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Cnm1 mediates nucleus–mitochondria contact site formation in response to phospholipid levels
Author(s) -
Michal EisenbergBord,
Naama Zung,
Javier Collado,
Layla Drwesh,
Emma Fenech,
Amir Fadel,
Nili Dezorella,
Yury S. Bykov,
Doron Rapaport,
Rubén FernándezBusnadiego,
Maya Schuldiner
Publication year - 2021
Publication title -
the journal of cell biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.414
H-Index - 380
eISSN - 1540-8140
pISSN - 0021-9525
DOI - 10.1083/jcb.202104100
Subject(s) - organelle , mitochondrion , nucleus , microbiology and biotechnology , crosstalk , inner membrane , biology , cell nucleus , biophysics , chemistry , physics , optics
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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