Abstract
MOPC-460 mouse plasmacytoma cells produce intracellular A-type particles and extracellular oncornavirus-like particles ("myeloma-associated virus," abbreviated MAV). The genomes of these two particles are closely related. During attempts to establish infections with MOPC-460 extracellular particles, we isolated ecotropic and xenotropic infectious forms of murine leukemia virus. We have investigated the relation of these isolates to A-type particles and to MAV by nucleic acid hybridization. Using complementary DNA probes prepared from the two isolates, we found that these infectious murine leukemia viruses differ from A-type particles and from MAV. Moreover, we found that MAV is the predominant extracellular component: the ecotropic and xenotropic forms of murine leukemia virus were present at only low levels (less than 5%) in MAV preparations. Neither the SC-1 cells infected with ectropic murine leukemia virus nor the mink cells infected with xenotropic murine leukemia virus showed any A-type particles in their cytoplasm when examined by electron microscopy. Our inability to demonstrate infection by the A-type particle-related component, MAV, suggests that these may be defective.
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Selected References
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- Aoki T., Potter M., Sturm M. M. Analysis by immunoelectron microscopy of type-C viruses associated with primary and short-term transplanted mouse plasma cell tumors. J Natl Cancer Inst. 1973 Nov;51(5):1609–1617. doi: 10.1093/jnci/51.5.1609. [DOI] [PubMed] [Google Scholar]
- Aoki T., Takahashi T. Viral and cellular surface antigens of murine leukemias and myelomas. Serological analysis by immunoelectron microscopy. J Exp Med. 1972 Mar 1;135(3):443–457. doi: 10.1084/jem.135.3.443. [DOI] [PMC free article] [PubMed] [Google Scholar]
- August J. T., Bolognesi D. P., Fleissner E., Gilden R. V., Nowinski R. C. A proposed nomenclature for the virion proteins of oncogenic RNA viruses. Virology. 1974 Aug;60(2):595–600. doi: 10.1016/0042-6822(74)90356-0. [DOI] [PubMed] [Google Scholar]
- Baluda M. A., Shoyab M., Markham P. D., Evans R. M., Droham W. N. Base sequence complexity of 35S avian myeloblastosis virus RNA determined by molecular hybridization kinetics. Cold Spring Harb Symp Quant Biol. 1975;39(Pt 2):869–874. doi: 10.1101/sqb.1974.039.01.101. [DOI] [PubMed] [Google Scholar]
- Besmer P., Olshevsky U., Baltimore D., Dolberg D., Fan H. Virus-like 30S RNA in mouse cells. J Virol. 1979 Mar;29(3):1168–1176. doi: 10.1128/jvi.29.3.1168-1176.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bishop J. O., Morton J. G., Rosbash M., Richardson M. Three abundance classes in HeLa cell messenger RNA. Nature. 1974 Jul 19;250(463):199–204. doi: 10.1038/250199a0. [DOI] [PubMed] [Google Scholar]
- Callahan R., Benveniste R. E., Lieber M. M., Todaro G. J. Nucleic acid homology of murine type-C viral genes. J Virol. 1974 Dec;14(6):1394–1403. doi: 10.1128/jvi.14.6.1394-1403.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chamberlin M. E., Galau G. A., Britten R. J., Davidson E. H. Studies on nucleic acid reassociation kinetics: V. Effects of disparity in tracer and driver fragment lengths. Nucleic Acids Res. 1978 Jun;5(6):2073–2094. doi: 10.1093/nar/5.6.2073. [DOI] [PMC free article] [PubMed] [Google Scholar]
- East J. L., Knesek J. E., Chan J. C., Dmochowski L. Quantitative nucleotide sequence relationships of mammalian RNA tumor viruses. J Virol. 1975 Jun;15(6):1396–1408. doi: 10.1128/jvi.15.6.1396-1408.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hall W. T., Hartley J. W., Sanford K. K. Characteristics of and relationship between C particles and intracisternal A particles in cloned cell strains. J Virol. 1968 Mar;2(3):238–247. doi: 10.1128/jvi.2.3.238-247.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hartley J. W., Rowe W. P. Clonal cells lines from a feral mouse embryo which lack host-range restrictions for murine leukemia viruses. Virology. 1975 May;65(1):128–134. doi: 10.1016/0042-6822(75)90013-6. [DOI] [PubMed] [Google Scholar]
