Evidence map›Paper›PMID 30523653›Full record

ArticleJournal of evolutionary biology2019

Sexually dimorphic gene expression and transcriptome evolution provide mixed evidence for a fast-Z effect in Heliconius.

Ana Pinharanda, Marjolaine Rousselle, Simon H Martin, Joe J Hanly, John W Davey, Sujai Kumar, Nicolas Galtier, Chris D Jiggins

Abstract read
In one paragraph

Article in Journal of evolutionary biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Reconciling theories of dominance with the relative rates of adaptive substitution on sex chromosomes and autosomes.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  10. Neural divergence and hybrid disruption between ecologically isolatedProceedings of the National Academy of Sciences of the United States of America · 2021
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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

8 authors.

Ana PinharandaDepartment of Zoology, University of Cambridge, Cambridge, UK.ORCID 0000-0002-4696-9218
Marjolaine RousselleUMR 5554 Institut des Sciences de l'Evolution, CNRS, IRD, EPHE, Université de Montpellier, Montpellier, France.
Simon H MartinDepartment of Zoology, University of Cambridge, Cambridge, UK.
Joe J HanlyDepartment of Zoology, University of Cambridge, Cambridge, UK.
John W DaveyDepartment of Zoology, University of Cambridge, Cambridge, UK.
Sujai KumarInstitute of Evolutionary Biology, University of Edinburgh, Edinburgh, UK.
Nicolas GaltierDepartment of Ecology and Evolutionary Biology and Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, New Jersey.
Chris D JigginsDepartment of Zoology, University of Cambridge, Cambridge, UK.ORCID 0000-0002-7809-062X

Funding

Biotechnology and Biological Sciences Research Council BB/K020161/1Wellcome Trust
6 · The paper itself

Abstract

Sex chromosomes have different evolutionary properties compared to autosomes due to their hemizygous nature. In particular, recessive mutations are more readily exposed to selection, which can lead to faster rates of molecular evolution. Here, we report patterns of gene expression and molecular evolution for a group of butterflies. First, we improve the completeness of the Heliconius melpomene reference annotation, a neotropical butterfly with a ZW sex determination system. Then, we analyse RNA from male and female whole abdomens and sequence female ovary and gut tissue to identify sex- and tissue-specific gene expression profiles in H. melpomene. Using these expression profiles, we compare (a) sequence divergence and polymorphism; (b) the strength of positive and negative selection; and (c) rates of adaptive evolution, for Z and autosomal genes between two species of Heliconius butterflies, H. melpomene and H. erato. We show that the rate of adaptive substitutions is higher for Z than autosomal genes, but contrary to expectation, it is also higher for male-biased than female-biased genes. Additionally, we find no significant increase in the rate of adaptive evolution or purifying selection on genes expressed in ovary tissue, a heterogametic-specific tissue. Our results contribute to a growing body of literature from other ZW systems that also provide mixed evidence for a fast-Z effect where hemizygosity influences the rate of adaptive substitutions.

Indexed as

Adaptation, BiologicalEvolution, MolecularSelection, GeneticSex ChromosomesAnimalsButterfliesFemaleGastrointestinal TractGene ExpressionMaleOvarySex CharacteristicsTranscriptomegene expressiongenomicsinsectsmolecular evolutionsex chromosomes

Identifiers

PMID30523653
PMCPMC6850379

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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.