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作 者:张中林[1] 山松[1] 陈曦[1] 苏宁[1] 吴祥甫[2] 钱凯先[3] 沈桂芳[1]
机构地区:[1]中国农业科学院生物技术研究中心,北京100081 [2]中国科学院上海生物化学研究所,上海200031 [3]浙江大学生物科学与技术系,杭州310027
出 处:《遗传》1999年第6期1-6,共6页Hereditas(Beijing)
摘 要:用PCR 方法从丙型肝炎病毒(HCV) cDNA 文库中克隆了两段DNA 片段,即HCV 基因组非结构NS3区抗原基因(约0.7 kb)和核心抗原C区抗原基因(约0.6 kb)的cDNA 片段。在两段cDNA 间加入连接肽Ser- Pro- Gly- Ser 的密码子序列,构建成融合抗原基因NS3- C。将该融合基因与衣藻叶绿体基因atpA 的启动子和rbcL 基因的3′末端连接,得到丙肝病毒融合抗原基因NS3- C表达盒,再将该表达盒与选择标记基因aadA 表达盒和衣藻叶绿体基因组同源片段连接,构建成衣藻叶绿体转化载体pSS6。基因枪法转化衣藻叶绿体,经壮观霉素筛选获得转化再生的单藻落,对转基因衣藻的PCR 和Southern 杂交分析表明,融合抗原基因NS3- C已整合到衣藻叶绿体基因组中。Two DNA fragments encoding the nucleocapsid (C) region protein and the non-structural region 3 (NS 3 ) protein of hepatitis C virus(HCV) were amplified from cDNA library by using PCR method. The 5′ terminal of C cDNA fragment was linked up with the 3′ terminal of NS 3 cDNA fragment by a oligonucleotide linker Ser-Pro-Gly-Ser to form a chimeric gene NS 3 -C, which was placed under the control of the chloroplast atpA promoter and rbcL 3′ region of Chlamydomonas reinhardtii to construct the chimeric gene NS 3 -C cassette. Then the NS 3 -C cassette was linked with selectable gene aadA cassette and the chloroplast homologous fragments of Chlamydomonas reinhardtii to generate transformation vector pSS6. Chloroplasts of Chlamydomonas reinhardtii were transformed by particle bombardment. Plastid transformants were selected by their resistance to 100 mg/L of spectinomycin. PCR and Southern hybridization analysis showed that the chimeric gene NS 3 -C had been integrated into chloroplast genome of Chlamydomonas reinhardtii.
关 键 词:丙型肝炎病毒 基因融合 叶绿体转化 aadA基因 衣藻
分 类 号:Q78[生物学—分子生物学] R373.21[医药卫生—病原生物学]
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