Keravala Annahita, Calos Michele P
Department of Genetics, Stanford University School of Medicine, Stanford, CA.
Methods Mol Biol. 2008;435:165-73. doi: 10.1007/978-1-59745-232-8_12.
phiC31 integrase is a site-specific recombinase from a bacteriophage that has become a useful tool in mammalian cells. The enzyme normally performs precise, unidirectional recombination between two attachment or att sites called attB and attP. We have shown that an attP site preintegrated into a mammalian chromosome can serve as a target for integration of an introduced plasmid carrying an attB site. Recombination leads to precise integration of the plasmid into the chromosome at the attP site. This reaction is useful for placing introduced genes into the same chromosomal environment, in order to minimize position effects associated with random integration. Because phiC31 integrase can also mediate integration at endogenous sequences that resemble attP, called pseudo attP sites, a selection system is used that yields integration only at the desired preintegrated attP site. This chapter provides a protocol that features a simple antibiotic selection to isolate cell lines in which the introduced plasmid has integrated at the desired attP site. A polymerase chain reaction assay is also presented to verify correct chromosomal placement of the introduced plasmid. This integration system based on phiC31 integrase supplies a simple method to obtain repeated integration at the same chromosomal site in mammalian cells.
phiC31整合酶是一种来自噬菌体的位点特异性重组酶,已成为哺乳动物细胞中一种有用的工具。该酶通常在两个称为attB和attP的附着或att位点之间进行精确的单向重组。我们已经表明,预先整合到哺乳动物染色体中的attP位点可以作为携带attB位点的导入质粒整合的靶标。重组导致质粒在attP位点精确整合到染色体中。该反应对于将导入的基因置于相同的染色体环境中很有用,以便最小化与随机整合相关的位置效应。由于phiC31整合酶也可以介导在类似于attP的内源性序列(称为假attP位点)处的整合,因此使用一种选择系统,该系统仅在所需的预先整合的attP位点产生整合。本章提供了一种方案,其特点是通过简单的抗生素选择来分离导入质粒已在所需的attP位点整合的细胞系。还介绍了一种聚合酶链反应测定法,以验证导入质粒在染色体上的正确位置。这种基于phiC31整合酶的整合系统提供了一种简单的方法,可在哺乳动物细胞的同一染色体位点获得重复整合。