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A phage integrase directs efficient site-specific integration in human cells.

The integrase from the Streptomyces phage phiC31 carries out efficient recombination between the attP site in the phage genome and the attB site in the host bacterial chromosome. In this paper, we show that the enzyme also functions in human cells. A plasmid assay system was constructed that measured intramolecular integration of attP into attB. This assay was used to demonstrate that in the presence of the phiC31 integrase, precise unidirectional integration occurs with an efficiency of 100% in Escherichia coli and >50% in human cells. This assay system was also used to define the minimal sizes of attB and attP at 34 bp and 39 bp, respectively. Furthermore, precise and efficient intermolecular integration of an incoming plasmid bearing attP into an established Epstein-Barr virus plasmid bearing attB was documented in human cells. This work is a demonstration of efficient, site-specific, unidirectional integration in mammalian cells. These observations form the basis for site-specific integration strategies potentially useful in a broad range of genetic engineering applications.

Pubmed ID: 10801973 RIS Download

Mesh terms: Bacteriophages | Base Sequence | Cells, Cultured | Chromosomes, Human | Escherichia coli | Genetic Engineering | Genetic Vectors | Herpesvirus 4, Human | Humans | Integrases | Molecular Sequence Data | Species Specificity | Streptomyces | Substrate Specificity | Viral Proteins | Virus Integration

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Associated grants

  • Agency: NCI NIH HHS, Id: T32 CA009302
  • Agency: NCI NIH HHS, Id: 5 T32 CA09302
  • Agency: NIDDK NIH HHS, Id: DK51834

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