Modeling the Leigh syndrome nt8993 T-->C mutation in Escherichia coli F1F0 ATP synthase

Int J Biochem Cell Biol. 1999 Jul;31(7):769-76. doi: 10.1016/s1357-2725(99)00029-1.

Abstract

The mutations in human mitochondrial DNA at nt8993 are associated with a range of neuromuscular disorders. One mutation encodes a proline in place of a leucine conserved in all animal mitochondrial ATPase-6 subunits and bacterial a subunits of F1F0 ATP synthases. This conserved site is leu-156 and leu-207 in humans and Escherichia coli, respectively. An aleu-207-->pro substitution mutation has been constructed in the E. coli F1F0 ATP synthase in order to model the biochemical basis of the human disease mutation. The phenotype of the aleu-207-->pro substitution has been compared to that of the previously studied aleu-207-->arg substitution (Hartzog and Cain, 1993, Journal of Biological Chemistry 268, 12250-12252). The leu-207-->pro mutation resulted in approximately a 35% decrease in the number of intact enzyme complexes as determined by N, N'-dicyclohexylcarbodiimide-sensitive membrane associated ATP hydrolysis activity and western analysis using an anti-a subunit antibody. A 75% reduction in the efficiency of proton translocation through F1F0 ATP synthase was observed in ATP-driven proton pumping assays. Interestingly, the loss in F1F0 ATP synthase activity resulting from the leu-207-->pro substitution was markedly less dramatic than had been observed for the leu-207-->arg mutation studied earlier. By analogy, the human enzyme may also be affected by the leu-156-->pro substitution to a lesser extent than the leu-156-->arg substitution, and this would account for the milder clinical manifestations of the human leu-156-->pro disease mutations.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • DNA, Mitochondrial / genetics
  • Escherichia coli / enzymology*
  • Escherichia coli / genetics
  • Genetic Complementation Test
  • Humans
  • Leigh Disease / enzymology*
  • Leigh Disease / genetics*
  • Plasmids / genetics
  • Point Mutation*
  • Proton-Translocating ATPases / chemistry
  • Proton-Translocating ATPases / genetics*
  • Proton-Translocating ATPases / metabolism
  • Syndrome

Substances

  • DNA, Mitochondrial
  • Proton-Translocating ATPases