Abstract
Spontaneous, transplantable leukemias of DBA/2 mice express an antigen (ML) which cross-reacts with antigens of murine mammary tumor virus (MuMTV). The MuMTV cross-reactive antigen of the DBA/2 leukemias (ML cells) was found to be a glycoprotein of 78,000 molecular weight containing antigenic determinants of the major MuMTV glycoprotein gp52. No MuMTV particles were produced by the ML cells, although they did contain type A particles--the pronucleocapsids of MuMTV. The ML antigen appeared to be an aberrant form of the intracellular MuMTV env precursor molecular prgp70, which was not processed properly but instead acquired extra carbohydrate groups and was expressed in uncleaved form on the cell surface. Isolation of MuMTV core protein p28 from the leukemic cells and subsequent tryptic peptide mapping analysis showed that the p28 from leukemia cells differed from the p28 of MuMTV isolated from DBA/2 mouse milk. These observations indicate that the MuMTV expressed in DBA/2 leukemic spleen cells is of a different strain than the virus secreted in lactating mammary glands of DBA/2 mice and probably represents the expression of an endogenous DBA/2 provirus.
Full text
PDF









Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Calafat J., Buijs F., Hageman P. C., Links J., Hilgers J., Hekman A. Distribution of virus particles and mammary tumor virus antigens in mouse mammary tumors, transformed BALB-c mouse kidney cells, and GR ascites leukemia cells. J Natl Cancer Inst. 1974 Oct;53(4):977–992. doi: 10.1093/jnci/53.4.977. [DOI] [PubMed] [Google Scholar]
- Cohen J. C., Varmus H. E. Endogenous mammary tumour virus DNA varies among wild mice and segregates during inbreeding. Nature. 1979 Mar 29;278(5703):418–423. doi: 10.1038/278418a0. [DOI] [PubMed] [Google Scholar]
- Dickson C., Atterwill M. Polyproteins related to the major core protein of mouse mammary tumor virus. J Virol. 1978 Jun;26(3):660–672. doi: 10.1128/jvi.26.3.660-672.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dickson C., Atterwill M. Structure and processing of the mouse mammary tumor virus glycoprotein precursor pr73env. J Virol. 1980 Aug;35(2):349–361. doi: 10.1128/jvi.35.2.349-361.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Elder J. H., Pickett R. A., 2nd, Hampton J., Lerner R. A. Radioiodination of proteins in single polyacrylamide gel slices. Tryptic peptide analysis of all the major members of complex multicomponent systems using microgram quantities of total protein. J Biol Chem. 1977 Sep 25;252(18):6510–6515. [PubMed] [Google Scholar]
- Gahmberg C. G. External labeling of human erythrocyte glycoproteins. Studies with galactose oxidase and fluorography. J Biol Chem. 1976 Jan 25;251(2):510–515. [PubMed] [Google Scholar]
- Hilgers J., Haverman J., Nusse R., van Blitterswijk W. J., Cleton F. J., Hageman P. C., van Nie P., Calafat J. Immunologic, virologic, and genetic aspects of mammary tumor virus-induced cell-surface antigens: presence of these antigens and the Thy 1.2 antigen on murine mammary gland and tumor cells. J Natl Cancer Inst. 1975 Jun;54(6):1323–1333. doi: 10.1093/jnci/54.6.1323. [DOI] [PubMed] [Google Scholar]
- Karande K. A., Joshi B. J., Talageri V. R., Dumaswala R. U., Ranadive K. J. Intracytoplasmic type A particles from mammary tumours and leukaemias of strain ICRC mice. Br J Cancer. 1979 Feb;39(2):132–142. doi: 10.1038/bjc.1979.23. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kennel S. J., Tsakeres F., Kelly P. A., Allison D. P. Defective C-type retrovirus particles secreted by L1210 leukemia cells. Cancer Res. 1978 Dec;38(12):4574–4579. [PubMed] [Google Scholar]
- Livingston D. M. Immunoaffinity chromatography of proteins. Methods Enzymol. 1974;34:723–731. doi: 10.1016/s0076-6879(74)34094-3. [DOI] [PubMed] [Google Scholar]
- Marcus S. L., Kopelman R., Sarkar N. H. Simultaneous purification of murine mammary tumor virus structural proteins: analysis of antigenic reactivities of native gp34 by radioimmunocompetition assays. J Virol. 1979 Aug;31(2):341–349. doi: 10.1128/jvi.31.2.341-349.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marcus S. L., Smith S. W., Racevskis J., Sarkar N. H. The relative hydrophobicity of oncornaviral structural proteins. Virology. 1978 May 15;86(2):398–412. doi: 10.1016/0042-6822(78)90080-6. [DOI] [PubMed] [Google Scholar]
- Massey R. J., Schochetman G. Gene order of mouse mammary tumor virus precusor polyproteins and their interaction leading to the formation of a virus. Virology. 1979 Dec;99(2):358–371. doi: 10.1016/0042-6822(79)90015-1. [DOI] [PubMed] [Google Scholar]
- Murray M. J., Kabat D. Genetic and sialylation sources of heterogeneity of the murine leukemia virus membrane envelope glycoproteins gp69/71. J Biol Chem. 1979 Feb 25;254(4):1340–1348. [PubMed] [Google Scholar]
