Literature DB >> 29237729

The mammalian phosphate carrier SLC25A3 is a mitochondrial copper transporter required for cytochrome c oxidase biogenesis.

Aren Boulet1, Katherine E Vest2, Margaret K Maynard2, Micah G Gammon2, Antoinette C Russell2, Alexander T Mathews2, Shelbie E Cole2, Xinyu Zhu2, Casey B Phillips2, Jennifer Q Kwong3, Sheel C Dodani4, Scot C Leary1, Paul A Cobine5.   

Abstract

Copper is required for the activity of cytochrome c oxidase (COX), the terminal electron-accepting complex of the mitochondrial respiratory chain. The likely source of copper used for COX biogenesis is a labile pool found in the mitochondrial matrix. In mammals, the proteins that transport copper across the inner mitochondrial membrane remain unknown. We previously reported that the mitochondrial carrier family protein Pic2 in budding yeast is a copper importer. The closest Pic2 ortholog in mammalian cells is the mitochondrial phosphate carrier SLC25A3. Here, to investigate whether SLC25A3 also transports copper, we manipulated its expression in several murine and human cell lines. SLC25A3 knockdown or deletion consistently resulted in an isolated COX deficiency in these cells, and copper addition to the culture medium suppressed these biochemical defects. Consistent with a conserved role for SLC25A3 in copper transport, its heterologous expression in yeast complemented copper-specific defects observed upon deletion of PIC2 Additionally, assays in Lactococcus lactis and in reconstituted liposomes directly demonstrated that SLC25A3 functions as a copper transporter. Taken together, these data indicate that SLC25A3 can transport copper both in vitro and in vivo.
© 2018 by The American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  copper; copper transport; cytochrome c oxidase (complex IV); membrane transport; mitochondria

Mesh:

Substances:

Year:  2017        PMID: 29237729      PMCID: PMC5808751          DOI: 10.1074/jbc.RA117.000265

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  64 in total

1.  Mitochondrial phosphate-carrier deficiency: a novel disorder of oxidative phosphorylation.

Authors:  Johannes A Mayr; Olaf Merkel; Sepp D Kohlwein; Boris R Gebhardt; Hansjosef Böhles; Ulrike Fötschl; Johannes Koch; Michaela Jaksch; Hanns Lochmüller; Rita Horváth; Peter Freisinger; Wolfgang Sperl
Journal:  Am J Hum Genet       Date:  2007-01-10       Impact factor: 11.025

2.  Expression in Escherichia coli, functional characterization, and tissue distribution of isoforms A and B of the phosphate carrier from bovine mitochondria.

Authors:  G Fiermonte; V Dolce; F Palmieri
Journal:  J Biol Chem       Date:  1998-08-28       Impact factor: 5.157

3.  HL-1 cells: a cardiac muscle cell line that contracts and retains phenotypic characteristics of the adult cardiomyocyte.

Authors:  W C Claycomb; N A Lanson; B S Stallworth; D B Egeland; J B Delcarpio; A Bahinski; N J Izzo
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-17       Impact factor: 11.205

4.  Mutations in SCO2 are associated with a distinct form of hypertrophic cardiomyopathy and cytochrome c oxidase deficiency.

Authors:  M Jaksch; I Ogilvie; J Yao; G Kortenhaus; H G Bresser; K D Gerbitz; E A Shoubridge
Journal:  Hum Mol Genet       Date:  2000-03-22       Impact factor: 6.150

5.  Homozygosity (E140K) in SCO2 causes delayed infantile onset of cardiomyopathy and neuropathy.

Authors:  M Jaksch; R Horvath; N Horn; D P Auer; C Macmillan; J Peters; K D Gerbitz; I Kraegeloh-Mann; A Muntau; V Karcagi; R Kalmanchey; H Lochmuller; E A Shoubridge; P Freisinger
Journal:  Neurology       Date:  2001-10-23       Impact factor: 9.910

6.  Natural and Induced Mitochondrial Phosphate Carrier Loss: DIFFERENTIAL DEPENDENCE OF MITOCHONDRIAL METABOLISM AND DYNAMICS AND CELL SURVIVAL ON THE EXTENT OF DEPLETION.

