Interactions between Double-Stranded RNA Regulators and the Protein Kinase DAI

REFERENCES

• Baglioni, C., and P. A. Maroney. 1981. Inhibition of doublestranded ribonucleic acid activated protein kinase and 2′,5′- oligo(adenylic acid) polymerase by ethidium bromide. Biochemistry 20: 758–762.
   PubMedGoogle Scholar
• Baglioni, C., M. A. Minks, and E. DeClercq. 1981. Structural requirements of polynucleotides for the activation of (2′-5′)An polymerase and protein kinase. Nucleic Acids Res. 9: 4939–4950.
   PubMedGoogle Scholar
• Berry, M. J., G. S. Knutson, S. R. Laskey, S. M. Munemitsu, and C. E. Samuel. 1985. Purification and substrate specificities of the double-stranded RNA-dependent protein kinase from untreated and interferon-treated mouse fibroblasts. J. Biol. Chem. 260: 11240–11247.
   PubMedGoogle Scholar
• Bhat, R. A., and B. Thimmappaya. 1985. Construction and analysis of additional adenovirus substitution mutants confirm the complementation of VAI RNA function by two small RNAs encoded by Epstein-Barr virus. J. Virol. 56: 750–756.
   PubMedGoogle Scholar
• Bischoff, J. R., and C. E. Samuel. 1989. Mechanism of interferon action. Activation of the human Pl/eIF-2α protein kinase by individual reovirus s-class mRNAs: s1 mRNA is a potent activator relative to s4 mRNA. Virology 172: 106–115.
   PubMedGoogle Scholar
• Chong, K. L., L. Feng, K. Schappert, E. Meurs, T. F. Donahue, J. D. Friesen, A. G. Hovenessian, and B. R.G. Williams. 1992. Human p68 kinase exhibits growth suppression in yeast and homology to the translational regulator GCN2. EMBO J. 11: 1553–1562.
   PubMed Web of Science ®Google Scholar
• Clarke, P. A., N. A. Sharp, and M. J. Clemens. 1990. Translational control by the Epstein-Barr virus small RNA EBER-1. Reversal of the double-stranded RNA-induced inhibition of protein synthesis in reticulocyte lysates. Eur. J. Biochem. 193: 635–641.
   PubMedGoogle Scholar
• deBenedetti, A., and C. Baglioni. 1984. Inhibition of mRNA binding to ribosomes by localized activation of dsRNA-depen- dent protein kinase. Nature (London) 311: 79–81.
   PubMed Web of Science ®Google Scholar
• Dever, T. E., L. Feng, R. C. Wek, A. M. Cigan, T. F. Donahue, and A. G. Hinnebusch. 1992. Phosphorylation of initiation factor 2α by protein kinase GCN2 mediates gene-specific translational control of GCN4 in yeast. Cell 68: 585–596.
   PubMed Web of Science ®Google Scholar
• Dubois, M.-F., J. Galabru, P. Lebon, B. Safer, and A. G. Hovanessian. 1989. Reduced activity of the interferon-induced double-stranded RNA-dependent protein kinase during a heat shock stress. J. Biol. Chem. 264: 12165–12171.
   PubMedGoogle Scholar
• Farrell, P. J., K. Balkow, T. Hunt, and R. J. Jackson. 1977. Phosphorylation of initiation factor eIF-2 and the control of reticulocyte protein synthesis. Cell 11: 187–200.
   PubMed Web of Science ®Google Scholar
• Feng, G.-S., K. Chong, A. Kumar, and B. R.G. Williams. 1992. Identification of double-stranded RNA-binding domains in the interferon-induced double-stranded RNA-activated p68 kinase. Proc. Natl. Acad. Sci. USA 89: 5447–5451.
   PubMed Web of Science ®Google Scholar
• Galabru, J., and A. Hovanessian. 1985. Two interferon-induced proteins are involved in the protein kinase complex dependent on double-stranded RNA. Cell 43: 685–694.
   PubMedGoogle Scholar
• Galabru, J., and A. Hovanessian. 1987. Autophosphorylation of the protein kinase dependent on double-stranded RNA. J. Biol. Chem. 262: 15538–15544.
   PubMedGoogle Scholar
• Galabru, J., M. G. Katze, N. Robert, and A. G. Hovanessian. 1989. The binding of double-stranded RNA and adenovirus VAI RNA to the interferon-induced protein kinase. Eur. J. Biochem. 178: 581–589.
