Radford I R, Martin R F, Finch L R
Biochim Biophys Acta. 1982 Feb 26;696(2):145-53. doi: 10.1016/0167-4781(82)90022-7.
The effect of the anti-metabolite hydroxyurea on DNA synthesis in mouse L-cells has been examined. It was shown previously that when DNA synthesis was diminished to very low levels by treatment with the drug there was preferential incorporation of added [3H]dThd into low molecular weight fragments (Martin, R.F., Radford, I. And Pardee, M. (1977) Biochem. Biophys. Res. Commun. 74, 9-15). On the basis of several criteria it is concluded here that these fragments are a product of semi-conservative nuclear DNA replication. The preferential labelling of DNA fragments, but not their size, is shown to be dependent on the hydroxyurea concentration used. These DNA fragments are also shown, by comparison with normal DNA replication intermediates, to comprise a heterogeneous population of 'larger-than-normal' fragments. Different models to account for these findings are considered and it is concluded that the results are compatible with a loss of coordination of DNA synthesis following drug treatment.
已对抗代谢物羟基脲对小鼠L细胞中DNA合成的影响进行了研究。先前的研究表明,当用该药物将DNA合成降低到非常低的水平时,添加的[³H]胸苷([³H]dThd)会优先掺入低分子量片段中(Martin, R.F., Radford, I. 和 Pardee, M. (1977) Biochem. Biophys. Res. Commun. 74, 9 - 15)。基于多个标准,在此得出结论,这些片段是半保留核DNA复制的产物。已表明DNA片段的优先标记而非其大小取决于所用的羟基脲浓度。通过与正常DNA复制中间体比较还表明,这些DNA片段由“大于正常”的片段组成的异质群体。考虑了用于解释这些发现的不同模型,得出的结论是,结果与药物处理后DNA合成协调性的丧失相符。