Salzman L A, Fabisch P, Parr R, Garon C, Wali T
J Virol. 1978 Sep;27(3):784-90. doi: 10.1128/JVI.27.3.784-790.1978.
Double-stranded, full-length linear DNA was synthesized in vitro by using single-stranded linear DNA as a self-priming template from the parvovirus Kilham rat virus and Escherichia coli DNA polymerase "large fragment" as the polymerizing enzyme. To ascertain the order of the synthesis of the cleavage fragments and to assess the accuracy of the in vitro synthesis, restriction endonuclease cleavage sites with known recognition sequences were mapped on the DNA. Comparing the cleavage pattern of the synthesized DNA with that of double-stranded viral DNA isolated from infected cells confirms that the in vitro synthesis produces a faithful copy of the viral single-stranded genome. Electron micrographs of the in vitro product reveal it to be a double-stranded linear molecule.
以细小病毒基尔汉姆大鼠病毒的单链线性DNA为自引发模板,使用大肠杆菌DNA聚合酶“大片段”作为聚合酶,在体外合成了双链全长线性DNA。为了确定切割片段的合成顺序并评估体外合成的准确性,将具有已知识别序列的限制性内切酶切割位点定位在DNA上。将合成的DNA的切割模式与从感染细胞中分离的双链病毒DNA的切割模式进行比较,证实体外合成产生了病毒单链基因组的忠实拷贝。体外产物的电子显微镜照片显示它是一个双链线性分子。