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Alternative oxidase confers nutritional limitation on Drosophila development
The mitochondrial alternative oxidase, AOX, present in most eukaryotes apart from vertebrates and insects, catalyzes the direct oxidation of ubiquinol by oxygen, by‐passing the terminal proton‐motive steps of the respiratory chain. Its physiological role is not fully understood, but it is proposed t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617715/ https://www.ncbi.nlm.nih.gov/pubmed/31218852 http://dx.doi.org/10.1002/jez.2274 |
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author | Saari, Sina Kemppainen, Esko Tuomela, Tea Oliveira, Marcos T. Dufour, Eric Jacobs, Howard T. |
author_facet | Saari, Sina Kemppainen, Esko Tuomela, Tea Oliveira, Marcos T. Dufour, Eric Jacobs, Howard T. |
author_sort | Saari, Sina |
collection | PubMed |
description | The mitochondrial alternative oxidase, AOX, present in most eukaryotes apart from vertebrates and insects, catalyzes the direct oxidation of ubiquinol by oxygen, by‐passing the terminal proton‐motive steps of the respiratory chain. Its physiological role is not fully understood, but it is proposed to buffer stresses in the respiratory chain similar to those encountered in mitochondrial diseases in humans. Previously, we found that the ubiquitous expression of AOX from Ciona intestinalis in Drosophila perturbs the development of flies cultured under low‐nutrient conditions (media containing only glucose and yeast). Here we tested the effects of a wide range of nutritional supplements on Drosophila development, to gain insight into the physiological mechanism underlying this developmental failure. On low‐nutrient medium, larvae contained decreased amounts of triglycerides, lactate, and pyruvate, irrespective of AOX expression. Complex food supplements, including treacle (molasses), restored normal development to AOX‐expressing flies, but many individual additives did not. Inhibition of AOX by treacle extract was excluded as a mechanism, since the supplement did not alter the enzymatic activity of AOX in vitro. Furthermore, antibiotics did not influence the organismal phenotype, indicating that commensal microbes were not involved. Fractionation of treacle identified a water‐soluble fraction with low solubility in ethanol, rich in lactate and tricarboxylic acid cycle intermediates, which contained the critical activity. We propose that the partial activation of AOX during metamorphosis impairs the efficient use of stored metabolites, resulting in developmental failure. |
format | Online Article Text |
id | pubmed-6617715 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66177152019-07-22 Alternative oxidase confers nutritional limitation on Drosophila development Saari, Sina Kemppainen, Esko Tuomela, Tea Oliveira, Marcos T. Dufour, Eric Jacobs, Howard T. J Exp Zool A Ecol Integr Physiol Research Papers The mitochondrial alternative oxidase, AOX, present in most eukaryotes apart from vertebrates and insects, catalyzes the direct oxidation of ubiquinol by oxygen, by‐passing the terminal proton‐motive steps of the respiratory chain. Its physiological role is not fully understood, but it is proposed to buffer stresses in the respiratory chain similar to those encountered in mitochondrial diseases in humans. Previously, we found that the ubiquitous expression of AOX from Ciona intestinalis in Drosophila perturbs the development of flies cultured under low‐nutrient conditions (media containing only glucose and yeast). Here we tested the effects of a wide range of nutritional supplements on Drosophila development, to gain insight into the physiological mechanism underlying this developmental failure. On low‐nutrient medium, larvae contained decreased amounts of triglycerides, lactate, and pyruvate, irrespective of AOX expression. Complex food supplements, including treacle (molasses), restored normal development to AOX‐expressing flies, but many individual additives did not. Inhibition of AOX by treacle extract was excluded as a mechanism, since the supplement did not alter the enzymatic activity of AOX in vitro. Furthermore, antibiotics did not influence the organismal phenotype, indicating that commensal microbes were not involved. Fractionation of treacle identified a water‐soluble fraction with low solubility in ethanol, rich in lactate and tricarboxylic acid cycle intermediates, which contained the critical activity. We propose that the partial activation of AOX during metamorphosis impairs the efficient use of stored metabolites, resulting in developmental failure. John Wiley and Sons Inc. 2019-06-20 2019-07-01 /pmc/articles/PMC6617715/ /pubmed/31218852 http://dx.doi.org/10.1002/jez.2274 Text en © 2019 The Authors. Journal of Experimental Zoology Part A: Ecological Genetics and Physiology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Papers Saari, Sina Kemppainen, Esko Tuomela, Tea Oliveira, Marcos T. Dufour, Eric Jacobs, Howard T. Alternative oxidase confers nutritional limitation on Drosophila development |
title | Alternative oxidase confers nutritional limitation on Drosophila development |
title_full | Alternative oxidase confers nutritional limitation on Drosophila development |
title_fullStr | Alternative oxidase confers nutritional limitation on Drosophila development |
title_full_unstemmed | Alternative oxidase confers nutritional limitation on Drosophila development |
title_short | Alternative oxidase confers nutritional limitation on Drosophila development |
title_sort | alternative oxidase confers nutritional limitation on drosophila development |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6617715/ https://www.ncbi.nlm.nih.gov/pubmed/31218852 http://dx.doi.org/10.1002/jez.2274 |
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