Four myriapod relatives - but who are sisters? No end to debates on relationships among the four major myriapod subgroups.

Arthropod phylogeny Conflict Confounding signal Internal rooting Phylogenetics Phylogenomics Quartet topology RNA-Seq Transcriptomes

Journal

BMC evolutionary biology
ISSN: 1471-2148
Titre abrégé: BMC Evol Biol
Pays: England
ID NLM: 100966975

Informations de publication

Date de publication:
04 11 2020
Historique:
received: 16 05 2020
accepted: 30 09 2020
entrez: 5 11 2020
pubmed: 6 11 2020
medline: 26 11 2020
Statut: epublish

Résumé

Phylogenetic relationships among the myriapod subgroups Chilopoda, Diplopoda, Symphyla and Pauropoda are still not robustly resolved. The first phylogenomic study covering all subgroups resolved phylogenetic relationships congruently to morphological evidence but is in conflict with most previously published phylogenetic trees based on diverse molecular data. Outgroup choice and long-branch attraction effects were stated as possible explanations for these incongruencies. In this study, we addressed these issues by extending the myriapod and outgroup taxon sampling using transcriptome data. We generated new transcriptome data of 42 panarthropod species, including all four myriapod subgroups and additional outgroup taxa. Our taxon sampling was complemented by published transcriptome and genome data resulting in a supermatrix covering 59 species. We compiled two data sets, the first with a full coverage of genes per species (292 single-copy protein-coding genes), the second with a less stringent coverage (988 genes). We inferred phylogenetic relationships among myriapods using different data types, tree inference, and quartet computation approaches. Our results unambiguously support monophyletic Mandibulata and Myriapoda. Our analyses clearly showed that there is strong signal for a single unrooted topology, but a sensitivity of the position of the internal root on the choice of outgroups. However, we observe strong evidence for a clade Pauropoda+Symphyla, as well as for a clade Chilopoda+Diplopoda. Our best quartet topology is incongruent with current morphological phylogenies which were supported in another phylogenomic study. AU tests and quartet mapping reject the quartet topology congruent to trees inferred with morphological characters. Moreover, quartet mapping shows that confounding signal present in the data set is sufficient to explain the weak signal for the quartet topology derived from morphological characters. Although outgroup choice affects results, our study could narrow possible trees to derivatives of a single quartet topology. For highly disputed relationships, we propose to apply a series of tests (AU and quartet mapping), since results of such tests allow to narrow down possible relationships and to rule out confounding signal.

Sections du résumé

BACKGROUND
Phylogenetic relationships among the myriapod subgroups Chilopoda, Diplopoda, Symphyla and Pauropoda are still not robustly resolved. The first phylogenomic study covering all subgroups resolved phylogenetic relationships congruently to morphological evidence but is in conflict with most previously published phylogenetic trees based on diverse molecular data. Outgroup choice and long-branch attraction effects were stated as possible explanations for these incongruencies. In this study, we addressed these issues by extending the myriapod and outgroup taxon sampling using transcriptome data.
RESULTS
We generated new transcriptome data of 42 panarthropod species, including all four myriapod subgroups and additional outgroup taxa. Our taxon sampling was complemented by published transcriptome and genome data resulting in a supermatrix covering 59 species. We compiled two data sets, the first with a full coverage of genes per species (292 single-copy protein-coding genes), the second with a less stringent coverage (988 genes). We inferred phylogenetic relationships among myriapods using different data types, tree inference, and quartet computation approaches. Our results unambiguously support monophyletic Mandibulata and Myriapoda. Our analyses clearly showed that there is strong signal for a single unrooted topology, but a sensitivity of the position of the internal root on the choice of outgroups. However, we observe strong evidence for a clade Pauropoda+Symphyla, as well as for a clade Chilopoda+Diplopoda.
CONCLUSIONS
Our best quartet topology is incongruent with current morphological phylogenies which were supported in another phylogenomic study. AU tests and quartet mapping reject the quartet topology congruent to trees inferred with morphological characters. Moreover, quartet mapping shows that confounding signal present in the data set is sufficient to explain the weak signal for the quartet topology derived from morphological characters. Although outgroup choice affects results, our study could narrow possible trees to derivatives of a single quartet topology. For highly disputed relationships, we propose to apply a series of tests (AU and quartet mapping), since results of such tests allow to narrow down possible relationships and to rule out confounding signal.

