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人乳头瘤病毒16型癌蛋白对角质形成细胞分化相关基因的转录调控

Transcriptional regulation of genes involved in keratinocyte differentiation by human papillomavirus 16 oncoproteins.

作者信息

Gyöngyösi Eszter, Szalmás Anita, Ferenczi Annamária, Póliska Szilárd, Kónya József, Veress György

机构信息

Department of Medical Microbiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

出版信息

Arch Virol. 2015 Feb;160(2):389-98. doi: 10.1007/s00705-014-2305-y. Epub 2014 Dec 7.

Abstract

The life cycle of human papillomaviruses (HPVs) is strictly linked to the differentiation of their natural host cells. The HPV E6 and E7 oncoproteins can delay the normal differentiation program of keratinocytes; however, the exact mechanisms responsible for this have not yet been identified. The goal of this study was to investigate the effects of HPV16 oncoproteins on the expression of genes involved in keratinocyte differentiation. Primary human keratinocytes transduced by LXSN (control) retroviruses or virus vectors expressing HPV16 E6, E7 or E6/E7 genes were subjected to gene expression profiling. The results of microarray analysis showed that HPV 16 E6 and E7 have the capacity to downregulate the expression of several genes involved in keratinocyte differentiation. Quantitative real-time polymerase chain reaction (qRT-PCR) assays were performed to confirm the microarray data. To investigate the effects of the HPV oncoproteins on the promoters of selected keratinocyte differentiation genes, luciferase reporter assays were performed. Our results suggest that the HPV 16 E6 and/or E7 oncogenes are able to downregulate the expression of several genes involved in keratinocyte differentiation (such as desmocollin 1, keratin 4, S100 calcium-binding protein A8 and small proline-rich protein 1A), at least partially by downregulating their promoter activity. This activity of the HPV oncoproteins may have a role in the productive virus life cycle, and also in virus-induced carcinogenesis.

摘要

人乳头瘤病毒(HPV)的生命周期与它们天然宿主细胞的分化严格相关。HPV E6和E7癌蛋白可延缓角质形成细胞的正常分化程序;然而,其确切机制尚未明确。本研究的目的是调查HPV16癌蛋白对参与角质形成细胞分化的基因表达的影响。用LXSN(对照)逆转录病毒或表达HPV16 E6、E7或E6/E7基因的病毒载体转导的原代人角质形成细胞进行基因表达谱分析。微阵列分析结果显示,HPV 16 E6和E7有能力下调几个参与角质形成细胞分化的基因的表达。进行定量实时聚合酶链反应(qRT-PCR)测定以确认微阵列数据。为了研究HPV癌蛋白对所选角质形成细胞分化基因启动子的影响,进行了荧光素酶报告基因测定。我们的结果表明,HPV 16 E6和/或E7癌基因能够下调几个参与角质形成细胞分化的基因(如桥粒芯蛋白1、角蛋白4、S100钙结合蛋白A8和富含脯氨酸的小蛋白1A)的表达,至少部分是通过下调它们的启动子活性。HPV癌蛋白的这种活性可能在病毒的有效生命周期中起作用,也在病毒诱导的致癌作用中起作用。

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