A Single Adaptable Cochaperone-Scaffold Complex Delivers Nascent Iron-Sulfur Clusters to Mammalian Respiratory Chain Complexes I-III

Cell Metab. 2017 Apr 4;25(4):945-953.e6. doi: 10.1016/j.cmet.2017.03.010.

Abstract

The iron-sulfur (Fe-S) cluster of the Rieske protein, UQCRFS1, is essential for Complex III (CIII) activity, though the mechanism for Fe-S cluster transfer has not previously been elucidated. Recent studies have shown that the co-chaperone HSC20, essential for Fe-S cluster biogenesis of SDHB, directly binds LYRM7, formerly described as a chaperone that stabilizes UQCRFS1 prior to its insertion into CIII. Here we report that a transient subcomplex involved in CIII assembly, composed of LYRM7 bound to UQCRFS1, interacts with components of an Fe-S transfer complex, consisting of HSC20, its cognate chaperone HSPA9, and the holo-scaffold ISCU. Binding of HSC20 to the LYR motif of LYRM7 in a pre-assembled UQCRFS1-LYRM7 intermediate in the mitochondrial matrix facilitates Fe-S cluster transfer to UQCRFS1. The five Fe-S cluster subunits of Complex I also interact with HSC20 to acquire their clusters, highlighting the crucial role of HSC20 in the assembly of the mitochondrial respiratory chain.

Keywords: Complex I; Complex II; Complex III; HSC20; HSPA9; ISCU; LYRM7; iron sulfur biogenesis; mitochondrial respiratory chain.

MeSH terms

  • Amino Acid Motifs
  • Animals
  • Electron Transport
  • Electron Transport Chain Complex Proteins / metabolism*
  • Gene Knockout Techniques
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Iron-Sulfur Proteins / metabolism*
  • Mammals / metabolism*
  • Mitochondria / metabolism
  • Mitochondrial Proteins / chemistry
  • Mitochondrial Proteins / metabolism
  • Molecular Chaperones / chemistry
  • Molecular Chaperones / metabolism*
  • Protein Binding

Substances

  • Electron Transport Chain Complex Proteins
  • HSCB protein, human
  • Iron-Sulfur Proteins
  • LYRM7 protein, human
  • Mitochondrial Proteins
  • Molecular Chaperones
  • UQCRFS1 protein, human