Mutagenicity of the 1-Nitropyrene−DNA Adduct N-(Deoxyguanosin-8-yl)-1-aminopyrene in Escherichia coli Located in a Nonrepetitive CGC Sequence
Citations Over Time
Abstract
1-Nitropyrene, a common environmental pollutant, forms a major DNA adduct, N-(deoxyguanosin-8-yl)-1-aminopyrene (dG(AP)). Mutational spectra of randomly introduced dG(AP) in Escherichia coli included many different types of mutations. However, a prior site-specific study in a CGCG(AP)CG sequence showed only CpG deletions and +1 frame shifts. To further explore the context effects of dG(AP) in mutagenesis, in this work this adduct was incorporated into a nonrepetitive CGC sequence in single-stranded M13mp7L2 DNA. Upon replication of this construct in repair-competent E. coli, one-base deletions and base substitutions were detected. The -1 frame shifts, whose frequency increased 3-6-fold with SOS (to an average frequency of 1.5%), involved deletion of the adjacent C residues. The base substitutions ( approximately 2.2%) included targeted G-to-T and G-to-C transversions, whose frequencies did not increase with SOS. This suggests that dG(AP) mutagenesis is highly dependent on the local DNA sequence.
Related Papers
- → trans-3,4-Dihydroxy-anti-1,2-epoxy-1,2,3,4-tetrahydrodi- benz[a,j]acridine Involvement in Dibenz[a,j]acridine DNA Adduct Formation in Mouse Skin Consistent with Ha-ras Mutation Patterns in Tumors(2001)3 cited
- → Effect of conformation of the arylamine-DNA adduct on the sensitivity of [Ru(phen)2(dppz)]2+ complex(2016)6 cited
- → Aromatic DNA adducts in lymphocytes of humans working at high and low traffic density areas(1996)34 cited
- → 32P-postlabelling analysis of DNA adducts from Fischer-344 rats administered 2,4-diaminotoluene(1992)15 cited
- → Analysis of an RNA adduct formed from aminophenylnorharman(2009)2 cited