Chemistry: molecular biology and microbiology – Process of mutation – cell fusion – or genetic modification
Reexamination Certificate
2007-09-18
2007-09-18
Kaushal, Sumesh (Department: 1633)
Chemistry: molecular biology and microbiology
Process of mutation, cell fusion, or genetic modification
C435S455000, C435S462000, C435S463000, C435S468000, C435S477000, C435S478000
Reexamination Certificate
active
10152994
ABSTRACT:
An isolated DNA encoding the enzyme I-SceI is provided. The DNA sequence can be incorporated in cloning and expression vectors, transformed cell lines and transgenic animals. The vectors are useful in gene mapping and site-directed insertion of genes.
REFERENCES:
patent: 5162215 (1992-11-01), Bosselman et al.
patent: 5474896 (1995-12-01), Dujon et al.
patent: 5545808 (1996-08-01), Hew et al.
patent: 5792632 (1998-08-01), Dujon et al.
patent: 5866361 (1999-02-01), Dujon et al.
patent: 5948678 (1999-09-01), Dujon et al.
patent: 5962327 (1999-10-01), Dujon et al.
patent: 6238924 (2001-05-01), Dujon et al.
patent: 6395959 (2002-05-01), Dujon et al.
patent: 6610545 (2003-08-01), Dujon et al.
patent: WO96 04397 (1996-02-01), None
Juengst BMJ, 326:1410-11, 2003.
Check Nature 422:7, 2003.
Rosenberg et al, Science 287:1751, 2000.
Friedmann, Science 287(5461):2163-5, 2000.
Anderson, WF, Nature 392:25-30, 1998.
Verma et al Nature 389: 239-242, 1997.
Touchette, Nat. Med. 2(1) 7-8, 1996.
Jasin et al., “Targeted Transgenesis,” Proc. Natl. Acad. Sci., USA, 93:17, pp. 8804-8804, (Aug. 20, 1996).
Rouet, et al., “Introduction of Double-Strand Breaks into the Genome of Mouse Cells by Expression of a Rare-Cutting Endonuclease,” Molecular and Cellular Biology, pp. 8096-8106 (Dec. 1994).
Rouet et al., “Expression of a Site-Specific Endonuclease Stimulates Homologous Recombination in Mammalian Cells,” Proc. Natl. Acad. Sci., USA, 99:6064-6068 (Jun. 1994).
Lukasovich, et al., “Repair of a Specific Double-Strand Break Generated within a Mammalian Chromosome by Yeast Endonuclease 1-Sce1,” Nucleic Acids Research, 22:25, pp. 5649-5657 (1994).
Smith et al., “Double-Strand Breaks at the Target Locus Stimulate Gene Targeting in Embryonic Stem Cells,” Nucleic Acids Research, 23(24): 5012-5019 (1995).
Moynahan, et al., “A Model for Testing Recombinogenic Sequences in the Mouse Germline,” Human Molecular Genetics, 5(7):875-886 (1996).
Jasin, “Genetic Manipulation of Genomes with Rare-Cutting Endonucleases,” Trends in Genetics, 12(6):224-228 (Jun. 1996).
Colleaux et al., “Universal Code Equivalent of a Yeast Mitochrondril Intron Reading Frame is Expressed intoE. Colias a Specific Double Strand Endonuclease,” Cell, 44:521-533 (1986).
Colleaux et al., “Recognition and Cleavage Site of the Intron-Encoded Omega Transposase,” Proc. Natl. Acad. Sci., USA, 85:6022-6026 (1988).
Colleaux et al., “The Apocytochrome b Gene ofChlamydomonas smithiiContains a Mobile Intron Related to Both Saccharomyces and Neurospora Introns,” Mol. Gen. Genet., 223:288-296 (1990).
Colleaux et al., “Rapid Mapping of YAC Inserts . . . I,” Human Mol. Genet., 2(3):265-271 (1993).
Dujon et al., “Sequence of the Intron and Flanking Exons of the Mitochrondrial 21s rRNA Gene of Yeast Strains Having Different Alleles at the ω and rib-1 Loci,” Cell, 20:185-187 (1980).
Dujon et al., Mitochrondria, Walter de Gruyer & Co., pp. 389-403 (1983).
Dujon et al., “In Achievements and Perspectives of Mitochrondrial Research,” Biogenesis, Elsevier Science Publishers, 2:215-225 (1985).
Dujon et al., “In Extrachromosomal Elements in Lower Eukaryotes,” Plenum Publishing Corporation, pp. 5-27 (1986).
Dujon et al., “Group I Introns as Mobile Genetic Elements: Facts and Mechanistic Speculations—A Review,” Gene, 82:91-114 (1989).
Dujon et al., “Mobile Introns: Definition of Terms and Recommended Nomenclature,” Gene, 82:115-118 (1989).
Dujon et al., “Mobile Itrons,” Abstract presented at EMBO Workshop, Roscoff, France, Jun. 24-28, 1990.
