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通过在大肠杆菌中进行功能选择从哺乳动物细胞中拯救转染基因。

Rescue of transfected genes from mammalian cells by functional selection in Escherichia coli.

作者信息

Strauss M, Kiessling U, Kaehler R

出版信息

Mol Gen Genet. 1985;201(2):277-81. doi: 10.1007/BF00425671.

Abstract

We have established procedures for reisolating a transfected gene from mammalian cells by selection in Escherichia coli for the function of the gene product using the Herpes simplex virus thymidine kinase gene as a model. Rescue of the gene is accomplished by three different methods. The tk gene is recloned into a plasmid in which it is hooked up by either the lac promoter or a lac/tk hybrid promoter, or the original plasmid is cut out of the host cell DNA. As the lac/tk hybrid gene can be expressed and selected both in the mammalian and E. coli cells, this type of gene rescue allows investigations on mutagenesis and methylation processes. Additionally, it offers a simple way of studying the integration of the transfected gene into the mammalian genome.

摘要

我们已经建立了从哺乳动物细胞中重新分离转染基因的程序,以单纯疱疹病毒胸苷激酶基因作为模型,通过在大肠杆菌中筛选基因产物的功能来实现。基因的拯救通过三种不同的方法完成。tk基因被重新克隆到一个质粒中,在该质粒中它通过lac启动子或lac/tk杂交启动子连接,或者原始质粒从宿主细胞DNA中切出。由于lac/tk杂交基因可以在哺乳动物细胞和大肠杆菌细胞中表达和筛选,这种类型的基因拯救允许对诱变和甲基化过程进行研究。此外,它提供了一种研究转染基因整合到哺乳动物基因组中的简单方法。

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