László Brigitta, Ferenczi Annamária, Madar László, Gyöngyösi Eszter, Szalmás Anita, Szakács Levente, Veress György, Kónya József
Department of Medical Microbiology, Faculty of Medicine, University of Debrecen, Nagyerdei krt. 98, Debrecen, 4032, Hungary.
Department of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Nagyerdei krt. 98, Debrecen, 4032, Hungary.
Virus Genes. 2016 Aug;52(4):552-5. doi: 10.1007/s11262-016-1338-6. Epub 2016 Apr 20.
The mechanisms that regulate papillomavirus gene expression include DNA methylation. The transcription of papillomavirus oncogenes E6 and E7 is controlled by certain regulatory elements in the LCR, which include binding sites for the E2 protein, a viral regulator of oncogene expression. In HPV-31-infected exfoliated cervical cells, the CpG methylation of the entire LCR was determined by next-generation sequencing after bisulfite modification. Six of the 22 cases had methylated CpG sites in the HPV-31 LCR, including position 7479 and/or 7485, at the promoter distal E2 binding site, thus suggesting a potential regulatory mechanism for papillomavirus transcription.
调节乳头瘤病毒基因表达的机制包括DNA甲基化。乳头瘤病毒致癌基因E6和E7的转录受长控制区(LCR)中某些调控元件的控制,这些调控元件包括E2蛋白的结合位点,E2蛋白是致癌基因表达的病毒调节因子。在人乳头瘤病毒31型(HPV-31)感染的宫颈脱落细胞中,经亚硫酸氢盐修饰后通过二代测序确定了整个LCR的CpG甲基化情况。22例病例中有6例在HPV-31 LCR中存在CpG位点甲基化,包括启动子远端E2结合位点处的7479位和/或7485位,从而提示了乳头瘤病毒转录的一种潜在调控机制。