H3S10ph broadly marks early-replicating domains in interphase ESCs and shows reciprocal antagonism with H3K9me2

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Figure 3.
Figure 3.

Overexpression of H3S10A in ESCs promotes H3K9me2 accumulation in early-replicating regions. (A) ChIP enrichment of YFP (RPKM) around transcription start sites (TSS ±500 bp) in WT and S10A H3.3-YFP-expressing lines, clustered by genic expression quartiles. (B) Genome browser screen shot spanning Cpeb4 to Fbxw11 loci on Chromosome 11 (31,696,800–32,668,200) with YFP and H3K9me2 ChIP enrichment in H3.3-YFP WT and S10A mutant lines presented, as well as previously published RT (Yokochi et al. 2009) and H3.3-HA (Elsässer et al. 2015) tracks. (C) Histogram showing the global density distribution of H3K9me2 in H3.3-YFP WT and S10A lines. (D) 2D scatterplot comparing the gain or loss (z-score) of H3K9me2 in the S10A.2 mutant line with WT H3K9me2 enrichment levels (RPKM). (E) Comparison of YFP incorporation levels with the change in H3K9me2 enrichment in H3.3-YFP S10A.2 relative to WT cells (z-score). Heat map and data-point size represent the range of WT H3S10ph enrichment levels. Note that gain of H3K9me2 occurs predominantly within regions that are enriched for H3S10ph in WT ESCs.

This Article

  1. Genome Res. 28: 37-51

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