• Media type: E-Article
  • Title: DNA methylation signatures follow preformed chromatin compartments in cardiac myocytes
  • Contributor: Nothjunge, Stephan; Nührenberg, Thomas G.; Grüning, Björn A.; Doppler, Stefanie A.; Preissl, Sebastian; Schwaderer, Martin; Rommel, Carolin; Krane, Markus; Hein, Lutz; Gilsbach, Ralf
  • Published: Springer Science and Business Media LLC, 2017
  • Published in: Nature Communications, 8 (2017) 1
  • Language: English
  • DOI: 10.1038/s41467-017-01724-9
  • ISSN: 2041-1723
  • Origination:
  • Footnote:
  • Description: AbstractStorage of chromatin in restricted nuclear space requires dense packing while ensuring DNA accessibility. Thus, different layers of chromatin organization and epigenetic control mechanisms exist. Genome-wide chromatin interaction maps revealed large interaction domains (TADs) and higher order A and B compartments, reflecting active and inactive chromatin, respectively. The mutual dependencies between chromatin organization and patterns of epigenetic marks, including DNA methylation, remain poorly understood. Here, we demonstrate that establishment of A/B compartments precedes and defines DNA methylation signatures during differentiation and maturation of cardiac myocytes. Remarkably, dynamic CpG and non-CpG methylation in cardiac myocytes is confined to A compartments. Furthermore, genetic ablation or reduction of DNA methylation in embryonic stem cells or cardiac myocytes, respectively, does not alter genome-wide chromatin organization. Thus, DNA methylation appears to be established in preformed chromatin compartments and may be dispensable for the formation of higher order chromatin organization.
  • Access State: Open Access