Chemistry: molecular biology and microbiology – Process of mutation – cell fusion – or genetic modification – Introduction of a polynucleotide molecule into or...
Reexamination Certificate
2006-06-13
2006-06-13
Sullivan, Daniel M. (Department: 1636)
Chemistry: molecular biology and microbiology
Process of mutation, cell fusion, or genetic modification
Introduction of a polynucleotide molecule into or...
C435S468000, C435S471000, C435S325000, C536S024200, C514S04400A
Reexamination Certificate
active
07060499
ABSTRACT:
To provide DNA comprising mutant FRT sequence which causes recombination reaction between two mutant FRT sequences having an identical sequence to each other but does not cause recombination reaction with a wild-type FRT sequence, in the presence of FLP recombinase; and a method for performing high-efficiency, gene insertion or gene replacement. A DNA comprising a mutant FRT sequence. A DNA comprising a mutant FRT sequence possessing (A) causing no specific DNA recombination reaction with wild type FRT, even if FLP recombinase is present, and (B) causing specific DNA recombination reaction with another mutant FRT sequence having an identical sequence thereto in the presence of recombinase FLP; gene replacement method using the DNA in the presence of recombinase FLP; and a specific DNA recombination method, characterized in that a specific DNA recombination reaction is carried out by using two mutant FRT sequences in the presence of recombinase FLP.
REFERENCES:
Dymecki SM. Flp recombinase promotes site-specific DNA recombination in embryonic stem cells and transgenic mice. Proc Natl Acad Sci U S A. Jun. 11, 1996;93(12):6191-6.
Emanueli et al. Angiogenesis gene therapy to rescue ischaemic tissues: achievements and future directions.Br J Pharmacol. Aug. 2001;133(7):951-8.
Marshall E. Gene therapy's growing pains. Science. Aug. 25, 1995;269(5227):1050, 1052-5.
Rissanen et al. Gene therapy for therapeutic angiogenesis in critically ischaemic lower limb—on the way to the clinic. Eur J Clin Invest. Aug. 2001;31(8):651-66.
Ross et al. Gene therapy in the United States: a five-year status report. Hum Gene Ther. Sep. 10, 1996;7(14):1781-90.
Rubanyi GM. The future of human gene therapy. Mol Aspects Med. Jun. 2001;22(3):113-42.
Schwaab et al. Gene therapy of hemophilia. Semin Thromb Hemost. Aug. 2001;27(4):417-24.
Sigmund CD. Viewpoint: are studies in genetically altered mice out of control? Arterioscler Thromb Vasc Biol. Jun. 2000;20(6):1425-9.
Verma et al. Gene therapy—promises, problems and prospects. Nature. Sep. 18, 1997;389(6648):239-42.
Vooijs et al. Flp-mediated tissue-specific inactivation of the retinoblastoma tumor suppressor gene in the mouse. Oncogene. Jul. 9, 1998;17(1):1-12.
Eck et al. (1996) Goodman & Gilman's The Pharmacological Basis of Therapeutics, 9th Edition, Chapter 5, McGraw-Hill, NY.
Orkin et al. (1995) Report and recommendations of the panel to assess the NIH investment in research on gene therapy, available through the National Institutes of Health and at http://www.nih.gov
ews/panelrep.html.
Seibler et al., Biochemistry, vol. 36, No. 7, pp. 1740-1747 (1997).
Schlake et al., Biochemistry, vol. 33, pp. 12746-12751 (1994).
Seibler et al., Biochemistry, vol. 37, pp. 6229-6234 (1998).
Umlauf et al., The EMBO Journal, vol. 7, No. 6, pp. 1845-1852 (1988).
Saito Izumu
Saito Yumi
Birch & Stewart Kolasch & Birch, LLP
Dainippon Sumitomo Pharma Co. ,Ltd.
Saito Izumu
Sullivan Daniel M.
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