Evidence map›Paper›PMID 40796329›Full record

ArticleGenome biology and evolution2025

Gene Family Evolution Suggests Correlated Dietary Adaptations in Butterflies and Moths.

Yi-Ming Weng, Jose I Martinez, Amanda Markee, David Plotkin, Yash Sondhi, Andrew J Mongue, Paul B Frandsen, Akito Y Kawahara

Abstract read
In one paragraph

Article in Genome biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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.

Yi-Ming WengMcGuire Center for Lepidoptera & Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL, USA.ORCID 0000-0002-8243-5061
Jose I MartinezMcGuire Center for Lepidoptera & Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL, USA.ORCID 0000-0003-4368-2729
Amanda MarkeeAmerican Museum of Natural History, Richard Gilder Graduate School, New York, NY, USA.ORCID 0000-0001-7421-6339
David PlotkinMcGuire Center for Lepidoptera & Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL, USA.ORCID 0000-0002-2339-655X
Yash SondhiMcGuire Center for Lepidoptera & Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL, USA.ORCID 0000-0002-7704-3944
Andrew J MongueDepartment of Entomology and Nematology, University of Florida, Gainesville, FL, USA.ORCID 0000-0002-8487-9248
Paul B FrandsenDepartment of Plant and Wildlife Sciences, Brigham Young University, Provo, UT, USA.ORCID 0000-0002-4801-7579
Akito Y KawaharaMcGuire Center for Lepidoptera & Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL, USA.ORCID 0000-0002-3724-4610

Funding

National Science Foundation #2426250National Science Foundation DEB #1541500National Science Foundation EF #2217159National Science Foundation IOS #1920895
6 · The paper itself

Abstract

Butterflies and moths (Lepidoptera) are a megadiverse lineage of approximately 160,000 described species. Their evolutionary success is thought to be closely linked to the radiation of flowering plants and represents a classic example of co-evolution. However, mechanisms by which these insects evolved to feed on such diverse plant hosts remain largely unknown. Previous studies found emergent gene families of odorant receptors and peptidases in the ancestor of Lepidoptera, suggesting these genetic innovations may be linked to Lepidoptera diversification. Here, we examined 431 genomes and identified lineage-specific gene families within Lepidoptera and 3 key nested clades. We found 54, 88, 77, and 4 functionally annotated gene families specific to Lepidoptera, Glossata, Ditrysia, and Apoditrysia, respectively. These gene families are involved in chemosensation, digestion, detoxification, immunity, and other functions. There was a marked increase in gene families presumably associated with chemosensation and immunity in Glossata and Ditrysia, clades which encompass more than 98% of Lepidoptera species diversity. We also identified horizontal gene transfer (HGT) events involving two putative digestion-related gene families (Catalytic LigB subunit of aromatic ring-opening dioxygenase and Glycosyl hydrolases family 32) and a detoxification gene family (Cysteine synthase-like), likely acquired in the common ancestors of Lepidoptera and Ditrysia, respectively. These HGT events likely played a pivotal role in facilitating dietary transitions from algae, diatoms, and aquatic plant debris to fungi and early terrestrial plants, ultimately enabling Lepidoptera to adapt to and diversify on angiosperm hosts.

Indexed as

ButterfliesEvolution, MolecularMothsMultigene FamilyAnimalsDietGene Transfer, HorizontalGenome, InsectPhylogenyangiosperm terrestrial revolutioncomparative genomicsDitrysiahorizontal gene transferLepidoptera

Identifiers

PMID40796329
PMCPMC12477841

What Socratic holds

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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 Socratic graph.