Phenotypic diversity and epigenomic variation - The utility of mass spectrometric analysis of DNA methylation

被引:3
作者
McLean, Cameron [1 ]
Gluckman, Peter [1 ,2 ]
Sheppard, Allan [1 ]
机构
[1] Univ Auckland, Liggins Inst, Auckland 1, New Zealand
[2] Natl Univ Singapore, Singapore Inst Clin Sci, Singapore, Singapore
关键词
Epigenetics; Programming; Phenotypic variation; DE-NOVO METHYLATION; NON-CPG METHYLATION; EPIGENETIC INHERITANCE; DEVELOPMENTAL ORIGINS; BINDING-PROTEINS; DEMETHYLATION; GENE; PATTERNS; 5-HYDROXYMETHYLCYTOSINE; METHYLTRANSFERASES;
D O I
10.1016/j.jprot.2012.01.036
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Epigenomic variation may underlie phenotypic diversity that is not attributable to differences in genomic sequence. Such processes provide an organism the flexibility to respond to changing environmental cues within its lifetime, and perhaps its offspring's lifetime, and would therefore be expected to confer a selective advantage in evolutionary terms. Analysis of epigenomic variation within a population may be both a useful measure of developmental exposures and an indicator of future phenotype. A key molecular indicator of epigenomic variation in organisms is the chemical modification of DNA by methylation at specific nucleotide residues in the genome. Here we discuss how mass spectrometry can be utilised to provide quantitative analysis of DNA methylation patterns across populations. This article is part of a Special Section entitled: Understanding genome regulation and genetic diversity by mass spectrometry. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:3400 / 3409
页数:10
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