Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1784603212037226496 |
---|---|
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. |
format | Online Article Text |
id | pubmed-8610998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ilamathihemasaranya anewautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT ouelletmathieu anewautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT sabounyrasha anewautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT desrochersgoyettejustine anewautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT linesmatthewa anewautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT pfeffergerald anewautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT shutttimothye anewautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT germainmarc anewautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT ilamathihemasaranya newautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT ouelletmathieu newautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT sabounyrasha newautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT desrochersgoyettejustine newautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT linesmatthewa newautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT pfeffergerald newautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT shutttimothye newautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks AT germainmarc newautomatedtooltoquantifynucleoiddistributionwithinmitochondrialnetworks |