First Author | Nothjunge S | Year | 2017 |
Journal | Nat Commun | Volume | 8 |
Issue | 1 | Pages | 1667 |
PubMed ID | 29162810 | Mgi Jnum | J:257207 |
Mgi Id | MGI:6106119 | Doi | 10.1038/s41467-017-01724-9 |
Citation | Nothjunge S, et al. (2017) DNA methylation signatures follow preformed chromatin compartments in cardiac myocytes. Nat Commun 8(1):1667 |
abstractText | Storage 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. |