A thermodynamic limit constrains complexity and primitive social function

Detalhes bibliográficos
Autor(a) principal: Gerrish, Philip J.
Data de Publicação: 2019
Outros Autores: Ferreira, Claudia P. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1017/S1473550418000149
http://hdl.handle.net/11449/196555
Resumo: The evolutionary trend toward increasing complexity and social function is ultimately the result of natural selection's paradoxical tendency to foster cooperation through competition. Cooperating populations ranging from complex societies to somatic tissue are constantly under attack, however, by non-cooperating mutants or transformants, called 'cheaters'. Structure in these populations promotes the formation of cooperating clusters whose competitive superiority can alone be sufficient to thwart outgrowths of cheaters and thereby maintain cooperation. But we find that when cheaters appear too frequently - exceeding a threshold mutation or transformation rate - their scattered outgrowths infiltrate and break up cooperating clusters, resulting in a cascading loss of social cohesiveness, a switch to net positive selection for cheaters and ultimately in the loss of cooperation. Our findings imply that a critically low mutation rate had to be achieved (perhaps through the advent of proofreading and repair mechanisms) before complex cooperative functions, such as those required for multicellularity and social behaviour, could have evolved and persisted. When mutation rate in our model is also allowed to evolve, the threshold is crossed spontaneously after thousands of generations, at which point cheaters rapidly invade. Probing extrapolations of these findings suggest: (1) in somatic tissue, it is neither social retro-evolution alone nor mutation rate evolution alone but the interplay between these two that ultimately leads to oncogenic transitions; the rate of this coevolution might thereby provide an indicator of lifespan of species, terrestrial or not; (2) the likelihood that extraterrestrial life can be expected to be multicellular and social should be affected by ultraviolet and other mutagenic factors.
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spelling A thermodynamic limit constrains complexity and primitive social functionCancercomplexitycooperationextraterrestrial lifegame theorymulticellularityphase transitionsocial evolutionThe evolutionary trend toward increasing complexity and social function is ultimately the result of natural selection's paradoxical tendency to foster cooperation through competition. Cooperating populations ranging from complex societies to somatic tissue are constantly under attack, however, by non-cooperating mutants or transformants, called 'cheaters'. Structure in these populations promotes the formation of cooperating clusters whose competitive superiority can alone be sufficient to thwart outgrowths of cheaters and thereby maintain cooperation. But we find that when cheaters appear too frequently - exceeding a threshold mutation or transformation rate - their scattered outgrowths infiltrate and break up cooperating clusters, resulting in a cascading loss of social cohesiveness, a switch to net positive selection for cheaters and ultimately in the loss of cooperation. Our findings imply that a critically low mutation rate had to be achieved (perhaps through the advent of proofreading and repair mechanisms) before complex cooperative functions, such as those required for multicellularity and social behaviour, could have evolved and persisted. When mutation rate in our model is also allowed to evolve, the threshold is crossed spontaneously after thousands of generations, at which point cheaters rapidly invade. Probing extrapolations of these findings suggest: (1) in somatic tissue, it is neither social retro-evolution alone nor mutation rate evolution alone but the interplay between these two that ultimately leads to oncogenic transitions; the rate of this coevolution might thereby provide an indicator of lifespan of species, terrestrial or not; (2) the likelihood that extraterrestrial life can be expected to be multicellular and social should be affected by ultraviolet and other mutagenic factors.NIHNational Aeronautics and Space AdministrationEuropean CommissionFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)CNRSNIH (ARRA Supplement)Georgia Tech, Sch Biol, 310 Ferst Dr NW, Atlanta, GA 30332 USALos Alamos Natl Lab, Theoret Biol & Biophys, Los Alamos, NM 87545 USAUniv Autonoma Ciuadad Juarez, Inst Ciencias Biomed, Chihuahua 32310, MexicoUniversidade Estadual Paulista, Dept Bioestat, Inst Biociencias, BR-18618000 Botucatu, SP, BrazilUniversidade Estadual Paulista, Dept Bioestat, Inst Biociencias, BR-18618000 Botucatu, SP, BrazilNIH: R01 GM079483National Aeronautics and Space Administration: NNA15BB04AEuropean Commission: FP7 231807FAPESP: FAPESP 16/23738-3Cambridge Univ PressGeorgia TechLos Alamos Natl LabUniv Autonoma Ciuadad JuarezUniversidade Estadual Paulista (Unesp)Gerrish, Philip J.Ferreira, Claudia P. [UNESP]2020-12-10T19:48:42Z2020-12-10T19:48:42Z2019-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article329-335http://dx.doi.org/10.1017/S1473550418000149International Journal Of Astrobiology. New York: Cambridge Univ Press, v. 18, n. 4, p. 329-335, 2019.1473-5504http://hdl.handle.net/11449/19655510.1017/S1473550418000149WOS:00051136680000720527496982046170000-0002-9404-6098Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Journal Of Astrobiologyinfo:eu-repo/semantics/openAccess2021-11-18T19:23:13Zoai:repositorio.unesp.br:11449/196555Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T23:58:10.256127Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv A thermodynamic limit constrains complexity and primitive social function
title A thermodynamic limit constrains complexity and primitive social function
spellingShingle A thermodynamic limit constrains complexity and primitive social function
Gerrish, Philip J.
