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乳头瘤病毒E2蛋白与参与角质形成细胞分化的C/EBP因子结合并协同作用。

The Papillomavirus E2 protein binds to and synergizes with C/EBP factors involved in keratinocyte differentiation.

作者信息

Hadaschik Dirk, Hinterkeuser Korinna, Oldak Monika, Pfister Herbert J, Smola-Hess Sigrun

机构信息

Institute of Virology, University of Cologne, Germany.

出版信息

J Virol. 2003 May;77(9):5253-65. doi: 10.1128/jvi.77.9.5253-5265.2003.

Abstract

The papillomavirus life cycle is closely linked to the differentiation program of the host keratinocyte. Thus, late gene expression and viral maturation are restricted to terminally differentiated keratinocytes. A variety of cellular transcription factors including those of the C/EBP family are involved in the regulation of keratinocyte differentiation. In this study we show that the papillomavirus transcription factor E2 cooperates with C/EBPalpha and -beta in transcriptional activation. This synergism was independent of an E2 binding site. E2 and C/EBP factors synergistically transactivated a synthetic promoter construct containing classical C/EBPbeta sites and the C/EBPalpha-responsive proximal promoter of the involucrin gene, which is naturally expressed in differentiating keratinocytes. C/EBPalpha or -beta coprecipitated with E2 proteins derived from human papillomavirus type 8 (HPV8), HPV16, HPV18, and bovine papillomavirus type 1 in vitro and in vivo, indicating complex formation by the cellular and viral factors. The interaction domains could be mapped to the C terminus of E2 and amino acids 261 to 302 located within the bZIP motif of C/EBPbeta. Our data suggest that E2, via its interaction with C/EBP factors, may contribute to enhancing keratinocyte differentiation, which is suppressed by the viral oncoproteins E6 and E7 in HPV-induced lesions.

摘要

乳头瘤病毒的生命周期与宿主角质形成细胞的分化程序密切相关。因此,晚期基因表达和病毒成熟仅限于终末分化的角质形成细胞。多种细胞转录因子,包括C/EBP家族的转录因子,参与角质形成细胞分化的调控。在本研究中,我们发现乳头瘤病毒转录因子E2与C/EBPα和-β在转录激活中协同作用。这种协同作用不依赖于E2结合位点。E2和C/EBP因子协同反式激活了一个合成启动子构建体,该构建体包含经典的C/EBPβ位点和在分化角质形成细胞中自然表达的内披蛋白基因的C/EBPα反应性近端启动子。在体外和体内,C/EBPα或-β与源自人乳头瘤病毒8型(HPV8)、HPV16、HPV18和牛乳头瘤病毒1型的E2蛋白共沉淀,表明细胞和病毒因子形成了复合物。相互作用结构域可定位到E2的C末端以及位于C/EBPβ的bZIP基序内的第261至302位氨基酸。我们的数据表明,E2通过与C/EBP因子相互作用,可能有助于增强角质形成细胞的分化,而在HPV诱导的病变中,这种分化受到病毒癌蛋白E6和E7的抑制。

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