Evidence map›Paper›PMID 36148939›Full record

ArticleEvolution; international journal of organic evolution2022

Meiotic drive is associated with sexual incompatibility in Neurospora.

Aaron A Vogan, Jesper Svedberg, Magdalena Grudzinska-Sterno, Hanna Johannesson

Abstract read
In one paragraph

Article in Evolution; international journal of organic evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Molecular Mechanisms and Evolutionary Consequences of Spore Killers in Ascomycetes.Microbiology and molecular biology reviews : MMBR · 2021
    Review
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.

Aaron A VoganDepartment of Organismal Biology, Uppsala University, Uppsala, SE-75236, Sweden.ORCID 0000-0003-2013-7445
Jesper SvedbergDepartment of Organismal Biology, Uppsala University, Uppsala, SE-75236, Sweden.ORCID 0000-0002-0951-3019
Magdalena Grudzinska-SternoDepartment of Organismal Biology, Uppsala University, Uppsala, SE-75236, Sweden.
Hanna JohannessonDepartment of Organismal Biology, Uppsala University, Uppsala, SE-75236, Sweden.ORCID 0000-0001-6359-9856

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evolution of Bateson-Dobzhansky-Muller (BDM) incompatibilities is thought to represent a key step in the formation of separate species. They are incompatible alleles that have evolved in separate populations and are exposed in hybrid offspring as hybrid sterility or lethality. In this study, we reveal a previously unconsidered mechanism promoting the formation of BDM incompatibilities, meiotic drive. Theoretical studies have evaluated the role that meiotic drive, the phenomenon whereby selfish elements bias their transmission to progeny at ratios above 50:50, plays in speciation, and have mostly concluded that drive could not result in speciation on its own. Using the model fungus Neurospora, we demonstrate that the large meiotic drive haplotypes, Sk-2 and Sk-3, contain putative sexual incompatibilities. Our experiments revealed that although crosses between Neurospora intermedia and Neurospora metzenbergii produce viable progeny at appreciable rates, when strains of N. intermedia carry Sk-2 or Sk-3 the proportion of viable progeny drops substantially. Additionally, it appears that Sk-2 and Sk-3 have accumulated different incompatibility phenotypes, consistent with their independent evolutionary history. This research illustrates how meiotic drive can contribute to reproductive isolation between populations, and thereby speciation.

Indexed as

NeurosporaAllelesPhenotypeReproductive IsolationBateson-Dobzhansky-Muller incompatibilitymeiotic driveNeurosporasexual incompatibilityspeciation

Identifiers

PMID36148939
PMCPMC9828778

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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.