- Hartley J. W., Rowe W. P., Huebner R. J. Host-range restrictions of murine leukemia viruses in mouse embryo cell cultures. J Virol. 1970 Feb;5(2):221–225. doi: 10.1128/jvi.5.2.221-225.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hartley J. W., Wolford N. K., Old L. J., Rowe W. P. A new class of murine leukemia virus associated with development of spontaneous lymphomas. Proc Natl Acad Sci U S A. 1977 Feb;74(2):789–792. doi: 10.1073/pnas.74.2.789. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hopkins N., Schindler J., Gottlieb P. D. Evidence for recombination between N- and B-tropic murine leukemia viruses. J Virol. 1977 Mar;21(3):1074–1078. doi: 10.1128/jvi.21.3.1074-1078.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krueger R. G. Host range studies of FLOPC-1 murine myeloma C particles. J Virol. 1975 Nov;16(5):1137–1145. doi: 10.1128/jvi.16.5.1137-1145.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Krueger R. G. Intracisternal A particles from FLOPC-1 BALB/c myeloma: presence of high-molecular-weight RNA and RNA-dependent DNA polymerase. J Virol. 1976 May;18(2):745–756. doi: 10.1128/jvi.18.2.745-756.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kuff E. L., Lueders K. K., Scolnick E. M. Nucleotide sequence relationship between intracisternal type A particles of Mus musculus and an endogenous retrovirus (M432) of Mus cervicolor. J Virol. 1978 Oct;28(1):66–74. doi: 10.1128/jvi.28.1.66-74.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kuff E. L., Wivel N. A., Lueders K. K. The extraction of intracisternal A-particles from a mouse plasma-cell tumor. Cancer Res. 1968 Oct;28(10):2137–2148. [PubMed] [Google Scholar]
- Linial M., Medeiros E., Hayward W. S. An avian oncovirus mutant (SE 21Q1b) deficient in genomic RNA: biological and biochemical characterization. Cell. 1978 Dec;15(4):1371–1381. doi: 10.1016/0092-8674(78)90062-4. [DOI] [PubMed] [Google Scholar]
- Potter M. Immunoglobulin-producing tumors and myeloma proteins of mice. Physiol Rev. 1972 Jul;52(3):631–719. doi: 10.1152/physrev.1972.52.3.631. [DOI] [PubMed] [Google Scholar]
- Robertson D. L., Baenziger N. L., Dobbertin D. C., Thach R. E. Characterization of DNA polymerase and RNA associated with A-type particles from murine myeloma cells. J Virol. 1975 Feb;15(2):407–415. doi: 10.1128/jvi.15.2.407-415.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robertson D. L., Jhabvala P. S., Godefroy-Colburn T., Thach R. E. Characterization of the proteins of intracisternal type A and extracellular oncornavirus-like particles produced by MOPC-460 myeloma cells. J Virol. 1979 Oct;32(1):114–122. doi: 10.1128/jvi.32.1.114-122.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Robertson D. L., Yau P., Dobbertin D. C., Sweeney T. K., Thach S. S., Brendler T., Thach R. E. Relationships between intracisternal type A and extracellular oncornavirus-like particles produced in murine MOPC-460 myeloma cells. J Virol. 1976 Apr;18(1):344–355. doi: 10.1128/jvi.18.1.344-355.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rowe W. P., Pugh W. E., Hartley J. W. Plaque assay techniques for murine leukemia viruses. Virology. 1970 Dec;42(4):1136–1139. doi: 10.1016/0042-6822(70)90362-4. [DOI] [PubMed] [Google Scholar]
- Stephenson J. R., Tronick S. R., Aaronson S. A. Isolation from BALB/c mouse cells of a structural polypeptide of a third endogenous type C virus. Cell. 1974 Dec;3(4):347–353. doi: 10.1016/0092-8674(74)90049-x. [DOI] [PubMed] [Google Scholar]
- Syrewicz J. J., Naso R. B., Wang C. S., Arlinghaus R. B. Purification of large amounts of murine ribonucleic acid tumor viruses produced in roller bottle cultures. Appl Microbiol. 1972 Sep;24(3):488–494. doi: 10.1128/am.24.3.488-494.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Volkman L. E., Krueger R. G. Characterization of C-type particles produced by a tissue culture-adapted murine myeloma. J Virol. 1973 Dec;12(6):1589–1597. doi: 10.1128/jvi.12.6.1589-1597.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Watson J., Ralph P., Sarkar S., Cohn M. Leukemia viruses associated with mouse myeloma cells. Proc Natl Acad Sci U S A. 1970 Jun;66(2):344–351. doi: 10.1073/pnas.66.2.344. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wetmur J. G. Hybridization and renaturation kinetics of nucleic acids. Annu Rev Biophys Bioeng. 1976;5:337–361. doi: 10.1146/annurev.bb.05.060176.002005. [DOI] [PubMed] [Google Scholar]
- Wivel N. A., Smith G. H. Distribution of intracisternal A-particles in a variety of normal and neoplastic mouse tissues. Int J Cancer. 1971 Jan 15;7(1):167–175. doi: 10.1002/ijc.2910070119. [DOI] [PubMed] [Google Scholar]
- Wong-Staal F., Reitz M. S., Jr, Trainor C. D., Gallo R. C. Murine intracisternal type A particles: a biochemical characterization. J Virol. 1975 Oct;16(4):887–896. doi: 10.1128/jvi.16.4.887-896.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yang S. S., Wivel N. A. Analysis of high-molecular-weight ribonucleic acid associated with intracisternal A particles. J Virol. 1973 Feb;11(2):287–298. doi: 10.1128/jvi.11.2.287-298.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yang S. S., Wivel N. A. Characterization of an endogenous RNA-dependent DNA polymerase associated with murine intracisternal A particles. J Virol. 1974 Mar;13(3):712–720. doi: 10.1128/jvi.13.3.712-720.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
