A twin approach to unraveling epigenetics

被引:235
|
作者
Bell, Jordana T. [1 ,2 ]
Spector, Tim D. [1 ]
机构
[1] St Thomas Hosp, Univ London Kings Coll, Dept Twin Res & Genet Epidemiol, London SE1 7EH, England
[2] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
基金
英国惠康基金; 欧洲研究理事会;
关键词
GENETICALLY COMPLEX TRAITS; EMBRYONIC STEM-CELLS; DNA METHYLATION; MONOZYGOTIC TWINS; LINKAGE STRATEGIES; CPG ISLAND; HISTONE MODIFICATIONS; RHEUMATOID-ARTHRITIS; MISSING HERITABILITY; GENE-EXPRESSION;
D O I
10.1016/j.tig.2010.12.005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The regulation of gene expression plays a pivotal role in complex phenotypes, and epigenetic mechanisms such as DNA methylation are essential to this process. The availability of next-generation sequencing technologies allows us to study epigenetic variation at an unprecedented level of resolution. Even so, our understanding of the underlying sources of epigenetic variability remains limited. Twin studies have played an essential role in estimating phenotypic heritability, and these now offer an opportunity to study epigenetic variation as a dynamic quantitative trait. High monozygotic twin discordance rates for common diseases suggest that unexplained environmental or epigenetic factors could be involved. Recent genome-wide epigenetic studies in disease-discordant monozygotic twins emphasize the power of this design to successfully identify epigenetic changes associated with complex traits. We describe how large-scale epigenetic studies of twins can improve our understanding of how genetic, environmental and stochastic factors impact upon epigenetics, and how such studies can provide a comprehensive understanding of how epigenetic variation affects complex traits.
引用
收藏
页码:116 / 125
页数:10
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