Tumor suppressor gene merlin

Chemistry: molecular biology and microbiology – Vector – per se

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435 691, 536 235, 536 241, C12N 1512, C12N 1500, C12N 1509

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057078637

ABSTRACT:
A novel tumor suppressor protein, merlin, is described, including DNA sequences encoding merlin, and recombinant vectors and hosts capable of expressing merlin. Method for the diagnosis and treatment of merlin-associated tumors, and for the diagnosis and treatment of the disease neurofibromatosis 2 (NF2) are also provided.

REFERENCES:
Seizinger, B.R., et al., "Tumor Suppressor Genes and Neural Crest-Derived Neoplasms: Toward the Isolation of the Gene Causing Neurofibromatosis Type 2 (NF2)," Keytstone Symposium on Melanoma and Biology of the Neural Crest, Taos, NM, Feb. 1-8, 1992, J. Cell. Biochem. Suppl. 0 (16 Part B):306, Abstract No. K 026 (Feb. 1992).
A copy of the Partial European Search Report for the corresponding European Patent Application, EPO Application No. EP 94 30 1367.
Lankes et al. 1991. PNAS USA 86: 8297-8301.
Sambrook et al. 1989. Molecular Cloning, 2nd ed., Cold Spring Harbor Press, NY, pp. 11.7-11.8.
Trofatter, J. et al., GenBank Entry of Human Merlin (Hummerlin) locus. Accession No. L11353 (May 8, 1993).
Basu, T. et al., Aberrant Regulation of ras Proteins in malignant Tumour Cells from Type 1 Neurofibromatosis Patients, Nature 356:713-715 (1992).
Bernal, S. et al., Cytoskeleton-Associated Proteins: Their Role as Cellular Integrators in the Neoplastic Process, Crit. Rev. Oncol. Hematol. 3(3):191-204 (1985).
Bijlsma, E. et al. Molecular Characterization of Chromosome 22 Deletions in Schwannomas, Genes, Chromosomes & Cancer 5:201-205 (1992).
Birgbauer, E. et al., Association of Ezrin Isoforms with the Nueronal Cytoskeleton, J. Neuroscience Research 30:232-241 (1991).
Breakefield, X. et al., Herpes Simplex Virus for Gene Delivery to Neurons, The New Biologist 3(3):203-218 (1991).
Buckler, A. J. et al., Exon amplification: A strategy to isolate mammalian genes based on RNA splicing, Proc. Natl. Acad. Sci. USA 88:4005-4009 (1991).
Correas, I. et al., Identification of the Functional Site of Eryhtrocyte Protein 4.1 Involved in Spectrin-Actin Associations, J. Biol. Chem. 261(7):3310-3315 (1986).
Couturier, J. et al., Assessment of Chromosome 22 Anomalies in Neurinomas by Combined Karyotype and RFLP Analyses, Cancer Genet. Cytogenet. 45:55-62 (1990).
DeClue, J. et al., Abnormal Regulation of Mammalian p21.sup.ras Contributes to Malignant Tumor Growth in von Recklinghausen (Type 1) Neurofibromatosis, Cell 69:265-273 (1992).
Dryja, T. et al., Molecular Detection of Deletions Involving Band q14 of Chromosome 13 in Retinoblastomas, Proc. Natl. Acad. Sci. USA 83:7391-7394 (1986).
Fiedler, W. et al., New Markers for the Neurofibromatosis-2 Region Generated by Microdissection of Chromosome 22, Genomics 10:786-791 (1991).
Fontaine, B. et al., Loss of Chromosome 22 Alleles in Human Sporadic Spinal Schwannomas, Ann. Neurol. 29 (2):183-186 (1991).
Fontaine, B. et al., Parental Origin of Chromosome 22 Loss in Sporadic and NF2 Neuromas, Genomics 10:280-283 (1991).
Francke, U. et al., Aniridia-Wilms3 Tumor Association: Evidence for Specific Deletion of 11p13, Cytogenet. Cell Genet. 24:185-192 (1979).
Frazer, K. et al., A Radiation Hybrid Map of the Region on Human Chromosome 22 Containing the Neurofibromatosis Type 2 Locus, Genomics 14:574-584 (1992).
Furthmayr, H. et al., Moesin, a New Cytoskeletal Protein and Constituent of Filopodia: Its Role in Cellular Functions, Kidney International 41:665-670 (1992).
Gu, M. et al., Identification, Cloning, and Expression of a Cytosolic Megakaryocyte Protein-Tyrosine-Phosphatase with Sequence Homology to Cytoskeletal Protein 4.1, Proc. Natl. Acad. Sci. USA 88:5867-5871 (1991).
Hanzel, D. et al., The Secretion-Stimulated 80K Phosphoprotein of Parietal Cells is Ezrin, and has Properties of a Membrane Cytoskeletal Linker in the Induced Apical Microvilli, EMBO J. 10(9):2363-2373 (1991).
Huang, Q. et al., Introduction of a Foreign Gene (Escherichia coli lacZ) into Rat Neostriatal Neurons Using Herpes Simplex Virus Mutants: A Light and Electron Microscopic Study, Experimental Neurology 115:303-316 (1992).
