Li Guocai, Shi Weiqing, Chen Gang, Chen Hongju, Jiao Hongmei, Yan Hua, Ji Mingchun, Sun Huaichang
Department of Pathogeniology and Immunology, Yangzhou University School of Medicine, Yangzhou 225001, China; Jiangsu Key Laboratory of Zoonosis/Jiangsu Co-Innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou 225009, China; Jiangsu Key Laboratory of Integrated Traditional Chinese and Western Medicine for Prevention and Treatment of Senile Diseases, Yangzhou 225001, China.
Department of Pathology, Jiangsu Provincial Center for Disease Control and Prevention, Nanjing 210009, China.
Plasmid. 2014 Nov;76:47-53. doi: 10.1016/j.plasmid.2014.09.004. Epub 2014 Oct 2.
A mammary gland-specific expression vector p205C3 was constructed with the 5'- and 3'-flanking regions of β-lactoglobulin gene and the first intron of β-casein gene of Chinese dairy goat as regulatory sequences. Human lysozyme (hLYZ) cDNA from mammary gland was cloned into p205C3 and the recombinant vector was used to generate transgenic mice by microinjection. Based on the lysoplate assay, four female offspring of one male founder were detected expressing recombinant hLYZ in their milk at the levels of 5-200 mg/l, and the expressed protein had the same molecular weight as that of normal hLYZ. Besides mammary glands, ectopic expressions were also found in the spleens and the small intestines of the transgenic mice. Among the offspring, the female transgenic mice maintained and expressed the transgene stably with a highest expression level of 750 mg/l. Therefore, p205C3 could be used to develop animal mammary gland bioreactors expressing hLYZ.
构建了一种乳腺特异性表达载体p205C3,以中国奶山羊β-乳球蛋白基因的5'和3'侧翼区域以及β-酪蛋白基因的第一个内含子作为调控序列。将来自乳腺的人溶菌酶(hLYZ)cDNA克隆到p205C3中,并通过显微注射将重组载体用于生成转基因小鼠。基于溶菌平板试验,检测到一只雄性奠基者的四只雌性后代在其乳汁中表达重组hLYZ,表达水平为5 - 200毫克/升,且表达的蛋白与正常hLYZ具有相同的分子量。除了乳腺外,在转基因小鼠的脾脏和小肠中也发现了异位表达。在后代中,雌性转基因小鼠稳定维持并表达转基因,最高表达水平为750毫克/升。因此,p205C3可用于开发表达hLYZ的动物乳腺生物反应器。