Evidence map›Paper›PMID 35344560›Full record

ArticlePLoS genetics2022

Imbalanced segregation of recombinant haplotypes in hybrid populations reveals inter- and intrachromosomal Dobzhansky-Muller incompatibilities.

Juan Li, Molly Schumer, Claudia Bank

Abstract read
In one paragraph

Article in PLoS genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

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0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. The Ecology of Hybrid Incompatibilities.Cold Spring Harbor perspectives in biology · 2024
    Review
  10. Fisher's Geometric Model as a Tool to Study Speciation.Cold Spring Harbor perspectives in biology · 2024
    Review
  11. Article
  12. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Juan LiInstitute of Ecology and Evolution, University of Bern, Bern, Switzerland.ORCID 0000-0003-2643-0802
Molly SchumerDepartment of Biology, Stanford University, Stanford, California, United States of America.ORCID 0000-0002-2075-5668
Claudia BankInstitute of Ecology and Evolution, University of Bern, Bern, Switzerland.ORCID 0000-0003-4730-758X

Funding

The population genomics of hybridization: from genetic incompatibilities to genome evolutionR35GM133774 · NIGMS · STANFORD UNIVERSITY · PI Molly Schumer · 2019 to 2026
$3.3M
NIGMS NIH HHS R35 GM133774
6 · The paper itself

Abstract

Dobzhansky-Muller incompatibilities (DMIs) are a major component of reproductive isolation between species. DMIs imply negative epistasis and are exposed when two diverged populations hybridize. Mapping the locations of DMIs has largely relied on classical genetic mapping. Approaches to date are hampered by low power and the challenge of identifying DMI loci on the same chromosome, because strong initial linkage of parental haplotypes weakens statistical tests. Here, we propose new statistics to infer negative epistasis from haplotype frequencies in hybrid populations. When two divergent populations hybridize, the variance in heterozygosity at two loci decreases faster with time at DMI loci than at random pairs of loci. When two populations hybridize at near-even admixture proportions, the deviation of the observed variance from its expectation becomes negative for the DMI pair. This negative deviation enables us to detect intermediate to strong negative epistasis both within and between chromosomes. In practice, the detection window in hybrid populations depends on the demographic scenario, the recombination rate, and the strength of epistasis. When the initial proportion of the two parental populations is uneven, only strong DMIs can be detected with our method unless migration prevents parental haplotypes from being lost. We use the new statistics to infer candidate DMIs from three hybrid populations of swordtail fish. We identify numerous new DMI candidates, some of which are inferred to interact with several loci within and between chromosomes. Moreover, we discuss our results in the context of an expected enrichment in intrachromosomal over interchromosomal DMIs.

Indexed as

Genetic SpeciationModels, GeneticAnimalsHaplotypesHeterozygoteHybridization, GeneticReproductive Isolation

Identifiers

PMID35344560
PMCPMC8989332

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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.