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dc.contributor.authorNaseeb, S
dc.contributor.authorAmes, RM
dc.contributor.authorDelneri, D
dc.contributor.authorLovell, SC
dc.date.accessioned2017-09-26T12:10:26Z
dc.date.issued2017-08-23
dc.description.abstractDuplication of genes or genomes provides the raw material for evolutionary innovation. After duplication a gene may be lost, recombine with another gene, have its function modified or be retained in an unaltered state. The fate of duplication is usually studied by comparing extant genomes and reconstructing the most likely ancestral states. Valuable as this approach is, it may miss the most rapid evolutionary events. Here, we engineered strains of Saccharomyces cerevisiae carrying tandem and non-tandem duplications of the singleton gene IFA38 to monitor (i) the fate of the duplicates in different conditions, including time scale and asymmetry of gene loss, and (ii) the changes in fitness and transcriptome of the strains immediately after duplication and after experimental evolution. We found that the duplication brings widespread transcriptional changes, but a fitness advantage is only present in fermentable media. In respiratory conditions, the yeast strains consistently lose the non-tandem IFA38 gene copy in a surprisingly short time, within only a few generations. This gene loss appears to be asymmetric and dependent on genome location, since the original IFA38 copy and the tandem duplicate are retained. Overall, this work shows for the first time that gene loss can be extremely rapid and context dependent.en_GB
dc.description.sponsorshipThis work was generously supported by BBSRC grant no. BB/I020489/1 and the Wellcome Trust Institutional Strategic Support Award (WT105618MA).en_GB
dc.identifier.citationVol. 284 (1861), article 20171393en_GB
dc.identifier.doi10.1098/rspb.2017.1393
dc.identifier.urihttp://hdl.handle.net/10871/29542
dc.language.isoenen_GB
dc.publisherRoyal Societyen_GB
dc.rights© 2017 The Authors. Open access.Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.en_GB
dc.subjectgene duplicationen_GB
dc.subjectevolutionen_GB
dc.subjectfunctional innovationen_GB
dc.subjectgene expressionen_GB
dc.titleRapid functional and evolutionary changes follow gene duplication in yeasten_GB
dc.typeArticleen_GB
dc.date.available2017-09-26T12:10:26Z
dc.identifier.issn0962-8452
dc.descriptionThis is the author accepted manuscript. The final version is available from the Royal Society via the DOI in this record.en_GB
dc.identifier.journalProceedings of the Royal Society B: Biological Sciencesen_GB
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/


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© 2017 The Authors. Open access.Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
Except where otherwise noted, this item's licence is described as © 2017 The Authors. Open access.Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.