A mitochondrial ferredoxin is essential for biogenesis of cellular iron-sulfur proteins

Proc Natl Acad Sci U S A. 2000 Feb 1;97(3):1050-5. doi: 10.1073/pnas.97.3.1050.

Abstract

Iron-sulfur (Fe/S) cluster-containing proteins catalyze a number of electron transfer and metabolic reactions. The components and molecular mechanisms involved in the assembly of the Fe/S clusters have been identified only partially. In eukaryotes, mitochondria have been proposed to execute a crucial task in the generation of intramitochondrial and extramitochondrial Fe/S proteins. Herein, we identify the essential ferredoxin Yah1p of Saccharomyces cerevisiae mitochondria as a central component of the Fe/S protein biosynthesis machinery. Depletion of Yah1p by regulated gene expression resulted in a 30-fold accumulation of iron within mitochondria, similar to what has been reported for other components involved in Fe/S protein biogenesis. Yah1p was shown to be required for the assembly of Fe/S proteins both inside mitochondria and in the cytosol. Apparently, at least one of the steps of Fe/S cluster biogenesis within mitochondria requires reduction by ferredoxin. Our findings lend support to the idea of a primary function of mitochondria in the biosynthesis of Fe/S proteins outside the organelle. To our knowledge, Yah1p is the first member of the ferredoxin family for which a function in Fe/S cluster formation has been established. A similar role may be predicted for the bacterial homologs that are encoded within iron-sulfur cluster assembly (isc) operons of prokaryotes.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenodoxin*
  • Amino Acid Sequence
  • Apoproteins / metabolism
  • Bacterial Proteins / chemistry
  • Culture Media / pharmacology
  • Ferredoxins / chemistry
  • Ferredoxins / physiology*
  • Fungal Proteins / chemistry
  • Fungal Proteins / physiology*
  • Iron-Sulfur Proteins / biosynthesis*
  • Iron-Sulfur Proteins / genetics
  • Mitochondria / metabolism*
  • Molecular Sequence Data
  • Recombinant Fusion Proteins / metabolism
  • Saccharomyces cerevisiae / drug effects
  • Saccharomyces cerevisiae / growth & development
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins*
  • Sequence Alignment
  • Sequence Homology, Amino Acid

Substances

  • Apoproteins
  • Bacterial Proteins
  • Culture Media
  • Ferredoxins
  • Fungal Proteins
  • Iron-Sulfur Proteins
  • Recombinant Fusion Proteins
  • Saccharomyces cerevisiae Proteins
  • YAH1 protein, S cerevisiae
  • Adrenodoxin