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通过体内重组从黏粒文库中分离功能性人白细胞介素2基因。

Isolation of a functional human interleukin 2 gene from a cosmid library by recombination in vivo.

作者信息

Lindenmaier W, Dittmar K E, Hauser H, Necker A, Sebald W

出版信息

Gene. 1985;39(1):33-9. doi: 10.1016/0378-1119(85)90104-0.

Abstract

A method has been developed that allows the isolation of genomic clones from a cosmid library by homologous recombination in vivo. This method was used to isolate a human genomic interleukin 2 (IL2) gene. The genomic cosmid library was packaged in vivo into lambda phage particles. A recombination-proficient host strain carrying IL2 cDNA sequences in a non-homologous plasmid vector was infected by the packaged cosmid library. After in vivo packaging and reinfection, recombinants carrying the antibiotic resistance genes of both vectors were selected. From a recombinant cosmid clone the chromosomal IL2 gene was restored. After DNA mediated gene transfer into mouse Ltk- cells human IL2 was expressed constitutively.

摘要

已开发出一种方法,可通过体内同源重组从黏粒文库中分离基因组克隆。该方法用于分离人基因组白细胞介素2(IL2)基因。基因组黏粒文库在体内包装成λ噬菌体颗粒。携带非同源质粒载体中IL2 cDNA序列的重组缺陷宿主菌株被包装好的黏粒文库感染。经过体内包装和再次感染后,选择携带两种载体抗生素抗性基因的重组体。从一个重组黏粒克隆中恢复了染色体IL2基因。经DNA介导的基因转移到小鼠Ltk-细胞后,人IL2得以持续表达。

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