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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 plants(1,2), but their existence in mammals remains controversial(3-5). Here we demonstrate that mammalian mitochondria can take up intact NAD(+), and identify SLC25A51 (also known as MCART1)-an essential(6,7) 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.
The organisation of molecules into dynamic cells, and collaboration of many of those cells over a billion years led to the evolution of human life. During the last century, biologists then began to unravel the marvels of cellular organisation with ever in ...
Sonia Karaz, Umberto De Marchi, Vincenzo Sorrentino, Federico Sizzano