Some time ago I posted an item Everything relates to everything else – at least in the science of longevity. Recent research shows that applies to epigenomic information. For some time it has been known that epigenomic information can be stored as either patterns of DNA methylation or in the form of histone modifications. See the earlier posts Epigenetics, epigenomics and aging, DNA methylation, personalized medicine and longevity and Histone acetylase and deacetylase inhibitors. Both DNA methylation and histone modification can serve to silence genes and play important roles in the development of an organism. One paper comments “These modifications seem to be programmed for carrying out two separate biological functions: histone methylation blocks target-gene reactivation in the absence of transcriptional repressors, whereas DNA methylation prevents reprogramming to the undifferentiated state(ref).” Apparently, there can be significant crosstalk between these two forms of data storage. “It has recently become apparent that DNA methylation and histone modification pathways can be dependent on one another, and that this crosstalk can be mediated by biochemical interactions between SET domain histone methyltransferases and DNA methyltransferases. Relationships between DNA methylation and histone modification have implications for understanding normal development as well as somatic cell reprogramming and tumorigenesis(ref).”
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