The halogenated thymidine (dT) analogue, 5-bromodeoxy-uridine (BUdR), has a variety of effects on mammalian cells, including toxicity, suppression of differentiation, and mutagenesis. Although it is generally assumed that the effects of BUdR are due primarily to its presence in DNA, results from our laboratory have raised doubts about such assumptions1–4. We have shown, for example, that BUdR mutagenesis in mammalian cells is determined by the concentration of BUdR in the medium rather than in DNA3, and that mutagenesis can be suppressed by deoxycytidine (dC) without changing the amount of BUdR in DNA4. BUdR has also been shown to induce sister chromatid exchanges (SCEs) in mammalian cells5–7. Initial results suggested that the relationship between BUdR and SCEs might not be explained by a single factor5, and various correlations between BUdR and SCEs have been proposed8,9. However, the results to date have been inconclusive, because the experiments did not resolve as independent variables the concentration of BUdR in the medium and the amount of BUdR incorporated into nuclear DNA. We have now carried out experiments to resolve these two factors; the results indicate that the major factor in determining the frequency of SCEs is the concentration of BUdR in the medium.
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About this article
Influence of low doses of BrdU and estimation of spontaneous SCE in CHO chromosomes: three-way differential staining and an immunoperoxidase method
Human Genetics (1988)
Journal of Neuro-Oncology (1988)
Analysis of bromodeoxyuridine-induced single and twin sister chromatid exchanges in tetraploid Chinese hamster ovary cells
Detection of bromodeoxyuridine incorporation in mammalian chromosomes by a bromodeoxyuridine antibody