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  Origins of multicellular evolvability in snowflake yeast

Ratcliff, W. C., Fankhauser, J. D., Rogers, D. W., Greig, D., & Travisano, M. (2015). Origins of multicellular evolvability in snowflake yeast. Nature Communications, 6: 6102. doi:10.1038/ncomms7102.

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 Creators:
Ratcliff, William C., Author
Fankhauser, Johnathon D., Author
Rogers, David W.1, Author           
Greig, Duncan1, Author           
Travisano, Michael, Author
Affiliations:
1Max-Planck Research Group Experimental Evolution, Max Planck Institute for Evolutionary Biology, Max Planck Society, ou_1445640              

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Free keywords: Biological sciences; Evolution; Genetics
 Abstract: 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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Language(s): eng - English
 Dates: 2014-05-132014-12-152015-01-20
 Publication Status: Published online
 Pages: -
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 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1038/ncomms7102
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Title: Nature Communications
  Abbreviation : Nat. Commun.
Source Genre: Journal
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Publ. Info: London : Nature Publishing Group
Pages: 9 S. Volume / Issue: 6 Sequence Number: 6102 Start / End Page: - Identifier: ISSN: 2041-1723 (online)
CoNE: https://pure.mpg.de/cone/journals/resource/2041-1723