Knudson, A.B., Mutation and Cancer: Statistical Study of Retinoblastoma, Proc. Natl. Acad. Sci. USA 68(4):820-823 (1971).
Krieg, J. et al., Identification of the Two Major Epidermal Growth Factor-Induced Tyrosine Phosphorylation Sites in the Microvillar Core Protein Ezrin, J. Biol. Chem. 267(27):19258-19265 (1992).
Lees, J. et al., The Structure and Organization of the Human Heavy Neurofilament Subunit (NF-H) and the Gene Encoding It, EMBO J. 7(7):1947-1955 (1988).
Leto, T. et al., Structure and Function of Human Erythrocyte Cytoskeletal Protein 4.1, in Membrane Skeletons and Cytoskeletal-Membrane Associations, Alan R. Liss, Inc., pp. 201-209 (1986).
Luna, E. et al., Cytoskeleton-Plasma Membrane Interactions, Science 258:955-964 (1992).
MacCollin, M. et al., DNA Diagnosis of Neurofibromatosis 2: Altered Coding Sequence of the merlin Tumor Suppressor in an Extended Pedigree, J. Am. Med. Assoc. 270(19):2316-2320 (1993).
Martuza, R. et al., Neurofibromatosis 2, N. Engl. J. Med. 318(11):684-688 (1988).
Mulvihill, J. et al. Neurofibromatosis 1 (Recklinghausen Disease) and Neurofibromatosis 2 (Bilateral Acoustic Neurofiibromatosis), Ann. Internal Med. 113(1):39-52 (1990).
Narod, S. et al., Neurofibromatosis Type 2 Appears to be a Genetically Homogeneous Disease, Am. J. Hum. Genet. 51:486-496 (1992).
Orita, M. et al., Rapid and Sensitive Detection of Point Mutations and DNA Polymorphisms Using the Polymerase Chain Reaction, Genomics 5:874-879 (1989).
Pakkanen, R., Immunofluorescent and Immunochemical Evidence for the Expression of Cytovillin in the Microvilli of a Wide Range of Cultured Human Cells, J. Cell. Biochem. 38:65-75 (1988).
Rees, D. et al., Sequence and Domain Structure of Talin, Nature 347:685-689 (1990).
Riccardi, V. et al., Chromosomal Imbalance in the Aniridia-Wilms' Tumor Association: 11p Interstitial Deletion, Pediatrics 61(4):604-610 (1978).
Riccardi, V.M. et al., von Recklinghausen Neurofibromatosis, N. Engl. J. Med. 305(27):1617-1627 (1981).
Rouleau, G. et al., A Genetic Linkage Map of the Long Arm of Human Chromosome 22, Genomics 4:1-6 (1989).
Rouleau, G. et al., Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2, Nature 363:515-521 (1993).
Rouleau, G. et al., Flanking Markers Bracket the Neurofibromatosis Type 2 (NF2) Gene on Chromosome 22, Am. J. Hum. Genet. 46:323-328 (1990).
Rouleau, G. et al., Genetic Linkage of Bilateral Acoustic Neurofibromatosis to a DNA Marker on Chromosome 22, Nature 329:246-248 (1987).
Sato, N. et al., A Gene Family Consisting of Ezrin, Radixin and Moesin, J. Cell Sci. 103:131-143 (1992).
Sato, N. et al., Radixin, a Barbed End-Capping Actin-Modulating Protein, is Concentrated at the Cleavage Furrow During Cytokineses, J. Cell Biol. 113(2):321-330 (1991).
Seizinger, B. et al., Common Pathogenetic Mechanism for Three Tumor Types in Bilateral Acoustic Neurofibromatosis, Science 236:317-319 (1987).
Seizinger, B. et al., Loss of Genes on Chromosome 22 in Tumorigenesis of Human Acoustic Neuroma, Nature 322:644-647 (1986).
Seizinger, B. et al., Molecular Genetic Approach to Human Meningioma: Loss of Genes on Chromosome 22, Proc. Natl. Acad. Sci. USA 84:5419-5423 (1987).
Tchernia, G. et al., Deficiency of Skeletal Membrane Protein Band 4.1 in Homozygous Hereditary Elliptocytosis, J. Clin. Invest. 68:454-460 (1981).
Trofatter, J.A. et al., A Novel Moesin-, Ezrin-, Radixin-like Gene Is a Candidate for the Neurofibromatosis 2 Tumor Suppressor, Cell 72:791-800 (1993).
Viskochil, D. et al., Deletions and a Translocation Interrupt a Cloned Gene at the Neurofibromatosis Type 1 Locus, Cell 62:187-192 (1990).
Werteleki, W. et al., Neurofibromatosis 2: Clinical and DNA Linkage Studies of a Large Kindred, N. Engl. J. Med. 319(5):278-283 (1988).
Wolff, R. et al., Analysis of Chromosome 22 Deletions in Neurofibromatosis Type 2-Related Tumors, Am. J. Hum. Genet. 51:478-485 (1992).
Yang, Q. et al., Isolation of a cDNA Clone Encoding a Human Protein-Tyrosine Phosphatase with Homology to the Cytoskeletal-Associated Proteins Band 4.1, Ezrin, and Talin, Proc. Natl. Acad. Sci

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