Iron-sulfur protein biogenesis in eukaryotes: components and mechanisms

Annu Rev Cell Dev Biol. 2006:22:457-86. doi: 10.1146/annurev.cellbio.22.010305.104538.

Abstract

Iron-sulfur (Fe/S) clusters require a complex set of proteins to become assembled and incorporated into apoproteins in a living cell. Researchers have described three distinct assembly systems in eukaryotes that are involved in the maturation of cellular Fe/S proteins. Mitochondria are central for biogenesis. They contain the ISC-the iron-sulfur cluster assembly machinery that was inherited from a similar system of eubacteria in evolution and is involved in biogenesis of all cellular Fe/S proteins. The basic principle of mitochondrial (and bacterial) Fe/S protein maturation is the synthesis of the Fe/S cluster on a scaffold protein before the cluster is transferred to apoproteins. Biogenesis of cytosolic and nuclear Fe/S proteins is facilitated by the cytosolic iron-sulfur protein assembly (CIA) apparatus. This process requires the participation of mitochondria that export a still unknown component via the ISC export machinery, including an ABC transporter.

Publication types

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

MeSH terms

  • Animals
  • Bacteria / metabolism
  • Eukaryotic Cells / metabolism*
  • Ferredoxin-NADP Reductase / metabolism
  • Iron-Sulfur Proteins / biosynthesis*
  • Iron-Sulfur Proteins / metabolism
  • Mitochondria / metabolism
  • Saccharomyces cerevisiae / metabolism

Substances

  • Iron-Sulfur Proteins
  • Ferredoxin-NADP Reductase