A thermodynamic limit constrains complexity and primitive social function
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | |
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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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 |
|
_version_ |
1808129567978684416 |