trans-Lesion Synthesis Past Bulky Benzo[a]pyrene Diol Epoxide N2-dG and N6-dA Lesions Catalyzed by DNA Bypass Polymerases
Open Access
- 1 August 2002
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 277 (34) , 30488-30494
- https://doi.org/10.1074/jbc.m201167200
Abstract
No abstract availableKeywords
This publication has 66 references indexed in Scilit:
- Preferential Misincorporation of Purine Nucleotides by Human DNA Polymerase η Opposite Benzo[a]pyrene 7,8-Diol 9,10-Epoxide Deoxyguanosine AdductsPublished by Elsevier ,2002
- Total Synthesis, Mass Spectrometric Sequencing, and Stabilities of Oligonucleotide Duplexes with Singletrans-anti-BPDE-N6-dA Lesions in theN-rascodon 61 and Other Sequence ContextsPolycyclic Aromatic Compounds, 1999
- Primer Length Dependence of Binding of DNA Polymerase I Klenow Fragment to Template−Primer Complexes Containing Site-Specific Bulky LesionsBiochemistry, 1999
- How Stereochemistry Affects Mutagenesis by N2-Deoxyguanosine Adducts of 7,8-Dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene: Configuration of the Adduct Bond Is More Important Than Those of the Hydroxyl GroupsBiochemistry, 1997
- Replication Fork Bypass of a Pyrimidine Dimer Blocking Leading Strand DNA SynthesisJournal of Biological Chemistry, 1997
- Sequence Specific Mutagenesis of the Major (+)-anti-Benzo[a]pyrene Diol Epoxide−DNA Adduct at a Mutational Hot Spot in Vitro and in Escherichia coli CellsChemical Research in Toxicology, 1997
- Translesional synthesis on a DNA template containing a single stereoisomer of dG-(+)- or dG-(-)-anti-BPDE (7, 8-dihydroxy-anti-9, 10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyreneBiochemistry, 1993
- DNA polymerase action on benzo[a]pyrene—DNA adductsCarcinogenesis: Integrative Cancer Research, 1992
- Influence of benzo[a]pyrenediol epoxide chirality on solution conformations of DNA covalent adducts: the (-)-trans-anti-[BP]G.cntdot.C adduct structure and comparison with the (+)-trans-anti[BP]G.cntdot.C enantiomerBiochemistry, 1992
- Preparation and isolation of adducts in high yield derived from the binding of two benzo[a]pyrene-7,8-dihydroxy-9,10-oxide stereoisomers to the oligonucleotide d(ATATGTATA)Carcinogenesis: Integrative Cancer Research, 1990