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

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 ac...

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Autores principales: Winant, Mattias, Buhler, Kurt, Clements, Jason, De Groef, Sofie, Hens, Korneel, Vulsteke, Veerle, Callaerts, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499297/
https://www.ncbi.nlm.nih.gov/pubmed/36095003
http://dx.doi.org/10.1371/journal.pgen.1010380
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author Winant, Mattias
Buhler, Kurt
Clements, Jason
De Groef, Sofie
Hens, Korneel
Vulsteke, Veerle
Callaerts, Patrick
author_facet Winant, Mattias
Buhler, Kurt
Clements, Jason
De Groef, Sofie
Hens, Korneel
Vulsteke, Veerle
Callaerts, Patrick
author_sort Winant, Mattias
collection PubMed
description 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.
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spelling pubmed-94992972022-09-23 Genome-wide analysis identifies Homothorax and Extradenticle as regulators of insulin in Drosophila Insulin-Producing cells Winant, Mattias Buhler, Kurt Clements, Jason De Groef, Sofie Hens, Korneel Vulsteke, Veerle Callaerts, Patrick PLoS Genet Research Article 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. Public Library of Science 2022-09-12 /pmc/articles/PMC9499297/ /pubmed/36095003 http://dx.doi.org/10.1371/journal.pgen.1010380 Text en © 2022 Winant et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Winant, Mattias
Buhler, Kurt
Clements, Jason
De Groef, Sofie
Hens, Korneel
Vulsteke, Veerle
Callaerts, Patrick
Genome-wide analysis identifies Homothorax and Extradenticle as regulators of insulin in Drosophila Insulin-Producing cells
title Genome-wide analysis identifies Homothorax and Extradenticle as regulators of insulin in Drosophila Insulin-Producing cells
title_full Genome-wide analysis identifies Homothorax and Extradenticle as regulators of insulin in Drosophila Insulin-Producing cells
title_fullStr Genome-wide analysis identifies Homothorax and Extradenticle as regulators of insulin in Drosophila Insulin-Producing cells
title_full_unstemmed Genome-wide analysis identifies Homothorax and Extradenticle as regulators of insulin in Drosophila Insulin-Producing cells
title_short Genome-wide analysis identifies Homothorax and Extradenticle as regulators of insulin in Drosophila Insulin-Producing cells
title_sort genome-wide analysis identifies homothorax and extradenticle as regulators of insulin in drosophila insulin-producing cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499297/
https://www.ncbi.nlm.nih.gov/pubmed/36095003
http://dx.doi.org/10.1371/journal.pgen.1010380
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