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Regulated inositol synthesis is critical for balanced metabolism and development in Drosophila melanogaster
Myo-inositol is a precursor of the membrane phospholipid, phosphatidylinositol (PI). It is involved in many essential cellular processes including signal transduction, energy metabolism, endoplasmic reticulum stress, and osmoregulation. Inositol is synthesized from glucose-6-phosphate by myo-inosito...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565467/ https://www.ncbi.nlm.nih.gov/pubmed/34710213 http://dx.doi.org/10.1242/bio.058833 |
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author | Rivera, Maria J. Contreras, Altagracia Nguyen, LongThy T. Eldon, Elizabeth D. Klig, Lisa S. |
author_facet | Rivera, Maria J. Contreras, Altagracia Nguyen, LongThy T. Eldon, Elizabeth D. Klig, Lisa S. |
author_sort | Rivera, Maria J. |
collection | PubMed |
description | Myo-inositol is a precursor of the membrane phospholipid, phosphatidylinositol (PI). It is involved in many essential cellular processes including signal transduction, energy metabolism, endoplasmic reticulum stress, and osmoregulation. Inositol is synthesized from glucose-6-phosphate by myo-inositol-3-phosphate synthase (MIPSp). The Drosophila melanogaster Inos gene encodes MIPSp. Abnormalities in myo-inositol metabolism have been implicated in type 2 diabetes, cancer, and neurodegenerative disorders. Obesity and high blood (hemolymph) glucose are two hallmarks of diabetes, which can be induced in Drosophila melanogaster third-instar larvae by high-sucrose diets. This study shows that dietary inositol reduces the obese-like and high-hemolymph glucose phenotypes of third-instar larvae fed high-sucrose diets. Furthermore, this study demonstrates Inos mRNA regulation by dietary inositol; when more inositol is provided there is less Inos mRNA. Third-instar larvae with dysregulated high levels of Inos mRNA and MIPSp show dramatic reductions of the obese-like and high-hemolymph glucose phenotypes. These strains, however, also display developmental defects and pupal lethality. The few individuals that eclose die within two days with striking defects: structural alterations of the wings and legs, and heads lacking proboscises. This study is an exciting extension of the use of Drosophila melanogaster as a model organism for exploring the junction of development and metabolism. |
format | Online Article Text |
id | pubmed-8565467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-85654672021-11-04 Regulated inositol synthesis is critical for balanced metabolism and development in Drosophila melanogaster Rivera, Maria J. Contreras, Altagracia Nguyen, LongThy T. Eldon, Elizabeth D. Klig, Lisa S. Biol Open Research Article Myo-inositol is a precursor of the membrane phospholipid, phosphatidylinositol (PI). It is involved in many essential cellular processes including signal transduction, energy metabolism, endoplasmic reticulum stress, and osmoregulation. Inositol is synthesized from glucose-6-phosphate by myo-inositol-3-phosphate synthase (MIPSp). The Drosophila melanogaster Inos gene encodes MIPSp. Abnormalities in myo-inositol metabolism have been implicated in type 2 diabetes, cancer, and neurodegenerative disorders. Obesity and high blood (hemolymph) glucose are two hallmarks of diabetes, which can be induced in Drosophila melanogaster third-instar larvae by high-sucrose diets. This study shows that dietary inositol reduces the obese-like and high-hemolymph glucose phenotypes of third-instar larvae fed high-sucrose diets. Furthermore, this study demonstrates Inos mRNA regulation by dietary inositol; when more inositol is provided there is less Inos mRNA. Third-instar larvae with dysregulated high levels of Inos mRNA and MIPSp show dramatic reductions of the obese-like and high-hemolymph glucose phenotypes. These strains, however, also display developmental defects and pupal lethality. The few individuals that eclose die within two days with striking defects: structural alterations of the wings and legs, and heads lacking proboscises. This study is an exciting extension of the use of Drosophila melanogaster as a model organism for exploring the junction of development and metabolism. The Company of Biologists Ltd 2021-10-28 /pmc/articles/PMC8565467/ /pubmed/34710213 http://dx.doi.org/10.1242/bio.058833 Text en © 2021. Published by The Company of Biologists Ltd 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 that the original work is properly attributed. |
spellingShingle | Research Article Rivera, Maria J. Contreras, Altagracia Nguyen, LongThy T. Eldon, Elizabeth D. Klig, Lisa S. Regulated inositol synthesis is critical for balanced metabolism and development in Drosophila melanogaster |
title | Regulated inositol synthesis is critical for balanced metabolism and development in Drosophila melanogaster |
title_full | Regulated inositol synthesis is critical for balanced metabolism and development in Drosophila melanogaster |
title_fullStr | Regulated inositol synthesis is critical for balanced metabolism and development in Drosophila melanogaster |
title_full_unstemmed | Regulated inositol synthesis is critical for balanced metabolism and development in Drosophila melanogaster |
title_short | Regulated inositol synthesis is critical for balanced metabolism and development in Drosophila melanogaster |
title_sort | regulated inositol synthesis is critical for balanced metabolism and development in drosophila melanogaster |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565467/ https://www.ncbi.nlm.nih.gov/pubmed/34710213 http://dx.doi.org/10.1242/bio.058833 |
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