Evidence map›Paper›PMID 37824452›Full record

ArticlePLoS biology2023

Genomes from historical Drosophila melanogaster specimens illuminate adaptive and demographic changes across more than 200 years of evolution.

Max Shpak, Hamid R Ghanavi, Jeremy D Lange, John E Pool, Marcus C Stensmyr

Abstract read
In one paragraph

Article in PLoS biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Article
  3. The Evolution of Bees: Insights from 'Omic Studies.Genome biology and evolution · 2026
    Review
  4. The ongoing invasion of the endogenous retrovirusbioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Vertebrate and Invertebrate Animal Models for the Study of Down Syndrome.International journal of molecular sciences · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Pathogen prospecting of museums: Reconstructing malaria epidemiology.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Genomes of historical specimens reveal multiple invasions of LTR retrotransposons inProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Cellular and molecular organization of the Drosophila foregut.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  17. Article
  18. 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

5 authors.

Max ShpakLaboratory of Genetics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
Hamid R GhanaviDepartment of Biology, Lund University, Lund, Scania, Sweden.
Jeremy D LangeLaboratory of Genetics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
John E PoolLaboratory of Genetics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.ORCID 0000-0003-2968-9545
Marcus C StensmyrDepartment of Biology, Lund University, Lund, Scania, Sweden.ORCID 0000-0003-4009-9212

Funding

PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM007133 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI PERNA, NICOLE T · 1985 to 2023
$16.5M
The Architectures and Underpinnings of Adaptive Evolution and Reproductive IsolationR35GM136306 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI POOL, JOHN E · 2020 to 2025
$3.5M
NIGMS NIH HHS R35 GM136306NIGMS NIH HHS T32 GM007133
6 · The paper itself

Abstract

The ability to perform genomic sequencing on long-dead organisms is opening new frontiers in evolutionary research. These opportunities are especially notable in the case of museum collections, from which countless documented specimens may now be suitable for genomic analysis-if data of sufficient quality can be obtained. Here, we report 25 newly sequenced genomes from museum specimens of the model organism Drosophila melanogaster, including the oldest extant specimens of this species. By comparing historical samples ranging from the early 1800s to 1933 against modern-day genomes, we document evolution across thousands of generations, including time periods that encompass the species' initial occupation of northern Europe and an era of rapidly increasing human activity. We also find that the Lund, Sweden population underwent local genetic differentiation during the early 1800s to 1933 interval (potentially due to drift in a small population) but then became more similar to other European populations thereafter (potentially due to increased migration). Within each century-scale time period, our temporal sampling allows us to document compelling candidates for recent natural selection. In some cases, we gain insights regarding previously implicated selection candidates, such as ChKov1, for which our inferred timing of selection favors the hypothesis of antiviral resistance over insecticide resistance. Other candidates are novel, such as the circadian-related gene Ahcy, which yields a selection signal that rivals that of the DDT resistance gene Cyp6g1. These insights deepen our understanding of recent evolution in a model system, and highlight the potential of future museomic studies.

Indexed as

Drosophila melanogasterDrosophila ProteinsAnimalsDemographyGenome, InsectHumansInsecticide ResistanceDrosophila Proteins

Identifiers

PMID37824452
PMCPMC10569592

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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.