Expression of the Mouse Mammary Tumor Virus ORF Gene in Cultured Cells

References

• Dickson C., Peters G. Protein-coding potential of mouse mammary tumor virus genome RNA as examined by in vitro translation. J. Virol. 1981; 37: 36–47
   Google Scholar
• Dickson C., Smith R., Peters G. In-vitro synthesis of polypeptides encoded by the long terminal repeat region of mouse mammary tumor virus DNA. Nature 1981; 291: 511–513
   PubMedGoogle Scholar
• Donehower L. A., Huang A. L., Hager G. L. Regulatory and coding potential of the mouse mammary tumor virus long terminal redundancy. J. Virol. 1981; 37: 226–238
   PubMed Web of Science ®Google Scholar
• Sen G. C., Racevskis J., Sarkar N. H. Synthesis of murine mammary tumor viral proteins in vitro. J. Virol. 1981; 37: 963–975
   PubMedGoogle Scholar
• Fasel N., Pearson K., Buetti E., Diggelmann H. The region of mouse mammary tumor virus DNA containing the long terminal repeat includes a long coding sequence and signals for hormonally regulated transcription. EMBO J. 1982; 1: 3–7
   PubMed Web of Science ®Google Scholar
• Kennedy N., Knedlitschek G., Groner B., Hynes N. E., Herrlich P., Michalide R., van Ooyen A. J. J. Long terminal repeats of endogenous mouse mammary tumor virus contain a long open reading frame which extends into adjacent sequences. Nature 1982; 295: 622–624
   PubMedGoogle Scholar
• Peters G., Smith R., Brooks S., Dickson C. Conservation of protein coding potential in the long terminal repeats of exogenous and endogenous mouse mammary tumor viruses. J. Virol. 1982; 42: 880–888
   Google Scholar
• Donehower L. A., Fleurdelys B., Hager G. L. Further evidence for the protein coding potential of the mouse mammary tumor virus long terminal repeat: Nucleotide sequences of an endogenous proviral long terminal repeat. J. Virol. 1983; 45: 941–949
   PubMedGoogle Scholar
• Majors J. E., Varmus H. E. Nucleotide sequencing of an apparent proviral copy of env mRNA defines determinants of expression of the mouse mammary tumor virus env gene. J. Virol. 1983a; 47: 495–504
   Google Scholar
• Van Ooyen A. J. J., Michalides R. JA. M., Nusse R. Structural analysis of a 1.7-Kilobase mouse mammary tumor virus-specific RNA. J. Virol. 1983; 46: 362–370
   PubMedGoogle Scholar
• Wheeler D. A., Butel J. S., Medina D. M., Cardiff R. D., Hayes G. L. Transcription of mouse mammary tumor virus: identification of a candidate mRNA for the long terminal repeat gene product. J. Virol. 1983; 46: 42–49
   PubMedGoogle Scholar
• Racevskis J., Prakash O. Proteins encoded by the long terminal repeat region of mouse mammary tumor virus: Identification by hybrid selected translation. J. Virol. 1984; 51: 604–610
   Google Scholar
• Fasel N., Buetti E., Firzlaff J., Pearson K., Diggelmann H. Nucleotide sequence of the 5′ noncoding region and part of the gag gene of mouse mammary tumor virus; identification of the 5′ splicing site for subgenomic mRNA's. Nucleic Acids Res. 1983; 11: 6943–6955
   Google Scholar
• Cohen J. C., Majors J. E., Varmus H. E. Organization of mouse mammary tumor virus-specific DNA endogenous to BALB/c mice. J. Virol. 1979a; 32: 483–496
   PubMedGoogle Scholar
• Breznik T., Cohen J. C. Altered methylation of endogenous viral promoter sequences during mammary carcinogenesis. Nature 1982; 295: 255–257
   PubMedGoogle Scholar
• Graham D. E., Medina D., Smith G. H. Increased concentration of an indigenous proviral mouse mammary tumor virus long terminal repeat-containing transcript is associated with neoplastic transformation of mammary epithelium in C3H/Sm mice. J. Virol. 1984; 49: 819–827
   PubMedGoogle Scholar
