cDNA Structures and Regulation of Two Interferon-Induced Human Mx Proteins

LITERATURE CITED

• Arnheiter, H., and O. Haller. 1988. Antiviral state against influenza virus neutralized by microinjection of antibodies to interferon-induced Mx proteins. EMBO J. 7:1315–1320.
   PubMed Web of Science ®Google Scholar
• Auffrey, C., and F. Rougeon. 1980. Purification of mouse immunoglobulin heavy-chain messenger RNAs from total myeloma tumor RNA. Eur. J. Biochem. 107:303–314.
   PubMedGoogle Scholar
• Berk, A. J., and P. Sharp. 1977. Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonuclease- digested hybrids. Cell 12:721–732.
   PubMed Web of Science ®Google Scholar
• Chomczynski, P., and N. Sacchi. 1987. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162:156–159.
   PubMed Web of Science ®Google Scholar
• Dreiding, P., P. Staeheli, and O. Haller. 1985. Interferon-induced protein Mx accumulates in nuclei of mouse cells expressing resistance to influenza viruses. Virology 140:192–196.
   PubMedGoogle Scholar
• Goetschy, J.-F., H. Zeller, J. Content, and M. A. Horisberger. 1989. Regulation of the interferon-inducible IFI-78K gene, the human equivalent of the murine Mx gene, by interferons, double-stranded RNA, certain cytokines, and viruses. J. Virol. 63:2616–2622.
   PubMed Web of Science ®Google Scholar
• Gresser, I.. 1984. Role of interferon in resistance to viral infection in vivo, p. 221–246. In J. Vilcek, and E. De Maeyer (ed.), Interferon, vol. 2: interferons and the immune system. Elsevier Science Publishers B. V., Amsterdam.
   Google Scholar
• Gunning, P., P. Ponte, H. Okayama, J. Engel, H. Blau, and L. Kedes. 1983. Isolation and characterization of full-length cDNA clones for human α-, β-, and γ-actin mRNAs: skeletal but not cytoplasmic actins have an amino-terminal cysteine that is subsequently removed. Mol. Cell. Biol. 3:787–795.
   PubMed Web of Science ®Google Scholar
• Horisberger, M. A.. 1988. The action of recombinant bovine interferons on influenza virus replication correlates with the induction of two Mx-related proteins in bovine cells. Virology 162:181–186.
   PubMedGoogle Scholar
• Horisberger, M. A., and K. de Starinsky. 1985. Sensitivity of influenza A viruses to human interferons in human diploid cells. FEMS Microbiol. Lett. 29:207–210.
   Google Scholar
• Horisberger, M. A., and H. K. Hochkeppel. 1987. Production and use of monoclonal and polyclonal antibodies specific for an IFN-induced human 78 kDa protein. J. Interferon Res. 7:331–343.
   PubMedGoogle Scholar
• Horisberger, M. A., M. Wathelet, J. Szpirer, C. Szpirer, Q. Islam, G. Levan, G. Huez, and J. Content. 1988. cDNA cloning and assignment to chromosome 21 of IFN-78K gene, the human equivalent of murine Mx gene. Somatic Cell Mol. Genet. 14:123–131.
   PubMedGoogle Scholar
• Hug, H., M. Costas, P. Staeheli, M. Aebi, and C. Weissmann. 1988. Organization of the murine Mx gene and characterization of its interferon- and virus-inducible promoter. Mol. Cell. Biol. 8:3065–3079.
   PubMedGoogle Scholar
• Hugnh, T. V., R. A. Young, and R. W. Davis. 1984. Construction and screening cDNA libraries in λgt10 and λgt11, p. 49–78. In D. Glover (ed.), DNA cloning techniques: a practical approach. IRL Press, Oxford.
   Google Scholar
• Kozak, M.. 1987. An analysis of 5′-noncoding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Res. 15:8125–8148.
   PubMed Web of Science ®Google Scholar
• Krug, R. M., M. Shaw, B. Broni, G. Shapiro, and O. Haller. 1985. Inhibition of influenza viral mRNA synthesis in cells expressing the interferon-induced Mx gene product. J. Virol. 56:201–206.
   PubMed Web of Science ®Google Scholar
• Maniatis, T., E. F. Fritsch, and J. Sambrook. 1982. Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
   Google Scholar
• Maxam, A. M., and W. Gilbert. 1977. A new method for sequencing DNA. Proc. Natl. Acad. Sci. USA 74:560–564.
