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Synthesis of novel poly(dG)–poly(dG)–poly(dC) triplex structure by Klenow exo− fragment of DNA polymerase I

机译:DNA聚合酶I的Klenow exo-片段合成新型poly(dG)-poly(dG)-poly(dC)三重结构

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摘要

The extension of the G-strand of long (700 bp) poly(dG)–poly(dC) by the Klenow exo− fragment of DNA polymerase I yields a complete triplex structure of the H-DNA type. High-performance liquid chromatography analysis demonstrates that the length of the G-strand is doubled during the polymerase synthesis. Fluorescence resonance energy transfer analysis shows that the 5′ ends of the G- and the C-strands, labeled with fluorescein and TAMRA, respectively, are positioned close to each other in the product of the synthesis. Atomic force microscopy morphology imaging shows that the synthesized structures lack single-stranded fragments and have approximately the same length as the parent 700 bp poly(dG)–poly(dC). CD spectrum of the polymer has a large negative peak at 278 nm, which is characteristic of the poly(dG)–poly(dG)–poly(dC) triplex. The polymer is resistant to DNase and interacts much more weakly with ethidium bromide as compared with the double-stranded DNA.
机译:DNA聚合酶I的Klenow exo-片段延长了长(700 bp)poly(dG)-poly(dC)的G链,产生了H-DNA类型的完整三链体结构。高效液相色谱分析表明,在聚合酶合成过程中,G链的长度增加了一倍。荧光共振能量转移分析表明,分别用荧光素和TAMRA标记的G链和C链的5'端在合成产物中彼此靠近放置。原子力显微镜形态学成像显示,合成的结构没有单链片段,其长度与亲本700 bp poly(dG)–poly(dC)相同。聚合物的CD光谱在278 nm处有一个较大的负峰,这是poly(dG)-poly(dG)-poly(dC)三重态的特征。与双链DNA相比,该聚合物对DNase具有抗性,并且与溴化乙锭的相互作用弱得多。

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