Suggs J W, Wagner R W
Nucleic Acids Res. 1986 May 12;14(9):3703-16. doi: 10.1093/nar/14.9.3703.
The nuclease reactivity and specificity of a cloned tract of poly X (dA-dT) X poly(dA-dT) has been explored. Digestion with DNAse I, Mung Bean nuclease, S1 nuclease, DNAse II, and copper (1,10-phenanthroline)2 on a 256 base pair restriction fragment containing d(AT)14A revealed a dinucleotide repeat structure for the alternating sequence. Furthermore, conditions which wind or unwind the linear DNA had little effect on the reactivity of the AT insert. These preferred cleavages offer insights to structural alterations within the DNA helix which differ from A, B, or Z-DNA. Nucleation into flanking sequences by this structural alteration was not observed.
已对克隆的多聚X(dA-dT)X多聚(dA-dT)片段的核酸酶反应性和特异性进行了研究。用DNA酶I、绿豆核酸酶、S1核酸酶、DNA酶II以及铜(1,10-菲咯啉)2对一个含有d(AT)14A的256碱基对限制性片段进行消化,结果显示该交替序列具有二核苷酸重复结构。此外,使线性DNA缠绕或解旋的条件对AT插入片段的反应性影响很小。这些优先切割为DNA螺旋内不同于A、B或Z-DNA的结构改变提供了见解。未观察到这种结构改变向侧翼序列的成核现象。