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A new automated tool to quantify nucleoid distribution within mitochondrial networks

Mitochondrial DNA (mtDNA) maintenance is essential to sustain a functionally healthy population of mitochondria within cells. Proper mtDNA replication and distribution within mitochondrial networks are essential to maintain mitochondrial homeostasis. However, the fundamental basis of mtDNA segregati...

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Autores principales: Ilamathi, Hema Saranya, Ouellet, Mathieu, Sabouny, Rasha, Desrochers-Goyette, Justine, Lines, Matthew A., Pfeffer, Gerald, Shutt, Timothy E., Germain, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610998/
https://www.ncbi.nlm.nih.gov/pubmed/34815439
http://dx.doi.org/10.1038/s41598-021-01987-9
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author Ilamathi, Hema Saranya
Ouellet, Mathieu
Sabouny, Rasha
Desrochers-Goyette, Justine
Lines, Matthew A.
Pfeffer, Gerald
Shutt, Timothy E.
Germain, Marc
author_facet Ilamathi, Hema Saranya
Ouellet, Mathieu
Sabouny, Rasha
Desrochers-Goyette, Justine
Lines, Matthew A.
Pfeffer, Gerald
Shutt, Timothy E.
Germain, Marc
author_sort Ilamathi, Hema Saranya
collection PubMed
description Mitochondrial DNA (mtDNA) maintenance is essential to sustain a functionally healthy population of mitochondria within cells. Proper mtDNA replication and distribution within mitochondrial networks are essential to maintain mitochondrial homeostasis. However, the fundamental basis of mtDNA segregation and distribution within mitochondrial networks is still unclear. To address these questions, we developed an algorithm, Mitomate tracker to unravel the global distribution of nucleoids within mitochondria. Using this tool, we decipher the semi-regular spacing of nucleoids across mitochondrial networks. Furthermore, we show that mitochondrial fission actively regulates mtDNA distribution by controlling the distribution of nucleoids within mitochondrial networks. Specifically, we found that primary cells bearing disease-associated mutations in the fission proteins DRP1 and MYH14 show altered nucleoid distribution, and acute enrichment of enlarged nucleoids near the nucleus. Further analysis suggests that the altered nucleoid distribution observed in the fission mutants is the result of both changes in network structure and nucleoid density. Thus, our study provides novel insights into the role of mitochondria fission in nucleoid distribution and the understanding of diseases caused by fission defects.
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spelling pubmed-86109982021-11-24 A new automated tool to quantify nucleoid distribution within mitochondrial networks Ilamathi, Hema Saranya Ouellet, Mathieu Sabouny, Rasha Desrochers-Goyette, Justine Lines, Matthew A. Pfeffer, Gerald Shutt, Timothy E. Germain, Marc Sci Rep Article Mitochondrial DNA (mtDNA) maintenance is essential to sustain a functionally healthy population of mitochondria within cells. Proper mtDNA replication and distribution within mitochondrial networks are essential to maintain mitochondrial homeostasis. However, the fundamental basis of mtDNA segregation and distribution within mitochondrial networks is still unclear. To address these questions, we developed an algorithm, Mitomate tracker to unravel the global distribution of nucleoids within mitochondria. Using this tool, we decipher the semi-regular spacing of nucleoids across mitochondrial networks. Furthermore, we show that mitochondrial fission actively regulates mtDNA distribution by controlling the distribution of nucleoids within mitochondrial networks. Specifically, we found that primary cells bearing disease-associated mutations in the fission proteins DRP1 and MYH14 show altered nucleoid distribution, and acute enrichment of enlarged nucleoids near the nucleus. Further analysis suggests that the altered nucleoid distribution observed in the fission mutants is the result of both changes in network structure and nucleoid density. Thus, our study provides novel insights into the role of mitochondria fission in nucleoid distribution and the understanding of diseases caused by fission defects. Nature Publishing Group UK 2021-11-23 /pmc/articles/PMC8610998/ /pubmed/34815439 http://dx.doi.org/10.1038/s41598-021-01987-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ilamathi, Hema Saranya
Ouellet, Mathieu
Sabouny, Rasha
Desrochers-Goyette, Justine
Lines, Matthew A.
Pfeffer, Gerald
Shutt, Timothy E.
Germain, Marc
A new automated tool to quantify nucleoid distribution within mitochondrial networks
title A new automated tool to quantify nucleoid distribution within mitochondrial networks
title_full A new automated tool to quantify nucleoid distribution within mitochondrial networks
title_fullStr A new automated tool to quantify nucleoid distribution within mitochondrial networks
title_full_unstemmed A new automated tool to quantify nucleoid distribution within mitochondrial networks
title_short A new automated tool to quantify nucleoid distribution within mitochondrial networks
title_sort new automated tool to quantify nucleoid distribution within mitochondrial networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610998/
https://www.ncbi.nlm.nih.gov/pubmed/34815439
http://dx.doi.org/10.1038/s41598-021-01987-9
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