- Nowinski R. C., Boyse E. A., Old L. J., Carswell E. A. Influence of mammary tumor virus infection on the acceptance or rejection of transplanted ML+ leukemias. Proc Soc Exp Biol Med. 1968 Jan;127(1):20–25. doi: 10.3181/00379727-127-32611. [DOI] [PubMed] [Google Scholar]
- Nusse R., Janssen H., de Vries L., Michalides R. Analysis of secondary modifications of mouse mammary tumor virus proteins by two-dimensional gel electrophoresis. J Virol. 1980 Aug;35(2):340–348. doi: 10.1128/jvi.35.2.340-348.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nusse R., van der Ploeg L., van Duijn L., Michalides R., Hilgers J. Impaired maturation of mouse mammary tumor virus precursor polypeptides in lymphoid leukemia cells, producing intracytoplasmic A particles and no extracellular B-type virions. J Virol. 1979 Oct;32(1):251–258. doi: 10.1128/jvi.32.1.251-258.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- O'Farrell P. H. High resolution two-dimensional electrophoresis of proteins. J Biol Chem. 1975 May 25;250(10):4007–4021. [PMC free article] [PubMed] [Google Scholar]
- Racevskis J., Karande K. A., Sarkar N. H. Precursor product relationship between intracytoplasmic A particle and murine mammary tumor virus core proteins established by tryptic peptide analysis. Virology. 1981 Feb;109(1):201–204. doi: 10.1016/0042-6822(81)90488-8. [DOI] [PubMed] [Google Scholar]
- Racevskis J., Sarkar N. H. Synthesis and processing of precursor polypeptides to murine mammary tumor virus structural proteins. J Virol. 1978 Jan;25(1):374–383. doi: 10.1128/jvi.25.1.374-383.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- STUECK B., BOYSE E. A., OLD L. J., CARSWELL E. A. ML: A NEW ANTIGEN FOUND IN LEUKAEMIAS AND MAMMARY TUMOURS OF THE MOUSE. Nature. 1964 Sep 5;203:1033–1034. doi: 10.1038/2031033a0. [DOI] [PubMed] [Google Scholar]
- Sarkar N. H., Dion A. S. Polypeptides of the mouse mammary tumor virus. I. Characterization of two group-specific antigens. Virology. 1975 Apr;64(2):471–491. doi: 10.1016/0042-6822(75)90125-7. [DOI] [PubMed] [Google Scholar]
- Schochetman G., Fine D. L., Massey R. J. Mouse mammary tumor virus and murine leukemia virus cell surface antigens on virus producer and nonproducer mammary epithelial tumor cells. Virology. 1978 Jul 15;88(2):379–383. doi: 10.1016/0042-6822(78)90294-5. [DOI] [PubMed] [Google Scholar]
- Schochetman G., Fine D. L., Massey R. J. Mouse mammary tumor virus and murine leukemia virus cell surface antigens on virus producer and nonproducer mammary epithelial tumor cells. Virology. 1978 Jul 15;88(2):379–383. doi: 10.1016/0042-6822(78)90294-5. [DOI] [PubMed] [Google Scholar]
- Schultz A. M., Rabin E. H., Oroszlan S. Post-translational modification of Rauscher leukemia virus precursor polyproteins encoded by the gag gene. J Virol. 1979 Apr;30(1):255–266. doi: 10.1128/jvi.30.1.255-266.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sheffield J. B., Zacharchuk C. M., Taraschi N., Daly T. M. Effect of trypsin on mouse mammary tumor virus. J Virol. 1976 Jul;19(1):255–266. doi: 10.1128/jvi.19.1.255-266.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith G. H. Evidence for a precursor-product relationship between intracytoplasmic A particles and mouse mammary tumour virus cores. J Gen Virol. 1978 Oct;41(1):193–200. doi: 10.1099/0022-1317-41-1-193. [DOI] [PubMed] [Google Scholar]
- Tanaka H. Precursor-product relationship between nonglycosylated polypeptides of A and B particles of mouse mammary tumor virus. Virology. 1977 Feb;76(2):835–850. doi: 10.1016/0042-6822(77)90263-x. [DOI] [PubMed] [Google Scholar]
- Vaidya A. B., Long C. A., Sheffield J. B., Tamura A., Tanaka H. Murine mammary tumor virus deficient in the major glycoprotein: biochemical and biological studies on virions produced by a lymphoma cell line. Virology. 1980 Jul 30;104(2):279–293. doi: 10.1016/0042-6822(80)90333-5. [DOI] [PubMed] [Google Scholar]
- Van Blitterswijk W. J., Emmelot P., Hilgers J., Kamlag D., Nusse R., Feltkamp C. A. Quantitation of virus-induced (MLr) and normal (Thy.1.2) cell surface antigens in isolated plasma membranes and the extracellular ascites fluid of mouse leukemia cells. Cancer Res. 1975 Oct;35(10):2743–2751. [PubMed] [Google Scholar]
- Witte O. N., Weissman I. L. Oncornavirus budding: kinetics of formation and utilization of viral membrane glycoprotein. Virology. 1976 Feb;69(2):464–473. doi: 10.1016/0042-6822(76)90477-3. [DOI] [PubMed] [Google Scholar]
- Yang J., Tang R., Nandi S. Identification of the mammary tumor virus envelope glycoprotein (gp52) on mouse mammary epithelial cell surface. Biochem Biophys Res Commun. 1977 Jun 20;76(4):1044–1050. doi: 10.1016/0006-291x(77)90961-5. [DOI] [PubMed] [Google Scholar]
- Zak-Nejmark T., Steuden J., Radzikowski C. Mammary leukaemia (ML) antigen isolated from L 1210 leukaemia cells. Int J Cancer. 1978 Apr 15;21(4):490–495. doi: 10.1002/ijc.2910210415. [DOI] [PubMed] [Google Scholar]






