In the absence of the first membrane-spanning segment of subunit 4(b), the yeast ATP synthase is functional but does not dimerize or oligomerize

J Biol Chem. 2002 Mar 22;277(12):10739-45. doi: 10.1074/jbc.M111882200. Epub 2002 Jan 17.

Abstract

The N-terminal portion of the mitochondrial b-subunit is anchored in the inner mitochondrial membrane by two hydrophobic segments. We investigated the role of the first membrane-spanning segment, which is absent in prokaryotic and chloroplastic enzymes. In the absence of the first membrane-spanning segment of the yeast subunit (subunit 4), a strong decrease in the amount of subunit g was found. The mutant ATP synthase did not dimerize or oligomerize, and mutant cells displayed anomalous mitochondrial morphologies with onion-like structures. This phenotype is similar to that of the null mutant in the ATP20 gene that encodes subunit g, a component involved in the dimerization/oligomerization of ATP synthase. Our data indicate that the first membrane-spanning segment of the mitochondrial b-subunit is not essential for the function of the enzyme since its removal did not directly alter the oxidative phosphorylation. It is proposed that the unique membrane-spanning segment of subunit g and the first membrane-spanning segment of subunit 4 interact, as shown by cross-linking experiments. We hypothesize that in eukaryotic cells the b-subunit has evolved to accommodate the interaction with the g-subunit, an associated ATP synthase component only present in the mitochondrial enzyme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / metabolism
  • Amino Acid Sequence
  • Cell Membrane / metabolism
  • Cross-Linking Reagents / pharmacology
  • Dimerization
  • Dose-Response Relationship, Drug
  • Mitochondria / enzymology
  • Mitochondria / metabolism
  • Mitochondrial Proton-Translocating ATPases / chemistry*
  • Mitochondrial Proton-Translocating ATPases / metabolism*
  • Molecular Sequence Data
  • Mutation
  • Oxygen / metabolism
  • Phenotype
  • Phosphorylation
  • Protein Binding
  • Protein Structure, Tertiary
  • Rhodamine 123 / pharmacology
  • Sequence Homology, Amino Acid
  • Time Factors

Substances

  • Cross-Linking Reagents
  • Rhodamine 123
  • Adenosine Triphosphatases
  • Mitochondrial Proton-Translocating ATPases
  • Oxygen