Evidence map›Paper›PMID 34879263›Full record

ArticleDevelopmental cell2021

Rapid and robust optogenetic control of gene expression in Drosophila.

Florencia di Pietro, Sophie Herszterg, Anqi Huang, Floris Bosveld, Cyrille Alexandre, Lucas Sancéré, Stéphane Pelletier, Amina Joudat, Varun Kapoor, Jean-Paul Vincent and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Developmental cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 46 citations in OpenAlex.

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  8. Signal control during tissue regeneration in adult animals.Nature reviews. Molecular cell biology · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Protein design accelerates the development and application of optogenetic tools.Computational and structural biotechnology journal · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
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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

11 authors at 2 institutions in 2 countries.

Florencia di PietroInstitut Curie, Université PSL, Sorbonne Université, CNRS UMR 3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.
Sophie HersztergFrancis Crick Institute, 1 Midland Rd, London NW1 1AT, UK.
Anqi HuangFrancis Crick Institute, 1 Midland Rd, London NW1 1AT, UK.
Floris BosveldInstitut Curie, Université PSL, Sorbonne Université, CNRS UMR 3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.
Cyrille AlexandreFrancis Crick Institute, 1 Midland Rd, London NW1 1AT, UK.
Lucas SancéréInstitut Curie, Université PSL, Sorbonne Université, CNRS UMR 3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.
Stéphane PelletierInstitut Curie, Université PSL, Sorbonne Université, CNRS UMR 3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.
Amina JoudatInstitut Curie, Université PSL, Sorbonne Université, CNRS UMR 3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.
Varun KapoorInstitut Curie, Université PSL, Sorbonne Université, CNRS UMR 3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France.
Jean-Paul VincentFrancis Crick Institute, 1 Midland Rd, London NW1 1AT, UK. Electronic address: jp.vincent@crick.ac.uk.
Yohanns BellaïcheInstitut Curie, Université PSL, Sorbonne Université, CNRS UMR 3215, Inserm U934, Genetics and Developmental Biology, 75005 Paris, France. Electronic address: yohanns.bellaiche@curie.fr.
Centre National de la Recherche Scientifique · FRThe Francis Crick Institute · GB

Funding

Cancer Research UK FC001204Medical Research Council FC001204Wellcome Trust 206341/Z/17/ZWellcome Trust FC001204
6 · The paper itself

Abstract

Deciphering gene function requires the ability to control gene expression in space and time. Binary systems such as the Gal4/UAS provide a powerful means to modulate gene expression and to induce loss or gain of function. This is best exemplified in Drosophila, where the Gal4/UAS system has been critical to discover conserved mechanisms in development, physiology, neurobiology, and metabolism, to cite a few. Here we describe a transgenic light-inducible Gal4/UAS system (ShineGal4/UAS) based on Magnet photoswitches. We show that it allows efficient, rapid, and robust activation of UAS-driven transgenes in different tissues and at various developmental stages in Drosophila. Furthermore, we illustrate how ShineGal4 enables the generation of gain and loss-of-function phenotypes at animal, organ, and cellular levels. Thanks to the large repertoire of UAS-driven transgenes, ShineGal4 enriches the Drosophila genetic toolkit by allowing in vivo control of gene expression with high temporal and spatial resolutions.

Indexed as

Gene Expression Regulation, DevelopmentalOptogeneticsAnimalsBody PatterningDrosophila melanogasterLightOrgan SpecificityPupaTime FactorsDrosophilaGal4/UASgene expressionoptogenetics

Identifiers

PMID34879263
PMCPMC8693864
OpenAlexW4200216215

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.