Cell Engineering Department, Beijing Institute of Biotechnology, Beijing 100071, China.
Mol Biotechnol. 2012 Feb;50(2):137-44. doi: 10.1007/s12033-011-9428-0.
Transgene expression for the mammary gland bioreactor aimed at producing recombinant proteins requires optimized expression vector construction. Previously we presented a hybrid gene locus strategy, which was originally tested with human lactoferrin (hLF) as target transgene, and an extremely high-level expression of rhLF ever been achieved as to 29.8 g/l in mice milk. Here to demonstrate the broad application of this strategy, another 38.4 kb mWAP-htPA hybrid gene locus was constructed, in which the 3-kb genomic coding sequence in the 24-kb mouse whey acidic protein (mWAP) gene locus was substituted by the 17.4-kb genomic coding sequence of human tissue plasminogen activator (htPA), exactly from the start codon to the end codon. Corresponding five transgenic mice lines were generated and the highest expression level of rhtPA in the milk attained as to 3.3 g/l. Our strategy will provide a universal way for the large-scale production of pharmaceutical proteins in the mammary gland of transgenic animals.
为了实现生产重组蛋白的乳腺生物反应器的转基因表达,需要对表达载体进行优化构建。此前,我们提出了一种杂交基因座策略,最初用乳铁蛋白(hLF)作为目的转基因进行了测试,并在小鼠乳汁中实现了极高水平的 rhLF 表达,达到了 29.8 g/L。在这里,为了展示该策略的广泛应用,我们构建了另一个 38.4 kb 的 mWAP-htPA 杂交基因座,其中 24-kb 的小鼠乳清酸性蛋白(mWAP)基因座中的 3-kb 基因组编码序列被替换为人组织型纤溶酶原激活剂(htPA)的 17.4-kb 基因组编码序列,正好从起始密码子到终止密码子。生成了相应的五个转基因小鼠品系,在乳汁中获得了 rhtPA 的最高表达水平,达到了 3.3 g/L。我们的策略将为在转基因动物的乳腺中大规模生产药物蛋白提供一种通用的方法。