Evidence map›Paper›PMID 25136088›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2014

Introgression in hybrid ants is favored in females but selected against in males.

Jonna Kulmuni, Pekka Pamilo

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
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  5. Review
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  9. Article
  10. Species recognition limits mating between hybridizing ant species.Evolution; international journal of organic evolution · 2022
    Article
  11. Article
  12. Linked supergenes underlie split sex ratio and social organization in an ant.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Sexually antagonistic selection promotes genetic divergence between males and females in an ant.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  17. Hybridization increases population variation during adaptive radiation.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  18. Building a new research framework for social evolution: intralocus caste antagonism.Biological reviews of the Cambridge Philosophical Society · 2018
    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

2 authors at 2 institutions in 1 country.

Jonna KulmuniDepartment of Biosciences, Centre of Excellence in Biological Interactions and Tvärminne Zoological Station, Faculty of Biological and Environmental Sciences, University of Helsinki, 00014, Helsinki, Finland; and Department of Biology and Biocenter Oulu, University of Oulu, 90014, Oulu, Finland jonna.kulmuni@helsinki.fi.
Pekka PamiloDepartment of Biosciences, Centre of Excellence in Biological Interactions and Tvärminne Zoological Station, Faculty of Biological and Environmental Sciences, University of Helsinki, 00014, Helsinki, Finland; and.
University of Helsinki · FIUniversity of Oulu · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hybridization is not a mere reproductive dead end but has been suggested to play a central role in speciation, for example, by introducing adaptive genetic variation. Our previous study uncovered a unique consequence of hybridization in Formica ants. In a population including two isolated but partially introgressed genetic groups, the females have an apparent hybrid background, whereas the males do not. This situation results in large-scale differences between male and female genomes that are stable throughout generations. Here, we compare genotypes from different developmental stages to investigate how sex-specific introgression and genetic differences between sexes are maintained. We show that strong selection rather than sex-dependent transmission maintains the genetic differences between sexes. All genotype combinations are produced and observed in the eggs of both sexes, but the alleles acquired through hybridization disappear from the haploid males during development from egg to adult as their frequencies drop toward zero. However, the same introgressed alleles increase in frequency and are favored when heterozygous in the females. Genotypes eliminated from males most likely represent incompatibilities arising from hybridization. Our results show an unusual situation of opposite selection, where introgression is favored in diploid females but selected against in haploid males. This finding suggests that introgressed genomic regions harbor both fitness-enhancing and -reducing elements. Our work highlights the complex consequences of hybridization and provides a rare opportunity to observe natural selection in real time in nature.

Indexed as

Models, GeneticSelection, GeneticAnimalsAntsFemaleGenetic SpeciationGenomicsGenotypeHybridization, GeneticMaleReproductionSex Determination Processesadaptive introgressionHaldane's rulehaplodiploidHymenopteraspeciation continuum

Identifiers

PMID25136088
PMCPMC4156693
OpenAlexW1989721017

What OpenQuestion holds

Textmetadata
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.