Meneghini R
Biochim Biophys Acta. 1976 Apr 2;425(4):419-27. doi: 10.1016/0005-2787(76)90006-x.
DNA replication in ultraviolet-irradiated human cells was examined by treatment of the extracted DNA with a single-strand specific endonuclease from Neurospora crassa. WI38 cells were uniformly labeled with 32Pi for two generations before irradiation and then labeled with [3H]thymidine after irradiation. The isolated DNA was sedimented in neutral sucrose gradients after incubation with the endonuclease. The endonuclease treatment had no effect on the sedimentation profiles of either [32P]DNA or [3H]DNA from unirradiated control cultures. The endonuclease treatment also did not significantly alter the profile of [32P]DNA from irradiated cultures but did introduce breaks in the 3H pulse-labeled DNA synthesized after irradiation. These results indicate that DNA synthesis after ultraviolet irradiation proceeds in such fashion that gaps are formed along the newly made strand, leaving regions of single strandness in template DNA. As replication proceeds these gaps disappear and 2 h after irradiation (100-250 ergs/mm2) they are barely detectable by the endonuclease assay.
通过用来自粗糙脉孢菌的单链特异性核酸内切酶处理提取的DNA,研究了紫外线照射的人细胞中的DNA复制。WI38细胞在照射前用32Pi均匀标记两代,然后在照射后用[3H]胸苷标记。与核酸内切酶孵育后,分离的DNA在中性蔗糖梯度中沉降。核酸内切酶处理对未照射对照培养物的[32P]DNA或[3H]DNA的沉降图谱没有影响。核酸内切酶处理也没有显著改变照射培养物中[32P]DNA的图谱,但确实在照射后合成的3H脉冲标记DNA中引入了断裂。这些结果表明,紫外线照射后的DNA合成以这样的方式进行,即沿着新合成的链形成缺口,在模板DNA中留下单链区域。随着复制的进行,这些缺口消失,照射后2小时(100-250尔格/平方毫米),通过核酸内切酶测定几乎检测不到它们。