Genome-Wide Epigenetics

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Genome-Wide Epigenetics Brian C. Capell, Shelley L. Berger  Journal of Investigative Dermatology  Volume 133, Issue 6, Pages 1-4 (June 2013) DOI: 10.1038/jid.2013.173 Copyright © 2013 The Society for Investigative Dermatology, Inc Terms and Conditions

Figure 1 Major epigenetic modifications. (a) Histone modification. A total of 147 base pairs of DNA (depicted as yellow lines) wrap around eight histone proteins (depicted as blue cylinders) to form nucleosomes. When nucleosomes are packaged together, they form chromatin. Posttranslational modifications (e.g., addition of acetyl, methyl, or ubiquitin groups) of histones alter local chromatin conformation. Variability in chromatin compaction affects the accessibility of genes. Loosely condensed regions (euchromatin) are more actively expressed and tightly condensed regions (heterochromatin) are repressed. The image depicts histone acetylation, associated with loosening of local chromatin and more active gene expression. (b) DNA methylation. DNA methylation occurs through the addition of a methyl group to the C5 position of cytosine to form 5-methylcytosine, typically at cytosine phosphate guanine dinucleotides. In promoter regions, DNA methylation silences genes by interfering with transcription factor binding. DNA methylation is typically associated with tightly condensed chromatin. Reprinted with permission from Cheng and Cho, 2012. Journal of Investigative Dermatology 2013 133, 1-4DOI: (10.1038/jid.2013.173) Copyright © 2013 The Society for Investigative Dermatology, Inc Terms and Conditions

Figure 2 Basic epigenome browser view. This view highlights an ~9-Kb segment of the KRT5 gene, with the dark blue rectangles and lines depicting the gene structure. Profiled cells are primary cultured neonatal foreskin keratinocytes (KCs, top) and fibroblasts (bottom). These KCs express KRT5, whereas fibroblasts do not. Starting from the top, there are high levels of H3K4me3 histone modification signal (associated with active transcription) at the promoter in KCs (depicted in green). In pink, H3K27me3 signal (associated with gene repression) shows low levels in KCs. Regions of methylated DNA are depicted in brown, with minimal signal in KCs and high levels in fibroblasts. Unmethylated DNA is depicted with light blue vertical bars and shows a high number of sequencing peaks for KCs compared with a low number for fibroblasts. Reprinted with permission from Cheng and Cho, 2012. Journal of Investigative Dermatology 2013 133, 1-4DOI: (10.1038/jid.2013.173) Copyright © 2013 The Society for Investigative Dermatology, Inc Terms and Conditions

Journal of Investigative Dermatology 2013 133, 1-4DOI: (10. 1038/jid Copyright © 2013 The Society for Investigative Dermatology, Inc Terms and Conditions

Journal of Investigative Dermatology 2013 133, 1-4DOI: (10. 1038/jid Copyright © 2013 The Society for Investigative Dermatology, Inc Terms and Conditions