The maintenance of the precise chemical modifications to DNA and associated histone proteins that regulate gene expression without altering the underlying DNA sequence. Stable epigenomic marks are essential for correct cellular identity and function, while age-related epigenetic drift is a recognized hallmark of senescence. This stability ensures that the correct genes are turned on or off at the appropriate times, maintaining cellular health and tissue function.
Origin
The concept of the epigenome emerged from the fields of genetics and developmental biology, recognizing that phenotypic expression is controlled by factors beyond the primary DNA sequence. The term “epigenetics” itself was coined in the 1940s by Conrad Waddington. The clinical focus on “stability” reflects the modern understanding that maintaining the integrity of these regulatory marks is a critical component of biological longevity and disease prevention.
Mechanism
Hormonal signaling pathways directly influence the epigenome by modulating the activity of key epigenetic enzymes, such as DNA methyltransferases (DNMTs) and histone deacetylases (HDACs). For example, sex steroids can alter methylation patterns in promoter regions of target genes, influencing transcription. Maintaining epigenome stability involves counteracting the accumulation of aberrant methylation and histone modification patterns that disrupt normal gene silencing and activation, which is often observed with declining hormone levels in aging.
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