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A genetic strategy to measure insulin signaling regulation and physiology in Drosophila
Insulin regulation is a hallmark of health, and impaired insulin signaling promotes metabolic diseases like diabetes mellitus. However, current assays for measuring insulin signaling in all animals remain semi-quantitative and lack the sensitivity, tissue-specificity or temporal resolution needed to...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928101/ https://www.ncbi.nlm.nih.gov/pubmed/36730473 http://dx.doi.org/10.1371/journal.pgen.1010619 |
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author | Tsao, Deborah D. Chang, Kathleen R. Kockel, Lutz Park, Sangbin Kim, Seung K. |
author_facet | Tsao, Deborah D. Chang, Kathleen R. Kockel, Lutz Park, Sangbin Kim, Seung K. |
author_sort | Tsao, Deborah D. |
collection | PubMed |
description | Insulin regulation is a hallmark of health, and impaired insulin signaling promotes metabolic diseases like diabetes mellitus. However, current assays for measuring insulin signaling in all animals remain semi-quantitative and lack the sensitivity, tissue-specificity or temporal resolution needed to quantify in vivo physiological signaling dynamics. Insulin signal transduction is remarkably conserved across metazoans, including insulin-dependent phosphorylation and regulation of Akt/Protein kinase B. Here, we generated transgenic fruit flies permitting tissue-specific expression of an immunoepitope-labelled Akt (AktHF). We developed enzyme-linked immunosorption assays (ELISA) to quantify picomolar levels of phosphorylated (pAktHF) and total AktHF in single flies, revealing dynamic tissue-specific physiological regulation of pAktHF in response to fasting and re-feeding, exogenous insulin, or targeted genetic suppression of established insulin signaling regulators. Genetic screening revealed Pp1-87B as an unrecognized regulator of Akt and insulin signaling. Tools and concepts here provide opportunities to discover tissue-specific regulators of in vivo insulin signaling responses. |
format | Online Article Text |
id | pubmed-9928101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-99281012023-02-15 A genetic strategy to measure insulin signaling regulation and physiology in Drosophila Tsao, Deborah D. Chang, Kathleen R. Kockel, Lutz Park, Sangbin Kim, Seung K. PLoS Genet Research Article Insulin regulation is a hallmark of health, and impaired insulin signaling promotes metabolic diseases like diabetes mellitus. However, current assays for measuring insulin signaling in all animals remain semi-quantitative and lack the sensitivity, tissue-specificity or temporal resolution needed to quantify in vivo physiological signaling dynamics. Insulin signal transduction is remarkably conserved across metazoans, including insulin-dependent phosphorylation and regulation of Akt/Protein kinase B. Here, we generated transgenic fruit flies permitting tissue-specific expression of an immunoepitope-labelled Akt (AktHF). We developed enzyme-linked immunosorption assays (ELISA) to quantify picomolar levels of phosphorylated (pAktHF) and total AktHF in single flies, revealing dynamic tissue-specific physiological regulation of pAktHF in response to fasting and re-feeding, exogenous insulin, or targeted genetic suppression of established insulin signaling regulators. Genetic screening revealed Pp1-87B as an unrecognized regulator of Akt and insulin signaling. Tools and concepts here provide opportunities to discover tissue-specific regulators of in vivo insulin signaling responses. Public Library of Science 2023-02-02 /pmc/articles/PMC9928101/ /pubmed/36730473 http://dx.doi.org/10.1371/journal.pgen.1010619 Text en © 2023 Tsao 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 Tsao, Deborah D. Chang, Kathleen R. Kockel, Lutz Park, Sangbin Kim, Seung K. A genetic strategy to measure insulin signaling regulation and physiology in Drosophila |
title | A genetic strategy to measure insulin signaling regulation and physiology in Drosophila |
title_full | A genetic strategy to measure insulin signaling regulation and physiology in Drosophila |
title_fullStr | A genetic strategy to measure insulin signaling regulation and physiology in Drosophila |
title_full_unstemmed | A genetic strategy to measure insulin signaling regulation and physiology in Drosophila |
title_short | A genetic strategy to measure insulin signaling regulation and physiology in Drosophila |
title_sort | genetic strategy to measure insulin signaling regulation and physiology in drosophila |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928101/ https://www.ncbi.nlm.nih.gov/pubmed/36730473 http://dx.doi.org/10.1371/journal.pgen.1010619 |
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