Sherman L, Alloul N, Golan I, Durst M, Baram A
Department of Human Microbiology, Sackler School of Medicine, Tel-Aviv University, Israel.
Int J Cancer. 1992 Feb 1;50(3):356-64. doi: 10.1002/ijc.2910500305.
We have analysed the splicing patterns of human papillomavirus (HPV) type-16 mRNAs in a human epithelial cell line immortalized by HPV 16 (HPKII), in cell lines established from cervical carcinomas (SiHa and CaSki) and in pre-invasive and invasive carcinomas of the cervix. The presence of mRNA species previously described, which could encode the E6, E6I, E6II, E6III, E7, E2, E2C, E4, E5 and L1 proteins, was determined, using the RNA polymerase chain reaction (PCR) technique with primers that flank unique splice sites. The state of the viral DNA in the tumor biopsies was established by Southern blot analysis. The various HPV 16 transcripts could be detected in cell lines and in tumor biopsies. The size of the RNA PCR products were in agreement with the previously mapped splice sites. The full range of transcripts was revealed in the HPKII cell line and in a number of pre-invasive carcinomas. Messenger RNAs which could encode the E6III, E4 and E5 proteins were most prevalent in all types of tumor. The overall results of DNA and RNA analyses in cell lines and tumor specimens indicate that (1) expression of either of the early or late transcripts studied is not specifically related to (a) tumor stage or (b) the physical state of the viral genome; and (2) alterations in the splicing patterns of HPV 16 transcripts may not be involved in tumor progression.
我们分析了人乳头瘤病毒16型(HPV - 16)mRNA在由HPV 16永生化的人上皮细胞系(HPKII)、从宫颈癌建立的细胞系(SiHa和CaSki)以及宫颈的癌前病变和浸润性癌中的剪接模式。使用针对独特剪接位点侧翼的引物,通过RNA聚合酶链反应(PCR)技术确定了先前描述的可能编码E6、E6I、E6II、E6III、E7、E2、E2C、E4、E5和L1蛋白的mRNA种类的存在情况。通过Southern印迹分析确定肿瘤活检中病毒DNA的状态。在细胞系和肿瘤活检中均可检测到各种HPV 16转录本。RNA PCR产物的大小与先前绘制的剪接位点一致。在HPKII细胞系和一些癌前病变中发现了完整范围的转录本。可编码E6III、E4和E5蛋白的信使RNA在所有类型的肿瘤中最为普遍。细胞系和肿瘤标本中DNA和RNA分析的总体结果表明:(1)所研究的早期或晚期转录本的表达与(a)肿瘤分期或(b)病毒基因组的物理状态均无特异性关联;(2)HPV 16转录本剪接模式的改变可能与肿瘤进展无关。