Chromatin regulation upon recruitment of HOTAIR

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Chromatin regulation upon recruitment of HOTAIR Chromatin regulation upon recruitment of HOTAIR ChIP experiments with H3K27me3 and primers located along the luciferase reporter (left) or control regions (MYT1 and ACT) (right) in the cell lines indicated on the x‐axis of each graph (individual experiments and mean, n = 2). A H3K27me3 antibody of different origin was used in this assay as compared to Fig 3.ChIP experiments with H3K9me2 (top), H3K27ac (middle), or RNA polymerase II (bottom) in the cell lines indicated on the x‐axis of each graph. Primers used are indicated in the color legend (individual experiments and mean, n = 2).Analysis of DNA methylation. Schematic representation of the portion of the reporter construct analyzed for DNA methylation is displayed on top. It comprises the Gal4‐binding sites (5× UAS), the TK minimal promoter and part of the luciferase gene. DNA methylation analysis by bisulfite cloning is shown below in three different cell lines as indicated on the right. Black circles indicate methylated CpGs, and white circles indicate unmethylated CpGs. The percentage of methylated CpG is indicated below each condition.Data information: Correspondence between numbers and model cell lines is indicated at the bottom right.Source data are available online for this figure. Manuela Portoso et al. EMBO J. 2017;36:981-994 © as stated in the article, figure or figure legend