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Elife. 2014 Sep 26;3:e03397. doi: 10.7554/eLife.03397.

Synthetic CpG islands reveal DNA sequence determinants of chromatin structure.

Author information

  • 1The Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, United Kingdom.
  • 2Genomics and Biotechnology Centre, Technische Universitaet Dresden, Dresden, Germany.

Abstract

The mammalian genome is punctuated by CpG islands (CGIs), which differ sharply from the bulk genome by being rich in G + C and the dinucleotide CpG. CGIs often include transcription initiation sites and display 'active' histone marks, notably histone H3 lysine 4 methylation. In embryonic stem cells (ESCs) some CGIs adopt a 'bivalent' chromatin state bearing simultaneous 'active' and 'inactive' chromatin marks. To determine whether CGI chromatin is developmentally programmed at specific genes or is imposed by shared features of CGI DNA, we integrated artificial CGI-like DNA sequences into the ESC genome. We found that bivalency is the default chromatin structure for CpG-rich, G + C-rich DNA. A high CpG density alone is not sufficient for this effect, as A + T-rich sequence settings invariably provoke de novo DNA methylation leading to loss of CGI signature chromatin. We conclude that both CpG-richness and G + C-richness are required for induction of signature chromatin structures at CGIs.

KEYWORDS:

CpG islands; DNA methylation; bivalent chromatin; chromosomes; genes; histone modifications; mouse

Comment in

PMID:
25259796
PMCID:
PMC4204011
DOI:
10.7554/eLife.03397
[PubMed - indexed for MEDLINE]
Free PMC Article
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