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A novel classification system for evolutionary aging theories
Theories of lifespan evolution are a source of confusion amongst aging researchers. After a century of aging research the dispute over whether the aging process is active or passive persists and a comprehensive and universally accepted theoretical model remains elusive. Evolutionary aging theories p...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589719/ https://www.ncbi.nlm.nih.gov/pubmed/23508239 http://dx.doi.org/10.3389/fgene.2013.00025 |
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author | Trindade, Lucas S. Aigaki, Toshiro Peixoto, Alexandre A. Balduino, Alex Mânica da Cruz, Ivana B. Heddle, Jonathan G. |
author_facet | Trindade, Lucas S. Aigaki, Toshiro Peixoto, Alexandre A. Balduino, Alex Mânica da Cruz, Ivana B. Heddle, Jonathan G. |
author_sort | Trindade, Lucas S. |
collection | PubMed |
description | Theories of lifespan evolution are a source of confusion amongst aging researchers. After a century of aging research the dispute over whether the aging process is active or passive persists and a comprehensive and universally accepted theoretical model remains elusive. Evolutionary aging theories primarily dispute whether the aging process is exclusively adapted to favor the kin or exclusively non-adapted to favor the individual. Interestingly, contradictory data and theories supporting both exclusively programmed and exclusively non-programmed theories continue to grow. However, this is a false dichotomy; natural selection favors traits resulting in efficient reproduction whether they benefit the individual or the kin. Thus, to understand the evolution of aging, first we must understand the environment-dependent balance between the advantages and disadvantages of extended lifespan in the process of spreading genes. As described by distinct theories, different niches and environmental conditions confer on extended lifespan a range of fitness values varying from highly beneficial to highly detrimental. Here, we considered the range of fitness values for extended lifespan and develop a fitness-based framework for categorizing existing theories. We show that all theories can be classified into four basic types: secondary (beneficial), maladaptive (neutral), assisted death (detrimental), and senemorphic aging (varying between beneficial to detrimental). We anticipate that this classification system will assist with understanding and interpreting aging/death by providing a way of considering theories as members of one of these classes rather than consideration of their individual details. |
format | Online Article Text |
id | pubmed-3589719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35897192013-03-18 A novel classification system for evolutionary aging theories Trindade, Lucas S. Aigaki, Toshiro Peixoto, Alexandre A. Balduino, Alex Mânica da Cruz, Ivana B. Heddle, Jonathan G. Front Genet Genetics Theories of lifespan evolution are a source of confusion amongst aging researchers. After a century of aging research the dispute over whether the aging process is active or passive persists and a comprehensive and universally accepted theoretical model remains elusive. Evolutionary aging theories primarily dispute whether the aging process is exclusively adapted to favor the kin or exclusively non-adapted to favor the individual. Interestingly, contradictory data and theories supporting both exclusively programmed and exclusively non-programmed theories continue to grow. However, this is a false dichotomy; natural selection favors traits resulting in efficient reproduction whether they benefit the individual or the kin. Thus, to understand the evolution of aging, first we must understand the environment-dependent balance between the advantages and disadvantages of extended lifespan in the process of spreading genes. As described by distinct theories, different niches and environmental conditions confer on extended lifespan a range of fitness values varying from highly beneficial to highly detrimental. Here, we considered the range of fitness values for extended lifespan and develop a fitness-based framework for categorizing existing theories. We show that all theories can be classified into four basic types: secondary (beneficial), maladaptive (neutral), assisted death (detrimental), and senemorphic aging (varying between beneficial to detrimental). We anticipate that this classification system will assist with understanding and interpreting aging/death by providing a way of considering theories as members of one of these classes rather than consideration of their individual details. Frontiers Media S.A. 2013-03-06 /pmc/articles/PMC3589719/ /pubmed/23508239 http://dx.doi.org/10.3389/fgene.2013.00025 Text en Copyright © Trindade, Aigaki, Peixoto, Balduino, Mânica da Cruz and Heddle. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Genetics Trindade, Lucas S. Aigaki, Toshiro Peixoto, Alexandre A. Balduino, Alex Mânica da Cruz, Ivana B. Heddle, Jonathan G. A novel classification system for evolutionary aging theories |
title | A novel classification system for evolutionary aging theories |
title_full | A novel classification system for evolutionary aging theories |
title_fullStr | A novel classification system for evolutionary aging theories |
title_full_unstemmed | A novel classification system for evolutionary aging theories |
title_short | A novel classification system for evolutionary aging theories |
title_sort | novel classification system for evolutionary aging theories |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589719/ https://www.ncbi.nlm.nih.gov/pubmed/23508239 http://dx.doi.org/10.3389/fgene.2013.00025 |
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