This is the second revised application of CA46838 """"""""Analysis of Radiation Damage in DNA"""""""". Twenty-five different lesions have been identified in intact DNA oligomers. High resolution HPLC has served to isolate damaged oligomers bearing different lesions. The identification of these lesions has been accomplished through the use of NMR spectroscopy, complemented by fast atom bombardment (FAB) mass spectrometry. Additional lesions would be identified, especially in irradiated tetramers and hexamers. Preliminary studies have revealed stark differences between the HPLC product profile from irradiated single-stranded oligomer and the product profile from the same oligomer irradiated in duplex form. The double-stranded form manifestly interferes with the formation of particular lesions. An objective of the continuing research would be to identify these lesions. Radiation-modified DNA oligomers constitute an important resource. The behavior of a DNA oligomer bearing a specific lesion as substrate to endonucleases, kinases and polymerases can be studied. For example, it has been demonstrated in this laboratory that many radiation-induced lesions inhibit nuclease Pl. This phenomenon led to the design of a sensitive assay for the detection of Pl-resistant lesions in DNA. The assay has been implemented for the so-called formamido lesion. The assay would be further refined and extended to the analysis of DNA taken from exposed cells. The assay would also be extended to other lesions many of which are associated with oxidative stress as well as radiation damage. Another objective is to associate with each specific lesion a measure of the propensity of that lesion to induce mutation. An in vitro assay is proposed to evaluate the effect of the lesion on the -function of DNA polymerase. Again, the basic resource for the proposed experiments are oligomers bearing a specific lesion which are to be used as substrate for testing polymerase function.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA046838-06
Application #
2092330
Study Section
Radiation Study Section (RAD)
Project Start
1988-03-01
Project End
1996-04-30
Budget Start
1994-05-01
Budget End
1995-04-30
Support Year
6
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Roswell Park Cancer Institute Corp
Department
Type
DUNS #
City
Buffalo
State
NY
Country
United States
Zip Code
14263
Greene, Kellee F; Budzinski, Edwin E; Iijima, Herbert et al. (2007) Assessment of DNA damage at the dimer level: measurement of the formamide lesion. Radiat Res 167:146-51
Bailey, Douglas T; DeFedericis, Han-Chun C; Greene, Kellee F et al. (2006) A novel approach to DNA damage assessments: measurement of the thymine glycol lesion. Radiat Res 165:438-44
DeFedericis, Han-Chun; Patrzyc, Helen B; Rajecki, Michael J et al. (2006) Singlet oxygen-induced DNA damage. Radiat Res 165:445-51
Dawidzik, J B; Budzinski, E E; Patrzyc, H B et al. (2004) Dihydrothymine lesion in X-irradiated DNA: characterization at the molecular level and detection in cells. Int J Radiat Biol 80:355-61
Iijima, Herbert; Patrzyc, Helen B; Dawidzik, Jean B et al. (2004) Measurement of DNA adducts in cells exposed to cisplatin. Anal Biochem 333:65-71
Box, H C; Dawidzik, J B; Budzinski, E E (2001) Free radical-induced double lesions in DNA. Free Radic Biol Med 31:856-68
Box, H C; Budzinski, E E; Dawidzik, J et al. (2001) A novel double lesion in X-irradiated DNA consists of a strand break and a base modification. Radiat Res 156:215-9
Maccubbin, A E; Iijima, H; Ersing, N et al. (2000) Double-base lesions are produced in DNA by free radicals. Arch Biochem Biophys 375:119-23
Box, H C; Patrzyc, H B; Dawidzik, J B et al. (2000) Double base lesions in DNA X-irradiated in the presence or absence of oxygen. Radiat Res 153:442-6
Maccubbin, A E; Patrzyc, H B; Ersing, N et al. (1999) Assay for reactive oxygen species-induced DNA damage: measurement of the formamido and thymine glycol lesions. Biochim Biophys Acta 1454:80-8

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