Evidence map›Paper›PMID 31225876›Full record

ArticleMolecular biology and evolution2019

Ancestral Admixture Is the Main Determinant of Global Biodiversity in Fission Yeast.

Sergio Tusso, Bart P S Nieuwenhuis, Fritz J Sedlazeck, John W Davey, Daniel C Jeffares, Jochen B W Wolf

Abstract read
In one paragraph

Article in Molecular biology and evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

  1. Article
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  7. Review
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  9. Article
  10. The Fission Yeast Mating-Type Switching Motto: "One-for-Two" and "Two-for-One".Microbiology and molecular biology reviews : MMBR · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Article
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  18. Molecular Mechanisms and Evolutionary Consequences of Spore Killers in Ascomycetes.Microbiology and molecular biology reviews : MMBR · 2021
    Review
  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

6 authors.

Sergio TussoDivision of Evolutionary Biology, Faculty of Biology, LMU Munich, Planegg-Martinsried, Germany.
Bart P S NieuwenhuisDivision of Evolutionary Biology, Faculty of Biology, LMU Munich, Planegg-Martinsried, Germany.
Fritz J SedlazeckHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX.
John W DaveyBioscience Technology Facility, Department of Biology, University of York, York, United Kingdom.
Daniel C JeffaresDepartment of Biology, University of York, York, United Kingdom.
Jochen B W WolfDivision of Evolutionary Biology, Faculty of Biology, LMU Munich, Planegg-Martinsried, Germany.

Funding

Genomic Architecture of Common Disease in Diverse Populations: WGS of Ongoing Hemorrhagic Stroke Study SupplementUM1HG008898 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A · 2016 to 2020
$77.0M
NHGRI NIH HHS UM1 HG008898
6 · The paper itself

Abstract

Mutation and recombination are key evolutionary processes governing phenotypic variation and reproductive isolation. We here demonstrate that biodiversity within all globally known strains of Schizosaccharomyces pombe arose through admixture between two divergent ancestral lineages. Initial hybridization was inferred to have occurred ∼20-60 sexual outcrossing generations ago consistent with recent, human-induced migration at the onset of intensified transcontinental trade. Species-wide heritable phenotypic variation was explained near-exclusively by strain-specific arrangements of alternating ancestry components with evidence for transgressive segregation. Reproductive compatibility between strains was likewise predicted by the degree of shared ancestry. To assess the genetic determinants of ancestry block distribution across the genome, we characterized the type, frequency, and position of structural genomic variation using nanopore and single-molecule real-time sequencing. Despite being associated with double-strand break initiation points, over 800 segregating structural variants exerted overall little influence on the introgression landscape or on reproductive compatibility between strains. In contrast, we found strong ancestry disequilibrium consistent with negative epistatic selection shaping genomic ancestry combinations during the course of hybridization. This study provides a detailed, experimentally tractable example that genomes of natural populations are mosaics reflecting different evolutionary histories. Exploiting genome-wide heterogeneity in the history of ancestral recombination and lineage-specific mutations sheds new light on the population history of S. pombe and highlights the importance of hybridization as a creative force in generating biodiversity.

Indexed as

Genetic VariationHybridization, GeneticEpistasis, GeneticGenomic Structural VariationReproductive IsolationSchizosaccharomycesWhole Genome Sequencingepistasishybridizationreproductive isolationSchizosaccharomyces pombestructural variationtransgression

Identifiers

PMID31225876
PMCPMC6736153

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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.