   PubMedGoogle Scholar
• Green, S. R., and M. B. Mathews. Submitted for publication.
   Google Scholar
• Grodberg, J., and J. J. Dunn. 1988. ompT encodes the Escherichia coli outer membrane protease that cleaves T7 RNA polymerase during purification. J. Bacteriol. 170: 1245–1253.
   PubMed Web of Science ®Google Scholar
• Gunnery, S., A. P. Rice, H. D. Robertson, and M. B. Mathews. 1990. Tat-responsive region RNA of human immunodeficiency virus 1 can prevent activation of the double-stranded-RNA- activated protein kinase. Proc. Natl. Acad. Sci. USA 87: 8687–8691.
   PubMed Web of Science ®Google Scholar
• Hershey, J. W. B. 1989. Protein phosphorylation controls translation rates. J. Biol. Chem. 264: 20823–20826.
   PubMedGoogle Scholar
• Hershey, J. W. B. 1991. Translational control in mammalian cells. Annu. Rev. Biochem. 60: 717–755.
   PubMed Web of Science ®Google Scholar
• Hovanessian, A. G. 1989. The double stranded RNA-activated protein kinase induced by interferon: dsRNA-PK. J. Interferon Res. 9: 641–647.
   PubMedGoogle Scholar
• Hunter, T., T. Hunt, R. J. Jackson, and H. D. Robertson. 1975. The characteristics of inhibition of protein synthesis by doublestranded ribonucleic acid in reticulocyte lysates. J. Biol. Chem. 250: 409–417.
   PubMedGoogle Scholar
• Judware, R., and R. Petryshyn. 1991. Partial characterization of a cellular factor that regulates the double-stranded RNA-dependent eIF-2α kinase in 3T3-F442A fibroblasts. Mol. Cell. Biol. 11: 3259–3267.
   PubMed Web of Science ®Google Scholar
• Katze, M. G., B. M. Detjen, B. Safer, and R. M. Krug. 1986. Translational control by influenza virus: suppression of the kinase that phosphorylates the alpha subunit of initiation factor eIF-2 and selective translation of influenza viral messenger RNAs. Mol. Cell. Biol. 6: 1741–1750.
   PubMedGoogle Scholar
• Katze, M. G., M. Wambach, M.-L. Wong, M. Garfinkel, E. Meurs, K. Chong, B. R.G. Williams, A. G. Hovanessian, and G. N. Barber. 1991. Functional expression and RNA binding analysis of the interferon-induced, double-stranded RNA-activated, 68,000-Mr protein kinase in a cell-free system. Mol. Cell. Biol. 11: 5497–5505.
   PubMed Web of Science ®Google Scholar
• Kaufman, R. J., and P. Murtha. 1987. Translational control mediated by eukaryotic initiation factor-2 is restricted to specific mRNAs in transfected cells. Mol. Cell. Biol. 7: 1568–1571.
   PubMed Web of Science ®Google Scholar
• Kimchi, A., A. Zilberstein, A. Schmidt, L. Shulman, and M. Revel. 1979. The interferon-induced protein kinase PK-i from mouse L cells. J. Biol. Chem. 254: 9846–9853.
   PubMedGoogle Scholar
• Kitajewski, J., R. J. Schneider, B. Safer, S. M. Munemitsu, C. E. Samuel, B. Thimmappaya, and T. Shenk. 1986. Adenovirus VAI RNA antagonizes the antiviral action of the interferon by preventing activation of the interferon-induced eIF-2α kinase. Cell 45: 195–200.
   PubMed Web of Science ®Google Scholar
• Kostura, M., and M. B. Mathews. 1989. Purification and activation of the double-stranded RNA-dependent eIF-2 kinase DAI. Mol. Cell. Biol. 9: 1576–1586.
   PubMedGoogle Scholar
• Lasky, S. R., B. L. Jacobs, and C. E. Samuel. 1982. Characterization of the sites of phosphorylation in the interferon-induced phosphoprotein P1 from mouse fibroblasts: evidence for two forms of Pl. J. Biol. Chem. 257: 11087–11093.
   PubMedGoogle Scholar
• Laurent, A. G., B. Krust, J. Galabru, J. Svab, and A. G. Hovanessian. 1985. Monoclonal antibodies to an interferon- induced Mr 68,000 protein and their use for the detection of double-stranded RNA-dependent protein kinase in human cells. Proc. Natl. Acad. Sci. USA 82: 4341–4345.
