Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2036374 | Cell | 2011 | 14 Pages |
SummaryMammalian CpG islands are key epigenomic elements that were first characterized experimentally as genomic fractions with low levels of DNA methylation. Currently, CpG islands are defined based on their genomic sequences alone. Here, we develop evolutionary models to show that several distinct evolutionary processes generate and maintain CpG islands. One central evolutionary regime resulting in enriched CpG content is driven by low levels of DNA methylation and consequentially low rates of CpG deamination. Another major force forming CpG islands is biased gene conversion that stabilizes constitutively methylated CpG islands by balancing rapid deamination with CpG fixation. Importantly, evolutionary analysis and population genetics data suggest that selection for high CpG content is not a significant factor contributing to conservation of CpGs in differentially methylated regions. The heterogeneous, but not selective, origins of CpG islands have direct implications for the understanding of DNA methylation patterns in healthy and diseased cells.
Graphical AbstractFigure optionsDownload full-size imageDownload high-quality image (380 K)Download as PowerPoint slideHighlights► A novel evolutionary model for the origin of CpG islands ► Heterogeneous evolutionary processes generate and maintain CpG islands ► Lack of evidence for selection on CpGs at differentially methylated regions ► Epigenetics as a mechanism for emergence of genomic information without selection