Fig. 2 | Nature Communications

Fig. 2

From: Replication timing and epigenome remodelling are associated with the nature of chromosomal rearrangements in cancer

Fig. 2The alternative text for this image may have been generated using AI.

Replication timing correlates with DNA methylation in cancer. a DNA methylation (WGBS) density distributions for early (blue) and late (red) loci per cell line. Adjacent are scatterplots of DNA methylation in relation to replication timing (WA) for all measured 1 kb loci in PrEC and LNCaP. Blue dashed line indicates early (WA > 75) and red dashed line indicates late (WA < 20). b Representative examples of late-replicating regions common to both PrEC and LNCaP (shaded) that become hypomethylated in LNCaP. The correlation between DNA methylation and replication timing values increases from PrEC (Spearman’s 0.3073, p < 2.2e−16) to LNCaP (Spearman’s 0.4985, p < 2.2e−16). Scale bar represents 5 Mb. c Percentage (y-axis) of PrEC early and late regions (1 kb loci) that are hypermethylated (LNCaP-PrEC, ΔWGBS > 0.2) and hypomethylated (LNCaP-PrEC, ΔWGBS < −0.2). Asterisks indicate significantly different percentages between early and late (test of equal proportions, p < 2.2e−16). d Associations between genomic elements and hypo- and hypermethylated 1 kb loci. Association is above zero, and disassociation is below zero. Asterisks indicate significant associations (FDR < 0.05, Fisher’s exact test)

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