Epigenomics: a basis for understanding individual differences?

被引:36
作者
Mathers, John C. [1 ]
机构
[1] Univ Newcastle, Human Nutr Res Ctr, Sch Clin Med Sci, Inst Ageing & Hlth, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
基金
英国生物技术与生命科学研究理事会;
关键词
Epigenetic marks; DNA methylation; Histone modifications; Cellular memory; Inter-individual differences;
D O I
10.1017/S0029665108008744
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Epigenetics encompasses changes to marks on the genome that are copied from one cell generation to the next, which may alter gene expression but which do not involve changes in the primary DNA sequence. These marks include DNA methylation (methylation of cytosines within CpG dinucleotides) and post-translational modifications (acetylation, methylation, phosphorylation and ubiquitination) of the histone tails protruding from nucleosome cores. The sum of genome-wide epigenetic patterns is known as the epigenome. It is hypothesised that altered epigenetic marking is a means through which evidence of environmental exposures (including nutritional status and dietary exposure) is received and recorded by the genome. At least some of these epigenetic marks are remembered through multiple cell generations and their effects may be revealed in altered gene expression and cell function. Altered epigenetic marking allows plasticity of phenotype in a fixed genotype. Despite their identical genotypes, monozygotic twins show increasing epigenetic diversity with age and with divergent lifestyles. Differences in epigenetic markings may explain some inter-individual variation in disease risk and in response to nutritional interventions.
引用
收藏
页码:390 / 394
页数:5
相关论文
共 30 条
[1]  
[Anonymous], EPIGENETICS
[2]   Vernalization requires epigenetic silencing of FLC by histone methylation [J].
Bastow, R ;
Mylne, JS ;
Lister, C ;
Lippman, Z ;
Martienssen, RA ;
Dean, C .
NATURE, 2004, 427 (6970) :164-167
[3]   The methylome: approaches for global DNA methylation profiling [J].
Beck, Stephan ;
Rakyan, Vardhman K. .
TRENDS IN GENETICS, 2008, 24 (05) :231-237
[4]   The mammalian epigenome [J].
Bernstein, Bradley E. ;
Meissner, Alexander ;
Lander, Eric S. .
CELL, 2007, 128 (04) :669-681
[5]   The DNA methyltransferases of mammals [J].
Bestor, TH .
HUMAN MOLECULAR GENETICS, 2000, 9 (16) :2395-2402
[6]   Toward a human epigenome [J].
Brena, Romulo M. ;
Huang, Tim H-M ;
Plass, Christoph .
NATURE GENETICS, 2006, 38 (12) :1359-1360
[7]   Genetic variants in epigenetic genes and breast cancer risk [J].
Cebrian, Arancha ;
Pharoah, Paul D. ;
Ahmed, Shahana ;
Ropero, Santiago ;
Fraga, Mario F. ;
Smith, Paula L. ;
Conroy, Don ;
Luben, Robert ;
Perkins, Barbara ;
Easton, Douglas F. ;
Dunning, Alison M. ;
Esteller, Manel ;
Ponder, Bruce A. J. .
CARCINOGENESIS, 2006, 27 (08) :1661-1669
[8]   Maternal genistein alters coat color and protects Avy mouse offspring from obesity by modifying the fetal epigenome [J].
Dolinoy, DC ;
Weidman, JR ;
Waterland, RA ;
Jirtle, RL .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2006, 114 (04) :567-572
[9]   DNA methylation profiling of human chromosomes 6, 20 and 22 [J].
Eckhardt, Florian ;
Lewin, Joern ;
Cortese, Rene ;
Rakyan, Vardhman K. ;
Attwood, John ;
Burger, Matthias ;
Burton, John ;
Cox, Tony V. ;
Davies, Rob ;
Down, Thomas A. ;
Haefliger, Carolina ;
Horton, Roger ;
Howe, Kevin ;
Jackson, David K. ;
Kunde, Jan ;
Koenig, Christoph ;
Liddle, Jennifer ;
Niblett, David ;
Otto, Thomas ;
Pettett, Roger ;
Seemann, Stefanie ;
Thompson, Christian ;
West, Tony ;
Rogers, Jane ;
Olek, Alex ;
Berlin, Kurt ;
Beck, Stephan .
NATURE GENETICS, 2006, 38 (12) :1378-1385
[10]   Phenotypic plasticity and the epigenetics of human disease [J].
Feinberg, Andrew P. .
NATURE, 2007, 447 (7143) :433-440