Evidence map›Paper›PMID 30067846›Full record

ArticlePLoS genetics2018

bric à brac (bab), a central player in the gene regulatory network that mediates thermal plasticity of pigmentation in Drosophila melanogaster.

Sandra De Castro, Frédérique Peronnet, Jean-François Gilles, Emmanuèle Mouchel-Vielh, Jean-Michel Gibert

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. 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
1.5field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 45 citations in OpenAlex.

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  12. A genetic switch for male UV iridescence in an incipient species pair of sulphur butterflies.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

5 authors at 1 institution in 1 country.

Sandra De CastroSorbonne Université, CNRS, Laboratoire de Biologie du Développement -Institut de Biologie Paris Seine (LBD-IBPS), Team "Epigenetic control of developmental homeostasis and plasticity", Paris, France.
Frédérique PeronnetSorbonne Université, CNRS, Laboratoire de Biologie du Développement -Institut de Biologie Paris Seine (LBD-IBPS), Team "Epigenetic control of developmental homeostasis and plasticity", Paris, France.ORCID 0000-0003-1354-240X
Jean-François GillesSorbonne Université, CNRS, Core facility, Institut de Biologie Paris Seine (IBPS), Paris, France.
Emmanuèle Mouchel-VielhSorbonne Université, CNRS, Laboratoire de Biologie du Développement -Institut de Biologie Paris Seine (LBD-IBPS), Team "Epigenetic control of developmental homeostasis and plasticity", Paris, France.
Jean-Michel GibertSorbonne Université, CNRS, Laboratoire de Biologie du Développement -Institut de Biologie Paris Seine (LBD-IBPS), Team "Epigenetic control of developmental homeostasis and plasticity", Paris, France.ORCID 0000-0002-1579-0266
Centre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drosophila body pigmentation has emerged as a major Evo-Devo model. Using two Drosophila melanogaster lines, Dark and Pale, selected from a natural population, we analyse here the interaction between genetic variation and environmental factors to produce this complex trait. Indeed, pigmentation varies with genotype in natural populations and is sensitive to temperature during development. We demonstrate that the bric à brac (bab) genes, that are differentially expressed between the two lines and whose expression levels vary with temperature, participate in the pigmentation difference between the Dark and Pale lines. The two lines differ in a bab regulatory sequence, the dimorphic element (called here bDE). Both bDE alleles are temperature-sensitive, but the activity of the bDE allele from the Dark line is lower than that of the bDE allele from the Pale line. Our results suggest that this difference could partly be due to differential regulation by AbdB. bab has been previously reported to be a repressor of abdominal pigmentation. We show here that one of its targets in this process is the pigmentation gene tan (t), regulated via the tan abdominal enhancer (t_MSE). Furthermore, t expression is strongly modulated by temperature in the two lines. Thus, temperature sensitivity of t expression is at least partly a consequence of bab thermal transcriptional plasticity. We therefore propose that a gene regulatory network integrating both genetic variation and temperature sensitivity modulates female abdominal pigmentation. Interestingly, both bDE and t_MSE were previously shown to have been recurrently involved in abdominal pigmentation evolution in drosophilids. We propose that the environmental sensitivity of these enhancers has turned them into evolutionary hotspots.

Indexed as

Gene Regulatory NetworksAllelesAnimalsBase SequenceBinding SitesChromosomal Proteins, Non-HistoneDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEvolution, MolecularFemaleGene Expression RegulationGenetic VariationGenotyping TechniquesPigmentationSequence Analysis, DNABAB2 protein, DrosophilaBric-a-brac protein 1, DrosophilaChromosomal Proteins, Non-HistoneDNA-Binding ProteinsDrosophila Proteinst protein, DrosophilaTranscription Factors

Identifiers

PMID30067846
PMCPMC6089454
OpenAlexW2886002338

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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.