Maitland N J, Bromidge T, Cox M F, Crane I J, Prime S S, Scully C
Department of Pathology, Medical School, Bristol, UK.
Br J Cancer. 1989 May;59(5):698-703. doi: 10.1038/bjc.1989.146.
We have used the polymerase chain reaction to detect DNA sequences related to human papillomavirus type 16, by simultaneous priming with oligonucleotides from the E6 and L1/L2 open reading frames of the HPV16 genome. The HPV16-related sequence is present at low levels in normal oral tissue, in addition to biopsies and cell cultures from patients with benign and malignant disease. Ultimate analysis of the amplified sequences from the E6(120bp) and L1/L2(173bp) regions of HPV16 was achieved by gel electrophoresis and comparative nucleotide sequencing. The oral carcinoma biopsies and tissue cultures contained DNA sequences which were identical to the E6 region of HPV16, but only rarely contained sequences closely related to the L1/L2 region. The PCR technology should permit the detection, identification and cloning of latent viruses from extremely small tissue biopsies.
我们通过使用来自人乳头瘤病毒16型(HPV16)基因组E6和L1/L2开放阅读框的寡核苷酸同时引发,利用聚合酶链反应检测与HPV16相关的DNA序列。除了来自良性和恶性疾病患者的活检组织和细胞培养物外,HPV16相关序列在正常口腔组织中也以低水平存在。通过凝胶电泳和比较核苷酸测序对HPV16的E6(120bp)和L1/L2(173bp)区域的扩增序列进行了最终分析。口腔癌活检组织和组织培养物中含有与HPV16的E6区域相同的DNA序列,但很少含有与L1/L2区域密切相关的序列。聚合酶链反应技术应能从极小的组织活检中检测、鉴定和克隆潜伏病毒。