A unified framework for evolutionary genetic and physiological theories of aging
Résumé
Why and how we age are 2 intertwined questions that have fascinated scientists for many decades. However, attempts to answer these questions remain compartmentalized, preventing a comprehensive understanding of the aging process. We argue that the current lack of knowledge about the evolution of aging mechanisms is due to a lack of clarity regarding evolutionary theories of aging that explicitly involve physiological processes: the disposable soma theory (DST) and the developmental theory of aging (DTA). In this Essay, we propose a new hierarchical model linking genes to vital rates, enabling us to critically reevaluate the DST and DTA in terms of their relationship to evolutionary genetic theories of aging (mutation accumulation (MA) and antagonistic pleiotropy (AP)). We also demonstrate how these 2 theories can be incorporated in a unified hierarchical framework. The new framework will help to generate testable hypotheses of how the hallmarks of aging are shaped by natural selection.
Mots clés
AP
antagonistic pleiotropy DST
disposable soma theory DTA
developmental theory of aging ETA
evolutionary theory of aging IIS
insulin/IGF-1 signaling MA
mutation accumulation TOR
target of rapamycin
antagonistic pleiotropy
DST
disposable soma theory
DTA
developmental theory of aging
ETA
evolutionary theory of aging
IIS
insulin/IGF-1 signaling
MA
mutation accumulation
TOR
Domaines
Sciences du Vivant [q-bio]Origine | Fichiers éditeurs autorisés sur une archive ouverte |
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