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Overlap of copper and iron uptake systems in mitochondria in Saccharomyces cerevisiae
Author(s) -
Katherine E. Vest,
Jing Wang,
Micah G. Gammon,
Margaret K. Maynard,
Olivia L. White,
Jai A. Cobine,
Wilkerson K. Mahone,
Paul A. Cobine
Publication year - 2016
Publication title -
open biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.078
H-Index - 53
ISSN - 2046-2441
DOI - 10.1098/rsob.150223
Subject(s) - biology , mitochondrial matrix , copper , saccharomyces cerevisiae , mutant , cytochrome c oxidase , copper deficiency , mitochondrion , biochemistry , transport protein , respiratory chain , microbiology and biotechnology , yeast , gene , cytosol , materials science , enzyme , metallurgy
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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