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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...

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Autores principales: Ratcliff, William C., Fankhauser, Johnathon D., Rogers, David W., Greig, Duncan, Travisano, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2015
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.
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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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