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Origins of multicellular evolvability in snowflake yeast
Complex life has arisen through a series of ‘major transitions’ in which collectives of formerly autonomous individuals evolve into a single, integrated organism. A key step in this process is the origin of higher-level evolvability, but little is known about how higher-level entities originate and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309424/ https://www.ncbi.nlm.nih.gov/pubmed/25600558 http://dx.doi.org/10.1038/ncomms7102 |
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author | Ratcliff, William C. Fankhauser, Johnathon D. Rogers, David W. Greig, Duncan Travisano, Michael |
author_facet | Ratcliff, William C. Fankhauser, Johnathon D. Rogers, David W. Greig, Duncan Travisano, Michael |
author_sort | Ratcliff, William C. |
collection | PubMed |
description | Complex life has arisen through a series of ‘major transitions’ in which collectives of formerly autonomous individuals evolve into a single, integrated organism. A key step in this process is the origin of higher-level evolvability, but little is known about how higher-level entities originate and gain the capacity to evolve as an individual. Here we report a single mutation that not only creates a new level of biological organization, but also potentiates higher-level evolvability. Disrupting the transcription factor ACE2 in Saccharomyces cerevisiae prevents mother–daughter cell separation, generating multicellular ‘snowflake’ yeast. Snowflake yeast develop through deterministic rules that produce geometrically defined clusters that preclude genetic conflict and display a high broad-sense heritability for multicellular traits; as a result they are preadapted to multicellular adaptation. This work demonstrates that simple microevolutionary changes can have profound macroevolutionary consequences, and suggests that the formation of clonally developing clusters may often be the first step to multicellularity. |
format | Online Article Text |
id | pubmed-4309424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43094242015-02-09 Origins of multicellular evolvability in snowflake yeast Ratcliff, William C. Fankhauser, Johnathon D. Rogers, David W. Greig, Duncan Travisano, Michael Nat Commun Article Complex life has arisen through a series of ‘major transitions’ in which collectives of formerly autonomous individuals evolve into a single, integrated organism. A key step in this process is the origin of higher-level evolvability, but little is known about how higher-level entities originate and gain the capacity to evolve as an individual. Here we report a single mutation that not only creates a new level of biological organization, but also potentiates higher-level evolvability. Disrupting the transcription factor ACE2 in Saccharomyces cerevisiae prevents mother–daughter cell separation, generating multicellular ‘snowflake’ yeast. Snowflake yeast develop through deterministic rules that produce geometrically defined clusters that preclude genetic conflict and display a high broad-sense heritability for multicellular traits; as a result they are preadapted to multicellular adaptation. This work demonstrates that simple microevolutionary changes can have profound macroevolutionary consequences, and suggests that the formation of clonally developing clusters may often be the first step to multicellularity. Nature Pub. Group 2015-01-20 /pmc/articles/PMC4309424/ /pubmed/25600558 http://dx.doi.org/10.1038/ncomms7102 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ratcliff, William C. Fankhauser, Johnathon D. Rogers, David W. Greig, Duncan Travisano, Michael Origins of multicellular evolvability in snowflake yeast |
title | Origins of multicellular evolvability in snowflake yeast |
title_full | Origins of multicellular evolvability in snowflake yeast |
title_fullStr | Origins of multicellular evolvability in snowflake yeast |
title_full_unstemmed | Origins of multicellular evolvability in snowflake yeast |
title_short | Origins of multicellular evolvability in snowflake yeast |
title_sort | origins of multicellular evolvability in snowflake yeast |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309424/ https://www.ncbi.nlm.nih.gov/pubmed/25600558 http://dx.doi.org/10.1038/ncomms7102 |
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