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Synergistic cooperation promotes multicellular performance and unicellular free-rider persistence
The evolution of multicellular life requires cooperation among cells, which can be undermined by intra-group selection for selfishness. Theory predicts that selection to avoid non-cooperators limits social interactions among non-relatives, yet previous evolution experiments suggest that intra-group...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465372/ https://www.ncbi.nlm.nih.gov/pubmed/28580966 http://dx.doi.org/10.1038/ncomms15707 |
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author | Driscoll, William W Travisano, Michael |
author_facet | Driscoll, William W Travisano, Michael |
author_sort | Driscoll, William W |
collection | PubMed |
description | The evolution of multicellular life requires cooperation among cells, which can be undermined by intra-group selection for selfishness. Theory predicts that selection to avoid non-cooperators limits social interactions among non-relatives, yet previous evolution experiments suggest that intra-group conflict is an outcome, rather than a driver, of incipient multicellular life cycles. Here we report the evolution of multicellularity via two distinct mechanisms of group formation in the unicellular budding yeast Kluyveromyces lactis. Cells remain permanently attached following mitosis, giving rise to clonal clusters (staying together); clusters then reversibly assemble into social groups (coming together). Coming together amplifies the benefits of multicellularity and allows social clusters to collectively outperform solitary clusters. However, cooperation among non-relatives also permits fast-growing unicellular lineages to ‘free-ride' during selection for increased size. Cooperation and competition for the benefits of multicellularity promote the stable coexistence of unicellular and multicellular genotypes, underscoring the importance of social and ecological context during the transition to multicellularity. |
format | Online Article Text |
id | pubmed-5465372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54653722017-06-22 Synergistic cooperation promotes multicellular performance and unicellular free-rider persistence Driscoll, William W Travisano, Michael Nat Commun Article The evolution of multicellular life requires cooperation among cells, which can be undermined by intra-group selection for selfishness. Theory predicts that selection to avoid non-cooperators limits social interactions among non-relatives, yet previous evolution experiments suggest that intra-group conflict is an outcome, rather than a driver, of incipient multicellular life cycles. Here we report the evolution of multicellularity via two distinct mechanisms of group formation in the unicellular budding yeast Kluyveromyces lactis. Cells remain permanently attached following mitosis, giving rise to clonal clusters (staying together); clusters then reversibly assemble into social groups (coming together). Coming together amplifies the benefits of multicellularity and allows social clusters to collectively outperform solitary clusters. However, cooperation among non-relatives also permits fast-growing unicellular lineages to ‘free-ride' during selection for increased size. Cooperation and competition for the benefits of multicellularity promote the stable coexistence of unicellular and multicellular genotypes, underscoring the importance of social and ecological context during the transition to multicellularity. Nature Publishing Group 2017-06-05 /pmc/articles/PMC5465372/ /pubmed/28580966 http://dx.doi.org/10.1038/ncomms15707 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Driscoll, William W Travisano, Michael Synergistic cooperation promotes multicellular performance and unicellular free-rider persistence |
title | Synergistic cooperation promotes multicellular performance and unicellular free-rider persistence |
title_full | Synergistic cooperation promotes multicellular performance and unicellular free-rider persistence |
title_fullStr | Synergistic cooperation promotes multicellular performance and unicellular free-rider persistence |
title_full_unstemmed | Synergistic cooperation promotes multicellular performance and unicellular free-rider persistence |
title_short | Synergistic cooperation promotes multicellular performance and unicellular free-rider persistence |
title_sort | synergistic cooperation promotes multicellular performance and unicellular free-rider persistence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465372/ https://www.ncbi.nlm.nih.gov/pubmed/28580966 http://dx.doi.org/10.1038/ncomms15707 |
work_keys_str_mv | AT driscollwilliamw synergisticcooperationpromotesmulticellularperformanceandunicellularfreeriderpersistence AT travisanomichael synergisticcooperationpromotesmulticellularperformanceandunicellularfreeriderpersistence |