DNA encoding the heme-regulated eukaryotic initiation factor 2.a

Drug – bio-affecting and body treating compositions – Enzyme or coenzyme containing – Transferases

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

A61K 3845

Patent

active

056909306

ABSTRACT:
The cDNA which encodes heme-regulated eIF-2.alpha. kinase (HRI) has been cloned from a lambda Zap II cDNA library of rabbit reticulocytes. The rabbit HRI cDNA is highly homologous to human HRI and hybridizes to the human HRI DNA under moderately stringent conditions. The rabbit HRI cDNA contains 2729 amino acids. In vitro translation of HRI mRNA transcribed from HRI cDNA yields a 90 kDa polypeptide with eIF-2.alpha. kinase activity. Since HRI is a potent inhibitor of protein synthesis, it is anti-proliferative in nature. In addition, the unusually high degree of homology of HRI to three protein kinases involved in the regulation of cell division suggests that HRI plays a direct role in the regulation of cell division. Since regulation of protein synthesis is vital for cell growth and differentiation, the cDNA can be inserted into cells to manipulate proliferation and differentiation, especially of cells that are proliferating in an uncontrolled manner or characterized by arrested differentiation, such as some of the types of cancers. Initiation of protein synthesis can also be regulated by another eIF-2.alpha. kinase which is activated by double-stranded RNA (dsI) which represents an interferon-mediated response to viral infection. Deletion mutants of HRI cDNA can be constructed that are insensitive to regulation by heme, which should be more effective than native HRI in its anti-viral and anti-proliferative action.

