Kinds of mutations formed when a shuttle vector containing adducts of (+/-)-7 beta, 8 alpha-dihydroxy-9 alpha, 10 alpha-epoxy-7,8,9, 10-tetrahydrobenzo[a]pyrene replicates in human cells.
- 1 June 1987
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 84 (11) , 3787-3791
- https://doi.org/10.1073/pnas.84.11.3787
Abstract
We have investigated the kinds of mutations induced when a shuttle vector containing covalently bound residues of (.+-.)-7.beta.,8.alpha.-dihydroxy-9.alpha.,10.alpha.-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (BPDE) replicates in human cells. A human embryonic kidney cell line, 293, was used as the eukaryotic host. The target gene for mutation analysis, supF, codes for a tyrosine suppressor tRNA and is strategically located between the origin of replication of the plasmid in Escherichia coli and the gene for a selectable marker, so that the possibility of recovering supF mutants containing gross rearrangements is low. The frequency of supF mutants obtained when untreated plasmid replicated in 293 cells was 1.4 x 10-4. The frequency with BPDE-treated plasmid increased linearly as a function of the number of adducts, with 16 adducts per plasmid giving 38 x 10-4. Polyacrylamide gel and agarose gel electrophoresis analysis of 137 plasmids with mutations in the supF gene indicated that 70% (21/30) from untreated plasmids contained deletions or insertions or showed altered gel mobility, whereas only 28% (30/107) of those derived from BPDE-treated plasmids contained such alterations. Of the 86 unequivocally independent mutants derived from BPDE-treated plasmids that were analyzed by sequencing, the majority (60/86) exhibited base substitutions. Mutants exhibiting frameshifts (insertions or deletions of one, two or four base pairs) were also found, but they were a minority (11/86). In the progeny of BPDE-treated plasmids 61/71 base substitutions observed were transversions, with 45/61 G.cntdot.C .fwdarw. T.cntdot.A. Examination of the location of BPDE-induced mutations among the 85 base pairs in the structure of the tRNA revealed that 30% of the base substitutions occurred at two sites and 44% of the rest occurred at five other hot spots. Only 20% of all these base changes involved a site in which a guanine containing a BPDE adduct is predicted to be labile.sbd.i.e., a guanine that has a pyrimidine to its 5'' side.This publication has 38 references indexed in Scilit:
- Chemically induced mutagenesis in a shuttle vector with a low-background mutant frequency.Proceedings of the National Academy of Sciences, 1986
- Detection and analysis of UV-induced mutations in mammalian cell DNA using a lambda phage shuttle vector.Proceedings of the National Academy of Sciences, 1986
- The lacI shuttle: rapid analysis of the mutagenic specificity of ultraviolet light in human cells.Proceedings of the National Academy of Sciences, 1985
- Recombination and deletion of sequences in shuttle vector plasmids in mammalian cells.Molecular and Cellular Biology, 1985
- Depurination of benzo[a]pyrene-diolepoxide treated DNAChemico-Biological Interactions, 1985
- A shuttle vector plasmid for studying carcinogen-induced point mutations in mammalian cellsGene, 1985
- High spontaneous mutation frequency in shuttle vector sequences recovered from mammalian cellular DNA.Molecular and Cellular Biology, 1984
- Error-prone mutagenesis detected in mammalian cells by a shuttle vector containing the supF gene of Escherichia coli.Molecular and Cellular Biology, 1984
- Survival and mutagenesis of bacterial plasmids with localized carcinogen adductsMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1984
- On the nature of the mutations induced by the diolepoxide of benzo[a]pyrene in mammalian cellsCarcinogenesis: Integrative Cancer Research, 1984