Evidence map›Paper›PMID 41029729›Full record

ArticleMobile DNA2025

Gene and transposable element expression in response to stress in temperate and tropical populations of Drosophila.

Miriam Merenciano, Daniel S Oliveira, Judit Salces-Ortiz, Rita Rebollo, Bianca Manfré, Bianca Menezes, Gabriel Krasovec, Camille Simonet, Sonia Janillon, Nelly Burlet and 3 more

Abstract read
In one paragraph

Article in Mobile DNA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

13 authors.

Miriam Merenciano *Laboratoire de Biométrie et Biologie Évolutive, Université Claude Bernard Lyon 1, CNRS, UMR5558, Villeurbanne, Rhône-Alpes, 69100, France.
Daniel S Oliveira *Laboratoire de Biométrie et Biologie Évolutive, Université Claude Bernard Lyon 1, CNRS, UMR5558, Villeurbanne, Rhône-Alpes, 69100, France.
Judit Salces-OrtizLaboratoire de Biométrie et Biologie Évolutive, Université Claude Bernard Lyon 1, CNRS, UMR5558, Villeurbanne, Rhône-Alpes, 69100, France.
Rita RebolloUniv Lyon, INRAE, INSA-Lyon, BF2I, UMR 203, Villeurbanne, 69621, France.
Bianca ManfréInstitute of Biosciences, Humanities and Exact Sciences, São Paulo State University (Unesp), São José do Rio Preto, São Paulo, 15054-000, Brazil.
Bianca MenezesFederal Institute of Rio de Janeiro (IFRJ), Duque de Caxias, RJ, Brazil.
Gabriel KrasovecLaboratoire de Biométrie et Biologie Évolutive, Université Claude Bernard Lyon 1, CNRS, UMR5558, Villeurbanne, Rhône-Alpes, 69100, France.
Camille SimonetLaboratoire de Biométrie et Biologie Évolutive, Université Claude Bernard Lyon 1, CNRS, UMR5558, Villeurbanne, Rhône-Alpes, 69100, France.
Sonia JanillonLaboratoire de Biométrie et Biologie Évolutive, Université Claude Bernard Lyon 1, CNRS, UMR5558, Villeurbanne, Rhône-Alpes, 69100, France.
Nelly BurletLaboratoire de Biométrie et Biologie Évolutive, Université Claude Bernard Lyon 1, CNRS, UMR5558, Villeurbanne, Rhône-Alpes, 69100, France.
Claudia M A CararetoInstitute of Biosciences, Humanities and Exact Sciences, São Paulo State University (Unesp), São José do Rio Preto, São Paulo, 15054-000, Brazil.
Cristina VieiraLaboratoire de Biométrie et Biologie Évolutive, Université Claude Bernard Lyon 1, CNRS, UMR5558, Villeurbanne, Rhône-Alpes, 69100, France. cristina.vieira@univ-lyon1.fr.
Marie FabletLaboratoire de Biométrie et Biologie Évolutive, Université Claude Bernard Lyon 1, CNRS, UMR5558, Villeurbanne, Rhône-Alpes, 69100, France. marie.fablet@univ-lyon1.fr.

Funding

Agence Nationale de la Recherche ANR-20-CE02-0015Conselho Nacional de Desenvolvimento Científico e Tecnológico 308020/2021-9Coordenação de Aperfeiçoamento de Pessoal de Nível Superior 001Fondation pour la Recherche Médicale DEP20131128536HORIZON EUROPE Marie Sklodowska-Curie Actions 101065313
6 · The paper itself

Abstract

backgroundThe study of stress response in natural populations is crucial for understanding species local adaptation and evolution. In Drosophila, significant genetic diversity across populations from different geographical origins has been observed, emphasizing the influence of local environments.

resultsIn this study, we explored the impact of starvation and cold stress on the phenotypic and transcriptomic response of two natural populations of D. melanogaster and D. simulans from temperate and tropical regions. Additionally, we investigated the behavior and influence of transposable elements (TEs) in these types of stress, combining RNA-seq and ChIP-seq experiments, with high-quality long-read genome assemblies of all the strains. Our findings in D. melanogaster revealed that the transcriptomic response to stress is similar across geographical origins, whereas in D. simulans there is more variability. Notably, neither starvation nor cold induced a general activation of TEs in D. melanogaster or D. simulans, at least in the tissue and strains analysed in this study. Finally, we found three polymorphic TEs producing TE-chimeric transcripts associated with changes in nearby gene expression levels after stress.

conclusionsOverall, this study highlights the complexity of stress-TE interactions and their potential impact on adaptation. Understanding these dynamics contributes to the broader knowledge of how genetic and environmental factors interact to modulate gene expression, shaping an organism's ability to adapt to varying conditions.

Indexed as

DrosophilaEpigeneticsStressTranscriptomeTransposable elements

Identifiers

PMID41029729
PMCPMC12487357

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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.