   PubMed Web of Science ®Google Scholar
• Meier, E., J. Fäh, M. S. Grob, R. End, P. Staeheli, and O. Haller. 1988. A family of interferon-induced Mx-related mRNAs encode cytoplasmic and nuclear proteins in rat cells. J. Virol. 62:2386–2393.
   PubMedGoogle Scholar
• Meyer, T., and M. A. Horisberger. 1984. Combined action of mouse alpha and beta interferons in influenza virus-infected macrophages carrying the resistance gene Mx. J. Virol. 49:709–716.
   PubMedGoogle Scholar
• Noteborn, M., H. Arnheiter, L. Richter-Mann, H. Browning, and C. Weissmann. 1987. Transport of the murine Mx protein into the nucleus is dependent on a basic carboxy-terminal sequence. J. Interferon Res. 7:657–669.
   PubMedGoogle Scholar
• Okayama, H., and P. Berg. 1982. High-efficiency cloning of full-length cDNA. Mol. Cell. Biol. 2:161–170.
   PubMed Web of Science ®Google Scholar
• Ponte, P., S.-Y. Ng, J. Engel, P. Gunning, and L. Kedes. 1984. Evolutionary conservation in the untranslated regions of actin mRNAs: DNA sequence of a human beta-actin cDNA. Nucleic Acids Res. 12:1687–1696.
   PubMed Web of Science ®Google Scholar
• Rüther, U., and B. Muller-Hill. 1983. Easy identification of cDNA clones. EMBO J. 2:1791–1794.
   PubMedGoogle Scholar
• Samuel, C. E.. 1988. Mechanisms of the antiviral action of interferons. Prog. Nucleic Acid Res. Mol. Biol. 35:27–72.
   PubMed Web of Science ®Google Scholar
• Samuel, C. E.. 1989. Polycistronic animal virus RNAs. Prog. Nucleic Acid Res. Mol. Biol. 37:127–153.
   PubMedGoogle Scholar
• Sanger, F.. 1981. Determination of nucleotide sequences in DNA. Science 214:1205–1210.
   PubMed Web of Science ®Google Scholar
• Staeheli, P., P. Danielson, O. Haller, and J. G. Sutcliffe. 1986. Transcriptional activation of the mouse Mx gene by type I interferon. Mol. Cell. Biol. 6:4770–4774.
   PubMedGoogle Scholar
• Staeheli, P., and O. Haller. 1985. Interferon-induced human protein with homology to protein Mx of influenza virus-resistant mice. Mol. Cell. Biol. 5:2150–2153.
   PubMedGoogle Scholar
• Staeheli, P., and O. Haller. 1987. Interferon-induced Mx protein: a mediator of cellular resistance to influenza virus. Interferon 8:1–23.
   PubMedGoogle Scholar
• Staeheli, P., O. Haller, W. Boll, J. Lindenmann, and C. Weissmann. 1986. Mx protein: constitutive expression in 3T3 cells transformed with cloned Mx cDNA confers selective resistance to influenza virus. Cell 44:147–158.
   PubMed Web of Science ®Google Scholar
• Staeheli, P., and J. G. Sutcliffe. 1988. Identification of a second interferon-regulated murine Mx gene. Mol. Cell. Biol. 8:4524–4528.
   PubMedGoogle Scholar
• Staeheli, P., Y.-X. Yu, R. Grob, and O. Haller. 1989. A double-stranded RNA-inducible fish gene homologous to the murine influenza virus resistance gene Mx. Mol. Cell. Biol. 9:3117–3121.
   PubMedGoogle Scholar
• Stein, G. H.. 1979. T98G: an anchorage-independent human tumor cell line that exhibits stationary phase G1 arrest in vitro. J. Cell. Physiol. 99:43–54.
   PubMed Web of Science ®Google Scholar
• Stewart-Harris, C. H., and G. C. Schild. 1976. Influenza: The virus and the disease. Edward Arnold (Publishers) Ltd., London.
   Google Scholar
• Young, R. A., and R. W. Davies. 1983. Efficient isolation of genes by using antibody probes. Proc. Natl. Acad. Sci. USA 80:1194–1198.
   PubMed Web of Science ®Google Scholar