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Yeast homologs of human MCUR1 regulate mitochondrial proline metabolism.

Authors :
Zulkifli, Mohammad
Neff, John K.
Timbalia, Shrishiv A.
Garza, Natalie M.
Chen, Yingqi
Watrous, Jeramie D.
Murgia, Marta
Trivedi, Prachi P.
Anderson, Steven K.
Tomar, Dhanendra
Nilsson, Roland
Madesh, Muniswamy
Jain, Mohit
Gohil, Vishal M.
Source :
Nature Communications; 9/25/2020, Vol. 11 Issue 1, pN.PAG-N.PAG, 1p
Publication Year :
2020

Abstract

Mitochondria house evolutionarily conserved pathways of carbon and nitrogen metabolism that drive cellular energy production. Mitochondrial bioenergetics is regulated by calcium uptake through the mitochondrial calcium uniporter (MCU), a multi-protein complex whose assembly in the inner mitochondrial membrane is facilitated by the scaffold factor MCUR1. Intriguingly, many fungi that lack MCU contain MCUR1 homologs, suggesting alternate functions. Herein, we characterize Saccharomyces cerevisiae homologs Put6 and Put7 of MCUR1 as regulators of mitochondrial proline metabolism. Put6 and Put7 are tethered to the inner mitochondrial membrane in a large hetero-oligomeric complex, whose abundance is regulated by proline. Loss of this complex perturbs mitochondrial proline homeostasis and cellular redox balance. Yeast cells lacking either Put6 or Put7 exhibit a pronounced defect in proline utilization, which can be corrected by the heterologous expression of human MCUR1. Our work uncovers an unexpected role of MCUR1 homologs in mitochondrial proline metabolism. Although some fungal mitochondria lack the calcium uniporter, many intriguingly encode homologs of the uniporter assembly factor MCUR1. Here, the authors show that in budding yeast, the MCUR1 homologs Put6 and Put7 regulate mitochondrial proline metabolism, a function also conserved in human MCUR1. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
11
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
146081896
Full Text :
https://doi.org/10.1038/s41467-020-18704-1