Late-replicating heterochromatin is characterized by decreased cytosine methylation in the human genome

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 1.
Figure 1.

Cytosine methylation and replication timing correlate in broad genomic regions. (Top) Fibroblast data; (bottom) GM06690 lymphoblastoid cell line data. Cytosine methylation is shown as the HpaII/MspI log2 intensity ratio from the HELP assay. Positive values indicate relative hypomethylation, and negative values indicate hypermethylation of HpaII sites. DNA replication timing data are generated from raw sequence reads by an arctangent transformation of 1-kb counts comparing early (G1 and S1) and late (S4 and G2) cell samples, as described in the Methods section. Earlier replicated regions have higher values than later replicated regions.

This Article

  1. Genome Res. 21: 1833-1840

Preprint Server