Evidence map›Paper›PMID 20874735›Full record

ArticleEvolution; international journal of organic evolution2010

Sex linkage, sex-specific selection, and the role of recombination in the evolution of sexually dimorphic gene expression.

Tim Connallon, Andrew G Clark

Open access · greenAbstract read
In one paragraph

Article in Evolution; international journal of organic evolution, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
4.4field-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

69 citing papers in PubMed, 123 citations in OpenAlex.

  1. Article
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  6. Article
  7. On the resolution of sexual conflict over shared traits.Proceedings. Biological sciences · 2024
    Review
  8. Review
  9. Polygenic response of sex chromosomes to sexual antagonism.Evolution; international journal of organic evolution · 2024
    Article
  10. Article
  11. Article
  12. Intrinsic emergence and modulation of sex-specific dominance reversals in threshold traits.Evolution; international journal of organic evolution · 2022
    Article
  13. Article
  14. Searching for signatures of sexually antagonistic selection on stickleback sex chromosomes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  15. Article
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9 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Tim ConnallonDepartment of Molecular Biology & Genetics, Cornell University, Ithaca, New York 14853-2703, USA. tmc233@cornell.edu
Andrew G Clark
Cornell University · US

Funding

Molecular Evolution of Drosophila Y ChromosomeR01GM064590 · NIGMS · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI CARVALHO, ANTONIO BERNARDO, CLARK, ANDREW G · 2002 to 2012
$2.0M
NIGMS NIH HHS GM64590NIGMS NIH HHS R01 GM064590
6 · The paper itself

Abstract

Sex-biased genes--genes that are differentially expressed within males and females--are nonrandomly distributed across animal genomes, with sex chromosomes and autosomes often carrying markedly different concentrations of male- and female-biased genes. These linkage patterns are often gene- and lineage-dependent, differing between functional genetic categories and between species. Although sex-specific selection is often hypothesized to shape the evolution of sex-linked and autosomal gene content, population genetics theory has yet to account for many of the gene- and lineage-specific idiosyncrasies emerging from the empirical literature. With the goal of improving the connection between evolutionary theory and a rapidly growing body of genome-wide empirical studies, we extend previous population genetics theory of sex-specific selection by developing and analyzing a biologically informed model that incorporates sex linkage, pleiotropy, recombination, and epistasis, factors that are likely to vary between genes and between species. Our results demonstrate that sex-specific selection and sex-specific recombination rates can generate, and are compatible with, the gene- and species-specific linkage patterns reported in the genomics literature. The theory suggests that sexual selection may strongly influence the architectures of animal genomes, as well as the chromosomal distribution of fixed substitutions underlying sexually dimorphic traits.

Indexed as

Gene ExpressionModels, BiologicalSex CharacteristicsAnimalsEpistasis, GeneticFemaleGenetic LinkageGenetic PleiotropyGenetics, PopulationMaleMating Preference, AnimalRecombination, Genetic

Identifiers

PMID20874735
PMCPMC2998557
OpenAlexW1590291211

What OpenQuestion holds

Textmetadata
LicenceTDM
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.