Vogel F, Zimmermann W, Krause H, Scherneck S
Arch Geschwulstforsch. 1984;54(6):433-41.
The complete genome of the hamster papovavirus (HaPV) which was isolated from virions found in multiple skin tumors of the Syrian hamsters was measured by electron microscopy and cloned in Escherichia coli using the certified plasmid vector pBR322. The cloned viral DNA were characterized by digestion of the recombinant DNA with various restriction enzymes followed by comparison of their electrophoretic mobilities in agarose gels with that of similarly digested uncloned DNA and by electron microscopy to determine the genome size of cloned HaPV DNA. The restriction enzyme analysis of the cloned HaPV DNA showed the same cleavage pattern as the corresponding fragments from the uncloned DNA. No major insertions or deletions could be detected by heteroduplex analysis between cloned HaPV DNA and the starting material. The estimated genome size of 5.52 kb for HaPV DNA is approx. 300 bases larger than those determined for other known papovaviruses as SV40 or polyoma.
从叙利亚仓鼠多个皮肤肿瘤中发现的病毒粒子中分离出的仓鼠乳头瘤病毒(HaPV)的完整基因组,通过电子显微镜进行测量,并使用经过认证的质粒载体pBR322在大肠杆菌中进行克隆。通过用各种限制性内切酶消化重组DNA,然后将其在琼脂糖凝胶中的电泳迁移率与同样消化的未克隆DNA的电泳迁移率进行比较,并通过电子显微镜确定克隆的HaPV DNA的基因组大小,对克隆的病毒DNA进行了表征。克隆的HaPV DNA的限制性内切酶分析显示出与未克隆DNA的相应片段相同的切割模式。通过克隆的HaPV DNA与起始材料之间的异源双链分析,未检测到主要的插入或缺失。HaPV DNA估计的基因组大小为5.52 kb,比针对其他已知乳头瘤病毒(如SV40或多瘤病毒)确定的基因组大小大约300个碱基。