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机构地区:[1]中国科学院上海生物化学研究所
出 处:《病毒学报》1997年第3期215-223,共9页Chinese Journal of Virology
摘 要:构建了线性化的、从基本核心启动子(Cp)开始并有不同长度Cp上游顺序的、含完整转录单元的HBV基因组克隆,以研究Cp及其上游顺序对HBV基因表达的调控及对HBV子代DNA复制的影响。发现从基本核心启动子Cp开始的HBV转录单元能够有效地起始3.5kbmR-NA转录。Cp上游ENI顺序对子代DNA复制有极强的刺激作用,而ENⅡ更上游顺序对ENⅡ的刺激作用又有所抑制,证明Cp的转录受其上游顺序的正负双重调控。另外,Cp上游还存在与HBV基因表达的细胞专一性有关的调控顺序。In this study,linearized genome containing the entire HBV transcriptional units were constructed,which initiated from the basic core promoter (Cp) or its upstream regulatory sequences.The transcriptional unit from Cp was sufficient for the transcription,replication and expression of HBV genome.The upstream regulatory sequences of Cp,overlapping with EN Ⅱ,had a strong stimulating effect on the replication of HBV progeny DNA.However,a region upstream EN Ⅱ and Cp (nt 1403-1633) could suppress this activation.It indicated that the transcription and replication of HBV genome depended on both positive and negative regulation.In addition,there were regulatory elements located on upstream of Cp related to the hepatocyte specificity of HBV gene expression.
分 类 号:R373.21[医药卫生—病原生物学]
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