Halogenated hydrocarbons are major industrial chemicals and are of environmental and lexicological concern because of potential hazards to human health. Several of these compounds are bifunctional electrophiles and are bioactivated to crosslinking agents, linking glutathione (GSH) or the DMArepair protein C^-alklyguanine DNA-alkyltransferase (AGT) to DNA. Some compounds of interest in this group are ethylene and methylene dihalides and the related bis-electrophile butadiene diepoxide, a metabolite of the monomer butadiene. Wepropose to: (i) Characterize mechanisms of mutagenesis related to the AGT-DNA crosslinks, including the chemical characterization of DNA adducts and crosslinks, the possible involvement of translesion polymerases and nucleotide excision repair inmutagenic processing, and the relative contribution of the GSH and AGT pathways in producing mutationsin vivo, (ii) Characterize interactions of AGT with DNA and alkylated DNA, includingrates of AGT: DNA association and dissociation and of baseflipping,(iii) Search for other nuclear/DNA-binding proteins that also enhance Ws-electrophile-generated mutations via an AGT-like mechanism, both in bacteria and mammaliancells. Candidates are proliferating cell nuclear antigen (PCNA), uracil DNAglyosylase, and possibly OxyR. (iv) Quantify DNA adducts formed with GSH and CH2C12, CHzBr2, and ethylene dichloride in vitro and in vivo using rapid digestion, chromatography, and accelerator mass spectrometry for unstable DNA adducts.This information will be related to the halogen order, rates of GSH conjugation, and mutagenicity, and should be useful in assessments of the carcinogenic potentials of these and related compounds, (v) Characterize the mechanism by which GSH enhances the mutations produced by the Ms-functional electrophile butadiene diepoxide. Progress in the five Specific Aims described in this work will provide a better understanding of the interactions of these and other bis- functional electrophiles with DNA, and several aspects of the work have relevance :o the risk assessment of halogenated hydrocarbons.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES010546-08
Application #
7414775
Study Section
Cancer Etiology Study Section (CE)
Program Officer
Balshaw, David M
Project Start
2001-05-01
Project End
2011-04-30
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
8
Fiscal Year
2008
Total Cost
$427,685
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Biochemistry
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
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Su, Yan; Egli, Martin; Guengerich, F Peter (2017) Human DNA polymerase ? accommodates RNA for strand extension. J Biol Chem 292:18044-18051
Guengerich, F Peter (2016) Metals in Biology 2016: Molecular Basis of Selection of Metals by Enzymes. J Biol Chem 291:20838-20839
Choi, Jeong-Yun; Patra, Amritaj; Yeom, Mina et al. (2016) Kinetic and Structural Impact of Metal Ions and Genetic Variations on Human DNA Polymerase ?. J Biol Chem 291:21063-21073
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Xue, Qizhen; Zhong, Mengyu; Liu, Binyan et al. (2016) Kinetic analysis of bypass of 7,8-dihydro-8-oxo-2'-deoxyguanosine by the catalytic core of yeast DNA polymerase ?. Biochimie 121:161-9
Yeom, Mina; Kim, In-Hyeok; Kim, Jae-Kwon et al. (2016) Effects of Twelve Germline Missense Variations on DNA Lesion and G-Quadruplex Bypass Activities of Human DNA Polymerase REV1. Chem Res Toxicol 29:367-79
Su, Yan; Peter Guengerich, F (2016) Pre-Steady-State Kinetic Analysis of Single-Nucleotide Incorporation by DNA Polymerases. Curr Protoc Nucleic Acid Chem 65:7.23.1-7.23.10
Patra, Amitraj; Zhang, Qianqian; Guengerich, F Peter et al. (2016) Mechanisms of Insertion of dCTP and dTTP Opposite the DNA Lesion O6-Methyl-2'-deoxyguanosine by Human DNA Polymerase ?. J Biol Chem 291:24304-24313

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