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Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology
The steady-state morphology of the mitochondrial network is maintained by a balance of constitutive fission and fusion reactions. Disruption of this steady-state morphology results in either a fragmented or elongated network, both of which are associated with altered metabolic states and disease. Ho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147108/ https://www.ncbi.nlm.nih.gov/pubmed/32328629 http://dx.doi.org/10.1083/jcb.201911122 |
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author | Abrisch, Robert G. Gumbin, Samantha C. Wisniewski, Brett Taylor Lackner, Laura L. Voeltz, Gia K. |
author_facet | Abrisch, Robert G. Gumbin, Samantha C. Wisniewski, Brett Taylor Lackner, Laura L. Voeltz, Gia K. |
author_sort | Abrisch, Robert G. |
collection | PubMed |
description | The steady-state morphology of the mitochondrial network is maintained by a balance of constitutive fission and fusion reactions. Disruption of this steady-state morphology results in either a fragmented or elongated network, both of which are associated with altered metabolic states and disease. How the processes of fission and fusion are balanced by the cell is unclear. Here we show that mitochondrial fission and fusion are spatially coordinated at ER membrane contact sites (MCSs). Multiple measures indicate that the mitochondrial fusion machinery, Mitofusins, accumulate at ER MCSs where fusion occurs. Furthermore, fission and fusion machineries colocalize to form hotspots for membrane dynamics at ER MCSs that can persist through sequential events. Because these hotspots can undergo fission and fusion, they have the potential to quickly respond to metabolic cues. Indeed, we discover that ER MCSs define the interface between polarized and depolarized segments of mitochondria and can rescue the membrane potential of damaged mitochondria by ER-associated fusion. |
format | Online Article Text |
id | pubmed-7147108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71471082020-10-06 Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology Abrisch, Robert G. Gumbin, Samantha C. Wisniewski, Brett Taylor Lackner, Laura L. Voeltz, Gia K. J Cell Biol Article The steady-state morphology of the mitochondrial network is maintained by a balance of constitutive fission and fusion reactions. Disruption of this steady-state morphology results in either a fragmented or elongated network, both of which are associated with altered metabolic states and disease. How the processes of fission and fusion are balanced by the cell is unclear. Here we show that mitochondrial fission and fusion are spatially coordinated at ER membrane contact sites (MCSs). Multiple measures indicate that the mitochondrial fusion machinery, Mitofusins, accumulate at ER MCSs where fusion occurs. Furthermore, fission and fusion machineries colocalize to form hotspots for membrane dynamics at ER MCSs that can persist through sequential events. Because these hotspots can undergo fission and fusion, they have the potential to quickly respond to metabolic cues. Indeed, we discover that ER MCSs define the interface between polarized and depolarized segments of mitochondria and can rescue the membrane potential of damaged mitochondria by ER-associated fusion. Rockefeller University Press 2020-02-25 /pmc/articles/PMC7147108/ /pubmed/32328629 http://dx.doi.org/10.1083/jcb.201911122 Text en © 2020 Abrisch et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Abrisch, Robert G. Gumbin, Samantha C. Wisniewski, Brett Taylor Lackner, Laura L. Voeltz, Gia K. Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology |
title | Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology |
title_full | Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology |
title_fullStr | Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology |
title_full_unstemmed | Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology |
title_short | Fission and fusion machineries converge at ER contact sites to regulate mitochondrial morphology |
title_sort | fission and fusion machineries converge at er contact sites to regulate mitochondrial morphology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7147108/ https://www.ncbi.nlm.nih.gov/pubmed/32328629 http://dx.doi.org/10.1083/jcb.201911122 |
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