Evidence map›Paper›PMID 25317564›Full record

ArticleNature2015

Origins of major archaeal clades correspond to gene acquisitions from bacteria.

Shijulal Nelson-Sathi, Filipa L Sousa, Mayo Roettger, Nabor Lozada-Chávez, Thorsten Thiergart, Arnold Janssen, David Bryant, Giddy Landan, Peter Schönheit, Bettina Siebers and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed
15.9field-weighted citation impact, top 1% 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

141 citing papers in PubMed, 254 citations in OpenAlex.

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  17. Metabolic compatibility and the rarity of prokaryote endosymbioses.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  18. Article
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  20. Article

81 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 4 countries.

Shijulal Nelson-SathiInstitute of Molecular Evolution, Heinrich-Heine University, 40225 Düsseldorf, Germany.
Filipa L SousaInstitute of Molecular Evolution, Heinrich-Heine University, 40225 Düsseldorf, Germany.
Mayo RoettgerInstitute of Molecular Evolution, Heinrich-Heine University, 40225 Düsseldorf, Germany.
Nabor Lozada-ChávezInstitute of Molecular Evolution, Heinrich-Heine University, 40225 Düsseldorf, Germany.
Thorsten ThiergartInstitute of Molecular Evolution, Heinrich-Heine University, 40225 Düsseldorf, Germany.
Arnold JanssenMathematisches Institut, Heinrich-Heine University, 40225 Düsseldorf, Germany.
David BryantDepartment of Mathematics and Statistics, University of Otago, Dunedin 9054, New Zealand.
Giddy LandanGenomic Microbiology Group, Institute of Microbiology, Christian-Albrechts-Universität Kiel, 24118 Kiel, Germany.
Peter SchönheitInstitut für Allgemeine Mikrobiologie, Christian-Albrechts-Universität Kiel, 24118 Kiel, Germany.
Bettina SiebersFaculty of Chemistry, Biofilm Centre, Molecular Enzyme Technology and Biochemistry, University of Duisburg-Essen, 45117 Essen, Germany.
James O McInerneyDepartment of Biology, National University of Ireland, Maynooth, County Kildare, Ireland.
William F Martin1] Institute of Molecular Evolution, Heinrich-Heine University, 40225 Düsseldorf, Germany [2] Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, 2780-157 Oeiras, Portugal.
Heinrich Heine University Düsseldorf · DEKiel University · DENational University of Ireland, Maynooth · IEUniversidade Nova de Lisboa · PTUniversity of Duisburg-Essen · DEUniversity of Otago · NZ

Funding

European Research Council 232975European Research Council 281357
6 · The paper itself

Abstract

The mechanisms that underlie the origin of major prokaryotic groups are poorly understood. In principle, the origin of both species and higher taxa among prokaryotes should entail similar mechanisms--ecological interactions with the environment paired with natural genetic variation involving lineage-specific gene innovations and lineage-specific gene acquisitions. To investigate the origin of higher taxa in archaea, we have determined gene distributions and gene phylogenies for the 267,568 protein-coding genes of 134 sequenced archaeal genomes in the context of their homologues from 1,847 reference bacterial genomes. Archaeal-specific gene families define 13 traditionally recognized archaeal higher taxa in our sample. Here we report that the origins of these 13 groups unexpectedly correspond to 2,264 group-specific gene acquisitions from bacteria. Interdomain gene transfer is highly asymmetric, transfers from bacteria to archaea are more than fivefold more frequent than vice versa. Gene transfers identified at major evolutionary transitions among prokaryotes specifically implicate gene acquisitions for metabolic functions from bacteria as key innovations in the origin of higher archaeal taxa.

Indexed as

Evolution, MolecularArchaeaArchaeal ProteinsBacteriaGenes, ArchaealGenes, BacterialGene Transfer, HorizontalGenome, ArchaealPhylogenyArchaeal Proteins

Identifiers

PMID25317564
PMCPMC4285555
OpenAlexW1966317059

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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.