Fedor M J, Daniell E
Nucleic Acids Res. 1983 Jul 11;11(13):4417-34. doi: 10.1093/nar/11.13.4417.
Cleavage products resulting from DNase I treatment of adenoviral nucleoprotein were examined by gel electrophoresis, Southern blotting and hybridization to cloned restriction fragments derived from various regions of the viral genome. DNase I produced specific double-stranded cleavages in DNA of purified adenoviral cores and in DNA of intranuclear viral chromatin at early and late times of infection. At least some of these sites were also cleaved by DNase I in purified viral DNA, showing that sequence specificity of DNase I cleavage may contribute to the observation of specific double-stranded DNase I cleavage sites in adenoviral nucleoprotein. In addition, sites were observed which were specific either for cores or for intranuclear chromatin. In contrast to many cellular genes which have been characterized, there was no obvious relationship between DNase I cleavage sites and other features of the viral genome such as promoters or polyadenylation sites.
通过凝胶电泳、Southern印迹以及与源自病毒基因组不同区域的克隆限制性片段杂交,对经脱氧核糖核酸酶I(DNase I)处理腺病毒核蛋白产生的切割产物进行了检测。在感染的早期和晚期,DNase I在纯化的腺病毒核心DNA以及核内病毒染色质DNA中产生了特异性双链切割。这些位点中的至少一些在纯化的病毒DNA中也被DNase I切割,这表明DNase I切割的序列特异性可能有助于观察到腺病毒核蛋白中特异性双链DNase I切割位点。此外,还观察到了对核心或核内染色质具有特异性的位点。与许多已被表征的细胞基因不同,DNase I切割位点与病毒基因组的其他特征(如启动子或聚腺苷酸化位点)之间没有明显关系。