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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2021
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.
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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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