This refers to how sleep duration and quality influence reversible modifications to DNA and associated proteins, like histones, that alter gene expression without changing the underlying nucleotide sequence. This regulation is vital as it dictates the long-term plasticity of the endocrine and metabolic systems. Poor sleep can induce detrimental epigenetic marks associated with aging and dysfunction.
Origin
It integrates ‘Epigenetic Regulation,’ the field describing heritable changes in gene function, with ‘Sleep,’ the critical restorative period. This nomenclature reflects modern molecular biology’s understanding that environmental factors, like sleep patterns, directly communicate with the genome. We observe the molecular memory of sleep deprivation.
Mechanism
During deep sleep stages, specific enzymatic activities like DNA methyltransferases and histone deacetylases are highly active, potentially silencing or activating genes related to growth hormone release or circadian rhythmicity. For example, chronic sleep restriction can alter methylation at promoter regions controlling stress-response genes. This molecular sculpting dictates future cellular responsiveness.
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