乙型肝炎病毒前-S1蛋白反式激活蛋白2基因的克隆化研究  

Cloning of Human Gene 2 Transactivated by Pre-S1 Protein of Hepatitis B Virus

作　　者：郭江[1] 成军[1] 纪冬[1] 赵龙凤[1] 王建军[1] 刘妍[1] 刘蔚[1] 

机构地区：[1]中国人民解放军第302医院传染病研究所基因治疗研究中心,北京100039

出　　处：《中西医结合肝病杂志》2004年第4期212-215,共4页Chinese Journal of Integrated Traditional and Western Medicine on Liver Diseases

基　　金：军队回国留学人员启动基金资助课题(No98H038);国家自然科学基金攻关项目(NoC030114020;C30070689);军队"九.五"科技攻关项目(No98D063);军队"十.五"科技攻关青年基金项目(No01Q138);军队"十.五"科技攻关项目编号(No01B1

摘　　要：目的 :应用抑制性消减杂交 (SSH )技术及生物信息学 (bioinformatics)技术筛选并克隆乙型肝炎病毒(HBV)前 S1蛋白 (pre S1)反式激活新型靶基因 ,进一步阐明HBV感染相关疾病的发病机制。方法 :以HBV前 S1蛋白表达质粒 pcDNA3 1( -) pre S1转染HepG2细胞 ,以空载体 pcDNA3 1( -)为平行对照 ,提取mRNA并进行抑制性消减杂交分析。并应用分子生物学技术 ,结合生物信息学技术 ,克隆HBV前 S1反式激活作用的新的靶基因。结果 :对于所获基因片段序列分析表明 ,其中之一为新型基因片段。从HepG2细胞提取总RNA ,以逆转录多聚酶链反应 (RT PCR)技术扩增获得该新基因的全长序列 ,并测序证实 ,因其可以被前 S1蛋白反式激活 ,故命名为前 S1反式激活蛋白 2 (PS1TP2 ) ,已在GenBank中注册 ,注册号 :AY42 6673。PS1TP2基因的编码序列全长为 5 73个核苷酸 (nt) ,编码产物由 190个氨基酸残基 (aa)组成。结论 :HBV前 S1蛋白在HBV进入宿主细胞的过程中起着重要作用 ,最近的研究表明前 S1蛋白还具有反式激活的作用 ,上调宿主细胞某些基因的表达 ,从而改变宿主正常的免疫应答水平 ,引起病变。HBV前 S1反式激活新靶基因的发现 ,为进一步研究HBV前Objective:To screen and clone the target genes transactivated by hepatitis B virus (HBV) pre-S1 protein and to pave the way for elucidating the pathogenesis of HBV infection. Methods: Suppression subtractive hybridization (SSH) technique and bioinformatics technique were used, and the mRNA from HepG2 cells transfected with pcDNA3.1(-)-pre-S1 and pcDNA 3.1(-) empty vector was isolated, respectively, and SSH method was employed to analyze the differentially expressed DNA sequence between the two groups. The coding gene transactivated by HBV pre-S1 was cloned by bioinformatics methods.Results: The obtained sequences were searched for homologous DNA sequences from GenBank, one of which was a new gene with unknown function. The new gene with no homology with known genes in this database was confirmed and electric polymerase chain reaction (PCR) was conducted for the cloning of the full-length DNA for the new gene and in conjunction with Kozak role and exist of polyadenyl signal sequence. The reverse transcription PCR (RT-PCR) was used toamplify the new gene, named as PS1TP2, from the mRNA of HepG2 cells. The sequence for the PS1TP2 gene has been deposited into GenBank, the accession number is AY426673. Conclusion: HBV pre-S1 is a potential transactivator.These results willpave the way for the study of the molecular mechanism of the transactivating effects of HBV pre-S1 protein and the development of new therapy for chronic hepatitis B.

关 键 词：乙型肝炎病毒 前-S1蛋白 反式激活蛋白2 基因克隆化 

分 类 号：R346[医药卫生—基础医学]