The inactive X chromosome is epigenetically unstable and transcriptionally labile in breast cancer

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Figure 6.
Figure 6.

Chromatin landscape of the inactive X chromosome is disrupted in breast cancer cell lines. (A) Scheme of H3K27me3 enrichment (ChIP-seq) across the whole X chromosome. Red and green domains represent H3K27me3 and H3K9me3 enriched regions, respectively, as identified in normal human cells (Chadwick 2007). Regional loss of inactive X is indicated (and depicted by gray region). The two main enriched H3K27me3 domains’ loss in ZR-75-1 and MDA-MB-436 are depicted by the two red dotted rectangles. (B) H3K27me3 enrichment is detailed for three regions of the X chromosome carrying genes subjected (S) or escaping XCI (E). (C) Dot plots show variation of H3K27me3 enrichment along the X chromosome (1-Mb bins) of the three tumoral cell lines and WI-38 relative to HMEC. (D) TSS-centered plots (±1.5 kb) show RNA Pol II and H3K4me3 enrichment for the “cancer-specific” escapees (cf. Supplemental Table S1) of each tumoral cell line (red line) and HMEC (green line). The number of genes analyzed is indicated below each plot.

This Article

  1. Genome Res. 25: 488-503

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