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Cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels
Mitochondrial functions are tightly regulated by nuclear activity, requiring extensive communication between these organelles. One way by which organelles can communicate is through contact sites, areas of close apposition held together by tethering molecules. While many contacts have been character...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548916/ https://www.ncbi.nlm.nih.gov/pubmed/34694322 http://dx.doi.org/10.1083/jcb.202104100 |
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author | Eisenberg-Bord, Michal Zung, Naama Collado, Javier Drwesh, Layla Fenech, Emma J. Fadel, Amir Dezorella, Nili Bykov, Yury S. Rapaport, Doron Fernandez-Busnadiego, Ruben Schuldiner, Maya |
author_facet | Eisenberg-Bord, Michal Zung, Naama Collado, Javier Drwesh, Layla Fenech, Emma J. Fadel, Amir Dezorella, Nili Bykov, Yury S. Rapaport, Doron Fernandez-Busnadiego, Ruben Schuldiner, Maya |
author_sort | Eisenberg-Bord, Michal |
collection | PubMed |
description | Mitochondrial functions are tightly regulated by nuclear activity, requiring extensive communication between these organelles. One way by which organelles can communicate is through contact sites, areas of close apposition held together by tethering molecules. While many contacts have been characterized in yeast, the contact between the nucleus and mitochondria was not previously identified. Using fluorescence and electron microscopy in S. cerevisiae, we demonstrate specific areas of contact between the two organelles. Using a high-throughput screen, we uncover a role for the uncharacterized protein Ybr063c, which we have named Cnm1 (contact nucleus mitochondria 1), as a molecular tether on the nuclear membrane. We show that Cnm1 mediates contact by interacting with Tom70 on mitochondria. Moreover, Cnm1 abundance is regulated by phosphatidylcholine, enabling the coupling of phospholipid homeostasis with contact extent. The discovery of a molecular mechanism that allows mitochondrial crosstalk with the nucleus sets the ground for better understanding of mitochondrial functions in health and disease. |
format | Online Article Text |
id | pubmed-8548916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85489162021-11-05 Cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels Eisenberg-Bord, Michal Zung, Naama Collado, Javier Drwesh, Layla Fenech, Emma J. Fadel, Amir Dezorella, Nili Bykov, Yury S. Rapaport, Doron Fernandez-Busnadiego, Ruben Schuldiner, Maya J Cell Biol Article Mitochondrial functions are tightly regulated by nuclear activity, requiring extensive communication between these organelles. One way by which organelles can communicate is through contact sites, areas of close apposition held together by tethering molecules. While many contacts have been characterized in yeast, the contact between the nucleus and mitochondria was not previously identified. Using fluorescence and electron microscopy in S. cerevisiae, we demonstrate specific areas of contact between the two organelles. Using a high-throughput screen, we uncover a role for the uncharacterized protein Ybr063c, which we have named Cnm1 (contact nucleus mitochondria 1), as a molecular tether on the nuclear membrane. We show that Cnm1 mediates contact by interacting with Tom70 on mitochondria. Moreover, Cnm1 abundance is regulated by phosphatidylcholine, enabling the coupling of phospholipid homeostasis with contact extent. The discovery of a molecular mechanism that allows mitochondrial crosstalk with the nucleus sets the ground for better understanding of mitochondrial functions in health and disease. Rockefeller University Press 2021-10-25 /pmc/articles/PMC8548916/ /pubmed/34694322 http://dx.doi.org/10.1083/jcb.202104100 Text en © 2021 Eisenberg-Bord et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Eisenberg-Bord, Michal Zung, Naama Collado, Javier Drwesh, Layla Fenech, Emma J. Fadel, Amir Dezorella, Nili Bykov, Yury S. Rapaport, Doron Fernandez-Busnadiego, Ruben Schuldiner, Maya Cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels |
title | Cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels |
title_full | Cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels |
title_fullStr | Cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels |
title_full_unstemmed | Cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels |
title_short | Cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels |
title_sort | cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548916/ https://www.ncbi.nlm.nih.gov/pubmed/34694322 http://dx.doi.org/10.1083/jcb.202104100 |
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