. ;
Marks, Sophie M. ;
White, Helen E. ;
Acerini, Carlo L. ;
Boonen, Susanne E. ;
Dayanikli, Pinar ;
Firth, Helen V. ;
Goodship, Judith A. ;
Haemers, Andreas P. ;
Hahnemann, Johanne M. D. ;
Kordonouri, Olga ;
Masoud, Ahmed F. ;
Oestergaard, Elsebet ;
Storr, John ;
Ellard, Sian ;
Hattersley, Andrew T. ;
Robinson, David O. ;
Temple, I. Karen .
NATURE GENETICS, 2008, 40 (08) :949-951
[70]   SP1 SITES IN THE MOUSE APRT GENE PROMOTER ARE REQUIRED TO PREVENT METHYLATION OF THE CPG ISLAND [J].
MACLEOD, D ;
CHARLTON, J ;
MULLINS, J ;
BIRD, AP .
GENES & DEVELOPMENT, 1994, 8 (19) :2282-2292