Disruption of the DT diaphorase (NQO1) gene in mice leads to increased menadione toxicity

J Biol Chem. 1998 Mar 27;273(13):7382-9. doi: 10.1074/jbc.273.13.7382.

Abstract

NAD(P)H:quinone oxidoreductase 1 (NQO1) is a flavoenzyme that catalyzes two-electron reductive metabolism and detoxification of quinones and their derivatives leading to protection of cells against redox cycling and oxidative stress. To examine the in vivo role of NQO1, a NQO1-null mouse was produced using targeted gene disruption. Mice lacking NQO1 gene expression showed no detectable phenotype and were indistinguishable from wild-type mice. However, NQO1-null mice exhibited increased toxicity when administered menadione compared with wild-type mice. These results establish a role for NQO1 in protection against quinone toxicity. The NQO1-null mice are a model for NQO1 deficiency in humans and can be used to determine the role of this enzyme in sensitivity to toxicity and carcinogenesis.

Publication types

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

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Chromosome Mapping
  • DNA / chemistry
  • DNA / isolation & purification
  • Liver / enzymology
  • Liver / pathology
  • Mice
  • Mice, Knockout
  • NAD(P)H Dehydrogenase (Quinone) / genetics*
  • Phenotype
  • Rats
  • Recombination, Genetic
  • Vitamin K / toxicity*

Substances

  • Vitamin K
  • DNA
  • NAD(P)H Dehydrogenase (Quinone)
  • Aspartate Aminotransferases
  • Alanine Transaminase