SLC25A51 is a mammalian mitochondrial NAD+ transporter
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 controversia...
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creator | Luongo, Timothy S. Eller, Jared M. Lu, Mu-Jie Niere, Marc Raith, Fabio Perry, Caroline Bornstein, Marc R. Oliphint, Paul Wang, Lin McReynolds, Melanie R. Migaud, Marie E. Rabinowitz, Joshua D. Johnson, F. Brad Johnsson, Kai Ziegler, Mathias Cambronne, Xiaolu A. Baur, Joseph A. |
description | 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.
SLC25A51 is identified as a transporter of intact NAD
+
into mammalian mitochondria and is required to maintain the mitochondrial NAD
+
pool and respiratory function. |
doi_str_mv | 10.1038/s41586-020-2741-7 |
format | Article |
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+
) 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.
SLC25A51 is identified as a transporter of intact NAD
+
into mammalian mitochondria and is required to maintain the mitochondrial NAD
+
pool and respiratory function.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/s41586-020-2741-7</identifier><identifier>PMID: 32906142</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/106 ; 13/31 ; 14/19 ; 14/34 ; 42/41 ; 42/44 ; 631/443/319/333/1465 ; 631/80/642/333/1465 ; 82/1 ; 82/58 ; 96 ; 96/10 ; Adenine ; Animals ; Biological Transport ; Cell Line ; Cell Respiration - genetics ; Energy transduction ; Genetic Complementation Test ; Humanities and Social Sciences ; Humans ; Mammals ; Metabolism ; Metabolites ; Mice ; Mitochondria ; Mitochondria - genetics ; Mitochondria - metabolism ; Mitochondria - pathology ; Mitochondrial Proteins - deficiency ; Mitochondrial Proteins - genetics ; Mitochondrial Proteins - metabolism ; multidisciplinary ; NAD ; NAD - metabolism ; Nicotinamide ; Nicotinamide adenine dinucleotide ; Nucleotide Transport Proteins - genetics ; Organic Cation Transport Proteins - deficiency ; Organic Cation Transport Proteins - genetics ; Oxidative stress ; Proteins ; Respiration ; Saccharomyces cerevisiae - cytology ; Saccharomyces cerevisiae - genetics ; Saccharomyces cerevisiae - metabolism ; Saccharomyces cerevisiae Proteins - genetics ; Science ; Science (multidisciplinary) ; Stem cells ; Yeast ; Yeasts</subject><ispartof>Nature (London), 2020-12, Vol.588 (7836), p.174-179</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2020</rights><rights>Copyright Nature Publishing Group Dec 3, 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-7a65e37f826711e983462f459abc1bf64039a6843b987b5a475054f821e033003</citedby><cites>FETCH-LOGICAL-c507t-7a65e37f826711e983462f459abc1bf64039a6843b987b5a475054f821e033003</cites><orcidid>0000-0001-6961-2396 ; 0000-0001-7621-7992 ; 0000-0001-8262-6549 ; 0000-0002-7443-7227 ; 0000-0001-5427-2739 ; 0000-0002-3547-448X ; 0000-0002-1247-4727</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/s41586-020-2741-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/s41586-020-2741-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32906142$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luongo, Timothy S.</creatorcontrib><creatorcontrib>Eller, Jared M.</creatorcontrib><creatorcontrib>Lu, Mu-Jie</creatorcontrib><creatorcontrib>Niere, Marc</creatorcontrib><creatorcontrib>Raith, Fabio</creatorcontrib><creatorcontrib>Perry, Caroline</creatorcontrib><creatorcontrib>Bornstein, Marc R.</creatorcontrib><creatorcontrib>Oliphint, Paul</creatorcontrib><creatorcontrib>Wang, Lin</creatorcontrib><creatorcontrib>McReynolds, Melanie R.</creatorcontrib><creatorcontrib>Migaud, Marie E.</creatorcontrib><creatorcontrib>Rabinowitz, Joshua D.</creatorcontrib><creatorcontrib>Johnson, F. Brad</creatorcontrib><creatorcontrib>Johnsson, Kai</creatorcontrib><creatorcontrib>Ziegler, Mathias</creatorcontrib><creatorcontrib>Cambronne, Xiaolu A.</creatorcontrib><creatorcontrib>Baur, Joseph A.</creatorcontrib><title>SLC25A51 is a mammalian mitochondrial NAD+ transporter</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>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.
