首页> 美国卫生研究院文献>Journal of Virology >Identification of a differentiation-inducible promoter in the E7 open reading frame of human papillomavirus type 16 (HPV-16) in raft cultures of a new cell line containing high copy numbers of episomal HPV-16 DNA.
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Identification of a differentiation-inducible promoter in the E7 open reading frame of human papillomavirus type 16 (HPV-16) in raft cultures of a new cell line containing high copy numbers of episomal HPV-16 DNA.

机译:在包含高拷贝数的游离型HPV-16 DNA的新细胞系的筏培养中在人乳头瘤病毒16型(HPV-16)的E7开放阅读框中鉴定了诱导分化的启动子。

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摘要

Gene expression of human papillomaviruses (HPV) is tightly linked to differentiation processes within the pluristratified epithelium. To analyze changes in the transcription pattern of HPV-16 during epithelial cell differentiation, we established a permanently growing HPV-16 positive cell line, designated KG, from a vulvar intraepithelial neoplasm. KG cells of early passages harbored multiple copies of the HPV-16 DNA as episomes and were able to form a stratified epithelium in an organotypic raft culture system. Analysis of viral gene expression revealed the known transcription pattern of the early region of HPV-16 with the exception of a so far undefined mRNA class with start sites in the E7 open reading frame. Quantitative analysis of primer extension experiments with RNA from KG cells grown in monolayer and raft culture showed a strong induction of this transcript in differentiated KG cells, whereas the level of the mRNAs initiated at the early promoter P97 remained almost constant. Primer extension analyses with four different primers and direct sequencing of the extension product revealed that the differentiation-inducible transcript initiated at a novel promoter with a major start site around nucleotide position 670 (P670) in the E7 open reading frame of HPV-16. Sequence analysis of cDNAs derived from RNA of KG cells grown in raft culture suggested that the transcripts initiated at P670 have a coding potential for an E1E4 fusion protein and for the E5 protein.
机译:人乳头瘤病毒(HPV)的基因表达与多层次上皮细胞的分化过程紧密相关。为了分析上皮细胞分化过程中HPV-16转录模式的变化,我们从外阴上皮内肿瘤建立了一个永久生长的HPV-16阳性细胞系,称为KG。早期传代的KG细胞带有多个拷贝的HPV-16 DNA作为附加体,并且能够在器官型筏培养系统中形成分层的上皮。病毒基因表达的分析揭示了HPV-16早期区域的已知转录模式,但迄今未定义的mRNA类除外,其E7开放阅读框中有起始位点。用单层和筏式培养的KG细胞中的RNA进行引物延伸实验的定量分析表明,该转录本在分化的KG细胞中强烈诱导,而在早期启动子P97处起始的mRNA水平几乎保持恒定。用四种不同引物进行的引物延伸分析和延伸产物的直接测序表明,可诱导分化的转录物起始于一个新的启动子,该启动子在HPV-16的E7开放阅读框中的核苷酸位置670(P670)附近具有主要起始位点。对筏培养中生长的KG细胞的RNA衍生的cDNA的序列分析表明,在P670起始的转录本具有E1E4融合蛋白和E5蛋白的编码潜力。

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