Evidence map›Paper›PMID 27175796›Full record

ArticleBMC evolutionary biology2016

Sexually antagonistic selection on genetic variation underlying both male and female same-sex sexual behavior.

David Berger, Tao You, Maravillas R Minano, Karl Grieshop, Martin I Lind, Göran Arnqvist, Alexei A Maklakov

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
13.2field-weighted citation impact, top 2% 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

14 citing papers in PubMed, 42 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

David BergerAnimal Ecology, Department of Ecology and Genetics, Uppsala University, Evolutionary Biology Centre, Norbyvägen 18D, 75105, Uppsala, Sweden. david.berger@ebc.uu.se.
Tao YouAnimal Ecology, Department of Ecology and Genetics, Uppsala University, Evolutionary Biology Centre, Norbyvägen 18D, 75105, Uppsala, Sweden.
Maravillas R MinanoAnimal Ecology, Department of Ecology and Genetics, Uppsala University, Evolutionary Biology Centre, Norbyvägen 18D, 75105, Uppsala, Sweden.
Karl GrieshopAnimal Ecology, Department of Ecology and Genetics, Uppsala University, Evolutionary Biology Centre, Norbyvägen 18D, 75105, Uppsala, Sweden.
Martin I LindAnimal Ecology, Department of Ecology and Genetics, Uppsala University, Evolutionary Biology Centre, Norbyvägen 18D, 75105, Uppsala, Sweden.
Göran ArnqvistAnimal Ecology, Department of Ecology and Genetics, Uppsala University, Evolutionary Biology Centre, Norbyvägen 18D, 75105, Uppsala, Sweden.
Alexei A MaklakovAnimal Ecology, Department of Ecology and Genetics, Uppsala University, Evolutionary Biology Centre, Norbyvägen 18D, 75105, Uppsala, Sweden.
Uppsala University · SE

Funding

European Research Council 294333
6 · The paper itself

Abstract

backgroundIntralocus sexual conflict, arising from selection for different alleles at the same locus in males and females, imposes a constraint on sex-specific adaptation. Intralocus sexual conflict can be alleviated by the evolution of sex-limited genetic architectures and phenotypic expression, but pleiotropic constraints may hinder this process. Here, we explored putative intralocus sexual conflict and genetic (co)variance in a poorly understood behavior with near male-limited expression. Same-sex sexual behaviors (SSBs) generally do not conform to classic evolutionary models of adaptation but are common in male animals and have been hypothesized to result from perception errors and selection for high male mating rates. However, perspectives incorporating sex-specific selection on genes shared by males and females to explain the expression and evolution of SSBs have largely been neglected.

resultsWe performed two parallel sex-limited artificial selection experiments on SSB in male and female seed beetles, followed by sex-specific assays of locomotor activity and male sex recognition (two traits hypothesized to be functionally related to SSB) and adult reproductive success (allowing us to assess fitness consequences of genetic variance in SSB and its correlated components). Our experiments reveal both shared and sex-limited genetic variance for SSB. Strikingly, genetically correlated responses in locomotor activity and male sex-recognition were associated with sexually antagonistic fitness effects, but these effects differed qualitatively between male and female selection lines, implicating intralocus sexual conflict at both male- and female-specific genetic components underlying SSB.

conclusionsOur study provides experimental support for the hypothesis that widespread pleiotropy generates pervasive intralocus sexual conflict governing the expression of SSBs, suggesting that SSB in one sex can occur due to the expression of genes that carry benefits in the other sex.

Indexed as

AllelesAnimalsColeopteraEvolution, MolecularFemaleGenes, InsectGenetic PleiotropyGenetic VariationMalePhenotypeReproductionSelection, GeneticSex CharacteristicsSexual BehaviorArtificial selectionBehavioral syndromeB-matrixGenetic constraintsIntralocus sexual conflictMating strategyPleiotropySame-sex sexual behaviorSexual antagonismSexual selection

Identifiers

PMID27175796
PMCPMC4866275
OpenAlexW2343203922

What OpenQuestion holds

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LicenceCC BY
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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.