TY - JOUR
T1 - SLC25A51 is a mammalian mitochondrial NAD+ transporter
AU - Luongo, Timothy S.
AU - Eller, Jared M.
AU - Lu, Mu Jie
AU - Niere, Marc
AU - Raith, Fabio
AU - Perry, Caroline
AU - Bornstein, Marc R.
AU - Oliphint, Paul
AU - Wang, Lin
AU - McReynolds, Melanie R.
AU - Migaud, Marie E.
AU - Rabinowitz, Joshua D.
AU - Johnson, F. Brad
AU - Johnsson, Kai
AU - Ziegler, Mathias
AU - Cambronne, Xiaolu A.
AU - Baur, Joseph A.
N1 - Publisher Copyright:
© 2020, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2020/12/3
Y1 - 2020/12/3
N2 - Mitochondria require nicotinamide adenine dinucleotide (NAD+) to carry out the fundamental processes that fuel respiration and mediate cellular energy transduction. Mitochondrial NAD+ transporters have been identified in yeast and plants1,2, but their existence in mammals remains controversial3–5. Here we demonstrate that mammalian mitochondria can take up intact NAD+, and identify SLC25A51 (also known as MCART1)—an essential6,7 mitochondrial protein of previously unknown function—as a mammalian mitochondrial NAD+ transporter. Loss of SLC25A51 decreases mitochondrial—but not whole-cell—NAD+ content, impairs mitochondrial respiration, and blocks the uptake of NAD+ into isolated mitochondria. Conversely, overexpression of SLC25A51 or SLC25A52 (a nearly identical paralogue of SLC25A51) increases mitochondrial NAD+ levels and restores NAD+ uptake into yeast mitochondria lacking endogenous NAD+ transporters. Together, these findings identify SLC25A51 as a mammalian transporter capable of importing NAD+ into mitochondria.
AB - Mitochondria require nicotinamide adenine dinucleotide (NAD+) to carry out the fundamental processes that fuel respiration and mediate cellular energy transduction. Mitochondrial NAD+ transporters have been identified in yeast and plants1,2, but their existence in mammals remains controversial3–5. Here we demonstrate that mammalian mitochondria can take up intact NAD+, and identify SLC25A51 (also known as MCART1)—an essential6,7 mitochondrial protein of previously unknown function—as a mammalian mitochondrial NAD+ transporter. Loss of SLC25A51 decreases mitochondrial—but not whole-cell—NAD+ content, impairs mitochondrial respiration, and blocks the uptake of NAD+ into isolated mitochondria. Conversely, overexpression of SLC25A51 or SLC25A52 (a nearly identical paralogue of SLC25A51) increases mitochondrial NAD+ levels and restores NAD+ uptake into yeast mitochondria lacking endogenous NAD+ transporters. Together, these findings identify SLC25A51 as a mammalian transporter capable of importing NAD+ into mitochondria.
UR - http://www.scopus.com/inward/record.url?scp=85090431624&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85090431624&partnerID=8YFLogxK
U2 - 10.1038/s41586-020-2741-7
DO - 10.1038/s41586-020-2741-7
M3 - Article
C2 - 32906142
AN - SCOPUS:85090431624
SN - 0028-0836
VL - 588
SP - 174
EP - 179
JO - Nature
JF - Nature
IS - 7836
ER -