Cumming Sarah A, Repellin Claire E, McPhillips Maria, Radford Jonathan C, Clements J Barklie, Graham Sheila V
Institute of Virology, University of Glasgow, Glasgow G11 5JR, Scotland.
J Virol. 2002 Jun;76(12):5993-6003. doi: 10.1128/jvi.76.12.5993-6003.2002.
The papillomavirus life cycle is tightly linked to epithelial cell differentiation. Production of virus capsid proteins is restricted to the most terminally differentiated keratinocytes in the upper layers of the epithelium. However, mRNAs encoding the capsid proteins can be detected in less-differentiated cells, suggesting that late gene expression is controlled posttranscriptionally. Short sequence elements (less than 80 nucleotides in length) that inhibit gene expression in undifferentiated epithelial cells have been identified in the late 3' untranslated regions (UTRs) of several papillomaviruses, including the high-risk mucosal type human papillomavirus type 16 (HPV-16). Here we show that closely related high-risk mucosal type HPV-31 also contains elements that can act to repress gene expression in undifferentiated epithelial cells. However, the HPV-31 negative regulatory element is surprisingly complex, comprising a major inhibitory element of approximately 130 nucleotides upstream of the late polyadenylation site and a minor element of approximately 110 nucleotides mapping downstream. The first 60 nucleotides of the major element have 68% identity to the negative regulatory element of HPV-16, and these elements bind the same cellular proteins, CstF-64, U2AF(65), and HuR. The minor inhibitory element binds some cellular proteins in common with the major inhibitory element, though it also binds certain proteins that do not bind the upstream element.
乳头瘤病毒的生命周期与上皮细胞分化紧密相关。病毒衣壳蛋白的产生仅限于上皮上层中终末分化程度最高的角质形成细胞。然而,在分化程度较低的细胞中可检测到编码衣壳蛋白的mRNA,这表明晚期基因表达是在转录后受到调控的。在几种乳头瘤病毒的晚期3'非翻译区(UTR)中已鉴定出短序列元件(长度小于80个核苷酸),这些元件可抑制未分化上皮细胞中的基因表达,其中包括高危黏膜型人乳头瘤病毒16型(HPV-16)。在此我们表明,密切相关的高危黏膜型HPV-31也含有可在未分化上皮细胞中抑制基因表达的元件。然而,HPV-31负调控元件出人意料地复杂,包括位于晚期多聚腺苷酸化位点上游约130个核苷酸的主要抑制元件和位于下游约110个核苷酸的次要元件。主要元件的前60个核苷酸与HPV-16的负调控元件有68%的同源性,并且这些元件结合相同的细胞蛋白,即切割刺激因子64(CstF-64)、U2辅助因子65(U2AF(65))和HuR。次要抑制元件与主要抑制元件结合一些共同的细胞蛋白,尽管它也结合某些不与上游元件结合的蛋白。