Evidence map›Paper›PMID 30690715›Full record

ArticleEvolution; international journal of organic evolution2019

Meiotic drive shapes rates of karyotype evolution in mammals.

Heath Blackmon, Joshua Justison, Itay Mayrose, Emma E Goldberg

Abstract read
In one paragraph

Article in Evolution; international journal of organic evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Article
  2. Rapid centromere turnover and the adaptive radiation of lemurs.bioRxiv : the preprint server for biology · 2026
    Article
  3. The evolutionary genomics of meiotic drive.Molecular biology and evolution · 2026
    Article
  4. Article
  5. Article
  6. Centromeres drive and take a break.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Fast satellite DNA evolution in Nothobranchius annual killifishes.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2023
    Article
  16. Review
  17. Article
  18. High-density linkage maps and chromosome level genome assemblies unveil direction and frequency of extensive structural rearrangements in wood white butterflies (Leptidea spp.).Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2023
    Article
  19. The Chromosome Counts Database (CCDB).Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  20. Using ChromEvol to Determine the Mode of Chromosomal Evolution.Methods in molecular biology (Clifton, N.J.) · 2023
    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

4 authors.

Heath BlackmonDepartment of Biology, Texas A&M University, College Station, Texas 77843.ORCID 0000-0002-5433-4036
Joshua JustisonDepartment of Ecology, Evolution, and Behavior, University of Minnesota, Saint Paul, Minnesota 55108.
Itay MayroseSchool of Plant Sciences and Food Security, Tel Aviv University, Tel Aviv 69978, Israel.
Emma E GoldbergDepartment of Ecology, Evolution, and Behavior, University of Minnesota, Saint Paul, Minnesota 55108.

Funding

United States-Israel Binational Science Foundation BSF-2013286
6 · The paper itself

Abstract

Chromosome number is perhaps the most basic characteristic of a genome, yet generalizations that can explain the evolution of this trait across large clades have remained elusive. Using karyotype data from over 1000 mammals, we developed and applied a phylogenetic model of chromosome evolution that links chromosome number changes with karyotype morphology. Using our model, we infer that rates of chromosome number evolution are significantly lower in species with karyotypes that consist of either all bibrachial or all monobrachial chromosomes than in species with a mix of both types of morphologies. We suggest that species with homogeneous karyotypes may represent cases where meiotic drive acts to stabilize the karyotype, favoring the chromosome morphologies already present in the genome. In contrast, rapid bouts of chromosome number evolution in taxa with mixed karyotypes may indicate that a switch in the polarity of female meiotic drive favors changes in chromosome number. We do not find any evidence that karyotype morphology affects rates of speciation or extinction. Furthermore, we document that switches in meiotic drive polarity are likely common and have occurred in most major clades of mammals, and that rapid remodeling of karyotypes may be more common than once thought.

Indexed as

Biological EvolutionKaryotypeMeiosisAnimalsFemaleMammalsModels, GeneticChromosome numbermeiosismeiotic driveprobabilistic phylogenetic models

Identifiers

PMID30690715
PMCPMC6590138

What OpenQuestion holds

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LicenceCC BY-NC
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.