Disruption of the DT Diaphorase (NQO1) Gene in Mice Leads to Increased Menadione Toxicity

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 produce...

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Veröffentlicht in:The Journal of biological chemistry 1998-03, Vol.273 (13), p.7382-7389
Hauptverfasser: Radjendirane, V, Joseph, P, Lee, Y H, Kimura, S, Klein-Szanto, A J, Gonzalez, F J, Jaiswal, A K
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Sprache:eng
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Zusammenfassung: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.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.273.13.7382