DNA Base and Strand Damage in X-irradiated Monkey CV-1 Cells: Influence of Pretreatment Using Small Doses of Radiation
- 1 January 1990
- journal article
- research article
- Published by Taylor & Francis in International Journal of Radiation Biology
- Vol. 58 (1) , 35-54
- https://doi.org/10.1080/09553009014551421
Abstract
Base damage in αDNA from irradiated monkey CV-1 cells was determined by measuring release of 5′-32P-end labelled DNA fragments after digestion with endonuclease III of E. coli. The frequency and base sequence locations of the enzyme-sensitive sites were determined. Fragments were released from irradiated DNA at sequence sites of pyrimidines and guanines. The time for repair of half the single strand breaks was approximately 1·5 h. Repair of base damage as judged from loss of enzyme-sensitive sites in DNA was slower, with more than half of the damaged bases still detectable after 4 h of repair. Two important changes in the pattern of fragment release from DNA were produced when small radiation doses preceded the large ones needed to produce measurable DNA strand breaks and base damage. 5 Gy to cells incubated several hours before 320 Gy increased by five-fold the abundance of small DNA fragments with 3′-phosphoryl termini detected in high-resolution denaturing gels. These increases were detectable with doses as small as 0·2 Gy and were accompanied by the appearance of new species of DNA fragments of intermediate mobility at specific locations in the base sequence. The patterns resemble those produced by digesting DNA from heavily irradiated cells with endonuclease III.This publication has 36 references indexed in Scilit:
- Importance of thiols in the repair mechanisms of DNA containing AP (apurinic or apyrimidinic) sitesNucleic Acids Research, 1988
- Yeast redoxyendonuclease, a DNA repair enzyme similar to Escherichia coli endonuclease IIIBiochemistry, 1988
- Base Sequence Damage in DNA from X-irradiated Monkey CV-1 CellsInternational Journal of Radiation Biology, 1988
- Escherichia coli endonuclease III is not an endonuclease but a β-elimination catalystBiochemical Journal, 1987
- A highly conserved endonuclease activity present in Escherichia coli, bovine, and human cells recognizes oxidative DNA damage at sites of pyrimidines.Molecular and Cellular Biology, 1987
- Mechanism of action of a mammalian DNA repair endonucleaseBiochemistry, 1986
- Thymine lesions produced by ionizing radiation in double-stranded DNABiochemistry, 1985
- Endonuclease III (nth) mutants of Escherichia coli.Proceedings of the National Academy of Sciences, 1985
- Cleavage of pyrimidine dimers in specific DNA sequences by a pyrimidine dimer DNA-glycosylase of M. luteusNature, 1980
- Dissociation of histone and DNA synthesis in X-irradiated HeLa cells*1Experimental Cell Research, 1971