REFERENCES:
patent: 4594319 (1986-06-01), Sharma
patent: 4683195 (1987-07-01), Mullis et al.
patent: 5002874 (1991-03-01), Kaufman
Chen J.-J. et al., "Cloning of the cDNA of the heme-regulated eukaryotic initiation factor 2 alpha (eIF-2 alpha) kinase of rabbit reticulocytes: homology to yeast GCN2 protein kinase and human double-stranded-RNA-dependent eIF-2 alpha kinase" Proc. Natl. Acad. Sci. USA 88:7729-7733 (Sep. 1991).
Yang, J., et al., "Structure-function study of heme-regulated eukaryotic initiation factor 2 alpha kinase by site-directed mutagenesis" J. Cell Biol. 115:435A (Nov. 1991).
Chen, J.-J., et al., "Amino-acid microsequencing of internal tryptic peptides of heme-regulated eukaryotic initiation factor 2 alpha subunit kinase: homology to protein kinases" Proc. Natl. Acad. USA 88:315-319 (Jan. 1991).
Mendez, R., et al., "Regulation of heme-controlled eukaryotic polypeptide chain-initiation factor 2 alpha-subunit kinase of reticulocyte lysates" J. Biol. Chem. 267:11500-11507 (5 Jun. 1992).
Chen, J-J., et al., "Disulfide Bond Formation in the Regulation of eIF-2.alpha. Kinase by Heme"; J. Biol. Chem., 264:9559-9564 (1989).
Cigan, A.M., et al., "Yeast Translation Initiation Suppressor sui2 Encodes the .alpha.Subunit of Eukaryotic Initiation Factor 2 and Shares Sequence Identity with the Human .alpha. Subunit," Proc. Natl. Acad. Sci. USA, 86:2784-2788 (1989).
Dever, T.E., et al., "Phosphorylation of Initiation Factor 2.alpha. by Protein Kinase GCN2 Mediates Gene-Specific Translational Control of GCN4 in Yeast," Cell, 68, 585-596 (1992).
Ernst, H., et al., "Cloning and Sequencing of Complementary DNAs Encoding to .alpha.-Subunit of Translational Initiation Factor eIF-2," J. Biol. Chem., 262:1206-1212 (1987).
Fawcett, T.W., et al., "An Effective Method for Eliminating `Artifact Banding` When Sequencing Double-Stranded DNA Templates," BioTechniques, 9:46-48 (1990).
Felger, P.L., et al., "Lipofection: A Highly Efficient, Lipid-mediated DNA-Transfection Procedure", Proc. Natl. Acad. Sci., 84:7413-7417 (1987).
Frohman, M.A., et al., "Rapid Production of Full-length cDNAs from Rare Transcripts: Amplification Using a Single Gene-specific Oligonucleotide Primer," Proc. Natl. Acad. Sci. USA, 85, 8998-9002 (1988).
Gallie, D.R., et al., "A Comparison of Eukaryotic Viral 5'-Leader Sequences as Enhancers of mRNA Expression In Vivo," Nucl. Acids Res., 15, 8693-8711 (1987).
Gehrke, L., et al., "In: McCarthy, JEG Post-Transcriptional Regulation of Gene Expression, Series H: Cell Biology, ed. Tuite, M. (Springer Verlag Berlin)", 49:389-398 (1990).
Hanks, S.K., et al., "The Protein Kinase Family: Conserved Features and Deduced Phylogeny of the Catalytic Domains," Science, 241:42-52 (1988).
Maizel, J.V., Jr., et al., "Enhanced Graphic Matrix Analysis of Nucleic Acid and Protein Sequences," Proc. Natl. Acad. Sci., USA 78:7665-7669 (1981).
Maniatis, T., et al., Molecular Cloning, Cold Spring Harbor Laboratory Press (1989).
Meurs, E., et al., "Molecular Cloning and Characterization of the Human Double-Stranded RNA-Activated Protein Kinase Induced by Interferon," Cell, 62:379-390 (1990).
Miller, A.D., et al., "Improved Retroviral Vectors for Gene Transfer and Expression," BioTechniques, 7:980-990 (1989).
Pal, J.K., et al., "Tissue Distribution and Immunoreactivity of Heme-regulated eIF-1.alpha. Kinase Determined by Monoclonal Antibodies," Biochem. 30:2555-2562 (1991).
Patkak, V.K., et al., "Generation of a Mutant Form of Protein Synthesis Initiation Factor eIF-2 Lacking the Site of Phosphorylation by eIF-2 Kinases," Mol, Cell. Biol., 8:993-995 (1988).
Pearson, W.R., et al., "Improved Tool for Biological Sequence Comparison," Proc. Natl. Acad. Sci. U.S.A. 85:2444-2448 (1988).
Sanger, F., et al., "DNA Sequencing with Chain-terminating Inhibitors," Proc. Natl. Acad. Sci., USA, 74:5463-5467 (1977).
Tzamarias, D., et al., and Tzamarias, et al., Cell, 57:947-954 (1989).
Ullrich, A., et al., "Signal Transduction by Receptors with Tyrosine Kinase Activity," Cell, 61:302-212 (1990).
Wilson, J.M., et al., "Implantation of Vascular Grafts Lined With Genetically Modified Endothelial Cells", Science, 244:1344-1346 (1980).
Barnes, et al., "Human DNA ligase I cDNA: Cloning and functional expression in Saccharomyces cerevisae," Proc. Natl. Acad. Sci. USA 87:6679-6683 (1990).
Becker, et al., "A cDNA encoding a human CCAAT-binding protein cloned by functional complement in yeast," Proc. Natl. Acad. Sci. USA 88:1968-1972 (1991).
Benedetti and Baglioni, "Activation of Hemin-regulated Initiation Factor-2 Kinase in Heat-shocked HeLa Cells," J. Biol. Chem. 261:338-342 (1986).
Kranz and Holm, "Cloning by function: An alternative approach for identifying yeast homologs of genes from other organisms," Proc. Natl. Acad. Sci. USA 87:6629-6633 (1990).
Lee and Nurse, "Complementation used to clone a human homologue of the fission yeast cell cycle control gene cdc2," Nature 327:31-35 (1987).
Trachsel, et al., "Regulation of Protein Synthesis . . . " Proc. Natl. Acad. Sci. USA 75:3654-3658 (1978).
Wek, et al., "Juxtaposition of domains homologous to protein kinase and histidyl-tRNA synthetases in GCN2 protein suggests a mechanism for coupling GCN4 expression to amino acid availability," Proc. Natl. Acad. Sci. USA 86:4579-4583 (1989).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

DNA encoding the heme-regulated eukaryotic initiation factor 2.a does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with DNA encoding the heme-regulated eukaryotic initiation factor 2.a, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and DNA encoding the heme-regulated eukaryotic initiation factor 2.a will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2104439

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.