Barnett S W, Landaw E M, Dixon K
Biophys J. 1984 Sep;46(3):307-21. doi: 10.1016/S0006-3495(84)84027-8.
When mammalian cells are irradiated with ultraviolet light, semiconservative DNA replication is inhibited and the length of newly synthesized daughter strands is reduced. We have used the simian virus 40 (SV40) viral system to examine the molecular mechanism by which this inhibition of DNA replication occurs immediately following ultraviolet irradiation. We tested two models for DNA replication-inhibition by using a procedure first developed by Danna, K. J., and D. Nathans (1972, Proc. Natl. Acad. Sci. USA, 69:3097-3100) in which the distribution of 3H-label in segments of newly completed SV40 form-I molecules is measured after short pulse labeling with 3H-thymidine. Our experimental results were compared with those predicted by mathematical models that describe two possible molecular mechanisms of replication inhibition. Our data are best fit by a "blockage" model in which any pyrimidine dimer encountered by the replication fork prevents complete replication of the SV40 genome. An alternative model called "slowdown" in which DNA damage causes a generalized slowdown of replication fork movement on all genomes has more adjustable parameters but does not fit the data as well as the blockage model.
当哺乳动物细胞受到紫外线照射时,半保留DNA复制受到抑制,新合成的子链长度缩短。我们利用猿猴病毒40(SV40)病毒系统来研究紫外线照射后立即发生这种DNA复制抑制的分子机制。我们通过使用丹娜(Danna, K. J.)和内森斯(D. Nathans)(1972年,《美国国家科学院院刊》,69:3097 - 3100)首次开发的一种方法测试了两种DNA复制抑制模型,该方法是在用³H - 胸腺嘧啶进行短脉冲标记后,测量新完成的SV40 I型分子片段中³H标记的分布。我们将实验结果与描述两种可能的复制抑制分子机制的数学模型所预测的结果进行了比较。我们的数据最符合一种“阻断”模型,即复制叉遇到的任何嘧啶二聚体都会阻止SV40基因组的完全复制。另一种称为“减速”的模型认为DNA损伤会导致所有基因组上复制叉移动普遍减速,该模型有更多可调整参数,但与数据的拟合程度不如阻断模型。