Jacquier et al., “The Intron of the Mitochrondrial 21s rRNA Gene: Distribution in Different Yeast Species and Sequence Comparison BetweenKluyveromyces thermotleransandSaccharamyces cerevisiae,” Mol. Gen. Genet., 192:487-499 (1983).
Jacquier et al., “An Intron-Encoded Protein is Active in a Gene Conversion Process that Spreads an Intron into a Mitochrondrial Gene,” Cell, 41:383-394 (1985).
Michel et al., “Comparison of Fungal Mitochrondrial Introns Reveals Extensive Homologies in RNA Secondary Structure,” Biochemie, 64:867-881 (1982).
Michel et al., “Conservation of RNA Secondary Structure in Two Intron Families Including Mitochrondrial-, Chloroplast- and Nuclear-Encoded Members,” EMBO Journal, 2(1):33-38 (1983).
Michel et al., “Genetic Exchanges Between Bacteriophase T4 and Filamentous Fungi?,” Cell, 46:323 (1986).
Monteihet et al., “Purification and Characterization of the in vitro Activity of I-Scel, a Novel and Highly Specific Endonuclease Encoded by a Group 1 Intron,” Nucleic Acids Research, 18(6):1407-1413 (1990).
Muscarella et al., “A Mobile Group I Intron in the Nuclear rDNA of Physarum Polycephalum,” Cell, 56:433-454.
Plessis et al., “Site-Specific Recombination Determined by I-Sce I: A Mitochrondrial Group I Intron-Encoded Endonuclease Expressed in the Yeast Nucleus,” Genetics, 130(3):451-460 (1992).
Rudin et al., “Efficient Repart of HO-Induced Chromosomal Breaks inSaccharomyces cervisiaeby Recombination Between Flanking Homologous Sequence,” Mol, Cell Biol., 8:3918-3928.
Tartot et al., “Gene: New Cloning Vectors and Techniques . . . ,” Gene, 67:169-182 (1988).
Thierry et al., “Cleavage of Yeast and Bacteriophage T7 Genomes at a Single Site Using the Rare Cutter Endonuclease I-Sce I,” Nucleic Acid Research, 19(1):189-190 (1991).
Krimpenfort et al., “Generation of Transgenic Dairy Cattle Using ‘In Vitro’ Embryo Production,” Bio/Technology, 9:844-847 (Sep. 1991).
Orkin et al., “Report and Recommendations of the Panel to Assess the NIH Investment in Research on Gene Therapy,” Distributed by the national Institutes of Health, Bethesda, MD (Dec. 7, 1995).
Pursel et al., “Genetic Engineering of Livestock,” Science, 244:1281-1288 (Jun. 16, 1989).
Houdebine, “Production of Pharmaceutical Proteins from Transgenic Animals,” J. of Biotech., 34:269-287 (1994).
Michel et al., “Genetic Exchanges Between Bacteriophase T4 and Filamentous Fungi?,” Cell, 46:323 (1986).
Monteihet et al., “Purification and Characterization of the in vitro Activity of I-Scel, a Novel and Highly Specific Endonuclease Encoded by a Group 1 Intron,” Nucleic Acids Research, 18(6):1407-1413 (1990).
Muscarella et al., “A Mobile Group I Intron in the Nuclear rDNA of Physarum Polycephalum,” Cell, 56:433-454, 1989.
Plessis et al., “Site-Specific Recombination Determined by I-Sce I: A Mitochrondrial Group I Intron-Encoded Endonuclease Expressed in the Yeast Nucleus,” Genetics, 130(3):451-460 (1992).
Rudin et al., “Efficient Repart of HO-Induced Chromosomal Breaks inSaccharomyces cervisiaeby Recombination Between Flanking Homologous Sequence,” Mol, Cell Biol., 8:3918-3928, 1988.
Tartot et al., “Gene: New Cloning Vectors and Techniques . . . ,” Gene, 67:169-182 (1988).
Thierry et al., “Cleavage of Yeast and Bacteriophage T7 Genomes at a Single Site Using the Rare Cutter Endonuclease I-Sce I,” Nucleic Acid Research, 19(1):189-190 (1991).
Krimpenfort et al., “Generation of Transgenic Dairy Cattle Using ‘In Vitro’ Embryo Production,” Bio/Technology, 9:844-847 (Sep. 1991).
Orkin et al., “Report and Recommendations of the Panel to Assess the NIH Investment in Research on Gene Therapy,” Distributed by the national Institutes of Health, Bethesda, MD (Dec. 7, 1995).
Pursel et al., “Genetic Engineering of Livestock,” Science, 244:1281-1288 (Jun. 16, 1989).
Houdebine, “Production of Pharmaceutical Proteins from Transgenic Animals,” J. of Biotech., 34:269-287 (1994).
Choulika Andre
Dujon Bernard
Nicolas Jean-Francois
Perrin Arnaud
Finnegan Henderson Farabow Garrett & Dunner LLP
Institut Pasteur
Universite Pierre et Marie Curie
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