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UvrA and UvrB enhance mutations induced by oxidized deoxyribonucleotides.
Hori, Mika; Ishiguro, Chieko; Suzuki, Tetsuya; Nakagawa, Noriko; Nunoshiba, Tatsuo; Kuramitsu, Seiki; Yamamoto, Kazuo; Kasai, Hiroshi; Harashima, Hideyoshi; Kamiya, Hiroyuki.
Afiliação
  • Hori M; Faculty of Pharmaceutical Sciences, Hokkaido University, Kita-12, Nishi-6, Kita-ku, Sapporo 060-0812, Japan.
DNA Repair (Amst) ; 6(12): 1786-93, 2007 Dec 01.
Article em En | MEDLINE | ID: mdl-17709303
ABSTRACT
Oxidatively damaged DNA precursors (deoxyribonucleotides) are formed by reactive oxygen species. After the damaged DNA precursors are incorporated into DNA, they might be removed by DNA repair enzymes. In this study, to examine whether a nucleotide excision repair enzyme, Escherichia coli UvrABC, could suppress the mutations induced by oxidized deoxyribonucleotides in vivo, oxidized DNA precursors, 8-hydroxy-2'-deoxyguanosine 5'-triphosphate and 2-hydroxy-2'-deoxyadenosine 5'-triphosphate, were introduced into uvrA, uvrB, and uvrC E. coli strains, and mutations in the chromosomal rpoB gene were analyzed. Unexpectedly, these oxidized DNA precursors induced mutations only slightly in the uvrA and uvrB strains. In contrast, effect of the uvrC-deficiency was not observed. Next, mutT, mutT/uvrA, and mutT/uvrB E. coli strains were treated with H2O2, and the rpoB mutant frequencies were calculated. The frequency of the H2O2-induced mutations was increased in all of the strains tested; however, the increase was three- to four-fold lower in the mutT/uvrA and mutT/uvrB strains than in the mutT strain. Thus, UvrA and UvrB are involved in the enhancement, but not in the suppression, of the mutations induced by these oxidized deoxyribonucleotides. These results suggest a novel role for UvrA and UvrB in the processing of oxidative damage.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenosina Trifosfatases / DNA Helicases / Proteínas de Escherichia coli / Desoxirribonucleotídeos / Proteínas de Ligação a DNA / Mutação Idioma: En Revista: DNA Repair (Amst) Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Japão
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Adenosina Trifosfatases / DNA Helicases / Proteínas de Escherichia coli / Desoxirribonucleotídeos / Proteínas de Ligação a DNA / Mutação Idioma: En Revista: DNA Repair (Amst) Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA Ano de publicação: 2007 Tipo de documento: Article País de afiliação: Japão