Evidence map›Paper›PMID 24238092›Full record

ArticleBMC evolutionary biology2013

New phylogenomic data support the monophyly of Lophophorata and an Ectoproct-Phoronid clade and indicate that Polyzoa and Kryptrochozoa are caused by systematic bias.

Maximilian P Nesnidal, Martin Helmkampf, Achim Meyer, Alexander Witek, Iris Bruchhaus, Ingo Ebersberger, Thomas Hankeln, Bernhard Lieb, Torsten H Struck, Bernhard Hausdorf

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Article in BMC evolutionary biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

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43citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

43 citing papers in PubMed.

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  14. Evolutionary History of TOPIIA Topoisomerases in Animals.Journal of molecular evolution · 2022
    Article
  15. Article
  16. Review
  17. Review
  18. Are hyoliths Palaeozoic lophophorates?National science review · 2020
    Article
  19. Article
  20. EvoDevo · 2019
    Article
4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Maximilian P Nesnidal
Martin Helmkampf
Achim Meyer
Alexander Witek
Iris Bruchhaus
Ingo Ebersberger
Thomas Hankeln
Bernhard Lieb
Torsten H Struck
Bernhard HausdorfZoological Museum, University of Hamburg, Martin-Luther-King-Platz 3, D-20146 Hamburg, Germany. hausdorf@zoologie.uni-hamburg.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWithin the complex metazoan phylogeny, the relationships of the three lophophorate lineages, ectoprocts, brachiopods and phoronids, are particularly elusive. To shed further light on this issue, we present phylogenomic analyses of 196 genes from 58 bilaterian taxa, paying particular attention to the influence of compositional heterogeneity.

resultsThe phylogenetic analyses strongly support the monophyly of Lophophorata and a sister-group relationship between Ectoprocta and Phoronida. Our results contrast previous findings based on rDNA sequences and phylogenomic datasets which supported monophyletic Polyzoa (= Bryozoa sensu lato) including Ectoprocta, Entoprocta and Cycliophora, Brachiozoa including Brachiopoda and Phoronida as well as Kryptrochozoa including Brachiopoda, Phoronida and Nemertea, thus rendering Lophophorata polyphyletic. Our attempts to identify the causes for the conflicting results revealed that Polyzoa, Brachiozoa and Kryptrochozoa are supported by character subsets with deviating amino acid compositions, whereas there is no indication for compositional heterogeneity in the character subsets supporting the monophyly of Lophophorata.

conclusionOur results indicate that the support for Polyzoa, Brachiozoa and Kryptrochozoa gathered so far is likely an artifact caused by compositional bias. The monophyly of Lophophorata implies that the horseshoe-shaped mesosomal lophophore, the tentacular feeding apparatus of ectoprocts, phoronids and brachiopods is, indeed, a synapomorphy of the lophophorate lineages. The same may apply to radial cleavage. However, among phoronids also spiral cleavage is known. This suggests that the cleavage pattern is highly plastic and has changed several times within lophophorates. The sister group relationship of ectoprocts and phoronids is in accordance with the interpretation of the eversion of a ventral invagination at the beginning of metamorphosis as a common derived feature of these taxa.

Indexed as

PhylogenyAnimalsBryozoaInvertebratesProteinsSequence Analysis, ProteinUrochordataProteins

Identifiers

PMID24238092
PMCPMC4225663

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.