Evidence map›Paper›PMID 36095003›Full record

ArticlePLoS genetics2022

Genome-wide analysis identifies Homothorax and Extradenticle as regulators of insulin in Drosophila Insulin-Producing cells.

Mattias Winant, Kurt Buhler, Jason Clements, Sofie De Groef, Korneel Hens, Veerle Vulsteke, Patrick Callaerts

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2022. 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
0.3field-weighted citation impact, top 51% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Genomic and insulin-mediated control of metabolic homeostasis by the mosquito ecdysone-induced gene E93.Proceedings of the National Academy of Sciences of the United States of America · 2025
    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

7 authors at 2 institutions in 3 countries.

Mattias WinantLaboratory of Behavioral and Developmental Genetics, Department of Human Genetics, KU Leuven-University of Leuven, Leuven, Belgium.ORCID 0000-0003-2862-7908
Kurt BuhlerLaboratory of Behavioral and Developmental Genetics, Department of Human Genetics, KU Leuven-University of Leuven, Leuven, Belgium.ORCID 0000-0003-1236-4365
Jason ClementsLaboratory of Behavioral and Developmental Genetics, Department of Human Genetics, KU Leuven-University of Leuven, Leuven, Belgium.
Sofie De GroefLaboratory of Behavioral and Developmental Genetics, Department of Human Genetics, KU Leuven-University of Leuven, Leuven, Belgium.ORCID 0000-0002-9297-8406
Korneel HensCentre for Functional Genomics, Department of Biological and Medical Sciences, Faculty of Health and Life Sciences, Oxford Brooks University, Headington Campus, Oxford, United Kingdom.ORCID 0000-0002-0362-7007
Veerle VulstekeLaboratory of Behavioral and Developmental Genetics, Department of Human Genetics, KU Leuven-University of Leuven, Leuven, Belgium.
Patrick CallaertsLaboratory of Behavioral and Developmental Genetics, Department of Human Genetics, KU Leuven-University of Leuven, Leuven, Belgium.ORCID 0000-0003-4530-4561
Center for Human Genetics · USGenomics (United Kingdom) · GB

Funding

Biotechnology and Biological Sciences Research Council BB/N00230X/1
6 · The paper itself

Abstract

Drosophila Insulin-Producing Cells (IPCs) are the main production site of the Drosophila Insulin-like peptides or dilps which have key roles in regulating growth, development, reproduction, lifespan and metabolism. To better understand the signalling pathways and transcriptional networks that are active in the IPCs we queried publicly available transcriptome data of over 180 highly inbred fly lines for dilp expression and used dilp expression as the input for a Genome-wide association study (GWAS). This resulted in the identification of variants in 125 genes that were associated with variation in dilp expression. The function of 57 of these genes in the IPCs was tested using an RNAi-based approach. We found that IPC-specific depletion of most genes resulted in differences in expression of one or more of the dilps. We then elaborated further on one of the candidate genes with the strongest effect on dilp expression, Homothorax, a transcription factor known for its role in eye development. We found that Homothorax and its binding partner Extradenticle are involved in regulating dilp2, -3 and -5 expression and that genetic depletion of both TFs shows phenotypes associated with reduced insulin signalling. Furthermore, we provide evidence that other transcription factors involved in eye development are also functional in the IPCs. In conclusion, we showed that this expression level-based GWAS approach identified genetic regulators implicated in IPC function and dilp expression.

Indexed as

DrosophilaDrosophila ProteinsAnimalsDrosophila melanogasterGenome-Wide Association StudyInsulinTranscription FactorsDrosophila ProteinsInsulinTranscription Factors

Identifiers

PMID36095003
PMCPMC9499297
OpenAlexW4295880226

What OpenQuestion holds

Textmetadata
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.