SLC25A51 is identified as a transporter of intact NAD
+
into mammalian mitochondria and is required to maintain the mitochondrial NAD
+
pool and respiratory function.</description><subject>13/106</subject><subject>13/31</subject><subject>14/19</subject><subject>14/34</subject><subject>42/41</subject><subject>42/44</subject><subject>631/443/319/333/1465</subject><subject>631/80/642/333/1465</subject><subject>82/1</subject><subject>82/58</subject><subject>96</subject><subject>96/10</subject><subject>Adenine</subject><subject>Animals</subject><subject>Biological Transport</subject><subject>Cell Line</subject><subject>Cell Respiration - genetics</subject><subject>Energy transduction</subject><subject>Genetic Complementation Test</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Mammals</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Mice</subject><subject>Mitochondria</subject><subject>Mitochondria - genetics</subject><subject>Mitochondria - metabolism</subject><subject>Mitochondria - pathology</subject><subject>Mitochondrial Proteins - deficiency</subject><subject>Mitochondrial Proteins - genetics</subject><subject>Mitochondrial Proteins - metabolism</subject><subject>multidisciplinary</subject><subject>NAD</subject><subject>NAD - metabolism</subject><subject>Nicotinamide</subject><subject>Nicotinamide adenine dinucleotide</subject><subject>Nucleotide Transport Proteins - genetics</subject><subject>Organic Cation Transport Proteins - deficiency</subject><subject>Organic Cation Transport Proteins - genetics</subject><subject>Oxidative stress</subject><subject>Proteins</subject><subject>Respiration</subject><subject>Saccharomyces cerevisiae - cytology</subject><subject>Saccharomyces cerevisiae - genetics</subject><subject>Saccharomyces cerevisiae - metabolism</subject><subject>Saccharomyces cerevisiae Proteins - genetics</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Stem cells</subject><subject>Yeast</subject><subject>Yeasts</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kU1Lw0AQhhdRbK3-AC8S8CJIdPZ7cxFK_YSiB_W8bNJNm5Jk624q-O_d0lo_wLnMYZ55Z15ehI4xXGCg6jIwzJVIgUBKJMOp3EF9zKRImVByF_UBiEpBUdFDByHMAYBjyfZRj5IMBGakj8TzeET4kOOkColJGtM0pq5MmzRV54qZaye-MnXyOLw-Tzpv2rBwvrP-EO2Vpg72aNMH6PX25mV0n46f7h5Gw3FacJBdKo3glspSESExtpmiTJCS8czkBc5LwYBmRihG80zJnBsmOXAWcWyBUgA6QFdr3cUyb-yksG18otYLXzXGf2hnKv170lYzPXXvWkqsaKwBOtsIePe2tKHTTRUKW9emtW4ZNGEMC6CM8Yie_kHnbunbaC9SMiLRwkoQr6nCuxC8LbfPYNCrVPQ6FR1T0atUtIw7Jz9dbDe-YogAWQMhjtqp9d-n_1f9BIPclCE</recordid><startdate>20201203</startdate><enddate>20201203</enddate><creator>Luongo, Timothy S.</creator><creator>Eller, Jared M.</creator><creator>Lu, Mu-Jie</creator><creator>Niere, Marc</creator><creator>Raith, Fabio</creator><creator>Perry, Caroline</creator><creator>Bornstein, Marc R.</creator><creator>Oliphint, Paul</creator><creator>Wang, Lin</creator><creator>McReynolds, Melanie R.</creator><creator>Migaud, Marie E.</creator><creator>Rabinowitz, Joshua D.</creator><creator>Johnson, F. 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Brad ; Johnsson, Kai ; Ziegler, Mathias ; Cambronne, Xiaolu A. ; Baur, Joseph A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-7a65e37f826711e983462f459abc1bf64039a6843b987b5a475054f821e033003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>13/106</topic><topic>13/31</topic><topic>14/19</topic><topic>14/34</topic><topic>42/41</topic><topic>42/44</topic><topic>631/443/319/333/1465</topic><topic>631/80/642/333/1465</topic><topic>82/1</topic><topic>82/58</topic><topic>96</topic><topic>96/10</topic><topic>Adenine</topic><topic>Animals</topic><topic>Biological Transport</topic><topic>Cell Line</topic><topic>Cell Respiration - genetics</topic><topic>Energy transduction</topic><topic>Genetic Complementation Test</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Mammals</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Mice</topic><topic>Mitochondria</topic><topic>Mitochondria - genetics</topic><topic>Mitochondria - metabolism</topic><topic>Mitochondria - pathology</topic><topic>Mitochondrial Proteins - deficiency</topic><topic>Mitochondrial Proteins - genetics</topic><topic>Mitochondrial Proteins - metabolism</topic><topic>multidisciplinary</topic><topic>NAD</topic><topic>NAD - metabolism</topic><topic>Nicotinamide</topic><topic>Nicotinamide adenine dinucleotide</topic><topic>Nucleotide Transport Proteins - genetics</topic><topic>Organic Cation Transport Proteins - deficiency</topic><topic>Organic Cation Transport Proteins - genetics</topic><topic>Oxidative stress</topic><topic>Proteins</topic><topic>Respiration</topic><topic>Saccharomyces cerevisiae - cytology</topic><topic>Saccharomyces cerevisiae - genetics</topic><topic>Saccharomyces cerevisiae - metabolism</topic><topic>Saccharomyces cerevisiae Proteins - genetics</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Stem cells</topic><topic>Yeast</topic><topic>Yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luongo, Timothy S.