Université Lyon 1, CNRS, Laboratoire de Biométrie et Biologie Évolutive UMR 5558, Villeurbanne, France.
Institute of Ecology & Evolution, School of Biological Science, University of Edinburgh, Edinburgh, United Kingdom.
PLoS Biol. 2024 Feb 27;22(2):e3002513. doi: 10.1371/journal.pbio.3002513. eCollection 2024 Feb.
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.
为什么会衰老以及衰老的过程是两个让科学家们着迷了几十年的问题。然而,对于这些问题的解答尝试仍然是割裂的,这阻碍了人们对衰老过程的全面理解。我们认为,目前人们对衰老机制的进化缺乏了解,是因为在涉及到生理过程的衰老进化理论上,例如:躯体损耗理论(DST)和衰老的发育理论(DTA),还不够清晰。在这篇文章中,我们提出了一个新的层级模型,将基因与生命关键率联系起来,使我们能够根据与衰老的进化遗传理论(突变积累(MA)和拮抗多效性(AP))的关系,批判性地重新评估 DST 和 DTA。我们还展示了如何将这两个理论纳入一个统一的层级框架中。这个新的框架将有助于产生可检验的假说,说明衰老的特征是如何被自然选择塑造的。