Abstract
ULTRAVIOLET irradiation causes the formation of dimers between adjacent pyrimidines within a DNA strand. These dimers (predominantly thymine dimers) are highly deleterious to the cell; as evidence of their potential danger, most cells have several mechanisms for removing dimers1–3. In all cases, the implicit or explicit assumption is that dimers are formed randomly along the DNA chain. The distribution of repair regions in DNA after excision repair suggests that dimers are nonrandomly distributed4. In vitro studies also suggest that pyrimidine tracts are sites of increased dimer formation5. The preferential formation of dimers in pyrimidine tracts, particularly at low doses of ultraviolet, may have profound biological effects if the pyrimidine tracts are control regions of the DNA such as promoter sites or sites for the initiation of DNA synthesis6,7.
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References
Setlow, R. B., Swenson, P. A., and Carrier, W. L., Science, 142, 1464 (1963).
Setlow, J. K., in Current Topics in Radiation Research (edit. by Ebert, M., and Howard, A.), 2, 195 (North-Holland, Amsterdam, 1966).
Setlow, R. B., in Progress in Nucleic Acid Research and Molecular Biology (edit. by Davison, J. N., and Cohn, W. E.), 8, 257 (Academic Press, New York, 1968).
Brunk, C. F., and Hanawalt, P. C., Radiat. Res., 38, 285 (1969).
Setlow, R. B., Carrier, W. L., and Bollum, F. J., Biochim. Biophys. Acta, 91, 446 (1964).
Szybalski, W., Kubinski, H., and Sheldrick, P., Cold Spring Harbor Symp. Quant. Biol., 31, 123 (1966).
Scaife, J., and Beckwith, J. R., Cold Spring Harbor Symp. Quant. Biol., 31, 403 (1966).
Lamola, A. A., Photochem. Photobiol., 9, 291 (1969).
Burton, K., and Peterson, G. B., Biochem. J., 75, 17 (1960).
Tomlinson, R. V., and Tener, G. M., Biochemistry, 2, 697 (1963).
Brown, R. D., and Holt, C. E., Anal. Biochem., 20, 358 (1967).
Swartz, M. N., Trautner, T. A., and Kornberg, A., J. Biol. Chem., 237, 1961 (1962).
Guèron, M., and Shulman, R. G., Ann. Rev. Biochem., 37, 571 (1968).
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BRUNK, C. Distribution of Dimers in Ultraviolet-irradiated DNA. Nature New Biology 241, 74–76 (1973). https://doi.org/10.1038/newbio241074a0
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DOI: https://doi.org/10.1038/newbio241074a0
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