Evidence map›Paper›PMID 27149698›Full record

ArticlePLoS genetics2016

The Genomic Basis of Evolutionary Innovation in Pseudomonas aeruginosa.

Macarena Toll-Riera, Alvaro San Millan, Andreas Wagner, R Craig MacLean

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Evolution Under Thermal Stress AffectsbioRxiv : the preprint server for biology · 2024
    Article
  4. Analysis of soft rotFrontiers in microbiology · 2024
    Article
  5. Experimental evolution for cell biology.Trends in cell biology · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Co-evolutionary adaptations ofEvolutionary applications · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Experimental Evolution of Innovation and Novelty.Trends in ecology & evolution · 2019
    Review
  17. Article
  18. Article
  19. 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

4 authors at 2 institutions in 3 countries.

Macarena Toll-RieraDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
Alvaro San MillanDepartment of Zoology, University of Oxford, Oxford, United Kingdom.ORCID 0000-0001-8544-0387
Andreas WagnerInstitute of Evolutionary Biology and Environmental Studies, University of Zurich, Zürich, Switzerland.
R Craig MacLeanDepartment of Zoology, University of Oxford, Oxford, United Kingdom.
SIB Swiss Institute of Bioinformatics · CHUniversity of Oxford · GB

Funding

Medical Research Council G0900747Medical Research Council G090074791070Wellcome TrustWellcome Trust 090532/Z/09/Z
6 · The paper itself

Abstract

Novel traits play a key role in evolution, but their origins remain poorly understood. Here we address this problem by using experimental evolution to study bacterial innovation in real time. We allowed 380 populations of Pseudomonas aeruginosa to adapt to 95 different carbon sources that challenged bacteria with either evolving novel metabolic traits or optimizing existing traits. Whole genome sequencing of more than 80 clones revealed profound differences in the genetic basis of innovation and optimization. Innovation was associated with the rapid acquisition of mutations in genes involved in transcription and metabolism. Mutations in pre-existing duplicate genes in the P. aeruginosa genome were common during innovation, but not optimization. These duplicate genes may have been acquired by P. aeruginosa due to either spontaneous gene amplification or horizontal gene transfer. High throughput phenotype assays revealed that novelty was associated with increased pleiotropic costs that are likely to constrain innovation. However, mutations in duplicate genes with close homologs in the P. aeruginosa genome were associated with low pleiotropic costs compared to mutations in duplicate genes with distant homologs in the P. aeruginosa genome, suggesting that functional redundancy between duplicates facilitates innovation by buffering pleiotropic costs.

Indexed as

Evolution, MolecularGenomicsGene DuplicationGenetic PleiotropyGene Transfer, HorizontalGenome, BacterialMutationPseudomonas aeruginosaPseudomonas InfectionsTranscription, Genetic

Identifiers

PMID27149698
PMCPMC4858143
OpenAlexW2347123991

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.