Waterloh K, Fox K R
Department of Physiology & Pharmacology, University of Southhampton, UK.
Anticancer Drug Des. 1990 Feb;5(1):89-92.
The effect of actinomycin on DNA structure has been studied by nuclease digestion of a DNA fragment containing the sequence AAGCT(TA)6AGCTT. The drug enhances DNase I cleavage at ApT and TpA bonds closest to the drug binding site (GC). Large changes in the relative susceptibility of bonds to cleavage by micrococcal nuclease and DNase II are also observed. The changes suggest that actinomycin alters DNA structure around its binding site, facilitating the formation of an alternating DNA structure. When a similar TA sequence was inserted further from the actinomycin binding site no changes in nuclease susceptibility were observed.
通过对含有AAGCT(TA)6AGCTT序列的DNA片段进行核酸酶消化,研究了放线菌素对DNA结构的影响。该药物增强了DNase I在最接近药物结合位点(GC)的ApT和TpA键处的切割作用。还观察到微球菌核酸酶和DNase II切割键的相对敏感性发生了很大变化。这些变化表明放线菌素改变了其结合位点周围的DNA结构,促进了交替DNA结构的形成。当在距放线菌素结合位点较远的位置插入类似的TA序列时,未观察到核酸酶敏感性的变化。