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由 Fhx/P25 启动子驱动的 hIGF-I 基因在生殖丝腺和转 BmN 细胞中的表达。

Expression of the hIGF-I gene driven by the Fhx/P25 promoter in the silk glands of germline silkworm and transformed BmN cells.

机构信息

School of Biology and Basic Medical Sciences, Soochow University, 215123, Suzhou, People's Republic of China.

出版信息

Biotechnol Lett. 2011 Mar;33(3):489-94. doi: 10.1007/s10529-010-0462-y. Epub 2010 Nov 12.

Abstract

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.

摘要

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。

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