</creatorcontrib><creatorcontrib>Eller, Jared M.</creatorcontrib><creatorcontrib>Lu, Mu-Jie</creatorcontrib><creatorcontrib>Niere, Marc</creatorcontrib><creatorcontrib>Raith, Fabio</creatorcontrib><creatorcontrib>Perry, Caroline</creatorcontrib><creatorcontrib>Bornstein, Marc R.</creatorcontrib><creatorcontrib>Oliphint, Paul</creatorcontrib><creatorcontrib>Wang, Lin</creatorcontrib><creatorcontrib>McReynolds, Melanie R.</creatorcontrib><creatorcontrib>Migaud, Marie E.</creatorcontrib><creatorcontrib>Rabinowitz, Joshua D.</creatorcontrib><creatorcontrib>Johnson, F. 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luongo, Timothy S.</au><au>Eller, Jared M.</au><au>Lu, Mu-Jie</au><au>Niere, Marc</au><au>Raith, Fabio</au><au>Perry, Caroline</au><au>Bornstein, Marc R.</au><au>Oliphint, Paul</au><au>Wang, Lin</au><au>McReynolds, Melanie R.</au><au>Migaud, Marie E.</au><au>Rabinowitz, Joshua D.</au><au>Johnson, F. Brad</au><au>Johnsson, Kai</au><au>Ziegler, Mathias</au><au>Cambronne, Xiaolu A.</au><au>Baur, Joseph A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SLC25A51 is a mammalian mitochondrial NAD+ transporter</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2020-12-03</date><risdate>2020</risdate><volume>588</volume><issue>7836</issue><spage>174</spage><epage>179</epage><pages>174-179</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><abstract>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.
SLC25A51 is identified as a transporter of intact NAD
+
into mammalian mitochondria and is required to maintain the mitochondrial NAD
+
pool and respiratory function.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32906142</pmid><doi>10.1038/s41586-020-2741-7</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-6961-2396</orcidid><orcidid>https://orcid.org/0000-0001-7621-7992</orcidid><orcidid>https://orcid.org/0000-0001-8262-6549</orcidid><orcidid>https://orcid.org/0000-0002-7443-7227</orcidid><orcidid>https://orcid.org/0000-0001-5427-2739</orcidid><orcidid>https://orcid.org/0000-0002-3547-448X</orcidid><orcidid>https://orcid.org/0000-0002-1247-4727</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-0836 |
ispartof | Nature (London), 2020-12, Vol.588 (7836), p.174-179 |
issn | 0028-0836 1476-4687 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7718333 |
source | MEDLINE; Nature; SpringerLink Journals - AutoHoldings |
subjects | 13/106 13/31 14/19 14/34 42/41 42/44 631/443/319/333/1465 631/80/642/333/1465 82/1 82/58 96 96/10 Adenine Animals Biological Transport Cell Line Cell Respiration - genetics Energy transduction Genetic Complementation Test Humanities and Social Sciences Humans Mammals Metabolism Metabolites Mice Mitochondria Mitochondria - genetics Mitochondria - metabolism Mitochondria - pathology Mitochondrial Proteins - deficiency Mitochondrial Proteins - genetics Mitochondrial Proteins - metabolism multidisciplinary NAD NAD - metabolism Nicotinamide Nicotinamide adenine dinucleotide Nucleotide Transport Proteins - genetics Organic Cation Transport Proteins - deficiency Organic Cation Transport Proteins - genetics Oxidative stress Proteins Respiration Saccharomyces cerevisiae - cytology Saccharomyces cerevisiae - genetics Saccharomyces cerevisiae - metabolism Saccharomyces cerevisiae Proteins - genetics Science Science (multidisciplinary) Stem cells Yeast Yeasts |
title | SLC25A51 is a mammalian mitochondrial NAD+ transporter |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T14%3A12%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=SLC25A51%20is%20a%20mammalian%20mitochondrial%20NAD+%20transporter&rft.jtitle=Nature%20(London)&rft.au=Luongo,%20Timothy%20S.&rft.date=2020-12-03&rft.volume=588&rft.issue=7836&rft.spage=174&rft.epage=179&rft.pages=174-179&rft.issn=0028-0836&rft.eissn=1476-4687&rft_id=info:doi/10.1038/s41586-020-2741-7&rft_dat=%3Cproquest_pubme%3E2441603445%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2473447113&rft_id=info:pmid/32906142&rfr_iscdi=true |