Evidence map›Paper›PMID 31647561›Full record

ArticleMolecular biology and evolution2020

Convergent Evolution of Hydrogenosomes from Mitochondria by Gene Transfer and Loss.

William H Lewis, Anders E Lind, Kacper M Sendra, Henning Onsbring, Tom A Williams, Genoveva F Esteban, Robert P Hirt, Thijs J G Ettema, T Martin Embley

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology and evolution, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

31 citing papers in PubMed, 67 citations in OpenAlex.

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  3. Magnetotaxis in an anaerobic ciliate via tripartite syntrophy.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  9. Bioenergetics evolution: the link between Earth's and Life's history.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
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  19. Diverse signatures of convergent evolution in cacti-associated yeasts.bioRxiv : the preprint server for biology · 2023
    Article
  20. Article
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

9 authors at 4 institutions in 3 countries.

William H LewisInstitute for Cell and Molecular Biosciences, Newcastle University, Newcastle-Upon-Tyne, United Kingdom.
Anders E LindDepartment of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
Kacper M SendraInstitute for Cell and Molecular Biosciences, Newcastle University, Newcastle-Upon-Tyne, United Kingdom.
Henning OnsbringDepartment of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
Tom A WilliamsSchool of Biological Sciences, University of Bristol, Bristol, United Kingdom.
Genoveva F EstebanDepartment of Life and Environmental Sciences, Bournemouth University, Poole, United Kingdom.
Robert P HirtInstitute for Cell and Molecular Biosciences, Newcastle University, Newcastle-Upon-Tyne, United Kingdom.
Thijs J G EttemaDepartment of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.
T Martin EmbleyInstitute for Cell and Molecular Biosciences, Newcastle University, Newcastle-Upon-Tyne, United Kingdom.
Newcastle University · GBUppsala University · SEBournemouth University · GBUniversity of Bristol · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Hydrogenosomes are H2-producing mitochondrial homologs found in some anaerobic microbial eukaryotes that provide a rare intracellular niche for H2-utilizing endosymbiotic archaea. Among ciliates, anaerobic and aerobic lineages are interspersed, demonstrating that the switch to an anaerobic lifestyle with hydrogenosomes has occurred repeatedly and independently. To investigate the molecular details of this transition, we generated genomic and transcriptomic data sets from anaerobic ciliates representing three distinct lineages. Our data demonstrate that hydrogenosomes have evolved from ancestral mitochondria in each case and reveal different degrees of independent mitochondrial genome and proteome reductive evolution, including the first example of complete mitochondrial genome loss in ciliates. Intriguingly, the FeFe-hydrogenase used for generating H2 has a unique domain structure among eukaryotes and appears to have been present, potentially through a single lateral gene transfer from an unknown donor, in the common aerobic ancestor of all three lineages. The early acquisition and retention of FeFe-hydrogenase helps to explain the facility whereby mitochondrial function can be so radically modified within this diverse and ecologically important group of microbial eukaryotes.

Indexed as

AerobiosisAnaerobiosisCiliophoraEvolution, MolecularGene Expression ProfilingGene Transfer, HorizontalGenome, MitochondrialHydrogenMitochondriaPhylogenySequence Analysis, DNASequence Analysis, RNAHydrogenanaerobic metabolismevolutiongenomicshydrogenosomesmicrobial eukaryotesmitochondria

Identifiers

PMID31647561
PMCPMC6993867
OpenAlexW2981774379

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.