Evidence map›Paper›PMID 26247465›Full record

ArticlePloS one2015

Phylogeny of Echinoderm Hemoglobins.

Ana B Christensen, Joseph L Herman, Maurice R Elphick, Kord M Kober, Daniel Janies, Gregorio Linchangco, Dean C Semmens, Xavier Bailly, Serge N Vinogradov, David Hoogewijs

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 8 institutions in 4 countries.

Ana B ChristensenBiology Department, Lamar University, Beaumont, Texas, United States of America.
Joseph L HermanDepartment of Statistics, University of Oxford, Oxford, OX1 3TG, United Kingdom; Division of Mathematical Biology, National Institute of Medical Research, London, NW7 1AA, United Kingdom.
Maurice R ElphickSchool of Biological & Chemical Sciences, Queen Mary University of London, London E1 4NS, United Kingdom.
Kord M KoberDepartment of Ecology & Evolutionary Biology, University of California Santa Cruz, Santa Cruz, California, United States of America.
Daniel JaniesCollege of Computing and Informatics, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States of America.
Gregorio LinchangcoCollege of Computing and Informatics, University of North Carolina at Charlotte, Charlotte, North Carolina 28223, United States of America.
Dean C SemmensSchool of Biological & Chemical Sciences, Queen Mary University of London, London E1 4NS, United Kingdom.
Xavier BaillyMarine Plants and Biomolecules, Station Biologique de Roscoff, 2968 Roscoff, France.
Serge N VinogradovDepartment of Biochemistry and Molecular Biology, Wayne State University School of Medicine, Detroit, Michigan 48201, United States of America.
David HoogewijsInstitute of Physiology, University of Duisburg-Essen, Essen, Germany.
Queen Mary University of London · GBUniversity of North Carolina at Charlotte · USLamar University · USStation Biologique de Roscoff · FRUniversity of California, Santa Cruz · USUniversity of Duisburg-Essen · DEUniversity of Oxford · GBWayne State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent genomic information has revealed that neuroglobin and cytoglobin are the two principal lineages of vertebrate hemoglobins, with the latter encompassing the familiar myoglobin and α-globin/β-globin tetramer hemoglobin, and several minor groups. In contrast, very little is known about hemoglobins in echinoderms, a phylum of exclusively marine organisms closely related to vertebrates, beyond the presence of coelomic hemoglobins in sea cucumbers and brittle stars. We identified about 50 hemoglobins in sea urchin, starfish and sea cucumber genomes and transcriptomes, and used Bayesian inference to carry out a molecular phylogenetic analysis of their relationship to vertebrate sequences, specifically, to assess the hypothesis that the neuroglobin and cytoglobin lineages are also present in echinoderms.

resultsThe genome of the sea urchin Strongylocentrotus purpuratus encodes several hemoglobins, including a unique chimeric 14-domain globin, 2 androglobin isoforms and a unique single androglobin domain protein. Other strongylocentrotid genomes appear to have similar repertoires of globin genes. We carried out molecular phylogenetic analyses of 52 hemoglobins identified in sea urchin, brittle star and sea cucumber genomes and transcriptomes, using different multiple sequence alignment methods coupled with Bayesian and maximum likelihood approaches. The results demonstrate that there are two major globin lineages in echinoderms, which are related to the vertebrate neuroglobin and cytoglobin lineages. Furthermore, the brittle star and sea cucumber coelomic hemoglobins appear to have evolved independently from the cytoglobin lineage, similar to the evolution of erythroid oxygen binding globins in cyclostomes and vertebrates.

conclusionThe presence of echinoderm globins related to the vertebrate neuroglobin and cytoglobin lineages suggests that the split between neuroglobins and cytoglobins occurred in the deuterostome ancestor shared by echinoderms and vertebrates.

Indexed as

AnimalsBayes TheoremCytoglobinEchinodermataGlobinsLikelihood FunctionsModels, MolecularNerve Tissue ProteinsNeuroglobinPhylogenyProtein ConformationCytoglobinGlobinsNerve Tissue ProteinsNeuroglobin

Identifiers

PMID26247465
PMCPMC4527676
OpenAlexW1661585058

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Registered trials

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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.