Evidence map›Paper›PMID 32773032›Full record

ArticleeLife2020

Genomic architecture and evolutionary antagonism drive allelic expression bias in the social supergene of red fire ants.

Carlos Martinez-Ruiz, Rodrigo Pracana, Eckart Stolle, Carolina Ivon Paris, Richard A Nichols, Yannick Wurm

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Functional genetic elements of a butterfly mimicry supergene.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Radiation and hybridization underpin the spread of the fire ant social supergene.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  10. Iterative evolution of supergene-based social polymorphism in ants.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. A neutral model for the loss of recombination on sex chromosomes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2021
    Article
  15. Review
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Carlos Martinez-RuizSchool of Biological and Chemical Sciences, Queen Mary University of London, London, United Kingdom.ORCID https://orcid.org/0000-0002-4817-0565
Rodrigo PracanaSchool of Biological and Chemical Sciences, Queen Mary University of London, London, United Kingdom.
Eckart StolleSchool of Biological and Chemical Sciences, Queen Mary University of London, London, United Kingdom.
Carolina Ivon ParisDepartamento Ecología, Genética y Evolución, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Intendente Güiraldes 2160, Ciudad Universitaria, Buenos Aires, Argentina.
Richard A NicholsSchool of Biological and Chemical Sciences, Queen Mary University of London, London, United Kingdom.
Yannick WurmSchool of Biological and Chemical Sciences, Queen Mary University of London, London, United Kingdom.ORCID https://orcid.org/0000-0002-3140-2809
Queen Mary University of London · GBUniversidad de Buenos Aires · AR

Funding

BBSRC BB/K004204/1DAAD 570704 83European Commission Marie Curie Actions PIEF-GA-2013-623713NERC NE/L002485/1NERC NE/L00626X/1
6 · The paper itself

Abstract

Supergene regions maintain alleles of multiple genes in tight linkage through suppressed recombination. Despite their importance in determining complex phenotypes, our empirical understanding of early supergene evolution is limited. Here we focus on the young 'social' supergene of fire ants, a powerful system for disentangling the effects of evolutionary antagonism and suppressed recombination. We hypothesize that gene degeneration and social antagonism shaped the evolution of the fire ant supergene, resulting in distinct patterns of gene expression. We test these ideas by identifying allelic differences between supergene variants, characterizing allelic expression across populations, castes and body parts, and contrasting allelic expression biases with differences in expression between social forms. We find strong signatures of gene degeneration and gene-specific dosage compensation. On this background, a small portion of the genes has the signature of adaptive responses to evolutionary antagonism between social forms.

Indexed as

AntsSocial BehaviorAllelesAnimalsBehavior, AnimalBiological EvolutionChromosomesEvolution, MolecularGene ExpressionGenomicsSelection, Geneticallele-specific expressionantagonistic selectionantschromosomesevolutionary biologygene expressionsocial evolutionSolenopsis invictasupergenes

Identifiers

PMID32773032
PMCPMC7476760
OpenAlexW3048101824

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.