Mitochondrial deoxyguanosine kinase mutations and mitochondrial DNA depletion syndrome

FEBS Lett. 2003 Nov 20;554(3):319-22. doi: 10.1016/s0014-5793(03)01181-5.

Abstract

Mitochondrial deoxyguanosine kinase (dGK) catalyzes the initial phosphorylation of purine deoxynucleosides. Mutations in the dGK gene leading to deficiency in dGK activity is one of the causes of severe mitochondrial DNA depletion diseases. We used site-directed mutagenesis to introduce the clinically observed genetic alterations in the dGK gene and characterized the recombinant enzymes. The R142K enzyme had very low activity with deoxyguanosine and no activity with deoxyadenosine. The E227K mutant enzyme had unchanged K(m) values for all its substrates but very low V(max) values. C-terminal truncated dGK proteins were inactive. These results may help to define the role of dGK in mitochondrial DNA (mtDNA) precursor synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Binding Sites
  • DNA, Mitochondrial / genetics*
  • DNA, Mitochondrial / metabolism
  • Deoxyadenosines / metabolism
  • Deoxyguanosine / metabolism
  • Escherichia coli / enzymology
  • Escherichia coli / genetics
  • Heterozygote
  • Humans
  • Kinetics
  • Mitochondria / enzymology*
  • Mitochondria / genetics
  • Mitochondrial Diseases / enzymology
  • Mitochondrial Diseases / genetics*
  • Models, Molecular
  • Mutagenesis, Site-Directed
  • Phosphotransferases (Alcohol Group Acceptor) / deficiency
  • Phosphotransferases (Alcohol Group Acceptor) / genetics*
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism
  • Point Mutation*
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism

Substances

  • DNA, Mitochondrial
  • Deoxyadenosines
  • Recombinant Proteins
  • Adenosine Triphosphate
  • Phosphotransferases (Alcohol Group Acceptor)
  • deoxyguanosine kinase
  • Deoxyguanosine