cis-Acting Translational Effects of the 5′ Noncoding Region of c-myc mRNA

LITERATURE CITED

• Adams, J. M., S. Gerondakis, E. Webb, L. M. Corcoran, and S. Cory. 1983. Cellular myc oncogene is altered by chromosome translocation to an immunoglobulin locus in murine plasmacytomas and is rearranged similarly in human Burkitt lymphomas. Proc. Natl. Acad. Sci. USA 80:1982–1986.
   PubMed Web of Science ®Google Scholar
• Adams, J. M., A. N. Harris, C. A. Pinkert, L. M. Corcoran, N. S. Alexander, S. Cory, R. D. Palmiter, and R. L. Brinster. 1985. The c-myc oncogene driven by immunoglobulin enhancers induces lymphoid malignancy in transgenic mice. Nature (London) 318:533–538.
   PubMed Web of Science ®Google Scholar
• Baim, S. B., D. F. Pietras, D. C. Eustice, and F. Sherman. 1985. A mutation allowing an mRNA secondary structure diminishes translation of Saccharomyces cerevisiae iso-l-cytochrome c. Mol. Cell. Biol. 5:1839–1846.
   PubMedGoogle Scholar
• Bernard, O., S. Cory, S. Gerondakis, E. Webb, and J. M. Adams. 1983. Sequence of the murine and human cellular myc oncogenes and two modes of transcription resulting from chromosome translocation in B lymphoid tumors. EMBO J. 2:2375–2383.
   PubMed Web of Science ®Google Scholar
• Bishop, J. M. 1987. The molecular genetics of cancer. Science 235:305–311.
   PubMed Web of Science ®Google Scholar
• Butnick, N. Z., C. Miyamoto, R. Chizzonite, B. R. Cullen, G. Ju, and A.-M. Skalka. 1985. Regulation of human c-myc gene: 5′ noncoding sequences do not affect translation. Mol. Cell. Biol. 5:3009–3016.
   PubMedGoogle Scholar
• Colman, A. 1984. Expression of exogenous DNA in Xenopus oocytes, p. 49–69. In B. D. Hames and S. J. Higgins (ed.), Transcription and translation: a practical approach. IRL Press Ltd., Oxford.
   Google Scholar
• Colman, A. 1984. Translation of eukaryotic messenger RNA in Xenopus oocytes, p. 271–302. In B. D. Hames and S. J. Higgins (ed.), Transcription and translation: a practical approach. IRL Press Ltd., Oxford.
   Google Scholar
• Corcoran, L. M., S. Cory, and J. M. Adams. 1985. Transposition of the immunoglobulin heavy chain enhancer to the myc oncogene in a mouse plasmacytoma. Cell 40:71–79.
   PubMed Web of Science ®Google Scholar
• Cory, S. 1986. Activation of cellular oncogenes in hemopoietic cells by chromosome translocation. Adv. Cancer Res. 47:189–234.
   PubMed Web of Science ®Google Scholar
• Dani, C., J. M. Blanchard, M. Piechaczyk, S. El Sabouty, L. Marty, and P. Jeanteur. 1984. Extreme instability of myc mRNA in normal and transformed human cells. Proc. Natl. Acad. Sci. USA 81:7046–7050.
   PubMed Web of Science ®Google Scholar
• Dani, C., N. Mechti, M. Piechaczyk, B. Lebleu, P. Jeanteur, and J. M. Blanchard. 1985. Increased rate of degradation of c-myc in interferon-treated Daudi cells. Proc. Natl. Acad. Sci. USA 82:4896–4899.
   PubMed Web of Science ®Google Scholar
• Darveau, A., J. Pelletier, and N. Sonenberg. 1985. Differential efficiencies of in vitro translation of mouse c-myc transcripts differing in the 5′ untranslated region. Proc. Natl. Acad. Sci. USA 82:2315–2319.
   PubMed Web of Science ®Google Scholar
• Eisenman, R. N., C. Y. Tachibana, H. D. Abrams, and S. R. Hann. 1985. v-myc- and c-myc-encoded proteins are associated with the nuclear matrix. Mol. Cell. Biol. 5:114–126.
   PubMed Web of Science ®Google Scholar
• Erikson, J., D. A. Miller, O. J. Miller, P. W. Abcarian, R. M. Skurla, J. F. Mushinski, and C. M. Croce. 1985. The c-myc oncogene is translocated to the involved chromosome 12 in mouse plasmacytoma. Proc. Natl. Acad. Sci. USA 82:4212–4216.
   PubMed Web of Science ®Google Scholar
• Fahrlander, P. D., J. Sümegi, J.-Q. Yang, F. Weiner, K. B. Marcu, and G. Klein. 1985. Activation of the c-myc oncogene by the immunoglobulin heavy-chain gene enhancer after multiple switch region-mediated chromosome rearrangements in a murine plasmacytoma. Proc. Natl. Acad. Sci. USA 82:3746–3750.
