An essential function of the mitochondrial sulfhydryl oxidase Erv1p/ALR in the maturation of cytosolic Fe/S proteins

Biogenesis of Fe/S clusters involves a number of essential mitochondrial proteins. Here, we identify the essential Erv1p of Saccharomyces cerevisia mitochondria as a novel component that is specifically required for the maturation of Fe/S proteins in the cytosol, but not in mitochondria. Furthermore...

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Published in:EMBO reports Vol. 2; no. 8; pp. 715 - 720
Main Authors: Lange, Heike, Lisowsky, Thomas, Gerber, Jana, Mühlenhoff, Ulrich, Kispal, Gyula, Lill, Roland
Format: Journal Article
Language:English
Published: Chichester, UK John Wiley & Sons, Ltd 01-08-2001
Blackwell Publishing Ltd
Oxford University Press
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Summary:Biogenesis of Fe/S clusters involves a number of essential mitochondrial proteins. Here, we identify the essential Erv1p of Saccharomyces cerevisia mitochondria as a novel component that is specifically required for the maturation of Fe/S proteins in the cytosol, but not in mitochondria. Furthermore, Erv1p was found to be important for cellular iron homeostasis. The homologous mammalian protein ALR (‘augmenter of liver regeneration’), also termed hepatopoietin, can functionally replace defects in Erv1p and thus represents the mammalian orthologue of yeast Erv1p. Previously, a fragment of ALR was reported to exhibit an activity as an extracellular hepatotrophic growth factor. Both Erv1p and full‐length ALR are located in the mitochondrial intermembrane space and represent the first components of this compartment with a role in the biogenesis of cytosolic Fe/S proteins. It is likely that Erv1p/ALR operates downstream of the mitochondrial ABC transporter Atm1p/ABC7/Sta1, which also executes a specific task in this essential biochemical process.
Bibliography:istex:DA621D1D2ECC91EB131575E8277D4EBF7E5928F7
ArticleID:EMBR359
ark:/67375/WNG-1VV8TPXR-4
ObjectType-Article-1
SourceType-Scholarly Journals-1
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Corresponding author. Tel: +49 6421 286 6449; Fax: +49 6421 286 6414; E-mail: Lill@mailer.uni-marburg.de
ISSN:1469-221X
1469-3178
DOI:10.1093/embo-reports/kve161