Evidence map›Paper›PMID 40052482›Full record

ArticleDevelopment (Cambridge, England)2025

Lepidopteran scale cells derive from sensory organ precursors through a canonical lineage.

Ling S Loh, Kyle A DeMarr, Martina Tsimba, Christa Heryanto, Alejandro Berrio, Nipam H Patel, Arnaud Martin, W Owen McMillan, Gregory A Wray, Joseph J Hanly

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Morphological innovation without gene co-option: thebioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. 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

10 authors.

Ling S LohDepartment of Biological Sciences, The George Washington University, Washington, DC 20052, USA.ORCID 0000-0003-0981-7984
Kyle A DeMarrDepartment of Integrative Biology, University of California, Berkeley, CA 94720, USA.ORCID 0000-0002-2010-1576
Martina TsimbaDepartment of Biological Sciences, The George Washington University, Washington, DC 20052, USA.ORCID 0000-0002-9917-5710
Christa HeryantoDepartment of Biological Sciences, The George Washington University, Washington, DC 20052, USA.ORCID 0000-0002-2597-7550
Alejandro BerrioDepartment of Biology, Duke University, Durham, NC 27708, USA.ORCID 0000-0003-1259-2181
Nipam H PatelThe Marine Biological Laboratory, Woods Hole, MA 02543, USA.ORCID 0000-0003-4328-654X
Arnaud MartinDepartment of Biological Sciences, The George Washington University, Washington, DC 20052, USA.ORCID 0000-0002-5980-2249
W Owen McMillanSmithsonian Tropical Research Institute, Gamboa 0843-03092, Panama.ORCID 0000-0003-2805-2745
Gregory A WrayDepartment of Biology, Duke University, Durham, NC 27708, USA.ORCID 0000-0001-5634-5081
Joseph J HanlyDepartment of Biological Sciences, The George Washington University, Washington, DC 20052, USA.ORCID 0000-0002-9459-9776

Funding

Acquisition of Zeiss Cell Observer Spinning Disk Confocal SystemS10OD010710 · OD · GEORGE WASHINGTON UNIVERSITY · PI POPRATILOFF, ANASTAS · 2012 to 2012
$500k
George Washington UniversityNational Science Foundation IOS-2110532NIH HHS S10 OD010710Smithsonian Institution
6 · The paper itself

Abstract

The success of butterflies and moths is tightly linked to the origin of scales within the group. A long-standing hypothesis postulates that scales are homologous to the well-described mechanosensory bristles found in the fruit fly Drosophila melanogaster, as both derive from an epithelial precursor. Previous histological and candidate gene approaches identified parallels in genes involved in scale and bristle development. Here, we provide developmental and transcriptomic evidence that the differentiation of lepidopteran scales derives from the sensory organ precursor (SOP). Live imaging in lepidopteran pupae shows that SOP cells undergo two asymmetric divisions that first abrogate the neurogenic lineage, and then lead to a differentiated scale precursor and its associated socket cell. Single-nucleus RNA sequencing using early pupal wings revealed differential gene expression patterns that mirror SOP development, suggesting a shared developmental program. Additionally, we recovered a newly associated gene, the transcription factor pdm3, involved in the proper differentiation of butterfly wing scales. Altogether, these data open up avenues for understanding scale type specification and development, and illustrate how single-cell transcriptomics provide a powerful platform for understanding evolution of cell types.

Indexed as

Animal ScalesGene Expression Regulation, DevelopmentalLepidopteraStem CellsWings, AnimalAnimalsCell DifferentiationInsect ProteinsIntravital MicroscopyMalePupaSense OrgansSingle-Cell Gene Expression AnalysisTime-Lapse ImagingTranscription FactorsInsect ProteinsTranscription FactorsAsymmetric divisionCell type evolutionDifferentiationPatterningSensory organ precursorSerial homology

Identifiers

PMID40052482
PMCPMC11925400

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.