Vilarem M J, Gras M P, Larsen C J
Nucleic Acids Res. 1984 Nov 26;12(22):8653-65. doi: 10.1093/nar/12.22.8653.
The ability of BD-40, a DNA intercalative Ellipticine analogue, to induce DNA protein-cross links (DPLs) in mammalian cell DNA was studied by measuring DNA extractability with 0.5M KCl. Like Ellipticine, BD-40 was found to decrease the extractability of DNA, indicating the presence of DPLs, at inhibitory doses as well as at cytotoxic doses. Further analysis by alkaline sucrose gradient sedimentation of BD-40-induced DLPs indicated that the apparent size of DNA was not modified in comparison to that of control cell DNA. Abolition of DPLs by a prior proteinase K treatment of nuclear lysates resulted in DNA size reduction revealing the existence of hidden DNA strand breaks. In contrast, no proteolytic treatment was required to obtain a similar size reduction of DNA from Ellipticine-treated cells. These data suggest that BD-40 induced DPLs involve NaDodSO4+alkali-resistant DNA strand-protein bridges which maintain cohesiveness of adjacent DNA termini. Thus, BD-40 appears to be different from other DPL-inducing intercalative agents which have not been reported to induce DNA-protein bridges.
通过用0.5M KCl测量DNA的可提取性,研究了DNA嵌入性玫瑰树碱类似物BD - 40在哺乳动物细胞DNA中诱导DNA - 蛋白质交联(DPLs)的能力。与玫瑰树碱一样,发现BD - 40在抑制剂量和细胞毒性剂量下均会降低DNA的可提取性,表明存在DPLs。通过碱性蔗糖梯度沉降对BD - 40诱导的DPLs进行进一步分析表明,与对照细胞DNA相比,DNA的表观大小没有改变。用蛋白酶K预先处理核裂解物消除DPLs会导致DNA大小减小,揭示了隐藏的DNA链断裂的存在。相比之下,从玫瑰树碱处理的细胞中获得类似的DNA大小减小则不需要进行蛋白水解处理。这些数据表明,BD - 40诱导的DPLs涉及耐十二烷基硫酸钠+碱的DNA链 - 蛋白质桥,这些桥维持相邻DNA末端的粘性。因此,BD - 40似乎与其他未报道能诱导DNA - 蛋白质桥的DPL诱导嵌入剂不同。