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The ancestral levels of transcription and the evolution of sexual phenotypes in filamentous fungi

Changes in gene expression have been hypothesized to play an important role in the evolution of divergent morphologies. To test this hypothesis in a model system, we examined differences in fruiting body morphology of five filamentous fungi in the Sordariomycetes, culturing them in a common garden e...

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Autores principales: Trail, Frances, Wang, Zheng, Stefanko, Kayla, Cubba, Caitlyn, Townsend, Jeffrey P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509106/
https://www.ncbi.nlm.nih.gov/pubmed/28704372
http://dx.doi.org/10.1371/journal.pgen.1006867
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author Trail, Frances
Wang, Zheng
Stefanko, Kayla
Cubba, Caitlyn
Townsend, Jeffrey P.
author_facet Trail, Frances
Wang, Zheng
Stefanko, Kayla
Cubba, Caitlyn
Townsend, Jeffrey P.
author_sort Trail, Frances
collection PubMed
description Changes in gene expression have been hypothesized to play an important role in the evolution of divergent morphologies. To test this hypothesis in a model system, we examined differences in fruiting body morphology of five filamentous fungi in the Sordariomycetes, culturing them in a common garden environment and profiling genome-wide gene expression at five developmental stages. We reconstructed ancestral gene expression phenotypes, identifying genes with the largest evolved increases in gene expression across development. Conducting knockouts and performing phenotypic analysis in two divergent species typically demonstrated altered fruiting body development in the species that had evolved increased expression. Our evolutionary approach to finding relevant genes proved far more efficient than other gene deletion studies targeting whole genomes or gene families. Combining gene expression measurements with knockout phenotypes facilitated the refinement of Bayesian networks of the genes underlying fruiting body development, regulation of which is one of the least understood processes of multicellular development.
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spelling pubmed-55091062017-08-07 The ancestral levels of transcription and the evolution of sexual phenotypes in filamentous fungi Trail, Frances Wang, Zheng Stefanko, Kayla Cubba, Caitlyn Townsend, Jeffrey P. PLoS Genet Research Article Changes in gene expression have been hypothesized to play an important role in the evolution of divergent morphologies. To test this hypothesis in a model system, we examined differences in fruiting body morphology of five filamentous fungi in the Sordariomycetes, culturing them in a common garden environment and profiling genome-wide gene expression at five developmental stages. We reconstructed ancestral gene expression phenotypes, identifying genes with the largest evolved increases in gene expression across development. Conducting knockouts and performing phenotypic analysis in two divergent species typically demonstrated altered fruiting body development in the species that had evolved increased expression. Our evolutionary approach to finding relevant genes proved far more efficient than other gene deletion studies targeting whole genomes or gene families. Combining gene expression measurements with knockout phenotypes facilitated the refinement of Bayesian networks of the genes underlying fruiting body development, regulation of which is one of the least understood processes of multicellular development. Public Library of Science 2017-07-13 /pmc/articles/PMC5509106/ /pubmed/28704372 http://dx.doi.org/10.1371/journal.pgen.1006867 Text en © 2017 Trail et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Trail, Frances
Wang, Zheng
Stefanko, Kayla
Cubba, Caitlyn
Townsend, Jeffrey P.
The ancestral levels of transcription and the evolution of sexual phenotypes in filamentous fungi
title The ancestral levels of transcription and the evolution of sexual phenotypes in filamentous fungi
title_full The ancestral levels of transcription and the evolution of sexual phenotypes in filamentous fungi
title_fullStr The ancestral levels of transcription and the evolution of sexual phenotypes in filamentous fungi
title_full_unstemmed The ancestral levels of transcription and the evolution of sexual phenotypes in filamentous fungi
title_short The ancestral levels of transcription and the evolution of sexual phenotypes in filamentous fungi
title_sort ancestral levels of transcription and the evolution of sexual phenotypes in filamentous fungi
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509106/
https://www.ncbi.nlm.nih.gov/pubmed/28704372
http://dx.doi.org/10.1371/journal.pgen.1006867
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