首页> 美国卫生研究院文献>Journal of Virology >Genetic and Biochemical Analysis of cis Regulatory Elements within the Keratinocyte Enhancer Region of the Human Papillomavirus Type 31 Upstream Regulatory Region during Different Stages of the Viral Life Cycle
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Genetic and Biochemical Analysis of cis Regulatory Elements within the Keratinocyte Enhancer Region of the Human Papillomavirus Type 31 Upstream Regulatory Region during Different Stages of the Viral Life Cycle

机译:病毒生命周期不同阶段人乳头瘤病毒31型上游调控区角质形成细胞增强区内顺式调控元件的遗传和生化分析

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摘要

Using linker scanning mutational analysis, we recently identified potential cis regulatory elements contained within the 5′ upstream regulatory region (URR) domain and auxiliary enhancer (AE) region of the human papillomavirus type 31 (HPV31) URR involved in the regulation of E6/E7 promoter activity at different stages of the viral life cycle. For the present study, we extended the linker scanning mutational analysis to identify potential cis elements located in the keratinocyte enhancer (KE) region (nucleotides 7511 to 7762) of the HPV31 URR and to characterize cellular factors that bind to these elements under conditions representing different stages of the viral life cycle. The linker scanning mutational analysis identified viral cis elements located in the KE region that regulate transcription in the presence and absence of any viral gene products or viral DNA replication and determine the role of host tissue differentiation on viral transcriptional regulation. Using electrophoretic mobility shift assays, we illustrated defined reorganization in the composition of cellular transcription factors binding to the same cis regulatory elements at different stages of the HPV differentiation-dependent life cycle. Our studies provide an extensive map of functional elements in the KE region of the HPV31 URR, identify cis regulatory elements that exhibit significant transcription regulatory potential, and illustrate changes in specific protein-DNA interactions at different stages of the viral life cycle. The variable recruitment of transcription factors to the same cis element under different cellular conditions may represent a mechanism underlying the tight link between keratinocyte differentiation and E6/E7 expression.
机译:使用接头扫描突变分析,我们最近确定了人类乳头瘤病毒31型(HPV31)URR的5'上游调控区(URR)域和辅助增强子(AE)区域中所含的潜在顺式调控元件,参与了E6 / E7的调控病毒生命周期不同阶段的启动子活性。对于本研究,我们扩展了接头扫描突变分析,以鉴定位于HPV31 URR的角质形成细胞增强子(KE)区(核苷酸7511至7762)的潜在顺式元件,并表征在代表不同条件下与这些元件结合的细胞因子病毒生命周期的各个阶段。接头扫描突变分析确定了位于KE区的病毒顺式元件,该元件在存在和不存在任何病毒基因产物或病毒DNA复制的情况下调节转录,并确定宿主组织分化在病毒转录调控中的作用。使用电泳迁移率变动分析,我们说明了在HPV分化依赖型生命周期的不同阶段,与相同的顺式调控元件结合的细胞转录因子组成的重组。我们的研究为HPV31 URR的KE区提供了广泛的功能元件图谱,鉴定了具有明显转录调控潜能的顺式调控元件,并阐明了病毒生命周期不同阶段特定蛋白质-DNA相互作用的变化。在不同细胞条件下,转录因子向同一顺式元件的可变募集可能代表了角质形成细胞分化与E6 / E7表达之间紧密联系的基础机制。

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