DNA methylation patterns are set up in a relatively fixed programmed manner during normal embryonic development and are then stably maintained.  Using genome-wide analysis, we have discovered a postnatal pathway involving gender-specific demethylation that occurs exclusively in the male liver.  This demodification is programmed to take place at tissue-specific enhancer sequences, and our data show that the methylation state at these loci is associated with and appears to play a role in the transcriptional regulation of nearby genes.  This process is mediated by the secretion of testosterone at the time of sexual maturity, but the resulting methylation profile is stable and therefore can serve as an epigenetic memory even in the absence of this inducer.  These findings add a new dimension to our understanding of the role of DNA methylation in vivo and provide the foundations for deciphering how environment can impact on the epigenetic regulation of genes, in general. SOURCE: Howard Cedar The Hebrew University

Pluto Bioinformatics

GSE60012: Gender-specific post-natal demethylation and establishment of epigenetic memory