Evidence map›Paper›PMID 29048573›Full record

ArticleMolecular biology and evolution2018

The Rate of Evolution of Postmating-Prezygotic Reproductive Isolation in Drosophila.

David A Turissini, Joseph A McGirr, Sonali S Patel, Jean R David, Daniel R Matute

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
11.9field-weighted citation impact, top 1% 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

47 citing papers in PubMed, 117 citations in OpenAlex.

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  7. Regional specialization, polyploidy, and seminal fluid transcripts in theProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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

5 authors at 2 institutions in 2 countries.

David A TurissiniDepartment of Biology, University of North Carolina, Chapel Hill, NC.
Joseph A McGirrDepartment of Biology, University of North Carolina, Chapel Hill, NC.
Sonali S PatelDepartment of Biology, University of North Carolina, Chapel Hill, NC.
Jean R DavidLaboratoire Evolution, Génomes, Comportement, Ecologie (EGCE) CNRS, IRD, Univ. Paris-sud, Université Paris-Saclay, 91198 Gif sur Yvette, France.
Daniel R MatuteDepartment of Biology, University of North Carolina, Chapel Hill, NC.
University of North Carolina at Chapel Hill · USCentre National de la Recherche Scientifique · FR

Funding

The prevalence of genetic introgression in speciationR01GM121750 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MATUTE, DANIEL · 2017 to 2021
$1.7M
NIGMS NIH HHS R01 GM121750
6 · The paper itself

Abstract

Reproductive isolation is an intrinsic aspect of species formation. For that reason, the identification of the precise isolating traits, and the rates at which they evolve, is crucial to understanding how species originate and persist. Previous work has measured the rates of evolution of prezygotic and postzygotic barriers to gene flow, yet no systematic analysis has studied the rates of evolution of postmating-prezygotic (PMPZ) barriers. We measured the magnitude of two barriers to gene flow that act after mating occurs but before fertilization. We also measured the magnitude of a premating barrier (female mating rate in nonchoice experiments) and two postzygotic barriers (hybrid inviability and hybrid sterility) for all pairwise crosses of all nine known extant species within the melanogaster subgroup. Our results indicate that PMPZ isolation evolves faster than hybrid inviability but slower than premating isolation. Next, we partition postzygotic isolation into different components and find that, as expected, hybrid sterility evolves faster than hybrid inviability. These results lend support for the hypothesis that, in Drosophila, reproductive isolation mechanisms (RIMs) that act early in reproduction (or in development) tend to evolve faster than those that act later in the reproductive cycle. Finally, we tested whether there was evidence for reinforcing selection at any RIM. We found no evidence for generalized evolution of reproductive isolation via reinforcement which indicates that there is no pervasive evidence of this evolutionary process. Our results indicate that PMPZ RIMs might have important evolutionary consequences in initiating speciation and in the persistence of new species.

Indexed as

Reproductive IsolationAnimalsDrosophilaFemaleHybridization, GeneticMalePhylogenyconspecific sperm precedenceDrosophilagenomic alignmenthybridspostmating-prezygotic isolationpostzygotic isolationpremating isolation

Identifiers

PMID29048573
PMCPMC5850467
OpenAlexW2952072815

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.