• Kwon B. S., Weissman S. H. Mouse mammary tumor virus-related sequences in mouse lymphocytes are inducible by 12-o-Tetradecanoyl phorbol-13-acetate. J. Virol. 1984; 52: 1000–1004
   PubMedGoogle Scholar
• Michalides R., Wagenaar E., Weijers P. Rearrangements in the long terminal repeat of extra mammary tumor proviruses in T-cell leukemias of mouse strain GR result in a novel enhancer-like structure. Mol. Cell. Biol. 1985; 5: 823–830
   PubMedGoogle Scholar
• Darbre P., Dickson C., Peters G., Page M., Curtis S., King R. J. B. Androgen regulation of cell proliferation and expression of viral sequences in mouse mammary tumor cells. Nature 1983; 303: 431–433
   PubMedGoogle Scholar
• Allaz M. Thesis: Transformation of rabbit mammary epithelial cells. University of Lausanne, Medical Faculty. 1989; 1–63
   Google Scholar
• Smith G. H., Mirski M. A., Arthur L. O. DNA binding and unwinding activities associated with intracytoplasmic A particles isolated from mouse mammary tumors. J. Gen. Virol. 1980; 49: 263–272
   Google Scholar
• Van Klaveren P., Bentvelzen P. Transactivating potential of the 3′ open reading frame of murine mammary tumor virus. J. Virol. 1988; 62: 4410–4413
   Google Scholar
• Salmons B., Erfle V., Brem G., Günzburg W. H. naf, a trans-Regulating Negative-Acting Factor Encoded within the Mouse Mammary Tumor Virus Open Reading Frame Region. J. Virol. 1990; 64: 6355–6359
   PubMedGoogle Scholar
• Buetti E., Diggelmann H. Glucocorticold regulation of mouse mammary tumor virus: identification of a short essential DNA region. EMBO J. 1983; 2: 1423–1429
   PubMedGoogle Scholar
• Hynes N., van Ooyen A. J. J., Kennedy N., Herrlich P., Ponta H., Groner B. Subfragments of the large terminal repeat cause glucocorticoid-responsive expression of mouse mammary tumor virus and of an adjacent gene. Proc. Natl. Acad. Sci. USA 1983; 80: 3637–3641
   PubMedGoogle Scholar
• Majors J., Varmus H. E. A small region of the mouse mammary tumor virus long terminal repeat confers glucocorticoid hormone regulation on a linked heterologous gene. Proc. Natl. Acad. Sci. USA 1983b; 80: 5866–5870
   PubMedGoogle Scholar
• Scheidereit C., Geisse S., Westphal H. M., Beato M. The glucocorticoid receptor binds to defined nucleotide sequences near the promoter of mouse mammary tumor virus. Nature 1983; 304: 749–751
   PubMed Web of Science ®Google Scholar
• Gowland P. L., Buetti E. Mutations in the Hormone Regulatory Element of Mouse Mammary Tumor Virus Differentially Affect the Response to Progestins, Androgens, and Glucocorticoids. Mol. Cell. Biol. 1989; 9: 3999–4008
   PubMedGoogle Scholar
• Wellinger R., Garcia M., Vessaz A. L., Diggelmann H. Exogenous mouse mammary tumor virus proviral DNA isolated from a kidney adenocarcinoma contains alterations in the U3 region of the long terminal repeat. J. Virol. 1986; 60: 1–11
   PubMedGoogle Scholar
• Ball J. K., Diggelmann H., Dekaban G. A., Grossi G., Semmler R., Waight P. A., Fletcher R. F. Alterations in the U3 region of the LTR of an infectious thymotropic type B retrovirus. J. Virol. 1988; 62: 2985–2993
   PubMedGoogle Scholar
• Acha-Orbea H., Shakhov A. N., Scarpellino L., Kolb E., Müller V., Vessaz-Shaw A., Fuchs R., Blöchlinger K., Rollini P., Billotte J., Sarafidou M., MacDonald H. R., Diggelmann H. Clonal deletion of V-betal4 positive T cells in mammary tumor virus transgenic mice. Nature 1991; 350: 207–211
   PubMed Web of Science ®Google Scholar
• Choi Y., Kappler J. W., Marrack P. A superantigen encoded in the open reading frame of the 3′ long terminal repeat of mouse mammary tumor virus. Nature 1991; 350: 203–207
   PubMed Web of Science ®Google Scholar