Authors:  Erin L Seifert; Aniko Gál; Michelle G Acoba; Qipei Li; Lauren Anderson-Pullinger; Tunde Golenár; Cynthia Moffat; Neal Sondheimer; Steven M Claypool; György Hajnóczky
Journal:  J Biol Chem       Date:  2016-10-25       Impact factor: 5.157

Review 7.  The mitochondrial transporter family (SLC25): physiological and pathological implications.

Authors:  Ferdinando Palmieri
Journal:  Pflugers Arch       Date:  2003-11-04       Impact factor: 3.657

8.  The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A.

Authors:  T Tsukihara; H Aoyama; E Yamashita; T Tomizaki; H Yamaguchi; K Shinzawa-Itoh; R Nakashima; R Yaono; S Yoshikawa
Journal:  Science       Date:  1996-05-24       Impact factor: 47.728

9.  Human COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase.

Authors:  Myriam Bourens; Aren Boulet; Scot C Leary; Antoni Barrientos
Journal:  Hum Mol Genet       Date:  2014-01-08       Impact factor: 5.121

10.  The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission.

Authors:  Ruchika Anand; Timothy Wai; Michael J Baker; Nikolay Kladt; Astrid C Schauss; Elena Rugarli; Thomas Langer
Journal:  J Cell Biol       Date:  2014-03-10       Impact factor: 10.539

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  37 in total

1.  Reconstitution of a thermophilic Cu+ importer in vitro reveals intrinsic high-affinity slow transport driving accumulation of an essential metal ion.

Authors:  Brandon L Logeman; Dennis J Thiele
Journal:  J Biol Chem       Date:  2018-08-21       Impact factor: 5.157

2.  Filling the mitochondrial copper pool.

Authors:  Dennis R Winge
Journal:  J Biol Chem       Date:  2018-02-09       Impact factor: 5.157

3.  Omics Integration for Mitochondria Systems Biology.

Authors:  Xin Hu; Young-Mi Go; Dean P Jones
Journal:  Antioxid Redox Signal       Date:  2020-02-03       Impact factor: 8.401

Review 4.  Copper transporters and copper chaperones: roles in cardiovascular physiology and disease.

Authors:  Tohru Fukai; Masuko Ushio-Fukai; Jack H Kaplan
Journal:  Am J Physiol Cell Physiol       Date:  2018-06-06       Impact factor: 4.249

Review 5.  Non-cell autonomous mechanism of Parkinson's disease pathology caused by G2019S LRRK2 mutation in Ashkenazi Jewish patient: Single cell analysis.

Authors:  Jeffrey Kim; Marcel M Daadi
Journal:  Brain Res       Date:  2019-07-19       Impact factor: 3.252

6.  Copper dependent ERK1/2 phosphorylation is essential for the viability of neurons and not glia.

Authors:  Kaustav Chakraborty; Sumanta Kar; Bhawana Rai; Reshma Bhagat; Nabanita Naskar; Pankaj Seth; Arnab Gupta; Ashima Bhattacharjee
Journal:  Metallomics       Date:  2022-04-01       Impact factor: 4.526

7.  Splitting the functions of Rim2, a mitochondrial iron/pyrimidine carrier.

Authors:  Simon A B Knight; Heeyong Yoon; Ashutosh K Pandey; Jayashree Pain; Debkumar Pain; Andrew Dancis
Journal:  Mitochondrion       Date:  2019-01-18       Impact factor: 4.160

8.  Potential Diagnostic Significance of Salivary Copper Determination in Breast Cancer Patients: A Pilot Study.

Authors:  Lyudmila V Bel'skaya; Elena A Sarf; Sergey P Shalygin; Tatyana V Postnova; Victor K Kosenok
Journal:  Biol Trace Elem Res       Date:  2021-04-10       Impact factor: 3.738

Review 9.  Getting out what you put in: Copper in mitochondria and its impacts on human disease.

Authors:  Paul A Cobine; Stanley A Moore; Scot C Leary
Journal:  Biochim Biophys Acta Mol Cell Res       Date:  2020-10-02       Impact factor: 4.739

Review 10.  Copper metabolism as a unique vulnerability in cancer.

Authors:  Vinit C Shanbhag; Nikita Gudekar; Kimberly Jasmer; Christos Papageorgiou; Kamal Singh; Michael J Petris
Journal:  Biochim Biophys Acta Mol Cell Res       Date:  2020-10-20       Impact factor: 4.739

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