   PubMedGoogle Scholar
• Lebleu, B., G. C. Sen, S. Shaila, B. Cabrer, and P. Lengyel. 1976. Interferon, double-stranded RNA, and protein phosphorylation. Proc. Natl. Acad. Sci. USA 73: 3107–3111.
   PubMed Web of Science ®Google Scholar
• Lenz, J. R., and C. Baglioni. 1978. Inhibition of protein synthesis by double-stranded RNA and phosphorylation of initiation factor, eIF-2. J. Biol. Chem. 253: 4219–4223.
   PubMedGoogle Scholar
• Levin, D., and I. M. London. 1978. Regulation of protein synthesis: activation by double-stranded RNA of a protein kinase that phosphorylates eukaryotic initiation factor 2. Proc. Natl. Acad. Sci. USA 75: 1121–1125.
   PubMed Web of Science ®Google Scholar
• Levin, D. H., R. Petryshyn, and I. M. London. 1980. Characterization of double-stranded-RNA-activated kinase that phosphorylates α subunit of eukaryotic initiation factor 2 (eIF-2α) in reticulocyte lysates. Proc. Natl. Acad. Sci. USA 77: 832–836.
   PubMed Web of Science ®Google Scholar
• Mathews, M. B. 1991. Control of translation in adenovirus infected cells. Enzyme 44: 250–264.
   Google Scholar
• Mathews, M. B., S. Gunnery, L. Manche, K. H. Mellits, and T. Pe’ery. 1990. Control of protein synthesis by RNA regulators. NATO ASI (Adv Sci Inst) Ser H Cell Biol. 49: 377–388.
   Google Scholar
• Mathews, M. B., and T. Shenk. 1991. Adenovirus virus-associated RNA and translational control. J. Virol. 65: 5657–5662.
   PubMed Web of Science ®Google Scholar
• McCormack, S. J., D. C. Thomis, and C. E. Samuel. 1992. Mechanism of interferon action: identification of a RNA binding domain within the N-terminal region of the human RNA- dependent Pl/eIF-2α protein kinase. Virology 188: 47–56.
   PubMedGoogle Scholar
• Mellits, K. H., M. Kostura, and M. B. Mathews. 1990. Interaction of adenovirus VA RNAI with the protein kinase DAI: non-equivalence of binding and function. Cell 61: 843–852.
   PubMedGoogle Scholar
• Mellits, K. H., and M. B. Mathews. 1988. Effects of mutations in stem and loop regions on the structure and function of adenovirus VA RNAI EMBO J. 7: 2849–2859.
   PubMedGoogle Scholar
• Mellits, K. H., T. Pe’ery, L. Manche, H. D. Robertson, and M. B. Mathews. 1990. Removal of double-stranded contaminants from RNA transcripts: synthesis of adenovirus VA RNAI from a T7 vector. Nucleic Acids Res. 18: 5401–5406.
   PubMedGoogle Scholar
• Meurs, E., K. Chong, J. Galabru, N. S.B. Thomas, 1. M. Kerr, B. R.G. Williams, and A. G. Hovanessian. 1990. Molecular cloning and characterization of the human double-stranded RNA-activated protein kinase induced by interferon. Cell 62: 379–390.
   PubMed Web of Science ®Google Scholar
• Minks, M. A., D. K. West, S. Benvin, and C. Baglioni. 1979. Structural requirements of double-stranded RNA for the activation of 2′,5′-oligo(A) polymerase and protein kinase of interfer- on-treated HeLa cells. J. Biol. Chem. 254: 10180–10183.
   PubMed Web of Science ®Google Scholar
• Minks, M. A., D. K. West, S. Benvin, J. J. Greene, P. O.P. Ts’o, and C. Baglioni. 1980. Activation of 2′,5′-oligo(A) polymerase and protein kinase of interferon-treated HeLa cells by 2′-O- methylated poly (inosinic acid) • poly (cytidylic acid). J. Biol. Chem. 255: 6403–6407.
   PubMed Web of Science ®Google Scholar
• Ochoa, S. 1983. Regulation of protein synthesis initiation in eukaryotes. Arch. Biochem. Biophys. 223: 325–349.
