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Horizons in the evolution of aging

Between the 1930s and 50s, evolutionary biologists developed a successful theory of why organisms age, firmly rooted in population genetic principles. By the 1980s the evolution of aging had a secure experimental basis. Since the force of selection declines with age, aging evolves due to mutation ac...

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Detalles Bibliográficos
Autores principales: Flatt, Thomas, Partridge, Linda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100731/
https://www.ncbi.nlm.nih.gov/pubmed/30124168
http://dx.doi.org/10.1186/s12915-018-0562-z
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author Flatt, Thomas
Partridge, Linda
author_facet Flatt, Thomas
Partridge, Linda
author_sort Flatt, Thomas
collection PubMed
description Between the 1930s and 50s, evolutionary biologists developed a successful theory of why organisms age, firmly rooted in population genetic principles. By the 1980s the evolution of aging had a secure experimental basis. Since the force of selection declines with age, aging evolves due to mutation accumulation or a benefit to fitness early in life. Here we review major insights and challenges that have emerged over the last 35 years: selection does not always necessarily decline with age; higher extrinsic (i.e., environmentally caused) mortality does not always accelerate aging; conserved pathways control aging rate; senescence patterns are more diverse than previously thought; aging is not universal; trade-offs involving lifespan can be ‘broken’; aging might be ‘druggable’; and human life expectancy continues to rise but compressing late-life morbidity remains a pressing challenge.
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spelling pubmed-61007312018-08-27 Horizons in the evolution of aging Flatt, Thomas Partridge, Linda BMC Biol Review Between the 1930s and 50s, evolutionary biologists developed a successful theory of why organisms age, firmly rooted in population genetic principles. By the 1980s the evolution of aging had a secure experimental basis. Since the force of selection declines with age, aging evolves due to mutation accumulation or a benefit to fitness early in life. Here we review major insights and challenges that have emerged over the last 35 years: selection does not always necessarily decline with age; higher extrinsic (i.e., environmentally caused) mortality does not always accelerate aging; conserved pathways control aging rate; senescence patterns are more diverse than previously thought; aging is not universal; trade-offs involving lifespan can be ‘broken’; aging might be ‘druggable’; and human life expectancy continues to rise but compressing late-life morbidity remains a pressing challenge. BioMed Central 2018-08-20 /pmc/articles/PMC6100731/ /pubmed/30124168 http://dx.doi.org/10.1186/s12915-018-0562-z Text en © Partridge et al. 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Flatt, Thomas
Partridge, Linda
Horizons in the evolution of aging
title Horizons in the evolution of aging
title_full Horizons in the evolution of aging
title_fullStr Horizons in the evolution of aging
title_full_unstemmed Horizons in the evolution of aging
title_short Horizons in the evolution of aging
title_sort horizons in the evolution of aging
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6100731/
https://www.ncbi.nlm.nih.gov/pubmed/30124168
http://dx.doi.org/10.1186/s12915-018-0562-z
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