Moe J G, Reddy G R, Marnett L J, Stone M P
Department of Chemistry, Vanderbilt University, Nashville, Tennessee 37235.
Chem Res Toxicol. 1994 May-Jun;7(3):319-28. doi: 10.1021/tx00039a008.
The exocyclic lesion 1,N2-propano-2'-deoxyguanosine (PdG) was incorporated into 5'-d[ATCGC(PdG)CGGCATG]-3', derived from the hisD3052 gene of Salmonella typhimurium. The modified oligodeoxynucleotide was annealed with the complementary strand 5'-d[CATGCCGCGAT]-3' which contained a CpG deletion. The resulting duplex 5'-d[ATCGC(PdG)CGGCATG]-3'.5'-d[CATGCCGCGAT]-3' required PdG and one adjacent cytosine to be unpaired. Four thymine imino 1H NMR resonances were observed at temperatures below 25 degrees C, which demonstrated formation of a stable duplex with a two-base bulge. PdG was accommodated within the DNA helix, whereas the 3'-neighbor cytosine was poorly stacked and appeared to be extrahelical. The sequential nuclear Overhauser enhancement connectivities between aromatic and H1' protons along the modified strand were interrupted between PdG and the 3'-neighboring unpaired cytosine. On the complementary strand no interruptions were observed. An NOE was observed between the PdG methylene protons H8a,b and the imino proton of the 5'-neighbor base pair. Weaker NOEs were observed between the PdG H8a,b protons and the imino proton from guanine two nucleotides removed in the 3'-direction, and to the amino proton of cytosine located in the complementary strand two nucleotides removed in the 3'-direction. Chemical shift perturbations were also observed for the latter cytosine as compared to the corresponding cytosine in the unmodified fully complementary duplex. These observations provided evidence for a poorly stacked or an extrahelical conformation of this unpaired cytosine. The amino proton resonances of the 3'-neighbor cytosine were not observed, presumably due to increased exchange with solvent. The methylene protons from PdG were shifted upfield relative to the monomer PdG, probably as a result of aromatic ring current shielding, consistent with an intrahelical location. Multimeric derivative oligonucleotides containing the PdG bulge migrated anomalously on nondenaturing polyacrylamide gels, consistent with a structure in which the unpaired nucleotides induced a bend in the DNA.
外环损伤1,N2-丙基-2'-脱氧鸟苷(PdG)被掺入到源自鼠伤寒沙门氏菌hisD3052基因的5'-d[ATCGC(PdG)CGGCATG]-3'中。该修饰的寡脱氧核苷酸与包含一个CpG缺失的互补链5'-d[CATGCCGCGAT]-3'退火。所得的双链体5'-d[ATCGC(PdG)CGGCATG]-3'.5'-d[CATGCCGCGAT]-3'要求PdG和一个相邻的胞嘧啶不成对。在低于25摄氏度的温度下观察到四个胸腺嘧啶亚氨基1H NMR共振,这表明形成了具有两个碱基凸起的稳定双链体。PdG被容纳在DNA螺旋内,而3'-相邻的胞嘧啶堆积不良,似乎位于螺旋外。沿着修饰链的芳香族质子和H1'质子之间的顺序核Overhauser增强连接性在PdG和3'-相邻的不成对胞嘧啶之间中断。在互补链上未观察到中断。在PdG亚甲基质子H8a,b和5'-相邻碱基对的亚氨基质子之间观察到一个核Overhauser效应(NOE)。在PdG H8a,b质子与在3'-方向上相隔两个核苷酸的鸟嘌呤的亚氨基质子之间,以及与在3'-方向上相隔两个核苷酸的互补链中的胞嘧啶的氨基质子之间观察到较弱的NOE。与未修饰的完全互补双链体中的相应胞嘧啶相比,对于后一个胞嘧啶也观察到了化学位移扰动。这些观察结果为这个不成对胞嘧啶的堆积不良或螺旋外构象提供了证据。3'-相邻胞嘧啶的氨基质子共振未被观察到,可能是由于与溶剂的交换增加。来自PdG的亚甲基质子相对于单体PdG向高场移动,这可能是芳香环电流屏蔽的结果,与螺旋内位置一致。含有PdG凸起的多聚体衍生寡核苷酸在非变性聚丙烯酰胺凝胶上异常迁移,这与未配对核苷酸在DNA中诱导弯曲的结构的结构一致。