Denhardt D T, Miyamoto C
J Mol Biol. 1983 Apr 15;165(3):419-42. doi: 10.1016/s0022-2836(83)80211-3.
We have purified nascent DNA molecules from Escherichia coli pulse-labeled with 5-bromo[6-3H]deoxyuridine by repeated chromatography on nitrocellulose and isopycnic centrifugation in CsCl. The nascent molecules were labeled with 32P either at their 5' ends using polynucleotide kinase or at their 3' ends using terminal transferase. Compared to the non-nascent DNA of normal density, the nascent dense DNA contained a higher proportion of molecules terminated at their 5' ends with ribonucleotides. Exposure of the dense DNA to alkali generated 5' OH termini quantitatively equivalent to the number of molecules bearing 5' ribonucleotides. Experiments designed (1) to detect structures at the 5' ends of phosphatase-treated nascent DNA molecules that caused them to be resistant to hydrolysis by spleen exonuclease or (2) to detect polypeptides that were associated covalently with small DNA molecules and could be iodinated with the Bolton-Hunter reagent did not yield positive results. We conclude that many, if not all, of the intermediates in E. coli DNA replication are initiated with one or more ribonucleotides. The nascent molecules are outnumbered by small non-nascent DNA molecules in the cell, many of which appear to become slightly longer when cells are pulsed with thymidine. Many of the non-nascent DNA molecules behave as if they were self-complementary or crosslinked.
我们通过在硝酸纤维素上反复层析以及在氯化铯中进行等密度离心,从用5-溴[6-³H]脱氧尿苷脉冲标记的大肠杆菌中纯化出新生DNA分子。新生分子通过多核苷酸激酶在其5'末端用³²P标记,或者通过末端转移酶在其3'末端用³²P标记。与正常密度的非新生DNA相比,新生的高密度DNA中含有较高比例的在其5'末端以核糖核苷酸终止的分子。将高密度DNA暴露于碱中会产生与带有5'核糖核苷酸的分子数量在数量上相当的5'OH末端。旨在(1)检测经磷酸酶处理的新生DNA分子5'末端导致其对脾外切核酸酶水解具有抗性的结构,或(2)检测与小DNA分子共价结合并能用博尔顿-亨特试剂碘化的多肽的实验均未得到阳性结果。我们得出结论,大肠杆菌DNA复制中的许多(如果不是全部)中间体都是以一个或多个核糖核苷酸起始的。细胞中新生分子的数量少于小的非新生DNA分子,当用胸苷脉冲处理细胞时,其中许多非新生DNA分子似乎会变得稍微长一些。许多非新生DNA分子的行为就好像它们是自我互补或交联的。