Cancer
complexity
cooperation
extraterrestrial life
game theory
multicellularity
phase transition
social evolution
title_short A thermodynamic limit constrains complexity and primitive social function
title_full A thermodynamic limit constrains complexity and primitive social function
title_fullStr A thermodynamic limit constrains complexity and primitive social function
title_full_unstemmed A thermodynamic limit constrains complexity and primitive social function
title_sort A thermodynamic limit constrains complexity and primitive social function
author Gerrish, Philip J.
author_facet Gerrish, Philip J.
Ferreira, Claudia P. [UNESP]
author_role author
author2 Ferreira, Claudia P. [UNESP]
author2_role author
dc.contributor.none.fl_str_mv Georgia Tech
Los Alamos Natl Lab
Univ Autonoma Ciuadad Juarez
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Gerrish, Philip J.
Ferreira, Claudia P. [UNESP]
dc.subject.por.fl_str_mv Cancer
complexity
cooperation
extraterrestrial life
game theory
multicellularity
phase transition
social evolution
topic Cancer
complexity
cooperation
extraterrestrial life
game theory
multicellularity
phase transition
social evolution
description The evolutionary trend toward increasing complexity and social function is ultimately the result of natural selection's paradoxical tendency to foster cooperation through competition. Cooperating populations ranging from complex societies to somatic tissue are constantly under attack, however, by non-cooperating mutants or transformants, called 'cheaters'. Structure in these populations promotes the formation of cooperating clusters whose competitive superiority can alone be sufficient to thwart outgrowths of cheaters and thereby maintain cooperation. But we find that when cheaters appear too frequently - exceeding a threshold mutation or transformation rate - their scattered outgrowths infiltrate and break up cooperating clusters, resulting in a cascading loss of social cohesiveness, a switch to net positive selection for cheaters and ultimately in the loss of cooperation. Our findings imply that a critically low mutation rate had to be achieved (perhaps through the advent of proofreading and repair mechanisms) before complex cooperative functions, such as those required for multicellularity and social behaviour, could have evolved and persisted. When mutation rate in our model is also allowed to evolve, the threshold is crossed spontaneously after thousands of generations, at which point cheaters rapidly invade. Probing extrapolations of these findings suggest: (1) in somatic tissue, it is neither social retro-evolution alone nor mutation rate evolution alone but the interplay between these two that ultimately leads to oncogenic transitions; the rate of this coevolution might thereby provide an indicator of lifespan of species, terrestrial or not; (2) the likelihood that extraterrestrial life can be expected to be multicellular and social should be affected by ultraviolet and other mutagenic factors.
publishDate 2019
dc.date.none.fl_str_mv 2019-08-01
2020-12-10T19:48:42Z
2020-12-10T19:48:42Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1017/S1473550418000149
International Journal Of Astrobiology. New York: Cambridge Univ Press, v. 18, n. 4, p. 329-335, 2019.
1473-5504
http://hdl.handle.net/11449/196555
10.1017/S1473550418000149
WOS:000511366800007
2052749698204617
0000-0002-9404-6098
url http://dx.doi.org/10.1017/S1473550418000149
http://hdl.handle.net/11449/196555
identifier_str_mv International Journal Of Astrobiology. New York: Cambridge Univ Press, v. 18, n. 4, p. 329-335, 2019.
1473-5504
10.1017/S1473550418000149
WOS:000511366800007
2052749698204617
0000-0002-9404-6098
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Journal Of Astrobiology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 329-335
dc.publisher.none.fl_str_mv Cambridge Univ Press
publisher.none.fl_str_mv Cambridge Univ Press
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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