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HPV8 通过 Sp1/3 结合位点主要激活细胞基因表达。

HPV8 activates cellular gene expression mainly through Sp1/3 binding sites.

机构信息

Institute of Virology, University of Cologne, Faculty of Medicine and University Hospital of Cologne, Germany.

Department of Dermatology and Venereology, Medical University of Warsaw, Warsaw, Poland.

出版信息

Virology. 2019 Sep;535:136-143. doi: 10.1016/j.virol.2019.06.019. Epub 2019 Jul 1.

Abstract

The human papillomavirus type 8 (HPV8) is associated with skin cancer development. The goal of this study was to investigate the effects of HPV8 oncoproteins on cellular gene expression and the identification of key regulators. We performed affymetrix microarray analyses to identify differentially expressed genes and common sequence motifs and identified Sp1/3 binding sites as being crucial. In transient transfection assays, we confirmed that HPV8-E7 stimulates the activity of Sp1/3 promoters. Interestingly, the HPV8-E7 mutant, which cannot trigger keratinocyte invasion was unable to activate fibronectin gene expression. In skin models or HPV8 positive skin cancers we found a peculiar deposition of fibronectin in the dermal compartment, and a correlation of Sp3 and fibronectin in the nucleus of HPV8-positive keratinocytes. Taken together, we identified that HPV8-E7 exerts control over cellular gene expression through Sp1/3 binding motifs, which may contribute to HPV8-mediated keratinocyte transformation and subsequent fibronectin-dependent invasion.

摘要

人乳头瘤病毒 8 型(HPV8)与皮肤癌的发展有关。本研究的目的是研究 HPV8 致癌蛋白对细胞基因表达的影响,并确定关键调节因子。我们进行了 Affymetrix 微阵列分析,以鉴定差异表达的基因和常见的序列基序,并确定 Sp1/3 结合位点是至关重要的。在瞬时转染实验中,我们证实 HPV8-E7 可刺激 Sp1/3 启动子的活性。有趣的是,不能触发角质形成细胞侵袭的 HPV8-E7 突变体无法激活纤维连接蛋白基因表达。在皮肤模型或 HPV8 阳性皮肤癌中,我们发现纤维连接蛋白在真皮部分的沉积特别明显,并且 HPV8 阳性角质形成细胞核中的 Sp3 和纤维连接蛋白存在相关性。总之,我们发现 HPV8-E7 通过 Sp1/3 结合基序对细胞基因表达进行控制,这可能有助于 HPV8 介导的角质形成细胞转化和随后的纤维连接蛋白依赖性侵袭。

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