The collection of enzymatic processes and regulatory factors responsible for preserving the length and integrity of the telomeres, the protective caps on the ends of chromosomes. Maintaining these structures is fundamental to cellular replicative capacity and is a key focus in biological age management. Dysfunction in these pathways is strongly correlated with cellular senescence and age-related decline.
Origin
The term originates from molecular biology and genetics, where telomeres were identified as structures that shorten with each cell division, acting as a mitotic clock. “Maintenance pathways” denote the biological systems, primarily involving the enzyme telomerase, evolved to counteract this natural attrition. It anchors longevity science in fundamental genomic stability.
Mechanism
The primary mechanism involves the reactivation or upregulation of telomerase reverse transcriptase (TERT) activity, which synthesizes new telomeric repeats onto the chromosome ends. Furthermore, alternative lengthening of telomeres (ALT) pathways contribute to maintenance under specific cellular stress conditions. Optimizing these pathways ensures that essential genetic information is not lost during somatic cell division, thereby supporting tissue turnover and function.
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