Cargando…

Suicidal selection: Programmed cell death can evolve in unicellular organisms due solely to kin selection

ABSTRACT: Unicellular organisms can engage in a process by which a cell purposefully destroys itself, termed programmed cell death (PCD). While it is clear that the death of specific cells within a multicellular organism could increase inclusive fitness (e.g., during development), the origin of PCD...

Descripción completa

Detalles Bibliográficos
Autores principales: Vostinar, Anya E., Goldsby, Heather J., Ofria, Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706235/
https://www.ncbi.nlm.nih.gov/pubmed/31463010
http://dx.doi.org/10.1002/ece3.5460
_version_ 1783445674533060608
author Vostinar, Anya E.
Goldsby, Heather J.
Ofria, Charles
author_facet Vostinar, Anya E.
Goldsby, Heather J.
Ofria, Charles
author_sort Vostinar, Anya E.
collection PubMed
description ABSTRACT: Unicellular organisms can engage in a process by which a cell purposefully destroys itself, termed programmed cell death (PCD). While it is clear that the death of specific cells within a multicellular organism could increase inclusive fitness (e.g., during development), the origin of PCD in unicellular organisms is less obvious. Kin selection has been shown to help maintain instances of PCD in existing populations of unicellular organisms; however, competing hypotheses exist about whether additional factors are necessary to explain its origin. Those factors could include an environmental shift that causes latent PCD to be expressed, PCD hitchhiking on a large beneficial mutation, and PCD being simply a common pathology. Here, we present results using an artificial life model to demonstrate that kin selection can, in fact, be sufficient to give rise to PCD in unicellular organisms. Furthermore, when benefits to kin are direct—that is, resources provided to nearby kin—PCD is more beneficial than when benefits are indirect—that is, nonkin are injured, thus increasing the relative amount of resources for kin. Finally, when considering how strict organisms are in determining kin or nonkin (in terms of mutations), direct benefits are viable in a narrower range than indirect benefits. OPEN RESEARCH BADGES: [Image: see text] This article has been awarded Open Data and Open Materials Badges. All materials and data are publicly accessible via the Open Science Framework at https://github.com/anyaevostinar/SuicidalAltruismDissertation/tree/master/LongTerm.
format Online
Article
Text
id pubmed-6706235
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-67062352019-08-28 Suicidal selection: Programmed cell death can evolve in unicellular organisms due solely to kin selection Vostinar, Anya E. Goldsby, Heather J. Ofria, Charles Ecol Evol Original Research ABSTRACT: Unicellular organisms can engage in a process by which a cell purposefully destroys itself, termed programmed cell death (PCD). While it is clear that the death of specific cells within a multicellular organism could increase inclusive fitness (e.g., during development), the origin of PCD in unicellular organisms is less obvious. Kin selection has been shown to help maintain instances of PCD in existing populations of unicellular organisms; however, competing hypotheses exist about whether additional factors are necessary to explain its origin. Those factors could include an environmental shift that causes latent PCD to be expressed, PCD hitchhiking on a large beneficial mutation, and PCD being simply a common pathology. Here, we present results using an artificial life model to demonstrate that kin selection can, in fact, be sufficient to give rise to PCD in unicellular organisms. Furthermore, when benefits to kin are direct—that is, resources provided to nearby kin—PCD is more beneficial than when benefits are indirect—that is, nonkin are injured, thus increasing the relative amount of resources for kin. Finally, when considering how strict organisms are in determining kin or nonkin (in terms of mutations), direct benefits are viable in a narrower range than indirect benefits. OPEN RESEARCH BADGES: [Image: see text] This article has been awarded Open Data and Open Materials Badges. All materials and data are publicly accessible via the Open Science Framework at https://github.com/anyaevostinar/SuicidalAltruismDissertation/tree/master/LongTerm. John Wiley and Sons Inc. 2019-07-30 /pmc/articles/PMC6706235/ /pubmed/31463010 http://dx.doi.org/10.1002/ece3.5460 Text en © 2019 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Vostinar, Anya E.
Goldsby, Heather J.
Ofria, Charles
Suicidal selection: Programmed cell death can evolve in unicellular organisms due solely to kin selection
title Suicidal selection: Programmed cell death can evolve in unicellular organisms due solely to kin selection
title_full Suicidal selection: Programmed cell death can evolve in unicellular organisms due solely to kin selection
title_fullStr Suicidal selection: Programmed cell death can evolve in unicellular organisms due solely to kin selection
title_full_unstemmed Suicidal selection: Programmed cell death can evolve in unicellular organisms due solely to kin selection
title_short Suicidal selection: Programmed cell death can evolve in unicellular organisms due solely to kin selection
title_sort suicidal selection: programmed cell death can evolve in unicellular organisms due solely to kin selection
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6706235/
https://www.ncbi.nlm.nih.gov/pubmed/31463010
http://dx.doi.org/10.1002/ece3.5460
work_keys_str_mv AT vostinaranyae suicidalselectionprogrammedcelldeathcanevolveinunicellularorganismsduesolelytokinselection
AT goldsbyheatherj suicidalselectionprogrammedcelldeathcanevolveinunicellularorganismsduesolelytokinselection
AT ofriacharles suicidalselectionprogrammedcelldeathcanevolveinunicellularorganismsduesolelytokinselection