Identification of a Specific Pseudo attP Site for Phage phiC3 Integrase in the Genome of Chinese Hamster in CHO-K1 Cell Line

Authors

  • Kamran Ghaedi Department of Molecular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, IR Iran and Biology Department, School of Sciences, University of Isfahan, Isfahan, IR Iran
  • Kianoush Dormiani Department of Molecular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, IR Iran
  • Mahboubeh Foruzanfar Department of Molecular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, IR Iran
  • Mohammad Hossein Nasr Esfahani Department of Molecular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, IR Iran
  • Mohammad Reza Nassiri Department of Animal Science, Ferdowsi University of Mashhad, Mashhad, IR Iran
  • Mojtaba Tahmoorespur Department of Animal Science, Ferdowsi University of Mashhad, Mashhad, IR Iran
  • Morteza Hosseini Department of Reproductive Biotechnology, Reproductive Biomedicine Center, Royan Institute for Biotechnology, Isfahan, IR Iran
  • Yahya Khazaie Department of Molecular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, IR Iran
Abstract:

Background: PhiC31 integrase is a DNA site-specific recombinase integrates DNA into the chromosomes between the two sites of attB and attP. Several pseudo attPs have been identified in mammalian genomes with critical features for long-term expression of transgene. In this manuscript, we report a novel intrinsic pseudo attP site named CHOL1 in the Chinese hamster genome implementing an inverse Polymerase Chain Reaction (IPCR). Objectives:Identification of pseudo attP site(s) of Tenecteplase cDNA integration in the genome of stable transformed CHO cell line. Materials and Methods: First, genome was extracted from a stable transformed CHO cell line expressing Tenecteplase. By creating of minicircle DNA in the last step, sequenc‌ing was performed. Results: We obtained one band. BLAST analysis of the respective sequence of inverse PCR band identified a pseudo attP site. Conclusions: Data demonstrated that the phiC31 integrase provides a suitable insertion site in the genome to express the gene of interest.

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Journal title

volume 11  issue 1

pages  54- 8

publication date 2013-01-01

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