Evidence map›Paper›PMID 31665510›Full record

ArticleMolecular biology and evolution2020

Molecular Diversification of the Seminal Fluid Proteome in a Recently Diverged Passerine Species Pair.

Melissah Rowe, Emma Whittington, Kirill Borziak, Mark Ravinet, Fabrice Eroukhmanoff, Glenn-Peter Sætre, Steve Dorus

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Molecular biology and evolution, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.0field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

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  17. Nonadaptive molecular evolution of seminal fluid proteins in Drosophila.Evolution; international journal of organic evolution · 2021
    Article
  18. Article
  19. Article
  20. Seminal fluid and accessory male investment in sperm competition.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    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 2 institutions in 3 countries.

Melissah RoweNatural History Museum, University of Oslo, Oslo, Norway.
Emma WhittingtonCenter for Reproductive Evolution, Department of Biology, Syracuse University, Syracuse, NY.
Kirill BorziakCenter for Reproductive Evolution, Department of Biology, Syracuse University, Syracuse, NY.
Mark RavinetCentre for Ecological and Evolutionary Synthesis, Department of Biosciences, University of Oslo, Oslo, Norway.
Fabrice EroukhmanoffCentre for Ecological and Evolutionary Synthesis, Department of Biosciences, University of Oslo, Oslo, Norway.
Glenn-Peter SætreCentre for Ecological and Evolutionary Synthesis, Department of Biosciences, University of Oslo, Oslo, Norway.
Steve DorusCenter for Reproductive Evolution, Department of Biology, Syracuse University, Syracuse, NY.
University of Oslo · NOSyracuse University · US

Funding

Sperm Motility and Molecular Interactions in the Reproductive Tract R21HD088910 · NICHD · SYRACUSE UNIVERSITY · PI DORUS, STEPHEN · 2017 to 2018
$433k
NICHD NIH HHS R21 HD088910
6 · The paper itself

Abstract

Seminal fluid proteins (SFPs) mediate an array of postmating reproductive processes that influence fertilization and fertility. As such, it is widely held that SFPs may contribute to postmating, prezygotic reproductive barriers between closely related taxa. We investigated seminal fluid (SF) diversification in a recently diverged passerine species pair (Passer domesticus and Passer hispaniolensis) using a combination of proteomic and comparative evolutionary genomic approaches. First, we characterized and compared the SF proteome of the two species, revealing consistencies with known aspects of SFP biology and function in other taxa, including the presence and diversification of proteins involved in immunity and sperm maturation. Second, using whole-genome resequencing data, we assessed patterns of genomic differentiation between house and Spanish sparrows. These analyses detected divergent selection on immunity-related SF genes and positive selective sweeps in regions containing a number of SF genes that also exhibited protein abundance diversification between species. Finally, we analyzed the molecular evolution of SFPs across 11 passerine species and found a significantly higher rate of positive selection in SFPs compared with the rest of the genome, as well as significant enrichments for functional pathways related to immunity in the set of positively selected SF genes. Our results suggest that selection on immunity pathways is an important determinant of passerine SF composition and evolution. Assessing the role of immunity genes in speciation in other recently diverged taxa should be prioritized given the potential role for immunity-related proteins in reproductive incompatibilities in Passer sparrows.

Indexed as

AnimalsAvian ProteinsEvolution, MolecularGene Regulatory NetworksGenetic SpeciationImmunityMalePhylogenyProteomicsSparrowsSpermatozoaWhole Genome SequencingAvian Proteinscryptic female choicefertilityimmunitypositive selectionreproductionselective sweepsperm competition

Identifiers

PMID31665510
PMCPMC6993853
OpenAlexW2982434468

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.