That H3K27me3 is regulating the placement of DNAme in

That H3K27me3 is regulating the placement of DNAme in an indirect manner. Hierarchical GSK126 clustering of annotated mouse transcripts on the basis of DNAme patterns produced three main groups. One cluster had all of the genes with depleted DNAme, while the transcripts with increased DNAme were GSK2256098 chemical information divided into two groups (clusters 1 2, Figure 1E). The first cluster had peaks of increased DNAme upstream of the TSS, while the second had increased DNAme across the entire promoter. These two clusters also corresponded to GO annotation and promoter CpG content in wildtype ES cells. Genes with increased DNAme across the promoter were genes with functions in sensory perception and pheromone receptor activity, had ICP and LCP promoters and lacked H3K4/K27 methylation, while genes with increased DNAme upstream of the promoter were developmental genes with HCP promoters and were enriched for bivalent chromatin marks (Figure 1G ). We performed RNAseq on wildtype and Eed2/2 ES cells to determine if PRC2-dependent changes in DNAme led to expression level changes. While the gene ontology terms associated with genes with expression changes in Eed2/2 cells are enriched for developmental functions, as previously shown (Table S2) [24], we saw no significant change in expression in genes which have H3K27me3-dependent changes in DNAme (Figure 1J), suggesting that coordinate regulation of DNAme levels by PRC2 is not directly controlling gene expression, at least in undifferentiated ES cells. However, we note that it is possible this coordination might poise genes for properly controlled expression after differentiation. Our work thus far demonstrates that the patterns of changes in DNAme that occur as a consequence of loss of PRC2 activity correlate with a particular epigenetic state in wildtype ES cells and with specific gene functions.DNAme Globally Antagonizes the Placement of H3K27meAs a reciprocal experiment we investigated the effect loss of DNAme had on the placement of H3K27me3 by performing ChIP-seq for H3K27me3 on cells with severely depleted DNA methyltransferase (DNMT) activity. DNMT triple-knockout cells (DnmtTKO) lack genes for producing the two de novo DNMTs, DNMT3a and DNMT3b, and have the transcript of the maintenance DNMT, Dnmt1, depleted by stable expression of a shRNA [25]. The methylation level of these cells is 1.3 of that seen in wild type cells. We performed ChIP-seq on two biological replicates each for wildtype and DnmtTKO cells (Figure 2A, B). A comparison with published datasets shows our ChIP-seq results are comparable to previously published H3K27me3 levels in both wildtype and DnmtTKO cells (Figure S5). The first replicate generated 605,487 peaks of increased H3K27me3 in DnmtTKO cells, covering 887,929,154 bp. The second replicate had 563,216 peaks covering 870,300,855 bp. On average, our ChIP-seq showed that H3K27me3 is increased on 32.4 of the mouseDNAme and H3K27me3 in Mouse Embryonic Stem CellsDNAme and H3K27me3 in Mouse Embryonic Stem CellsFigure 1. Loss of PRC2 activity leads to changes in DNA methylation. a, Relative fluorescence ratios for each probe from three independent MeDIP-chip experiments across the Nkx2-1 promoter. The peak of increased DNA methylation is indicated under the probes (grey bar) and the first 1 kb of the gene is indicated on the bottom. b, Validation of the peak of increased DNA methylation by bisulfite PCR. Each line represents an individual clone. Methylated CpGs are indicated by filled-in circles.That H3K27me3 is regulating the placement of DNAme in an indirect manner. Hierarchical clustering of annotated mouse transcripts on the basis of DNAme patterns produced three main groups. One cluster had all of the genes with depleted DNAme, while the transcripts with increased DNAme were divided into two groups (clusters 1 2, Figure 1E). The first cluster had peaks of increased DNAme upstream of the TSS, while the second had increased DNAme across the entire promoter. These two clusters also corresponded to GO annotation and promoter CpG content in wildtype ES cells. Genes with increased DNAme across the promoter were genes with functions in sensory perception and pheromone receptor activity, had ICP and LCP promoters and lacked H3K4/K27 methylation, while genes with increased DNAme upstream of the promoter were developmental genes with HCP promoters and were enriched for bivalent chromatin marks (Figure 1G ). We performed RNAseq on wildtype and Eed2/2 ES cells to determine if PRC2-dependent changes in DNAme led to expression level changes. While the gene ontology terms associated with genes with expression changes in Eed2/2 cells are enriched for developmental functions, as previously shown (Table S2) [24], we saw no significant change in expression in genes which have H3K27me3-dependent changes in DNAme (Figure 1J), suggesting that coordinate regulation of DNAme levels by PRC2 is not directly controlling gene expression, at least in undifferentiated ES cells. However, we note that it is possible this coordination might poise genes for properly controlled expression after differentiation. Our work thus far demonstrates that the patterns of changes in DNAme that occur as a consequence of loss of PRC2 activity correlate with a particular epigenetic state in wildtype ES cells and with specific gene functions.DNAme Globally Antagonizes the Placement of H3K27meAs a reciprocal experiment we investigated the effect loss of DNAme had on the placement of H3K27me3 by performing ChIP-seq for H3K27me3 on cells with severely depleted DNA methyltransferase (DNMT) activity. DNMT triple-knockout cells (DnmtTKO) lack genes for producing the two de novo DNMTs, DNMT3a and DNMT3b, and have the transcript of the maintenance DNMT, Dnmt1, depleted by stable expression of a shRNA [25]. The methylation level of these cells is 1.3 of that seen in wild type cells. We performed ChIP-seq on two biological replicates each for wildtype and DnmtTKO cells (Figure 2A, B). A comparison with published datasets shows our ChIP-seq results are comparable to previously published H3K27me3 levels in both wildtype and DnmtTKO cells (Figure S5). The first replicate generated 605,487 peaks of increased H3K27me3 in DnmtTKO cells, covering 887,929,154 bp. The second replicate had 563,216 peaks covering 870,300,855 bp. On average, our ChIP-seq showed that H3K27me3 is increased on 32.4 of the mouseDNAme and H3K27me3 in Mouse Embryonic Stem CellsDNAme and H3K27me3 in Mouse Embryonic Stem CellsFigure 1. Loss of PRC2 activity leads to changes in DNA methylation. a, Relative fluorescence ratios for each probe from three independent MeDIP-chip experiments across the Nkx2-1 promoter. The peak of increased DNA methylation is indicated under the probes (grey bar) and the first 1 kb of the gene is indicated on the bottom. b, Validation of the peak of increased DNA methylation by bisulfite PCR. Each line represents an individual clone. Methylated CpGs are indicated by filled-in circles.