Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Recombinant dna technique included in method of making a...
Patent
1995-09-27
1998-03-03
Carlson, Karen C.
Chemistry: molecular biology and microbiology
Micro-organism, tissue cell culture or enzyme using process...
Recombinant dna technique included in method of making a...
530350, C12P 2106, C07K 14435
Patent
active
057233136
ABSTRACT:
The INK4A (MTS1, CDKN2) gene encodes a specific inhibitor (InK4a-p16) of the cyclin D-dependent kinases CDK4 and CDK6. InK4a-p16 can block these kinase from phosphorylating the retinoblastoma protein (pRb), preventing exit from the G1 phase of the cell cycle. Deletions and mutations involving the gene encoding InK4a-p16, INK4A, occur frequently in cancer cells, implying that INK4a-p16, like pRb, suppresses tumor formulation. However, a completely unrelated protein (ARF-p19) arises in major part from an alternative reading frame of the mouse INK4A gene. Expression of an ARF-p19 cDNA (SEQ ID NO:1) in rodent fibroblasts induces both G1 and G2 phase arrest.
REFERENCES:
patent: 4965188 (1990-10-01), Mullis et al.
patent: 5174986 (1992-12-01), Berns
patent: 5185260 (1993-02-01), Crissman et al.
Duro, D. et al., "A new type of p16.sup.INK4 /MTS1 gene transcript expressed in B-cell malignancies," Oncogene 11:21-29 (Jul. 1995).
Kamb, A. et al., "A Cell Cycle Regulator Potentially Involved in Genesis of Many Tumor Types," Science 264:436-440 (Apr. 1994).
Nobori, T. et al., "Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers," Nature 368:753-756 (Apr. 1994).
Okamoto, A. et al., "Mutations and altered expression of p16.sup.INK4 in human cancer," Proc. Natl. Acad. Sci. USA 91:11045-11049 (Nov. 1994).
Quelle, D. E. et al., "Alternative Reading Frames of the INK4a Tumor Suppressor Gene Encode Two Unrelated Proteins Capable of Inducing Cell Cycle Arrest," Cell 83:993-1000 (Dec. 1995).
Quelle, D. E. et al., "Cloning and characterization of murine p16.sup.INK4a and p15.sup.INK4b genes," Oncogene 11:635-645 (Aug. 1995).
Baldin, V., et al., "Cyclin D1 is a Nuclear Protein Required for Cell Cycle Progression in G.sub.1," Genes & Devel. 7:812-821 (May 1993).
Bates, S., et al., "Absence of Cyclin D/cdk Complexes in Cells Lacking Functional Retinoblastoma Protein," Oncogene 9(6):1633-1640 (Jun. 1994).
Dowdy, S. F., et al., "Physical Interaction of the Retinoblastoma Protein with Human D Cyclins," Cell 73(3):499-511 (May 7, 1993).
El-Deiry, W.S., et al., "WAF1, a Potential Mediator of p.53 Tumor Suppression," Cell 75 (4):817-825 (Nov. 19, 1993).
Ewen, M.E., et al., "Functional Interactions of the Retinoblastoma Protein with Mammalian D-Type Cycline," Cell 73(3):487-497 (May 7, 1993).
Gu, Y., et al., "Inhbition of CDK2 Activity in vivo by an Associated 20K Regulatory Subunit," Nature 366:707-710 (Dec. 16, 1993).
Guan, K.-L., et al., "Growth Suppression by p18, a p.16.sup.INK4/MTS1 -and p14.sup.INK4B/MTS2 -Related CDK6 Inhibitor, Correlates with Wild-type pRb Function," Genes & Devel. 8(24):2939-2952 (Dec. 15, 1994).
Hannon, G.J., and Beach, D., "p15.sup.INK4B is a Potential of TGF-.beta.-induced Cell Cycle Arrest," Nature 37:257-261 (Sep. 15, 1994).
Harper, J.W., et al., "The p21 Cdk-Interacting Protein Cip1 Is a Potent Inhibitor of G1 Cyclin-Dependent Kinases," Cell 75(4):805-816 (Nov. 19, 1993).