   PubMed Web of Science ®Google Scholar
• Godeau, F., H. Persson, H. E. Gray, and A. B. Pardee. 1986. c-myc expression is dissociated from DNA synthesis and cell division in Xenopus oocyte and early embryonic development. EMBO J. 5:3571–3577.
   PubMedGoogle Scholar
• Gorman, C. M., L. F. Moffat, and B. H. Howard. 1982. Recombinant genomes which express chloramphenicol acetyltransferase in mammalian cells. Mol. Cell. Biol. 2:1044–1051.
   PubMed Web of Science ®Google Scholar
• Graham, F. L., and A. J. Van der Eb. 1973. A new technique for the assay of infectivity of human adenovirus 5 DNA. Virology 52:465–467.
   Google Scholar
• Hann, S. R., and R. N. Eisenman. 1984. Proteins encoded by the human c-myc oncogene: differential expression in neoplastic cells. Mol. Cell. Biol. 4:2486–2497.
   PubMed Web of Science ®Google Scholar
• Hann, S. R., M. W. King, D. L. Bentley, C. W. Anderson, and R. N. Eisenman. 1988. A non-AUG translational initiation in c-myc exon 1 generates an N-terminally distinct protein whose synthesis is disrupted in Burkitt's lymphomas. Cell 52:185–195.
   PubMed Web of Science ®Google Scholar
• Jones, T. R., and M. D. Cole. 1987. Rapid cytoplasmic turnover of c-myc mRNA: requirement of the 3′ untranslated sequences. Mol. Cell. Biol. 7:4513–4521.
   PubMed Web of Science ®Google Scholar
• Kaufman, R. 1985. Identification of the components necessary for adenovirus translational control and their utilization in cDNA expression vectors. Proc. Natl. Acad. Sci. USA 82:689–693.
   PubMed Web of Science ®Google Scholar
• Kelly, K., B. H. Cochran, C. D. Stiles, and P. Leder. 1983. Cell specific regulation of the c-myc gene by lymphocyte mitogens and platelet-derived growth factor. Cell 35:603–610.
   PubMed Web of Science ®Google Scholar
• Krieg, P. A., and D. A. Melton. 1984. Functional messenger RNAs are produced by SP6 in vitro transcription of cloned cDNAs. Nucleic Acids Res. 12:7057–7070.
   PubMed Web of Science ®Google Scholar
• Lachman, H. M., and H. I. Skoultchi. 1984. Expression of c-myc changes during differentiation of mouse erythroleukemia cells. Nature (London) 310:592–594.
   PubMed Web of Science ®Google Scholar
• Laemmli, U. K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature (London) 227:680–685.
   PubMed Web of Science ®Google Scholar
• Land, H., A. C. Chen, J. P. Morgenstern, L. F. Parada, and R. A. Weinberg. 1986. Behavior of myc and ras oncogenes in transformation of rat embryo fibroblasts. Mol. Cell. Biol. 6:1917–1925.
   PubMed Web of Science ®Google Scholar
• Land, H., L. Parada, and R. Weinberg. 1983. Tumorigenic conversion of primary embryo fibroblasts requires at least two cooperating oncogenes. Nature (London) 304:596–602.
   PubMed Web of Science ®Google Scholar
• Leder, P., J. Battey, G. Lenoir, C. Moulding, W. Murphy, H. Potter, T. Stewart, and R. Taub. 1983. Translocation among antibody genes in human cancer. Science 222:765–771.
   PubMed Web of Science ®Google Scholar
• Lee, K. A. W., and N. Sonenberg. 1982. Inactivation of capbinding proteins accompanies the shut-off of host protein synthesis by poliovirus. Proc. Natl. Acad. Sci. USA 79:3447–3451.
   PubMedGoogle Scholar
• Lombardi, L., E. W. Newcomb, and R. Dalla Favera. 1987. Pathogenesis of Burkitt lymphoma: expression of an activated c-myc oncogene causes the tumorigenic conversion of EBV-infected human B lymphoblasts. Cell 49:161–170.
   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
• Marcu, K. B., L. J. Harris, L. W. Stanton, J. Erikson, R. Watt, and C. M. Croce. 1983. Transcriptionally active c-myc oncogene is contained within NIARD, a DNA sequence associated with chromosome translocation in B cell neoplasia. Proc. Natl. Acad. Sci. USA 80:519–523.
   PubMed Web of Science ®Google Scholar
• McGarry, T. J., and S. Lindquist. 1985. The preferential translation of Drosophila hsp70 mRNA requires sequences in the untranslated leader. Cell 42:903–911.
   PubMedGoogle Scholar
• Mellon, P., V. Parker, Y. Gluzman, and T. Maniatis. 1981. Identification of DNA sequences required for transcription of the human α1-globin gene in a new SV40 host-vector system. Cell 27:279–288.
   PubMed Web of Science ®Google Scholar
• Melton, D. A., P. A. Krieg, M. R. Rebagliati, T. Maniatis, K. Zinn, and M. R. Green. 1984. Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. Nucleic Acids Res. 12:7035–7056.
