Dentify regions with altered levels of H3K27me3. Finally, we

Dentify regions with altered levels of H3K27me3. Finally, we perform RNAseq analysis in both cell types to try to associate gene expression changes with changes in the placement of either mark. We show that PRC2 activity is required for proper placement of DNAme at a number of developmentally important genes. We also demonstrate that DNAme is Mirin site globally repressing the placement of H3K27me3. Our expression studies show that the coordinate regulation between these marks does not appear to have a direct effect on gene expression in the undifferentiated cells, but we show that the indirect effects on gene expression of loss of PRC2 or DNA methyltransferase have a remarkable similarity.Results Changes in DNAme in H3K27me3-deficient ES CellsIn order to investigate changes in DNAme that occur as a consequence of loss of H3K27me3 we globally assayed DNAme using Methyl DNA immunoprecipitation followed by hybridization to a promoter microarray (MeDIP) in ES cells derived from Eed17Rn5?354SB (Eed2/2) mutant mice. EED is one of the three components of the PRC2 complex and is required for normal H3K27 trimethylation. EED binds to histone tails carrying trimethyl-lysine residues and activates the methyltransferase activity of PRC2 [21]. Without EED, H3K27me3 is undetectable, while there is no difference in H3K9me3 [22]. We performed three independent MeDIP experiments and identified 2,296 regions with significant changes in DNAme as a consequence of loss of H3K27me3. Pairwise Pearson correlations showed good correlation of peak ZK-36374 price intensities between the three arrays (Figure S1). These peaks correspond to 2,933 promoters and 1,413 genes according to the Ensembl annotation of the NCBIM37 assembly of the mouse genome (Table S1). Of the 1,413 genes with changes in DNAme 861 showed increased DNAme and 552 showed decreased DNAme. Peaks were validated by sequencing .15 independent clones of PCR-amplified bisulfite-treated DNA and testing for changes in DNA methylation using a Fisher’s exact test (Figure 1A , Figure S2). In total, 7 peaks from 6 genes were validated. Interestingly 23 promoters showed peaks of both increased and decreased DNAme within the same promoter (Figure S2E-F), demonstrating that loss of PRC2 activity can have opposite effects on DNAme at close proximity, consistent with an earlier report of DNAme changes at the Cdkn1c and Grb10 loci in eed2/2 mice [23]. In order to examine whether changes in DNAme tend to happen in a focused location relative to the transcriptional start site (TSS) we aligned all genes with or without changes of DNAme and averaged the enrichment scores for all probes in 100-bp bins (Figure 1D). We see that changes in DNAme are distributed acrossthe promoter with the greatest level of enrichment at between 1 and 2 kb upstream of the TSS. Gene ontology analysis of genes with changes in DNAme showed that genes with decreased DNAme in Eed2/2 cells tended to be involved in chromatin organization while genes with increased DNAme were either involved in sensory perception or were developmentally important genes (Figure 1F). Genes with decreased DNAme also tended to be enriched for high-CpG-content (HCP) promoters and bivalent chromatin marks, while genes with increased DNAme tended to be genes with low- (LCP) or intermediate-CpG-content promoters (ICP) that lacked H3K4me3 and H3K27me3 in wildtype ES cells (Figure 1H,I). It is interesting to note that the lack of H3K27me3 in the promoter of genes with increased DNAme may indicate.Dentify regions with altered levels of H3K27me3. Finally, we perform RNAseq analysis in both cell types to try to associate gene expression changes with changes in the placement of either mark. We show that PRC2 activity is required for proper placement of DNAme at a number of developmentally important genes. We also demonstrate that DNAme is globally repressing the placement of H3K27me3. Our expression studies show that the coordinate regulation between these marks does not appear to have a direct effect on gene expression in the undifferentiated cells, but we show that the indirect effects on gene expression of loss of PRC2 or DNA methyltransferase have a remarkable similarity.Results Changes in DNAme in H3K27me3-deficient ES CellsIn order to investigate changes in DNAme that occur as a consequence of loss of H3K27me3 we globally assayed DNAme using Methyl DNA immunoprecipitation followed by hybridization to a promoter microarray (MeDIP) in ES cells derived from Eed17Rn5?354SB (Eed2/2) mutant mice. EED is one of the three components of the PRC2 complex and is required for normal H3K27 trimethylation. EED binds to histone tails carrying trimethyl-lysine residues and activates the methyltransferase activity of PRC2 [21]. Without EED, H3K27me3 is undetectable, while there is no difference in H3K9me3 [22]. We performed three independent MeDIP experiments and identified 2,296 regions with significant changes in DNAme as a consequence of loss of H3K27me3. Pairwise Pearson correlations showed good correlation of peak intensities between the three arrays (Figure S1). These peaks correspond to 2,933 promoters and 1,413 genes according to the Ensembl annotation of the NCBIM37 assembly of the mouse genome (Table S1). Of the 1,413 genes with changes in DNAme 861 showed increased DNAme and 552 showed decreased DNAme. Peaks were validated by sequencing .15 independent clones of PCR-amplified bisulfite-treated DNA and testing for changes in DNA methylation using a Fisher’s exact test (Figure 1A , Figure S2). In total, 7 peaks from 6 genes were validated. Interestingly 23 promoters showed peaks of both increased and decreased DNAme within the same promoter (Figure S2E-F), demonstrating that loss of PRC2 activity can have opposite effects on DNAme at close proximity, consistent with an earlier report of DNAme changes at the Cdkn1c and Grb10 loci in eed2/2 mice [23]. In order to examine whether changes in DNAme tend to happen in a focused location relative to the transcriptional start site (TSS) we aligned all genes with or without changes of DNAme and averaged the enrichment scores for all probes in 100-bp bins (Figure 1D). We see that changes in DNAme are distributed acrossthe promoter with the greatest level of enrichment at between 1 and 2 kb upstream of the TSS. Gene ontology analysis of genes with changes in DNAme showed that genes with decreased DNAme in Eed2/2 cells tended to be involved in chromatin organization while genes with increased DNAme were either involved in sensory perception or were developmentally important genes (Figure 1F). Genes with decreased DNAme also tended to be enriched for high-CpG-content (HCP) promoters and bivalent chromatin marks, while genes with increased DNAme tended to be genes with low- (LCP) or intermediate-CpG-content promoters (ICP) that lacked H3K4me3 and H3K27me3 in wildtype ES cells (Figure 1H,I). It is interesting to note that the lack of H3K27me3 in the promoter of genes with increased DNAme may indicate.