| Literature DB >> 31078719 |
Ornella Affinito1, Domenico Palumbo2, Annalisa Fierro3, Mariella Cuomo4, Giulia De Riso4, Antonella Monticelli5, Gennaro Miele6, Lorenzo Chiariotti7, Sergio Cocozza2.
Abstract
The tendency of individual CpG sites to be methylated is distinctive, non-random and well-regulated throughout the genome. We investigated the structural and spatial factors influencing CpGs methylation by performing an ultra-deep targeted methylation analysis on human, mouse and zebrafish genes. We found that methylation is not a random process and that closer neighboring CpG sites are more likely to share the same methylation status. Moreover, if the distance between CpGs increases, the degree of co-methylation decreases. We set up a simulation model to analyze the contribution of both the intrinsic susceptibility and the distance effect on the probability of a CpG to be methylated. Our finding suggests that the establishment of a specific methylation pattern follows a universal rule that must take into account of the synergistic and dynamic interplay of these two main factors: the intrinsic methylation susceptibility of specific CpG and the nucleotide distance between two CpG sites.Entities:
Keywords: Co-methylation; DNA methylation; Intrinsic methylation susceptibility; Nearby CpG sites; Nucleotide distance effect
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Year: 2019 PMID: 31078719 DOI: 10.1016/j.ygeno.2019.05.007
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736