The cell nucleus is a highly structured compartment where nuclear components are thought to localize in non-random positions. Correct positioning of large chromatin domains may have a direct impact on the localization of other nuclear components, and can therefore influence the global functionality of the nuclear compartment. DNA methylation of cytosine residues in CpG dinucleotides is a prominent epigenetic modification of the chromatin fiber. DNA methylation, in conjunction with the biochemical modification pattern of histone tails, is known to lock chromatin in a close and transcriptionally inactive conformation. The relationship between DNA methylation and large-scale organization of nuclear architecture, however, is poorly understood. Here we briefly summarize present concepts of nuclear architecture and current data supporting a link between DNA methylation and the maintenance of large-scale nuclear organization.
Santos A. Susín, Éric Daugas, L Ravagnan, Kumiko Samejima, Naoufal Zamzami, Markus Loeffler, Paola Costantini, Karine F. Ferri, Théano Irinopoulou, Marie-Christine Prévost, Greg Brothers, Tak W. Mak, Josef Penninger, William C. Earnshaw, Guido Guido Kroemer
Discussion(0)
No comments yet. Be the first to comment.