Stable Ethnic Variations in DNA Methylation Patterns of Human Skin

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Stable Ethnic Variations in DNA Methylation Patterns of Human Skin Marc Winnefeld, Bodo Brueckner, Elke Grönniger, Franz Stäb, Horst Wenck, Frank Lyko  Journal of Investigative Dermatology  Volume 132, Issue 2, Pages 466-468 (February 2012) DOI: 10.1038/jid.2011.323 Copyright © 2012 The Society for Investigative Dermatology, Inc Terms and Conditions

Figure 1 Relationships of epidermal methylation patterns from three distinct ethnicities. Unsupervised hierarchical clustering of 30 methylation profiles, each consisting of >27,000 markers, shows a close relationship of samples from specific ethnic groups. Microarray data are available in the ArrayExpress database (http://www.ebi.ac.uk/arrayexpress) under accession number E-MTAB-625 (username: Reviewer_E-MTAB-625, password: nmrwmhuq). Journal of Investigative Dermatology 2012 132, 466-468DOI: (10.1038/jid.2011.323) Copyright © 2012 The Society for Investigative Dermatology, Inc Terms and Conditions

Figure 2 Identification of ethnic methylation differences. (a) Pairwise comparisons of genomic DNA methylation profiles from African, Caucasian, and Asian epidermis samples. Red lines indicate significant methylation changes (∣Δβ∣>∣0.15∣ and P<0.01). (b) Validation of array-predicted methylation differences by 454 bisulfite sequencing. Red vertical lines represent individual CpG dinucleotides of the PCR amplicons analyzed. Arrowheads highlight CpGs represented on the array, with their distance relative to the transcriptional start site indicated. PCR amplification was performed on equimolar sample pools, as decribed previously (Gronniger et al., 2010) and sequencing results are shown as heat maps. Each row represents one sequence read, individual red boxes represent methylated CpG dinucleotides, green boxes represent unmethylated CpG dinucleotides. Sequencing gaps are shown in white. Sequencing coverage ranged from 2,683 to 5,427 reads, as indicated. (c) The fraction of markers outside CpG islands is indicated for all markers on the array (all) and for the 205 markers showing ethnic methylation differences (EMD). (d) Principal component analysis of the nonredundant set of 205 markers that were differentially methylated across all three ethnicities. Journal of Investigative Dermatology 2012 132, 466-468DOI: (10.1038/jid.2011.323) Copyright © 2012 The Society for Investigative Dermatology, Inc Terms and Conditions