Identifiants

pubmed: 33148176
doi: 10.1186/s12862-020-01699-0
pii: 10.1186/s12862-020-01699-0
pmc: PMC7640414
doi:

Banques de données

Dryad
['10.5061/dryad.cvdncjt2r']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

144

Subventions

Organisme : Austrian Science Fund
ID : P 20497-B17
Pays : International
Organisme : Austrian Science Fund
ID : P 23251-B17
Pays : International
Organisme : Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
ID : PP00P3_170664
Pays : International
Organisme : European Research Council
ID : 754290
Pays : International

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Auteurs

Nikolaus U Szucsich (NU)

Department of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria. nikola.szucsich@univie.ac.at.
Central Research Laboratories, Natural History Museum of Vienna, A-1010, Vienna, Austria. nikola.szucsich@univie.ac.at.

Daniela Bartel (D)

Department of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria.

Alexander Blanke (A)

Institute for Zoology, Biocenter, University of Cologne, D-50674, Cologne, Germany.
Institute of Evolutionary Biology and Animal Ecology, University of Bonn, D-53121, Bonn, Germany.

Alexander Böhm (A)

Department of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria.

Alexander Donath (A)

Centre for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, D-53113, Bonn, Germany.

Makiko Fukui (M)

Department of Biology, Graduate School of Science and Engineering, Ehime University, Bunkyo-cho, Matsuyama, Ehime, 790-8577, Japan.

Simon Grove (S)

Invertebrate Zoology, Collections and Research Facility, Tasmanian Museum and Art Gallery, Rosny, Tasmania, 7018, Australia.

Shanlin Liu (S)

Department of Entomology, China Agricultural University, Beijing, 100193, People's Republic of China.

Oliver Macek (O)

Department of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria.
Central Research Laboratories, Natural History Museum of Vienna, A-1010, Vienna, Austria.

Ryuichiro Machida (R)

Sugadaira Research Station, Mountain Science Center, University of Tsukuba, Sugadaira, Ueda, Nagano, 386-2204, Japan.

Bernhard Misof (B)

Zoological Research Museum Alexander Koenig, D-53113, Bonn, Germany.

Yasutaka Nakagaki (Y)

Sugadaira Research Station, Mountain Science Center, University of Tsukuba, Sugadaira, Ueda, Nagano, 386-2204, Japan.

Lars Podsiadlowski (L)

Centre for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, D-53113, Bonn, Germany.

Kaoru Sekiya (K)

Sugadaira Research Station, Mountain Science Center, University of Tsukuba, Sugadaira, Ueda, Nagano, 386-2204, Japan.

Shigekazu Tomizuka (S)

Matsunoyamamatsuguchi, Tokamachi, Niigata, 942-1411, Japan.

Björn M Von Reumont (BM)

LOEWE Centre for Translational Biodiversity Genomics (LOEWE TBG), Senckenberganlage 25, 60325, Frankfurt, Germany.
Animal Venomics, Institute for Insect Biotechnology, University of Giessen, Heinrich Buff Ring 26-32, D-35394, Giessen, Germany.

Robert M Waterhouse (RM)

Department of Ecology and Evolution, University of Lausanne and Swiss Institute of Bioinformatics, 1015, Lausanne, Switzerland.

Manfred Walzl (M)

Department of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria.

Guanliang Meng (G)

Centre of Taxonomy and Evolutionary Research, Zoological Research Museum Alexander Koenig, D-53113, Bonn, Germany.

Xin Zhou (X)

Department of Entomology, China Agricultural University, Beijing, 100193, People's Republic of China.

Günther Pass (G)

Department of Evolutionary Biology, University of Vienna, A-1090, Vienna, Austria.

Karen Meusemann (K)

Centre for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, D-53113, Bonn, Germany. mail@karen-meusemann.de.
Department of Evolutionary Biology and Ecology, Institute of Biology I (Zoology), University of Freiburg, D-79104, Freiburg, Germany. mail@karen-meusemann.de.
Australian National Insect Collection, National Research Collections Australia, CSIRO, ACT, Canberra, 2601, Australia. mail@karen-meusemann.de.

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