Roychoudhury R, Tu C P, Wu R
Nucleic Acids Res. 1979 Apr;6(4):1323-33. doi: 10.1093/nar/6.4.1323.
We have analyzed the effect of base-pairing at the exposed ends of Hinc II fragments of SV40 DNA on the efficiency of ribonucleotide incorporation catalyzed by terminal transferase. Wide variations in the labeling efficiency of individual DNA fragments have been observed. To elucidate the nature of this variation at the molecular level, we have correlated this effect with nucleotide sequence adjacent to the cleavage site. We found that a G:C base pair right at the exposed end drastically reduces the incorporation of ribonucleotides. Furthermore, the higher the number of G:C base pairs adjacent to the exposed end, the greater the reduction in labeling efficiency. From these results, we conclude that the labeling efficiency is determined by the degree of 'terminal breathing' of the DNA molecule at the exposed end of the duplex.
我们分析了SV40 DNA的Hinc II片段暴露末端的碱基配对对末端转移酶催化的核糖核苷酸掺入效率的影响。已观察到各个DNA片段的标记效率存在很大差异。为了在分子水平上阐明这种变异的本质,我们将这种效应与切割位点相邻的核苷酸序列相关联。我们发现,暴露末端恰好有一个G:C碱基对会大幅降低核糖核苷酸的掺入。此外,与暴露末端相邻的G:C碱基对数量越多,标记效率的降低就越大。从这些结果中,我们得出结论,标记效率由双链体暴露末端DNA分子的“末端呼吸”程度决定。