Cloning and sequencing of a cDNA for human mitochondrial ubiquinone-binding protein of complex III

Biochem Biophys Res Commun. 1988 Oct 31;156(2):987-94. doi: 10.1016/s0006-291x(88)80941-0.

Abstract

The ubiquinone-binding protein (QP-C) is a nuclear-encoded component of ubiquinol-cytochrome c oxidoreductase in the mitochondrial respiratory chain and plays an important role in electron transfer as a ubiquinone-QP-C complex. We obtained a partial cDNA for rat liver QP-C by screening a lambda gt11 rat liver cDNA library using antiserum directed against bovine heart QP-C. Using this cDNA as a probe, a cDNA clone was isolated from a human fibroblast cDNA library by colony hybridization. The total length of the cloned cDNA was 518 base pairs with an open reading frame of 333 base pairs. The 111-amino acid sequence deduced from the nucleotide sequence of the cDNA is 85% homologous to that of bovine QP-C and contains only a single additional amino-terminal methionine. This implies that the human QP-C is synthesized without a presequence which is required for import of most nuclear-encoded mitochondrial proteins into mitochondria.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Carrier Proteins / genetics*
  • Cattle
  • Cloning, Molecular*
  • DNA / genetics*
  • Fibroblasts / analysis
  • Humans
  • Mitochondria / analysis
  • Molecular Sequence Data
  • Nucleic Acid Hybridization
  • Protein Conformation
  • Rats
  • Saccharomyces cerevisiae / genetics
  • Sequence Homology, Nucleic Acid
  • Ubiquinone

Substances

  • Carrier Proteins
  • ubiquinone-binding proteins
  • Ubiquinone
  • DNA

Associated data

  • GENBANK/M22348