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
相关论文
共 84 条
  • [11] Boom D, 2009, METHODS MOL BIOL
  • [12] UHRF1 plays a role in maintaining DNA methylation in mammalian cells
    Bostick, Magnolia
    Kim, Jong Kyong
    Esteve, Pierre-Olivier
    Clark, Amander
    Pradhan, Sriharsa
    Jacobsen, Steven E.
    [J]. SCIENCE, 2007, 317 (5845) : 1760 - 1764
  • [13] 5-HYDROXYMETHYLCYTOSINE DNA GLYCOSYLASE ACTIVITY IN MAMMALIAN TISSUE
    CANNON, SV
    CUMMINGS, A
    TEEBOR, GW
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 151 (03) : 1173 - 1179
  • [14] Linking DNA methylation and histone modification: patterns and paradigms
    Cedar, Howard
    Bergman, Yehudit
    [J]. NATURE REVIEWS GENETICS, 2009, 10 (05) : 295 - 304
  • [15] Transcription is required for establishment of germline methylation marks at imprinted genes
    Chotalia, Mita
    Smallwood, Sebastien A.
    Ruf, Nico
    Dawson, Claire
    Lucifero, Diana
    Frontera, Marga
    James, Katherine
    Dean, Wendy
    Kelsey, Gavin
    [J]. GENES & DEVELOPMENT, 2009, 23 (01) : 105 - 117
  • [16] DNA methylation: Bisulphite modification and analysis
    Clark, Susan J.
    Statham, Aaron
    Stirzaker, Clare
    Molloy, Peter L.
    Frommer, Marianne
    [J]. NATURE PROTOCOLS, 2006, 1 (05) : 2353 - 2364
  • [17] Methyl-CpG binding proteins: specialized transcriptional repressors or structural components of chromatin?
    Clouaire, T.
    Stancheva, I.
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2008, 65 (10) : 1509 - 1522
  • [18] Genomic profiling of CpG methylation and allelic specificity using quantitative high-throughput mass spectrometry: critical evaluation and improvements
    Coolen, Marcel W.
    Statham, Aaron L.
    Gardiner-Garden, Margaret
    Clark, Susan J.
    [J]. NUCLEIC ACIDS RESEARCH, 2007, 35 (18)
  • [19] DNA methylation and memory formation
    Day, Jeremy J.
    Sweatt, J. David
    [J]. NATURE NEUROSCIENCE, 2010, 13 (11) : 1319 - 1323
  • [20] Capturing the dynamic epigenome
    Deal, Roger B.
    Henikoff, Steven
    [J]. GENOME BIOLOGY, 2010, 11 (10)