Chang P J, Chang Y S, Liu S T
Institute of Microbiology and Immunology, National Yang-Ming University, Shih-Pai, Taipei, Taiwan.
J Gen Virol. 1998 Aug;79 ( Pt 8):2003-6. doi: 10.1099/0022-1317-79-8-2003.
The location of the BcLF1 promoter of Epstein-Barr virus (EBV) has been identified by primer extension, which indicates that the +1 site of the BcLF1 mRNA is located at nucleotide 137676 of the EBV genome. According to deletion analysis, the region upstream from nucleotide -38 is not essential for transcription of BcLF1. A 23 bp region in the promoter, from nucleotide -38 to -16, was identified as necessary for regulating the expression of BcLF1, i.e. the promoter activity is activated by 12-O-tetradecanoylphorbol 13-acetate but is repressed by phosphonoacetic acid. The results presented also demonstrate that the oriLyt sequence in cis is essential for enhancing the expression of BcLF1.
通过引物延伸法已确定了爱泼斯坦-巴尔病毒(EBV)的BcLF1启动子的位置,这表明BcLF1 mRNA的+1位点位于EBV基因组的第137676个核苷酸处。根据缺失分析,核苷酸-38上游的区域对于BcLF1的转录并非必需。启动子中一个从核苷酸-38到-16的23 bp区域被确定为调节BcLF1表达所必需,即启动子活性被12-O-十四酰佛波醇13-乙酸酯激活,但被膦甲酸抑制。所呈现的结果还表明,顺式oriLyt序列对于增强BcLF1的表达至关重要。