Evidence map›Paper›PMID 33739376›Full record

ArticleGenome biology and evolution2021

Gene Duplications Trace Mitochondria to the Onset of Eukaryote Complexity.

Fernando D K Tria, Julia Brueckner, Josip Skejo, Joana C Xavier, Nils Kapust, Michael Knopp, Jessica L E Wimmer, Falk S P Nagies, Verena Zimorski, Sven B Gould and 2 more

Abstract read
In one paragraph

Article in Genome biology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

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  10. Repeat sequences limit the effectiveness of lateral gene transfer and favored the evolution of meiotic sex in early eukaryotes.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

12 authors.

Fernando D K TriaInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.ORCID 0000-0003-4291-2115
Julia BruecknerInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.
Josip SkejoInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.
Joana C XavierInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.ORCID 0000-0001-9242-8968
Nils KapustInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.ORCID 0000-0001-8178-254X
Michael KnoppInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.
Jessica L E WimmerInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.
Falk S P NagiesInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.
Verena ZimorskiInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.
Sven B GouldInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.
Sriram G GargInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.
William F MartinInstitute for Molecular Evolution, Heinrich Heine University Düsseldorf, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The last eukaryote common ancestor (LECA) possessed mitochondria and all key traits that make eukaryotic cells more complex than their prokaryotic ancestors, yet the timing of mitochondrial acquisition and the role of mitochondria in the origin of eukaryote complexity remain debated. Here, we report evidence from gene duplications in LECA indicating an early origin of mitochondria. Among 163,545 duplications in 24,571 gene trees spanning 150 sequenced eukaryotic genomes, we identify 713 gene duplication events that occurred in LECA. LECA's bacterial-derived genes include numerous mitochondrial functions and were duplicated significantly more often than archaeal-derived and eukaryote-specific genes. The surplus of bacterial-derived duplications in LECA most likely reflects the serial copying of genes from the mitochondrial endosymbiont to the archaeal host's chromosomes. Clustering, phylogenies and likelihood ratio tests for 22.4 million genes from 5,655 prokaryotic and 150 eukaryotic genomes reveal no evidence for lineage-specific gene acquisitions in eukaryotes, except from the plastid in the plant lineage. That finding, and the functions of bacterial genes duplicated in LECA, suggests that the bacterial genes in eukaryotes are acquisitions from the mitochondrion, followed by vertical gene evolution and differential loss across eukaryotic lineages, flanked by concomitant lateral gene transfer among prokaryotes. Overall, the data indicate that recurrent gene transfer via the copying of genes from a resident mitochondrial endosymbiont to archaeal host chromosomes preceded the onset of eukaryotic cellular complexity, favoring mitochondria-early over mitochondria-late hypotheses for eukaryote origin.

Indexed as

Biological EvolutionGene DuplicationEukaryotaEvolution, MolecularGenes, ArchaealGenes, BacterialGene Transfer, HorizontalMitochondriaendosymbiosiseukaryote originevolutiongene duplicationgene transferparalogy

Identifiers

PMID33739376
PMCPMC8175051

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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.