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通过Cre重组酶将外源DNA靶向插入真核基因组。

Targeted insertion of exogenous DNA into the eukaryotic genome by the Cre recombinase.

作者信息

Sauer B, Henderson N

机构信息

E.I. DuPont de Nemours & Co., Inc., Central Research and Development Department, Wilmington, DE 19880-0328.

出版信息

New Biol. 1990 May;2(5):441-9.

PMID:2288914
Abstract

Cre is a 38-kD protein from bacteriophage P1 that catalyzes site-specific recombination between 34-bp loxP sequences. Our previous work has shown that Cre can perform site-specific excisive recombination not only in prokaryotes, but also in eukaryotes such as yeast and cultured mammalian cells. In this work we show that intermolecular Cre-mediated recombination can specifically direct the integration of a loxP-containing circular DNA into a chromosomal loxP site, both in yeast and in mammalian cells. The resulting integrants are predominantly simple single-copy insertions. Cre-mediated recombination thus provides a simple way to direct single-copy site-specific integration of exogenous DNA into the eukaryotic genome.

摘要

Cre是一种来自噬菌体P1的38-kD蛋白质,它催化34-bp loxP序列之间的位点特异性重组。我们之前的工作表明,Cre不仅可以在原核生物中进行位点特异性切除重组,还可以在酵母和培养的哺乳动物细胞等真核生物中进行。在这项工作中,我们表明分子间Cre介导的重组可以在酵母和哺乳动物细胞中特异性地指导含loxP的环状DNA整合到染色体loxP位点。产生的整合体主要是简单的单拷贝插入。因此,Cre介导的重组提供了一种将外源DNA单拷贝位点特异性整合到真核基因组中的简单方法。

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