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dc.contributor.authorKory, Nora
dc.contributor.authoruit de Bos, Jelmi
dc.contributor.authorvan der Rijt, Sanne
dc.contributor.authorJankovic, Nevena
dc.contributor.authorGüra, Miriam
dc.contributor.authorArp, Nicholas
dc.contributor.authorPena, Izabella A
dc.contributor.authorPrakash, Gyan
dc.contributor.authorChan, Sze Ham
dc.contributor.authorKunchok, Tenzin
dc.contributor.authorLewis, Caroline A
dc.contributor.authorSabatini, David M
dc.date.accessioned2021-10-27T20:22:48Z
dc.date.available2021-10-27T20:22:48Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/135285
dc.description.abstractThe nicotinamide adenine dinucleotide (NAD /NADH) pair is a cofactor in redox reactions and is particularly critical in mitochondria as it connects substrate oxidation by the tricarboxylic acid (TCA) cycle to adenosine triphosphate generation by the electron transport chain (ETC) and oxidative phosphorylation. While a mitochondrial NAD transporter has been identified in yeast, how NAD enters mitochondria in metazoans is unknown. Here, we mine gene essentiality data from human cell lines to identify MCART1 (SLC25A51) as coessential with ETC components. MCART1-null cells have large decreases in TCA cycle flux, mitochondrial respiration, ETC complex I activity, and mitochondrial levels of NAD and NADH. Isolated mitochondria from cells lacking or overexpressing MCART1 have greatly decreased or increased NAD uptake in vitro, respectively. Moreover, MCART1 and NDT1, a yeast mitochondrial NAD transporter, can functionally complement for each other. Thus, we propose that MCART1 is the long sought mitochondrial transporter for NAD in human cells. + + + +
dc.language.isoen
dc.publisherAmerican Association for the Advancement of Science (AAAS)
dc.relation.isversionof10.1126/SCIADV.ABE5310
dc.rightsCreative Commons Attribution NonCommercial License 4.0
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.sourceScience Advances
dc.titleMCART1/SLC25A51 is required for mitochondrial NAD transport
dc.typeArticle
dc.contributor.departmentWhitehead Institute for Biomedical Research
dc.contributor.departmentHoward Hughes Medical Institute
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.relation.journalScience Advances
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-07-23T18:31:09Z
dspace.orderedauthorsKory, N; uit de Bos, J; van der Rijt, S; Jankovic, N; Güra, M; Arp, N; Pena, IA; Prakash, G; Chan, SH; Kunchok, T; Lewis, CA; Sabatini, DM
dspace.date.submission2021-07-23T18:31:11Z
mit.journal.volume6
mit.journal.issue43
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Needed


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