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Mutagenesis by metal-induced oxygen radicals.
Reid, T M; Feig, D I; Loeb, L A.
Affiliation
  • Reid TM; Joseph Gottstein Memorial Cancer Research Laboratory, Department of Pathology, University of Washington School of Medicine, Seattle 98195.
Environ Health Perspect ; 102 Suppl 3: 57-61, 1994 Sep.
Article in En | MEDLINE | ID: mdl-7843138
ABSTRACT
To assess the contribution of reactive oxygen species (ROS) to metal-induced mutagenesis, we have determined the spectrum of mutations in the lacZ alpha gene after exposure of M13mp2 DNA to Fe2+, Cu2+, and Ni2+. With iron and copper ions, mutations are clustered and are predominantly single-base substitutions. Fe, Cu, and phorbol ester-stimulated neutrophils also produced tandem double CC-->TT mutations. This mutation may provide a marker for the role of oxidative damage in carcinogenesis. Mutagenesis by Ni2+ required the complexing of the metal to a tripeptide and the addition of H2O2. To assess the contribution of ROS in mammalian cells, we determined the spectrum of mutations produced when purified DNA polymerases-alpha and -beta synthesized DNA using a template that had been damaged by ROS. The mutation spectra produced by the two polymerases indicates that these enzymes substitute different nucleotides opposite the same lesions.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Reactive Oxygen Species / Copper / Iron / Mutagens / Nickel Limits: Humans Language: En Year: 1994 Type: Article

Full text: 1 Database: MEDLINE Main subject: Reactive Oxygen Species / Copper / Iron / Mutagens / Nickel Limits: Humans Language: En Year: 1994 Type: Article