Evidence map›Paper›PMID 31518398›Full record

ArticleGenome biology and evolution2019

Comparative Transcriptomics Provides Insights into Reticulate and Adaptive Evolution of a Butterfly Radiation.

Wei Zhang, Brian X Leon-Ricardo, Bas van Schooten, Steven M Van Belleghem, Brian A Counterman, W Owen McMillan, Marcus R Kronforst, Riccardo Papa

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Divergence of chemosensing during the early stages of speciation.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  5. Article
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 at 5 institutions in 4 countries.

Wei ZhangState Key Laboratory of Protein and Plant Gene Research, Peking-Tsinghua Center for Life Sciences, and School of Life Sciences, Peking University, Beijing, China.
Brian X Leon-RicardoDepartment of Biology, University of Puerto Rico.
Bas van SchootenDepartment of Biology, University of Puerto Rico.
Steven M Van BelleghemDepartment of Biology, University of Puerto Rico.
Brian A CountermanDepartment of Biological Sciences, Mississippi State University.
W Owen McMillanSmithsonian Tropical Research Institute, Gamboa, Panama.
Marcus R KronforstDepartment of Ecology and Evolution, University of Chicago.
Riccardo PapaDepartment of Biology, University of Puerto Rico.
University of Puerto Rico System · PRMississippi State University · USPeking University · CNSmithsonian Tropical Research Institute · PAUniversity of Chicago · US

Funding

SCIENCE AND TECHNOLOGY COMPETENCY & EDUCATION CORE (STCE)P20GM103475 · NIGMS · UNIVERSITY OF PUERTO RICO MED SCIENCES · PI Humberto Guillermo Ortiz-Zuazaga · 2012 to 2026
$52.9M
Characterizing the Molecular Basis of Supergene Mimicry in ButterfliesR35GM131828 · NIGMS · UNIVERSITY OF CHICAGO · PI Marcus Kronforst · 2019 to 2026
$3.3M
Characterizing the Molecular Basis of Supergene Mimicry in ButterfliesR01GM108626 · NIGMS · UNIVERSITY OF CHICAGO · PI KRONFORST, MARCUS · 2014 to 2018
$1.5M
NIGMS NIH HHS P20 GM103475NIGMS NIH HHS R01 GM108626NIGMS NIH HHS R35 GM131828
6 · The paper itself

Abstract

Butterfly eyes are complex organs that are composed of a diversity of proteins and they play a central role in visual signaling and ultimately, speciation, and adaptation. Here, we utilized the whole eye transcriptome to obtain a more holistic view of the evolution of the butterfly eye while accounting for speciation events that co-occur with ancient hybridization. We sequenced and assembled transcriptomes from adult female eyes of eight species representing all major clades of the Heliconius genus and an additional outgroup species, Dryas iulia. We identified 4,042 orthologous genes shared across all transcriptome data sets and constructed a transcriptome-wide phylogeny, which revealed topological discordance with the mitochondrial phylogenetic tree in the Heliconius pupal mating clade. We then estimated introgression among lineages using additional genome data and found evidence for ancient hybridization leading to the common ancestor of Heliconius hortense and Heliconius clysonymus. We estimated the Ka/Ks ratio for each orthologous cluster and performed further tests to demonstrate genes showing evidence of adaptive protein evolution. Furthermore, we characterized patterns of expression for a subset of these positively selected orthologs using qRT-PCR. Taken together, we identified candidate eye genes that show signatures of adaptive molecular evolution and provide evidence of their expression divergence between species, tissues, and sexes. Our results demonstrate: 1) greater evolutionary changes in younger Heliconius lineages, that is, more positively selected genes in the cydno-melpomene-hecale group as opposed to the sara-hortense-erato group, and 2) suggest an ancient hybridization leading to speciation among Heliconius pupal-mating species.

Indexed as

Evolution, MolecularTranscriptomeAnimalsButterfliesEyeFemaleGene Expression ProfilingGenes, InsectGenetic SpeciationMalePhylogenySelection, GeneticadaptationHeliconiushybrid speciationpositive selectiontranscriptome

Identifiers

PMID31518398
PMCPMC6821300
OpenAlexW2973180378

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.