Zettlmeissl G, Wirth M, Hauser H, Küpper H A
Research Laboratories of Behringwerke AG, Marburg/Lahn, W. Germany.
Behring Inst Mitt. 1988 Apr(82):26-34.
A DNA fragment carrying the enhancer of an immediate early gene of human cytomegalovirus (hCMV) was tested as a transcriptional control element by fusion downstream of a transcription unit for human antithrombin III (AT III) driven by the Simian virus (SV40) enhancer and promoter. Measurement of transient AT III expression in baby hamster kidney cells (BHK) shows that by the presence of the hCMV enhancer the synthesis of AT III is increased considerably (three to fourfold). The AT III expression vectors carrying the hCMV enhancer were used to establish stable BHK cell-lines by a new and fast G418/methotrexate selection protocol, which express up to 12 micrograms AT III/10(6) cells/24h after 40-50 days. The given system might be generally useful for the fast expression of recombinant proteins in mammalian cells, e.g. the screening of altered AT III molecules obtained by site directed mutagenesis.
携带人巨细胞病毒(hCMV)即刻早期基因增强子的DNA片段,作为转录控制元件进行了测试,方法是将其融合到由猴病毒(SV40)增强子和启动子驱动的人抗凝血酶III(AT III)转录单位的下游。对幼仓鼠肾细胞(BHK)中瞬时AT III表达的测量表明,由于hCMV增强子的存在,AT III的合成显著增加(三到四倍)。携带hCMV增强子的AT III表达载体,通过一种新的快速G418/甲氨蝶呤选择方案,用于建立稳定的BHK细胞系,该细胞系在40 - 50天后,每10⁶个细胞/24小时可表达高达12微克的AT III。给定的系统可能普遍适用于在哺乳动物细胞中快速表达重组蛋白,例如筛选通过定点诱变获得的改变的AT III分子。