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Image Search Results
Journal: Cancer research
Article Title: Identification of DNA methylation-independent epigenetic events underlying clear cell renal cell carcinoma
doi: 10.1158/0008-5472.CAN-15-2622
Figure Lengend Snippet: Tissues were obtained and processed as described in Materials and Methods. Tissues were processed and nuclei were either left untreated or were treated with the M.SssI methyltransferase enzyme. Endogenously methylated loci are unable to be interrogated (as illustrated). Following bisulfite conversion and HM450 analyses, untreated (endogenous) DNA methylation values from each sample were subtracted from respective enzyme-treated (exogenous) DNA methylation values, revealing chromatin accessibility changes.
Article Snippet: Acce SssI ble is rapid and cost-effective, only requiring 20 mg of tissue, the
Techniques: Methylation, DNA Methylation Assay
Journal: Nucleic Acids Research
Article Title: Functional DNA demethylation is accompanied by chromatin accessibility
doi: 10.1093/nar/gkt077
Figure Lengend Snippet: Majority of probes demethylated by 5-Aza-CdR are inaccessible to CpG methyltransferase M.SssI after 5-Aza-CdR treatment. ( A ) Schematic of the Acce SssI ble assay: after nuclei are treated with M.Sss1 (or a no-enzyme treatment control), DNA is extracted, bisulfite converted and assayed on the Illumina methylation 450 k beadchip. Endogenous DNA methylation status is obtained from the no-enzyme control (green indicating unmethylated and red methylated), and information on chromatin state for unmethylated probes is attained from the accessibility of the M.SssI methyltransferase to CpG dinucleotides (scaled from yellow to blue, with yellow as inaccessible and blue as highly accessible). ( B ) Kernel density scatter plot of delta-methylation (methylation in treated minus methylation in control) versus delta-accessibility (accessibility in treated minus accessibility in control) shows that majority of demethylated loci do not gain accessibility. Groups a and b are events that depict changes in chromatin accessibility independent of DNA methylation, whereas group c depicts regions that gain accessibility on DNA demethylation. ( C ) Bar graph depicting percentage of demethylated promoter- (9719), body- (1205) and enhancer-associated (28 348) probes that gain accessibility or remain inaccessible on demethylation. ( D ) Venn diagram of all promoter regions that are demethylated post-5-Aza-CdR treatment in HCT116 as well with those that gain accessibility. Results show that ∼90% of regions require demethylation to gain accessibility. ( E ) Volcano plot of genes whose promoters gain accessibility after treatment shows that most of these regions gain expression.
Article Snippet: We study this phenomenon globally using a novel assay that we have devised, using the
Techniques: Control, Methylation, DNA Methylation Assay, Expressing