Gasanova V K, Neschastnova A A, Belitskiĭ G A, Iakubovskaia M G
Mol Biol (Mosk). 2006 Jan-Feb;40(1):150-7.
Phenomenon of the interaction of a double-stranded DNA fragment with an oligonucleotide complementary to the end of the duplex strand was demonstrated to occur via formation of three-stranded DNA structure with an oligonucleotide invasion. It was shown that oligonucleotides complementary to the duplex ends inhibit Holliday junction formation in solutions of homologous linear DNA fragments. This effect depends on the oligonucleotide concentration, sequence and their complementarity to the duplex ends. Formation of three-stranded complexes was demonstrated using radiolabeled oligonucleotides by agarose gel-electrophoresis followed by autoradiography. Analysis of three-stranded DNA structures by chemical cleavage of non-canonical base pairs revealed that oligonucleotide invades into duplex ends via a sequential displacement mechanism and that the level of the invasion may vary considerably.
双链DNA片段与与双链链末端互补的寡核苷酸相互作用的现象被证明是通过寡核苷酸侵入形成三链DNA结构而发生的。结果表明,与双链末端互补的寡核苷酸在同源线性DNA片段溶液中抑制霍利迪连接的形成。这种效应取决于寡核苷酸的浓度、序列及其与双链末端的互补性。使用放射性标记的寡核苷酸通过琼脂糖凝胶电泳然后进行放射自显影来证明三链复合物的形成。通过对非规范碱基对进行化学切割来分析三链DNA结构,结果表明寡核苷酸通过顺序置换机制侵入双链末端,并且侵入水平可能有很大差异。