Evidence map›Paper›PMID 30649313›Full record

ArticleGenome biology and evolution2019

Repeated Evolution Versus Common Ancestry: Sex Chromosome Evolution in the Haplochromine Cichlid Pseudocrenilabrus philander.

Astrid Böhne, Alexandra Anh-Thu Weber, Jelena Rajkov, Michael Rechsteiner, Andrin Riss, Bernd Egger, Walter Salzburger

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Rapid turnover of sex-determining architecture in invasive mussels.bioRxiv : the preprint server for biology · 2026
    Article
  4. Sex Chromosome Evolution: Hallmarks and Question Marks.Molecular biology and evolution · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Repeated translocation of a supergene underlying rapid sex chromosome turnover inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Gene Variant ofInternational journal of molecular sciences · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. Disagreement in FMolecular ecology resources · 2020
    Article
  19. 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

7 authors at 1 institution in 2 countries.

Astrid BöhneDepartment of Environmental Sciences, Zoological Institute, University of Basel, Switzerland.
Alexandra Anh-Thu WeberDepartment of Environmental Sciences, Zoological Institute, University of Basel, Switzerland.
Jelena RajkovDepartment of Environmental Sciences, Zoological Institute, University of Basel, Switzerland.
Michael RechsteinerDepartment of Environmental Sciences, Zoological Institute, University of Basel, Switzerland.
Andrin RissDepartment of Environmental Sciences, Zoological Institute, University of Basel, Switzerland.
Bernd EggerDepartment of Environmental Sciences, Zoological Institute, University of Basel, Switzerland.
Walter SalzburgerDepartment of Environmental Sciences, Zoological Institute, University of Basel, Switzerland.
University of Basel · CH

Funding

European Research Council 617585
6 · The paper itself

Abstract

Why sex chromosomes turn over and remain undifferentiated in some taxa, whereas they degenerate in others, is still an area of ongoing research. The recurrent occurrence of homologous and homomorphic sex chromosomes in distantly related taxa suggests their independent evolution or continued recombination since their first emergence. Fishes display a great diversity of sex-determining systems. Here, we focus on sex chromosome evolution in haplochromines, the most species-rich lineage of cichlid fishes. We investigate sex-specific signatures in the Pseudocrenilabrus philander species complex, which belongs to a haplochromine genus found in many river systems and ichthyogeographic regions in northern, eastern, central, and southern Africa. Using whole-genome sequencing and population genetic, phylogenetic, and read-coverage analyses, we show that one population of P. philander has an XX-XY sex-determining system on LG7 with a large region of suppressed recombination. However, in a second bottlenecked population, we did not find any sign of a sex chromosome. Interestingly, LG7 also carries an XX-XY system in the phylogenetically more derived Lake Malawi haplochromine cichlids. Although the genomic regions determining sex are the same in Lake Malawi cichlids and P. philander, we did not find evidence for shared ancestry, suggesting that LG7 evolved as sex chromosome at least twice in haplochromine cichlids. Hence, our work provides further evidence for the labile nature of sex determination in fishes and supports the hypothesis that the same genomic regions can repeatedly and rapidly be recruited as sex chromosomes in more distantly related lineages.

Indexed as

Biological EvolutionSex ChromosomesSex Determination ProcessesAnimalsCichlidsFemaleMalegenome sequencingpopulation geneticssex determinationspeciationspecies complexteleost fish

Identifiers

PMID30649313
PMCPMC6375353
OpenAlexW2910400275

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.