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dc.contributor.authorRyu, JC-
dc.contributor.authorYoun, JY-
dc.contributor.authorKim, YJ-
dc.contributor.authorKwon, OS-
dc.contributor.authorSong, YS-
dc.contributor.authorKim, HT-
dc.contributor.authorCho, KH-
dc.contributor.authorChang, IM-
dc.date.accessioned2024-01-21T15:06:24Z-
dc.date.available2024-01-21T15:06:24Z-
dc.date.created2022-01-10-
dc.date.issued1999-09-
dc.identifier.issn1383-5718-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/141947-
dc.description.abstractThis paper describes the spectrum of mutations induced by 4-nitroquinoline N-oxide (4-NQO) in the lad target gene of the transgenic Big Blue(R) Rat2 cell line. There are only a few report for the mutational spectrum of 4-NQO in a mammalian system although its biological and genetic effects have been well studied. Big Blue(R) Rat2 cells were treated with 0.03125, 0.0625 or 0.125 mu g/ml of 4-NQO, the highest concentration giving 85% survival. Our results indicated that the mutant frequency (MF) induced by 4-NQO was dose-dependent with increases from three- to seven-fold. The DNA sequence analysis of lad mutants from the control and 4-NQO treatment groups revealed an obvious difference in the spectra of mutations. In spontaneous mutants, transition (60%) mutations, especially G:C --> A:T transition (45%), were most frequent. However, the major type of base substitution after treatment of 4-NQO was transversions (68.8%), especially G:C --> T:A (43.8%), while only 25% of mutants were transitions. These results are consistent with those produced by 4-NQO in other systems and the transgenic assay system will be a powerful tool to postulate more accurately the mechanism of chemical carcinogenesis involved. (C) 1999 Elsevier Science B.V, All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.titleMutation spectrum of 4-nitroquinoline N-oxide in the lacI transgenic Big Blue((R)) Rat2 cell line-
dc.typeArticle-
dc.identifier.doi10.1016/S1383-5718(99)00136-9-
dc.description.journalClass1-
dc.identifier.bibliographicCitationMUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, v.445, no.1, pp.127 - 135-
dc.citation.titleMUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS-
dc.citation.volume445-
dc.citation.number1-
dc.citation.startPage127-
dc.citation.endPage135-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000082839400012-
dc.identifier.scopusid2-s2.0-0032829015-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryGenetics & Heredity-
dc.relation.journalWebOfScienceCategoryToxicology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaGenetics & Heredity-
dc.relation.journalResearchAreaToxicology-
dc.type.docTypeArticle-
dc.subject.keywordPlusSHUTTLE VECTORS-
dc.subject.keywordPlusCOLORIMETRIC ASSAY-
dc.subject.keywordPlusESCHERICHIA-COLI-
dc.subject.keywordPlusMAMMALIAN-CELLS-
dc.subject.keywordPlusBLUE(R) RAT2-
dc.subject.keywordPlusP53 GENE-
dc.subject.keywordPlusDNA-
dc.subject.keywordPlusMICE-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlus1-OXIDE-
dc.subject.keywordAuthor4-nitroquinoline N-oxide-
dc.subject.keywordAuthorBig Blue((R)) Rat2 cell line-
dc.subject.keywordAuthorlacI gene-
dc.subject.keywordAuthormutational spectrum-
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