   PubMedGoogle Scholar
• O’Malley, R. P., R. F. Duncan, J. W.B. Hershey, and M. B. Mathews. 1989. Modification of protein synthesis initiation factors and shut-off of host protein synthesis in adenovirus- infected cells. Virology 168: 112–118.
   PubMedGoogle Scholar
• O’Malley, R. P., T. M. Mariano, J. Siekierka, and M. B. Mathews. 1986. A mechanism for the control of protein synthesis by adenovirus VA RNAI. Cell 44: 391–400.
   PubMedGoogle Scholar
• O’Malley, R. P., T. M. Mariano, J. Siekierka, W. C. Merrick, P. A. Reichel, and M. B. Mathews. 1986. The control of protein synthesis by adenovirus VA RNA. Cancer Cells 4: 291–301.
   Google Scholar
• Patel, R. C., and G. C. Sen. 1992. Identification of the doublestranded RNA-binding domain of the human interferon-inducible protein kinase. J. Biol. Chem. 267: 7671–7676.
   PubMed Web of Science ®Google Scholar
• Pestka, S., J. A. Langer, K. C. Zoon, and C. E. Samuel. 1987. Interferons and their actions. Annu. Rev. Biochem. 56: 727–777.
   PubMed Web of Science ®Google Scholar
• Petryshyn, R., J.-J. Chen, and I. M. London. 1984. Growth- related expression of a double-stranded RNA-dependent protein kinase in 3T3 cells. J. Biol. Chem. 259: 14736–14742.
   PubMedGoogle Scholar
• Rice, A. R., M. Kostura, and M. B. Mathews. 1989. Identification of a 90 KD polypeptide which associates with adenovirus VA RNAI and is phosphorylated by the double-stranded RNA dependent protein kinase. J. Biol. Chem. 264: 20632–20637.
   PubMedGoogle Scholar
• Samuel, C. E. 1991. Antiviral actions of interferon: interferon- regulated cellular proteins and their surprisingly selective antiviral activities. Virology 183: 1–11.
   PubMed Web of Science ®Google Scholar
• Schmedt, C., S. R. Green, and M. B. Mathews. Unpublished data.
   Google Scholar
• Schneider, R. J., and T. Shenk. 1987. Impact of virus infection on host cell protein synthesis. Annu. Rev. Biochem. 56: 317–332.
   PubMedGoogle Scholar
• Schweitz, H., and J. P. Ebel. 1971. A study of the mechanism of action of E. coli ribonuclease III. Biochimie 53: 585–593.
   PubMedGoogle Scholar
• Sen, G. C., H. Taira, and P. Lengyel. 1978. Interferon, doublestranded RNA, and protein phosphorylation. J. Biol. Chem. 253: 5915–5921.
   PubMed Web of Science ®Google Scholar
• Sonenberg, N. 1990. Measures and countermeasures in the modulation of initiation factor activities by viruses. New Biol. 2: 402–409.
   PubMedGoogle Scholar
• Svensson, C., and G. Akusjarvi. 1985. Adenovirus VA RNAI mediates a translational stimulation which is not restricted to the viral mRNAs. EMBO J. 4: 957–964.
   PubMedGoogle Scholar
• Tiwari, R. K., J. Kusari, R. Kumar, and G. C. Sen. 1988. Gene induction by interferons and double-stranded RNA: selective inhibition by 2-aminopurine. Mol. Cell. Biol. 8: 4289–4294.
   PubMed Web of Science ®Google Scholar
• Torrence, P. F., M. I. Johnston, D. A. Epstein, H. Jacobsen, and R. M. Friedman. 1981. Activation of human and mouse 2-5A synthetases and mouse protein P1 kinase by nucleic acids. FEBS Lett. 130: 291–296.
   PubMedGoogle Scholar
• Zilberstein, A., A. Kimchi, A. Schmidt, and M. Revel. 1978. Isolation of two interferon-induced translational inhibitors: a protein kinase and an oligo-isoadenylate synthetase. Proc. Natl. Acad. Sci. USA 75: 4734–4738.
   PubMed Web of Science ®Google Scholar
• Zinn, K., A. Keller, L.-A. Whitemore, and T. Maniatis. 1988. 2-Aminopurine selectively inhibits the induction of β-interferon, c-fos, and c-myc gene expression. Science 240: 210–213.
   PubMed Web of Science ®Google Scholar