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Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiae

In Saccharomyces cerevisiae, the mitochondrial carrier family protein Pic2 imports copper into the matrix. Deletion of PIC2 causes defects in mitochondrial copper uptake and copper-dependent growth phenotypes owing to decreased cytochrome c oxidase activity. However, copper import is not completely...

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Autores principales: Vest, Katherine E., Wang, Jing, Gammon, Micah G., Maynard, Margaret K., White, Olivia L., Cobine, Jai A., Mahone, Wilkerson K., Cobine, Paul A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736827/
https://www.ncbi.nlm.nih.gov/pubmed/26763345
http://dx.doi.org/10.1098/rsob.150223
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author Vest, Katherine E.
Wang, Jing
Gammon, Micah G.
Maynard, Margaret K.
White, Olivia L.
Cobine, Jai A.
Mahone, Wilkerson K.
Cobine, Paul A.
author_facet Vest, Katherine E.
Wang, Jing
Gammon, Micah G.
Maynard, Margaret K.
White, Olivia L.
Cobine, Jai A.
Mahone, Wilkerson K.
Cobine, Paul A.
author_sort Vest, Katherine E.
collection PubMed
description In Saccharomyces cerevisiae, the mitochondrial carrier family protein Pic2 imports copper into the matrix. Deletion of PIC2 causes defects in mitochondrial copper uptake and copper-dependent growth phenotypes owing to decreased cytochrome c oxidase activity. However, copper import is not completely eliminated in this mutant, so alternative transport systems must exist. Deletion of MRS3, a component of the iron import machinery, also causes a copper-dependent growth defect on non-fermentable carbon. Deletion of both PIC2 and MRS3 led to a more severe respiratory growth defect than either individual mutant. In addition, MRS3 expressed from a high copy number vector was able to suppress the oxygen consumption and copper uptake defects of a strain lacking PIC2. When expressed in Lactococcus lactis, Mrs3 mediated copper and iron import. Finally, a PIC2 and MRS3 double mutant prevented the copper-dependent activation of a heterologously expressed copper sensor in the mitochondrial intermembrane space. Taken together, these data support a role for the iron transporter Mrs3 in copper import into the mitochondrial matrix.
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spelling pubmed-47368272016-02-23 Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiae Vest, Katherine E. Wang, Jing Gammon, Micah G. Maynard, Margaret K. White, Olivia L. Cobine, Jai A. Mahone, Wilkerson K. Cobine, Paul A. Open Biol Research In Saccharomyces cerevisiae, the mitochondrial carrier family protein Pic2 imports copper into the matrix. Deletion of PIC2 causes defects in mitochondrial copper uptake and copper-dependent growth phenotypes owing to decreased cytochrome c oxidase activity. However, copper import is not completely eliminated in this mutant, so alternative transport systems must exist. Deletion of MRS3, a component of the iron import machinery, also causes a copper-dependent growth defect on non-fermentable carbon. Deletion of both PIC2 and MRS3 led to a more severe respiratory growth defect than either individual mutant. In addition, MRS3 expressed from a high copy number vector was able to suppress the oxygen consumption and copper uptake defects of a strain lacking PIC2. When expressed in Lactococcus lactis, Mrs3 mediated copper and iron import. Finally, a PIC2 and MRS3 double mutant prevented the copper-dependent activation of a heterologously expressed copper sensor in the mitochondrial intermembrane space. Taken together, these data support a role for the iron transporter Mrs3 in copper import into the mitochondrial matrix. The Royal Society 2016-01-13 /pmc/articles/PMC4736827/ /pubmed/26763345 http://dx.doi.org/10.1098/rsob.150223 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research
Vest, Katherine E.
Wang, Jing
Gammon, Micah G.
Maynard, Margaret K.
White, Olivia L.
Cobine, Jai A.
Mahone, Wilkerson K.
Cobine, Paul A.
Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiae
title Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiae
title_full Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiae
title_fullStr Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiae
title_full_unstemmed Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiae
title_short Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiae
title_sort overlap of copper and iron uptake systems in mitochondria in saccharomyces cerevisiae
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736827/
https://www.ncbi.nlm.nih.gov/pubmed/26763345
http://dx.doi.org/10.1098/rsob.150223
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