School of Biology and Basic Medical Sciences, Soochow University, 215123, Suzhou, People's Republic of China.
Biotechnol Lett. 2011 Mar;33(3):489-94. doi: 10.1007/s10529-010-0462-y. Epub 2010 Nov 12.
The expression of the human insulin-like growth factor (hIGF-I) gene driven by the Fhx/P25 promoter in the silk glands of transgenic silkworms (Bombyx mori) and in transformed silkworm cells, was achieved using BmN cells transfected with a piggyBac vector, pigA3GFP-Fhx/P25-hIGF-ie-neo containing a neomycin-resistance gene (neo), a green fluorescent protein gene (gfp), an hIGF-I gene, and a helper plasmid containing the piggyBac transposase sequence under the control of the B. mori actin 3 (A3) promoter. We selected stably transformed BmN cells expressing hIGF-I using the antibiotic G418. The expression level of hIGF-I was about 450 pg in 3 × 10(6) cells, determined by ELISA. The piggyBac vector was transferred into the silkworm eggs using sperm-mediated gene transfer. The expression level of hIGF-I per gram fresh posterior silk glands of G4 transgenic silkworms was approx. 150 ng.
利用转染了 piggyBac 载体的 BmN 细胞实现了丝氨酸羟甲基转移酶基因(fhx/p25)启动子驱动的人胰岛素样生长因子(hIGF-I)基因在转基因家蚕(Bombyx mori)的丝腺和转化的家蚕细胞中的表达。pigA3GFP-Fhx/P25-hIGF-ie-neo 载体中含有新霉素抗性基因(neo)、绿色荧光蛋白基因(gfp)、hIGF-I 基因和一个含有 piggyBac 转座酶序列的辅助质粒,该质粒受 B. mori 肌动蛋白 3(A3)启动子的控制。我们使用抗生素 G418 选择稳定表达 hIGF-I 的转染 BmN 细胞。通过 ELISA 测定,约 3×10(6)个细胞中 hIGF-I 的表达水平约为 450pg。使用精子介导的基因转移将 piggyBac 载体转入家蚕卵中。G4 转基因家蚕每克新鲜后丝腺中 hIGF-I 的表达水平约为 150ng。