Evidence map›Paper›PMID 29703975›Full record

ArticleNature communications2018

Transporter gene acquisition and innovation in the evolution of Microsporidia intracellular parasites.

P Dean, K M Sendra, T A Williams, A K Watson, P Major, S Nakjang, E Kozhevnikova, A V Goldberg, E R S Kunji, R P Hirt and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 103 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Treatment of MicrosporidiumMicroorganisms · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Germination of Microsporidian Spores: The Known and Unknown.Journal of fungi (Basel, Switzerland) · 2023
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

P DeanInstitute for Cell & Molecular Biosciences, Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK. p.dean@ncl.ac.uk.
K M SendraInstitute for Cell & Molecular Biosciences, Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
T A WilliamsInstitute for Cell & Molecular Biosciences, Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.ORCID http://orcid.org/0000-0003-1072-0223
A K WatsonInstitute for Cell & Molecular Biosciences, Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
P MajorInstitute for Cell & Molecular Biosciences, Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
S NakjangInstitute for Cell & Molecular Biosciences, Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
E KozhevnikovaInstitute for Cell & Molecular Biosciences, Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
A V GoldbergInstitute for Cell & Molecular Biosciences, Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
E R S KunjiMedical Research Council Building, Mitochondrial Biology Unit, University of Cambridge, Cambridge Biomedical Campus, Hills Road, Cambridge, CB2 0XY, UK.
R P HirtInstitute for Cell & Molecular Biosciences, Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
T M EmbleyInstitute for Cell & Molecular Biosciences, Medical School, University of Newcastle upon Tyne, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK. martin.embley@ncl.ac.uk.ORCID http://orcid.org/0000-0002-1484-340X
Newcastle University · GBUniversity of Bristol · GBUniversity of Cambridge · GB

Funding

Medical Research Council MC_U105663139Medical Research Council MC_UU_00015/1Wellcome Trust
6 · The paper itself

Abstract

The acquisition of genes by horizontal transfer can impart entirely new biological functions and provide an important route to major evolutionary innovation. Here we have used ancient gene reconstruction and functional assays to investigate the impact of a single horizontally transferred nucleotide transporter into the common ancestor of the Microsporidia, a major radiation of intracellular parasites of animals and humans. We show that this transporter provided early microsporidians with the ability to steal host ATP and to become energy parasites. Gene duplication enabled the diversification of nucleotide transporter function to transport new substrates, including GTP and NAD

Indexed as

Evolution, MolecularGene Transfer, HorizontalAnimalsCell LineGene DuplicationGenome, FungalHost-Pathogen InteractionsMetabolic Networks and PathwaysMicrosporidiaNucleotidesNucleotide Transport ProteinsPhylogenyRabbitsNucleotidesNucleotide Transport Proteins

Identifiers

PMID29703975
PMCPMC5923384
OpenAlexW2800669284

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.