Kremsdorf D, Jablonska S, Favre M, Orth G
J Virol. 1982 Aug;43(2):436-47. doi: 10.1128/JVI.43.2.436-447.1982.
The DNAs of the human papillomaviruses (HPVs) associated with the benign lesions of two patients suffering from epidermodysplasia verruciformis (patients JD and JK) were analyzed by using 12 restriction endonucleases. None of the restriction endonucleases were one-cut enzymes for the HPV DNA obtained from patient JD, referred to as the prototypical HPV-5, whereas five of them were one-cut enzymes for the DNA of the major virus found in patient JK, referred to as HPV-9. The molecular cloning of the two fragments resulting from the cleavage of HPV-5 DNA by endonuclease HindIII and of the single fragment obtained after treatment of HPV-9 DNA with endonuclease BamHI was performed in Escherichia coli after the fragments were inserted in plasmid pBR322. A cleavage map of the two cloned genomes was constructed. Little sequence homology (4 to 5%) was detected between HPV-5 and HPV-9 DNAs by DNA-DNA hybridization experiments in liquid phase at saturation; this homology was reproducibly higher than that (2 to 3%) detected under the same conditions between these DNAs and HPV-1a DNA. In addition, blot hybridization experiments performed under stringent conditions showed no or little sequence homology between the DNAs of HPV-5 and HPV-9 and those of HPV prototypes of types 1, 2, 3, 4, and 7 associated with skin warts. These results confirm that HPV-5 and HPV-9 are two distinct HPV types.
利用12种限制性内切酶对两名疣状表皮发育不良患者(JD和JK患者)良性病变相关的人乳头瘤病毒(HPV)DNA进行了分析。对于从JD患者获得的HPV DNA(称为典型的HPV - 5),没有一种限制性内切酶是单切点酶,而其中五种酶对于在JK患者中发现的主要病毒(称为HPV - 9)的DNA是单切点酶。在用内切酶HindIII切割HPV - 5 DNA产生的两个片段以及用内切酶BamHI处理HPV - 9 DNA后获得的单个片段插入质粒pBR322后,在大肠杆菌中进行了分子克隆。构建了两个克隆基因组的切割图谱。通过液相饱和DNA - DNA杂交实验检测到HPV - 5和HPV - 9 DNA之间的序列同源性很低(4%至5%);这种同源性在相同条件下可重复地高于这些DNA与HPV - 1a DNA之间检测到的同源性(2%至3%)。此外,在严格条件下进行的印迹杂交实验表明,HPV - 5和HPV - 9的DNA与1、2、3、4和7型与皮肤疣相关的HPV原型的DNA之间没有或只有很少的序列同源性。这些结果证实HPV - 5和HPV - 9是两种不同的HPV类型。