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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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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. |
format | Online Article Text |
id | pubmed-5509106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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