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Analysis of mitochondrial organization and function in the Drosophila blastoderm embryo
Mitochondria are inherited maternally as globular and immature organelles in metazoan embryos. We have used the Drosophila blastoderm embryo to characterize their morphology, distribution and functions in embryogenesis. We find that mitochondria are relatively small, dispersed and distinctly distrib...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511145/ https://www.ncbi.nlm.nih.gov/pubmed/28710464 http://dx.doi.org/10.1038/s41598-017-05679-1 |
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author | Chowdhary, Sayali Tomer, Darshika Dubal, Dnyanesh Sambre, Devashree Rikhy, Richa |
author_facet | Chowdhary, Sayali Tomer, Darshika Dubal, Dnyanesh Sambre, Devashree Rikhy, Richa |
author_sort | Chowdhary, Sayali |
collection | PubMed |
description | Mitochondria are inherited maternally as globular and immature organelles in metazoan embryos. We have used the Drosophila blastoderm embryo to characterize their morphology, distribution and functions in embryogenesis. We find that mitochondria are relatively small, dispersed and distinctly distributed along the apico-basal axis in proximity to microtubules by motor protein transport. Live imaging, photobleaching and photoactivation analyses of mitochondrially targeted GFP show that they are mobile in the apico-basal axis along microtubules and are immobile in the lateral plane thereby associating with one syncytial cell. Photoactivated mitochondria distribute equally to daughter cells across the division cycles. ATP depletion by pharmacological and genetic inhibition of the mitochondrial electron transport chain (ETC) activates AMPK and decreases syncytial metaphase furrow extension. In summary, we show that small and dispersed mitochondria of the Drosophila blastoderm embryo localize by microtubule transport and provide ATP locally for the fast syncytial division cycles. Our study opens the possibility of use of Drosophila embryogenesis as a model system to study the impact of maternal mutations in mitochondrial morphology and metabolism on embryo patterning and differentiation. |
format | Online Article Text |
id | pubmed-5511145 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55111452017-07-17 Analysis of mitochondrial organization and function in the Drosophila blastoderm embryo Chowdhary, Sayali Tomer, Darshika Dubal, Dnyanesh Sambre, Devashree Rikhy, Richa Sci Rep Article Mitochondria are inherited maternally as globular and immature organelles in metazoan embryos. We have used the Drosophila blastoderm embryo to characterize their morphology, distribution and functions in embryogenesis. We find that mitochondria are relatively small, dispersed and distinctly distributed along the apico-basal axis in proximity to microtubules by motor protein transport. Live imaging, photobleaching and photoactivation analyses of mitochondrially targeted GFP show that they are mobile in the apico-basal axis along microtubules and are immobile in the lateral plane thereby associating with one syncytial cell. Photoactivated mitochondria distribute equally to daughter cells across the division cycles. ATP depletion by pharmacological and genetic inhibition of the mitochondrial electron transport chain (ETC) activates AMPK and decreases syncytial metaphase furrow extension. In summary, we show that small and dispersed mitochondria of the Drosophila blastoderm embryo localize by microtubule transport and provide ATP locally for the fast syncytial division cycles. Our study opens the possibility of use of Drosophila embryogenesis as a model system to study the impact of maternal mutations in mitochondrial morphology and metabolism on embryo patterning and differentiation. Nature Publishing Group UK 2017-07-14 /pmc/articles/PMC5511145/ /pubmed/28710464 http://dx.doi.org/10.1038/s41598-017-05679-1 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chowdhary, Sayali Tomer, Darshika Dubal, Dnyanesh Sambre, Devashree Rikhy, Richa Analysis of mitochondrial organization and function in the Drosophila blastoderm embryo |
title | Analysis of mitochondrial organization and function in the Drosophila blastoderm embryo |
title_full | Analysis of mitochondrial organization and function in the Drosophila blastoderm embryo |
title_fullStr | Analysis of mitochondrial organization and function in the Drosophila blastoderm embryo |
title_full_unstemmed | Analysis of mitochondrial organization and function in the Drosophila blastoderm embryo |
title_short | Analysis of mitochondrial organization and function in the Drosophila blastoderm embryo |
title_sort | analysis of mitochondrial organization and function in the drosophila blastoderm embryo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5511145/ https://www.ncbi.nlm.nih.gov/pubmed/28710464 http://dx.doi.org/10.1038/s41598-017-05679-1 |
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