Kukimoto Iwao, Takeuchi Takamasa, Kanda Tadahito
Division of Molecular Genetics, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan.
Virology. 2006 Mar 1;346(1):98-107. doi: 10.1016/j.virol.2005.10.025. Epub 2005 Nov 22.
The P670 promoter of HPV16 directs transcription of the virus late genes in the differentiating epithelium. We found that CCAAT/enhancer binding protein beta (C/EBPbeta), a key transcription factor that induces the terminal differentiation of keratinocytes, enhanced the P670-driven transcription in transient reporter assays in HeLa cells and human primary keratinocytes, whereas it inhibited, as reported previously, the transcription from the early P97 promoter. An electrophoretic mobility shift analysis identified two binding sites in the upstream region of P670 for a bacterially expressed C/EBPbeta. A chromatin immunoprecipitation analysis demonstrated that C/EBPbeta bound to these sites of the P670 reporter plasmid in HeLa cells. Nucleotide substitutions in these sites in the reporter plasmid abrogated the enhancement by C/EBPbeta in the transient HeLa and keratinocyte assays, indicating that the C/EBPbeta-binding to these sites is required for the enhancement of transcription from P670. These results suggest that C/EBPbeta is involved in enhancing transcription from the P670 during keratinocyte differentiation.
人乳头瘤病毒16型(HPV16)的P670启动子指导病毒晚期基因在分化上皮细胞中的转录。我们发现,CCAAT/增强子结合蛋白β(C/EBPβ)是一种诱导角质形成细胞终末分化的关键转录因子,在HeLa细胞和人原代角质形成细胞的瞬时报告基因检测中,它增强了P670驱动的转录,而正如之前报道的那样,它抑制早期P97启动子的转录。电泳迁移率变动分析确定了细菌表达的C/EBPβ在P670上游区域的两个结合位点。染色质免疫沉淀分析表明,C/EBPβ在HeLa细胞中与P670报告质粒的这些位点结合。报告质粒中这些位点的核苷酸替换消除了C/EBPβ在瞬时HeLa细胞和角质形成细胞检测中的增强作用,表明C/EBPβ与这些位点的结合是增强P670转录所必需的。这些结果表明,C/EBPβ参与在角质形成细胞分化过程中增强P670的转录。