This term refers to the quantifiable, progressive alteration in the transcription of genetic information into functional proteins and RNA molecules that occurs naturally with chronological aging. It encompasses the shifting patterns of gene activity, where genes associated with cellular repair and anabolic processes tend to be downregulated, while those linked to inflammation and senescence are often upregulated. Understanding these shifts is central to addressing the molecular basis of age-related functional decline and hormonal changes. These expression changes influence cellular longevity and tissue maintenance throughout the body.
Origin
This concept originates from the field of molecular biology and gerontology, specifically leveraging advancements in genomics and transcriptomics to map the molecular signatures of aging. The recognition that aging is not merely wear-and-tear but involves programmed changes in gene regulation provided the foundation for this term. It is a direct application of genetic science to the physiology of human longevity and healthspan.
Mechanism
The mechanism involves epigenetic modifications, such as DNA methylation and histone acetylation, which alter chromatin structure and consequently influence the accessibility of genes to the transcriptional machinery. Furthermore, changes in microRNA regulation can affect the stability and translation of messenger RNA, thereby modulating protein synthesis in an age-dependent manner. These regulatory shifts directly impact the endocrine system’s sensitivity and the cellular response to key hormones, driving changes in metabolic and structural integrity over time.
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