   PubMed Web of Science ®Google Scholar
• Nepveu, A., K. B. Marcu, A. I. Skoultchi, and H. M. Lachman. 1987. Contributions of transcriptional and post-transcriptional mechanisms to the regulation of c-myc expression in mouse erythroleukemia cells. Genes Dev. 1:938–945.
   PubMedGoogle Scholar
• Nilsen, T. W., and P. A. Maroney. 1984. Translational efficiency of c-myc mRNA in Burkitt lymphoma cells. Mol. Cell. Biol. 4:2235–2238.
   PubMedGoogle Scholar
• Pelham, H. P. B., and R. J. Jackson. 1976. An efficient mRNA dependent translation system from reticulocyte lysates. Eur. J. Biochem. 67:247–256.
   PubMedGoogle Scholar
• Pelletier, J., and N. Sonenberg. 1985. Insertion mutagenesis to increase secondary structure within the 5′ noncoding region of a eucaryotic mRNA reduces translational efficiency. Cell 40:515–526.
   PubMed Web of Science ®Google Scholar
• Persson, H., and P. Leder. 1984. Nuclear localization and DNA binding properties of protein expressed by human c-myc oncogene. Science 225:718–721.
   PubMed Web of Science ®Google Scholar
• Piechaczyk, M., J.-M. Blanchard, and P. Jeanteur. 1987. c-myc gene regulation still holds its secret. Trends Genet. 3:47–51.
   Google Scholar
• Piechaczyk, M., W.-J. Yang, J.-M. Blanchard, P. Jeanteur, and K. B. Marcu. 1985. Post-transcriptional mechanisms are responsible for accumulation of truncated c-myc RNAs in murine plasma cell tumors. Cell 42:589–597.
   PubMed Web of Science ®Google Scholar
• Rabbitts, P. H., A. Forster, M. A. Stinson, and T. H. Rabbitts. 1985. Truncation of exon 1 from the c-myc gene results in prolonged c-myc mRNA stability. EMBO J. 4:3727–3733.
   PubMed Web of Science ®Google Scholar
• Ramsay, G., G. I. Evan, and J. M. Bishop. 1984. The protein encoded by the human proto-oncogene c-myc. Proc. Natl. Acad. Sci. USA 81:7742–7746.
   PubMed Web of Science ®Google Scholar
• Rose, J. K., H. Trachsel, K. Leong, and D. Baltimore. 1978. Inhibition of translation by poliovirus: inactivation of a specific initiation factor. Proc. Natl. Acad. Sci. USA 75:2732–2736.
   PubMedGoogle Scholar
• Saito, H., A. C. Hayday, K. Wiman, W. S. Hayward, and S. Tonegawa. 1983. Activation of the c-myc gene by translocation: a model for translational control. Proc. Natl. Acad. Sci. USA 80:7476–7480.
   PubMed Web of Science ®Google Scholar
• Stone, J., T. de Lange, G. Ramsay, E. Jakobovits, J. M. Bishop, H. Varmus, and W. Lee. 1987. Definition of regions in human c-myc that are involved in transformation and nuclear localization. Mol. Cell. Biol. 7:1697–1709.
   PubMed Web of Science ®Google Scholar
• Taub, R., C. Moulding, J. Battey, W. Murphy, T. Vasicek, G. M. Lenoir, and P. Leder. 1984. Activation and somatic mutation of the translocated c-myc gene in Burkitt lymphoma cells. Cell 36:339–348.
   PubMed Web of Science ®Google Scholar
• Taylor, M. V., M. Guzze, G. I. Evan, N. Dathan, and M. Mechali. 1986. Xenopus myc proto-oncogene during development: expression as a stable maternal mRNA uncoupled from cell division. EMBO J. 5:3563–3570.
   PubMedGoogle Scholar
• Watt, R., L. W. Stanton, K. B. Marcu, R. C. Gallo, C. M. Croce, and G. Rovera. 1983. Nucleotide sequence of cloned cDNA of human c-myc oncogene. Nature (London) 303:725–728.
   PubMed Web of Science ®Google Scholar
• Watt, R. A., A. R. Shatzman, and M. Rosenberg. 1985. Expression and characterization of the human c-myc DNA-binding protein. Mol. Cell. Biol. 5:448–456.
   PubMed Web of Science ®Google Scholar
• Wiman, K. G., B. Clarkson, A. C. Hayday, H. Saito, S. Tonegawa, and W. S. Hayward. 1984. Activation of a translocated c-myc gene: role of structural alterations in the upstream region. Proc. Natl. Acad. Sci. USA 81:6798–6802.
   PubMed Web of Science ®Google Scholar
• Yang, J.-Q., E. Remmers, and K. Marcu. 1986. The first exon of the c-myc proto-oncogene contains a novel positive control element. EMBO J. 5:3553–3562.
   PubMed Web of Science ®Google Scholar