Cloning of HBsAg-encoded genes in different vectors and their expression in eukaryotic cells

查看全文 作　　者：[3]ShanQin;[1]HongTang;Lian-[1]SanZhao;[1]FangHe;[1]YongLin;[1]LiLiu;Xiao-[2]MeiHe

机构地区：[1]KeyLaboratoryforMolecularBiologyofInfectiousDiseasesofSichuanProvince,WestChinaHospital,SichuanUniversity,Chengdu610041,Sichuan,China;[2]AnalyticalandTestingCenter,SichuanUniversity,Chengdu610064,Sichuan,China;[3]CenterforDiscoveryofDrugsandDiagnostics,BiomolecularScienceCenter,UniversityofCentralFlorida.12722ResearchParkway,Orlando,Florida32826.USA

出　　处：《World Journal of Gastroenterology》索引2003年第9卷第5期,共3页

基　　金：the National Science Foundation of China,No. 39670670 摘　　要：AIM: To compare the efficiency of different plasmids as DNA vectors by cloning three HBsAg-encoded genes into two eukaryotic expression vectors, pRc/CMV and pSG5UTPL/Flag, and to express HBsAg S, MS, and LS proteins in SP2/0 cells, and to establish monoclone SP2/0 cell strains that are capable of expressing S or S2S proteins stably.METHODS: Segments of S, preS2-S, preS1-preS2-S genes of Hepatitis B virus were amplified by routine PCR and preS1S fragment was amplified by Over-Lap Extension PCR. The amplified segments were cleaved with restricted endonuclease Hind Ⅲ/Not Ⅰ followed by ligation with pRc/CMV, or BamHI/EcoR Ⅰ followed by ligation with pSG5UTPL/Flag. After the plasmid vectors were cleaved with the correspond enzymes, the amplified segments were inserted into pRc/CMV or pSGSUTPL/Flag plasmid vectors with T4DNA ligase. KOZAK sequence was added before the initial ATG code of each fragment using specific primer. The inserted segments in the recombinant plasmids were sequenced after subcloning. BALB/c mice myeloma cells (SP2/0 cell line) were transfected with the recombinant plasmids. The expressions of the different recombinants were compared by Western-blot, using a monoclonal anti-HBs antibody as the primary antibody and peroxidase-labeled multi-linker as the secondary. Stable SP2/0-pRc/CMV-S or SP2/0- pRc/CMV-MS clones were established through clone screening with G418.RESULTS: Fragments with anticipated size were harvested after PCR. After recombination and screening, the sequences of the inserted segments in the recombinants were confirmed to be S, preS2S, preSl-preS2S and preSlS encoding genes,determined by sequencing. The results of Western-blot hybridization were positive for the anticipated proteins.Among them, pRc/CMV-S or pRc/CMV-MS demonstrated the highest expressing their respective antigen.CONCLUSION: Eight recombinant plasmids expressing S,M, L or preSlS proteins are obtained. For hepatitis surface antigen expression in eukaryotic cells, the vector pRc/CMV is superior to pSG5UTPL/Flag, and pRc/CMV-S and pRc/CMVMS are the most efficient in the pRc/CMV clones. SP2/0 cells stably expressing HBsAg are established, and may be used as target cells for evaluating the CTL activity of a DNA vaccine in vitro. 关键词：乙肝表面抗原编码基因真核细胞克隆乙型肝炎病毒病毒携带者

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Cloning of HBsAg-encoded genes in different vectors and their expression in eukaryotic cells

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