Charles K, Povirk L F
Department of Pharmacology and Toxicology, Medical College of Virginia, Virginia Commonwealth University, Richmond, Virginia 23298, USA.
Chem Res Toxicol. 1998 Dec;11(12):1580-5. doi: 10.1021/tx980154g.
Bleomycin-induced cleavage was examined in several nicked, gapped, or intact duplex DNA substrates, including a structure designed to mimic a proposed singly nicked intermediate in double-strand cleavage. This nicked structure appeared to correctly target the second cleavage event in the complementary strand, resulting in a blunt-ended double-strand break, similar to that induced directly by bleomycin alone in an intact duplex of the same sequence. A one-base-gapped structure was markedly less efficient in correctly targeting bleomycin attack in the complementary strand. The results are consistent with a model of bleomycin-induced double-strand cleavage in which the nick formed by the initial bleomycin attack serves to target secondary attack to a specific position in the complementary strand, resulting in a double-strand break with a defined geometry.
在几种有切口、有缺口或完整的双链DNA底物中检测了博来霉素诱导的切割,包括一种设计用于模拟双链切割中提议的单切口中间体的结构。这种有切口的结构似乎能正确地靶向互补链中的第二次切割事件,导致平端双链断裂,类似于相同序列的完整双链中仅由博来霉素直接诱导产生的双链断裂。单碱基缺口结构在正确靶向博来霉素对互补链的攻击方面效率明显较低。这些结果与博来霉素诱导双链切割的模型一致,在该模型中,最初博来霉素攻击形成的切口用于将二次攻击靶向互补链中的特定位置,从而产生具有特定几何形状的双链断裂。