• Kurjan J., Herskowitz I. Structure of a yeast pheromone gene (MFa): A putative alpha-factor precursor contains four tandem copies of mature alpha-factor. Cell 1982; 30: 933–943
   PubMed Web of Science ®Google Scholar
• Smith R. A., Duncan M. J., Moir D. T. Heterologous protein secretion from yeast. Science 1985; 229: 1219–1224
   PubMed Web of Science ®Google Scholar
• Woolford C. A., Daniels L. D., Park F. J., Jones E. W., Van Arsdell J. N., Innis M. A. The PEP4 gene encodes an aspartyl protease implicated in the posttranslational regulation of Saccharomyces cerevisiæ vacuolar hydrolases. Mol. Cell. Biol. 1984; 6: 2500–2510
   Google Scholar
• Ammerer G., Hunter C. P., Rothman J. H., Saari G. C., Valls L. A., Stevens T. PEP4 gene of Saccharomyces cerevisiæ encodes proteinase A, a vacuolar enzyme required for processing of vacuolar precursors. Mol. Cell. Biol. 1986; 6: 2490–2499
   PubMed Web of Science ®Google Scholar
• Kozak M. Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes. Cell 1986; 44: 283–292
   PubMed Web of Science ®Google Scholar
• Dobson M. J., Tuite M. F., Roberts N. A., Kingsman A. J., Kingsman S. M. Conservation of high efficiency promoter sequences in Saccharomyces cerevisiæ. Nucl. Acids Res. 1982; 10: 2625–2637
   PubMedGoogle Scholar
• Zsebo K. M., Hsieng-Sen L., Fieschko J. C., Goldstein L., Davis J., Duker K., Suggs S. V., Por-Hsiung L., Bitter G. A. Protein secretion from Saccharomyces cerevisiæ directed by the prepro-alpha-factor leader region. J. Biol. Chem. 1986; 261: 5858–5865
   PubMed Web of Science ®Google Scholar
• Garcia I., Sordat B., Rauccio-Farinon E., Dunand M., Kræhenbuhl J. P., Diggelmann H. Establishment of two rabbit mammary epithelial cell lines with distinct oncogenic potential and differentiated phenotype after microinjection of transforming genes. Mol. Cell. Biol. 1986; 6: 1974–1982
   PubMedGoogle Scholar
• Gritz L., Davies J. Plasmid-coded hygromycin B resistance: the sequence of hygromycin B phosphotransferase gene and its expression in Escherichia coli and Saccharomyces cerevisiæ. Gene 1983; 25: 179–188
   PubMed Web of Science ®Google Scholar
• Blochlinger K., Diggelmann H. Hygromycin B phosphotransferase as a selectable marker for DNA transfer experiments with higher eukaryotic cells. Mol. Cell. Biol. 1984; 4: 2929–2931
   PubMed Web of Science ®Google Scholar
• Brandt-Carlson C., Butel J. Detection and Characterization of a Glycoprotein Encoded by the Mouse Mammary Tumor Virus Long Terminal Repeat Gene. J. Virol. 1991; 65: 6051–6060
   PubMedGoogle Scholar
• Racevskis J. Expression of the protein product of the mouse mammary tumor virus long terminal repeat gene in phorbol ester-treated mouse T-cell-leukemia cells. J. Virol. 1986; 58: 441–449
   PubMedGoogle Scholar
• Sharon N. Glycoproteins. Trends in Biochem. Sci. 1984; 9: 198–202
   Web of Science ®Google Scholar
• Dyson P. J., Knight A. M., Fairchild S., Simpson E., Tomonari K. Genes encoding ligands for deletion of Vbetall T cells cosegregate with mammary tumor virus genomes. Nature 1991; 349: 531–532
   PubMed Web of Science ®Google Scholar
• Frankel W. N., Rudy C., Coffin J. M., Huber B. T. Linkage of Mls genes to endogenous mammary tumor virus of inbred mice. Nature 1991; 349: 526–528
   PubMed Web of Science ®Google Scholar
• Marrack P., Kushnir E., Kappler J. A maternally inherited superantigen encoded by a mammary tumor virus. Nature 1991; 349: 524–526
   PubMed Web of Science ®Google Scholar
• Woodland D., Happ M. P., Gallob K. J., Palmer E. P. An endogenous retrovirus mediating deletion of alpha-beta T cells?. Nature, 349: 529–530
   Google Scholar
• Acha-Orbea H., Palmer E. Mls-a retrovirus exploits the immune system. Immunology Today 1991; 12: 356–361
   PubMedGoogle Scholar