Hirai, H., et al., "Novel INK4 Proteins, p19 and p18, Are Specific Inhibitors of the Cyclin D-Dependent Kinases CDK4 and CDK6," Mol. Cell. Biol. 15(5):2672-2681 (May 1995).
Kato, J.-Y., et al., "Direct Binding of Cyclin D to the Retinoblastoma Gene Product (pRb) and pRb Phosphorylation by the Cyclin D-Dependent Kinase CDK4,"Genes & Devel. 7(3):331-342 Mar.1993.
Lukas, J., et al., "DNA Tumor Virus Oncorproteins and Retinoblastoma Gene Mutations Share The Ability to Relieve the Cell's Requirement for Cyclic D1 Funtion in G1," J. Cell Biol.125(3):625-638 (May 1994).
Mao, L., et al., "A Novel p16.sup.INK4A Transcript," Cancer Res. 55:2995-2997 Jul. 15, 1995).
Matsushime, H., et al., "Colony-Stimulating Factor 1 Regulates Novel Cyclins During the G1 Phase of the Cell Cycle," Cell 65(4):701-713 (May 17, 1991).
Matsushime, H., et al., "Identification and Properties of an Atypical Catalytic Subunit (p34.sup.PSK-J3 /cdk4) for Mammalian D Type G1 Cyclins," Cell 71(2):323-334 (Oct. 16, 1992).
Matsushime, H., et al., "D-Type Cyclin-Dependent Kinase Activity in Mammalian Cells," Mol. Cell. Biol. 14(3):2066-2076 (Mar. 1994).
Meyerson, M., and Harlow, E., "Identification of G.sub.1 Kinase Activity for cdk6, a Novel Cyclin D Partner," Mol. Cell. Biol. 14(3):2077-2086 (Mar. 1994).
Nasmyth, K., and Hunt, T., "Dams and Sluices,"Nature 366: 634-635 (Dec. 16, 1993).
Peters, G., "Stifled by Inhibitions," Nature 371:204-205 (Sep. 15, 1994).
Polyak, K., et al., "p27.sup.Kipl, a Cyclin-Cdk Inhibitor, Links Transforming Growth Factor-.beta. and Contact Inhibition to Cell Cycle Arrest," Genes & Devel. 8(11):9-22 (Jan. 1994).
Polyak, K., et al., "Cloning of p27.sup.Kipl, a Cyclin-Dependent Kinase Inhibitor and a Potential Mediator of Extracellular Antimitogenic Signal," Cell 78(1):59-66 (Jul. 15, 1994).
Quelle, D.E., et al., "Overexpression of Mouse D-type Cyclins Accelerates G.sub.1 Phase in Rodent Fibroblasts," Genes & Devel. 7(8):1559-1571 (Aug. 1993).
Serrano, M., et al., "A New Regulatory Motif in Cell-Cycle Control Causing Specific Inhibition of Cyclin D/CDK4," Nature 366:704-707 (Dec. 16, 1993).
Sherr, C.J., "Mammalian G.sub.1 Cyclins," Cell 73:1059-1065 (Jun. 18, 1993).
Stone, S., et al., "Complex Structure and Regulation of the P16 (MTS1) Locus," Cancer Res. 55:2988-2994 (Jul. 15, 1995).
Tam, S.W., et al., "Differential Expression and Regulation of Cyclic D1 Protein in Normal and Tumor Human Cells: Association with Cdk4 is Required for Cyclin D1 Function in G1 Progression," Oncogene 9(9):2663-2674 (Sep. 1994).
Toyoshima, H., and Hunter, T., "p27, a Novel Inhibitor of G1 Cyclin-Cdk Protein Kinase Activity, Is Related to p21," Cell 78(1):67-74 (Jul. 15, 1994).
Xiong, Y. et al., "Subunit Rearrangement of the Cyclin-Dependent Kinase is Associated with Cellular Transformation," Genes & Devel. 7(8):1572-1583 (Aug. 1993).
Xiong, Y., et al., "p21 Is a Universal Inhibitor of Cyclin Kinases," Nature 366:701-704 (Dec. 16, 1993).
Quelle Dawn E.
Sherr Charles J.
Carlson Karen C.
St. Jude Children's Research Hospital
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