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Nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation
Flatworms number among the most diverse invertebrate phyla and represent the most biomedically significant branch of the major bilaterian clade Spiralia, but to date, deep evolutionary relationships within this group have been studied using only a single locus (the rRNA operon), leaving the origins...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4398949/ https://www.ncbi.nlm.nih.gov/pubmed/25764302 http://dx.doi.org/10.7554/eLife.05503 |
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author | Laumer, Christopher E Hejnol, Andreas Giribet, Gonzalo |
author_facet | Laumer, Christopher E Hejnol, Andreas Giribet, Gonzalo |
author_sort | Laumer, Christopher E |
collection | PubMed |
description | Flatworms number among the most diverse invertebrate phyla and represent the most biomedically significant branch of the major bilaterian clade Spiralia, but to date, deep evolutionary relationships within this group have been studied using only a single locus (the rRNA operon), leaving the origins of many key clades unclear. In this study, using a survey of genomes and transcriptomes representing all free-living flatworm orders, we provide resolution of platyhelminth interrelationships based on hundreds of nuclear protein-coding genes, exploring phylogenetic signal through concatenation as well as recently developed consensus approaches. These analyses robustly support a modern hypothesis of flatworm phylogeny, one which emphasizes the primacy of the often-overlooked ‘microturbellarian’ groups in understanding the major evolutionary transitions within Platyhelminthes: perhaps most notably, we propose a novel scenario for the interrelationships between free-living and vertebrate-parasitic flatworms, providing new opportunities to shed light on the origins and biological consequences of parasitism in these iconic invertebrates. DOI: http://dx.doi.org/10.7554/eLife.05503.001 |
format | Online Article Text |
id | pubmed-4398949 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-43989492015-04-17 Nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation Laumer, Christopher E Hejnol, Andreas Giribet, Gonzalo eLife Genomics and Evolutionary Biology Flatworms number among the most diverse invertebrate phyla and represent the most biomedically significant branch of the major bilaterian clade Spiralia, but to date, deep evolutionary relationships within this group have been studied using only a single locus (the rRNA operon), leaving the origins of many key clades unclear. In this study, using a survey of genomes and transcriptomes representing all free-living flatworm orders, we provide resolution of platyhelminth interrelationships based on hundreds of nuclear protein-coding genes, exploring phylogenetic signal through concatenation as well as recently developed consensus approaches. These analyses robustly support a modern hypothesis of flatworm phylogeny, one which emphasizes the primacy of the often-overlooked ‘microturbellarian’ groups in understanding the major evolutionary transitions within Platyhelminthes: perhaps most notably, we propose a novel scenario for the interrelationships between free-living and vertebrate-parasitic flatworms, providing new opportunities to shed light on the origins and biological consequences of parasitism in these iconic invertebrates. DOI: http://dx.doi.org/10.7554/eLife.05503.001 eLife Sciences Publications, Ltd 2015-03-12 /pmc/articles/PMC4398949/ /pubmed/25764302 http://dx.doi.org/10.7554/eLife.05503 Text en © 2015, Laumer et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genomics and Evolutionary Biology Laumer, Christopher E Hejnol, Andreas Giribet, Gonzalo Nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation |
title | Nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation |
title_full | Nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation |
title_fullStr | Nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation |
title_full_unstemmed | Nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation |
title_short | Nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation |
title_sort | nuclear genomic signals of the ‘microturbellarian’ roots of platyhelminth evolutionary innovation |
topic | Genomics and Evolutionary Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4398949/ https://www.ncbi.nlm.nih.gov/pubmed/25764302 http://dx.doi.org/10.7554/eLife.05503 |
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