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Vesicular transport mediates the uptake of cytoplasmic proteins into mitochondria in Drosophila melanogaster
Mitochondrial aging, which results in mitochondrial dysfunction, is strongly linked to many age-related diseases. Aging is associated with mitochondrial enlargement and transport of cytosolic proteins into mitochondria. The underlying homeostatic mechanisms that regulate mitochondrial morphology and...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244744/ https://www.ncbi.nlm.nih.gov/pubmed/32444642 http://dx.doi.org/10.1038/s41467-020-16335-0 |
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author | Chen, Po-Lin Huang, Kai-Ting Cheng, Chu-Ya Li, Jian-Chiuan Chan, Hsiao-Yen Lin, Tzu-Yang Su, Matthew P. Yang, Wei-Yuan Chang, Henry C. Wang, Horng-Dar Chen, Chun-Hong |
author_facet | Chen, Po-Lin Huang, Kai-Ting Cheng, Chu-Ya Li, Jian-Chiuan Chan, Hsiao-Yen Lin, Tzu-Yang Su, Matthew P. Yang, Wei-Yuan Chang, Henry C. Wang, Horng-Dar Chen, Chun-Hong |
author_sort | Chen, Po-Lin |
collection | PubMed |
description | Mitochondrial aging, which results in mitochondrial dysfunction, is strongly linked to many age-related diseases. Aging is associated with mitochondrial enlargement and transport of cytosolic proteins into mitochondria. The underlying homeostatic mechanisms that regulate mitochondrial morphology and function, and their breakdown during aging, remain unclear. Here, we identify a mitochondrial protein trafficking pathway in Drosophila melanogaster involving the mitochondria-associated protein Dosmit. Dosmit induces mitochondrial enlargement and the formation of double-membraned vesicles containing cytosolic protein within mitochondria. The rate of vesicle formation increases with age. Vesicles originate from the outer mitochondrial membrane as observed by tracking Tom20 localization, and the process is mediated by the mitochondria-associated Rab32 protein. Dosmit expression level is closely linked to the rate of ubiquitinated protein aggregation, which are themselves associated with age-related diseases. The mitochondrial protein trafficking route mediated by Dosmit offers a promising target for future age-related mitochondrial disease therapies. |
format | Online Article Text |
id | pubmed-7244744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72447442020-06-03 Vesicular transport mediates the uptake of cytoplasmic proteins into mitochondria in Drosophila melanogaster Chen, Po-Lin Huang, Kai-Ting Cheng, Chu-Ya Li, Jian-Chiuan Chan, Hsiao-Yen Lin, Tzu-Yang Su, Matthew P. Yang, Wei-Yuan Chang, Henry C. Wang, Horng-Dar Chen, Chun-Hong Nat Commun Article Mitochondrial aging, which results in mitochondrial dysfunction, is strongly linked to many age-related diseases. Aging is associated with mitochondrial enlargement and transport of cytosolic proteins into mitochondria. The underlying homeostatic mechanisms that regulate mitochondrial morphology and function, and their breakdown during aging, remain unclear. Here, we identify a mitochondrial protein trafficking pathway in Drosophila melanogaster involving the mitochondria-associated protein Dosmit. Dosmit induces mitochondrial enlargement and the formation of double-membraned vesicles containing cytosolic protein within mitochondria. The rate of vesicle formation increases with age. Vesicles originate from the outer mitochondrial membrane as observed by tracking Tom20 localization, and the process is mediated by the mitochondria-associated Rab32 protein. Dosmit expression level is closely linked to the rate of ubiquitinated protein aggregation, which are themselves associated with age-related diseases. The mitochondrial protein trafficking route mediated by Dosmit offers a promising target for future age-related mitochondrial disease therapies. Nature Publishing Group UK 2020-05-22 /pmc/articles/PMC7244744/ /pubmed/32444642 http://dx.doi.org/10.1038/s41467-020-16335-0 Text en © The Author(s) 2020 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 Chen, Po-Lin Huang, Kai-Ting Cheng, Chu-Ya Li, Jian-Chiuan Chan, Hsiao-Yen Lin, Tzu-Yang Su, Matthew P. Yang, Wei-Yuan Chang, Henry C. Wang, Horng-Dar Chen, Chun-Hong Vesicular transport mediates the uptake of cytoplasmic proteins into mitochondria in Drosophila melanogaster |
title | Vesicular transport mediates the uptake of cytoplasmic proteins into mitochondria in Drosophila melanogaster |
title_full | Vesicular transport mediates the uptake of cytoplasmic proteins into mitochondria in Drosophila melanogaster |
title_fullStr | Vesicular transport mediates the uptake of cytoplasmic proteins into mitochondria in Drosophila melanogaster |
title_full_unstemmed | Vesicular transport mediates the uptake of cytoplasmic proteins into mitochondria in Drosophila melanogaster |
title_short | Vesicular transport mediates the uptake of cytoplasmic proteins into mitochondria in Drosophila melanogaster |
title_sort | vesicular transport mediates the uptake of cytoplasmic proteins into mitochondria in drosophila melanogaster |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244744/ https://www.ncbi.nlm.nih.gov/pubmed/32444642 http://dx.doi.org/10.1038/s41467-020-16335-0 |
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