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. 1988 Jun;62(6):1907–1916. doi: 10.1128/jvi.62.6.1907-1916.1988

Activation of thermosensitive RNA splicing and production of a heat-labile P85gag-mos kinase by the introduction of a specific deletion in murine sarcoma virus-124 DNA.

M de Mars 1, P E Cizdziel 1, E C Murphy Jr 1
PMCID: PMC253273  PMID: 2835496

Abstract

Murine sarcoma virus ts110 (MuSVts110) is a conditionally transformation-defective MuSV mutant lacking 1,487 bases found in its wild-type parent, MuSV-349 (MuSV-124). Expression of the MuSVts110 v-mos gene product, P85gag-mos, requires splicing of the viral transcript to align the gag and mos genes in frame. However, this splice event is restricted to growth temperatures of 33 degrees C or lower. No splicing of the viral RNA, no production of P85gag-mos, and, hence, no cell transformation is observed at growth temperatures above 33 degrees C. To determine whether thermosensitive splicing is an intrinsic property of To determine whether thermosensitive splicing is an intrinsic property of MuSVts110 RNA specified by the 1,487-base deletion or a result of a cellular defect, we examined an "equivalent" or MuSVts110 DNA (designated ts32 DNA) constructed by combining wild-type MuSV-124 DNA fragments with a synthetic oligonucleotide to yield an otherwise wild-type viral DNA containing the same 1,487-base deletion as authentic MuSVts110. As observed in control cells (6m2 cells) infected with the authentic MuSVts110 virus, NIH 3T3 cells transfected with ts32 DNA appeared morphologically transformed when grown at 33 degrees C, but were converted to a more normal, flattened shape within a few hours of a shift to 39 degrees C. In concert with these morphological changes, both the processing of the ts32 RNA transcripts and the production of ts32 p85gag-mos kinase were found to be optimal at growth temperatures from 28 to 33 degrees C, but dramatically reduced at 37 to 41 degrees C. Like authentic P85gag-mos, the ts32 P85gag-mos kinase activity was rapidly inactivated by brief exposure to 39 degrees C. These results suggested that the MuSVts110 equivalent is functionally indistinguishable from authentic MuSVts110 and that the novel temperature-sensitive splicing of MuSVts110 transcripts is specified by an intrinsic property of the viral RNA.

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Selected References

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  1. Arlinghaus R. B. The ts110 Moloney mouse sarcoma virus system: gag-mos gene products and cellular transformation. J Gen Virol. 1985 Sep;66(Pt 9):1845–1853. doi: 10.1099/0022-1317-66-9-1845. [DOI] [PubMed] [Google Scholar]
  2. Ball J., McCarter J. A., Sunderland S. M. Evidence for helper independent murine sarcoma virus. I. Segregation of replication-defective and transformation-defective viruses. Virology. 1973 Nov;56(1):268–284. doi: 10.1016/0042-6822(73)90305-x. [DOI] [PubMed] [Google Scholar]
  3. Biggart N. W., Gallick G. E., Murphy E. C., Jr Nickel-induced heritable alterations in retroviral transforming gene expression. J Virol. 1987 Aug;61(8):2378–2388. doi: 10.1128/jvi.61.8.2378-2388.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Biggart N. W., Murphy E. C., Jr Analysis of metal-induced mutations altering the expression or structure of a retroviral gene in a mammalian cell line. Mutat Res. 1988 Mar;198(1):115–129. doi: 10.1016/0027-5107(88)90047-4. [DOI] [PubMed] [Google Scholar]
  5. Blair D. G., Hull M. A., Finch E. A. The isolation and preliminary characterization of temperature-sensitive transformation mutants of Moloney sarcoma virus. Virology. 1979 Jun;95(2):303–316. doi: 10.1016/0042-6822(79)90486-0. [DOI] [PubMed] [Google Scholar]
  6. Brown R. L., Horn J. P., Wible L., Arlinghaus R. B., Brinkley B. R. Sequence of events in the transformation process in cells infected with a temperature-sensitive transformation mutant of Moloney murine sarcoma virus. Proc Natl Acad Sci U S A. 1981 Sep;78(9):5593–5597. doi: 10.1073/pnas.78.9.5593. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Chen E. Y., Seeburg P. H. Supercoil sequencing: a fast and simple method for sequencing plasmid DNA. DNA. 1985 Apr;4(2):165–170. doi: 10.1089/dna.1985.4.165. [DOI] [PubMed] [Google Scholar]
  8. Cizdziel P. E., Nash M. A., Blair D. G., Murphy E. C., Jr Molecular basis underlying phenotypic revertants of Moloney murine sarcoma virus MuSVts110. J Virol. 1986 Jan;57(1):310–317. doi: 10.1128/jvi.57.1.310-317.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Cizdziel P. E., de Mars M., Murphy E. C., Jr Exploitation of a thermosensitive splicing event to study pre-mRNA splicing in vivo. Mol Cell Biol. 1988 Apr;8(4):1558–1569. doi: 10.1128/mcb.8.4.1558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Gallick G. E., Hamelin R., Maxwell S., Duyka D., Arlinghaus R. B. The gag-mos hybrid protein of ts110 Moloney murine sarcoma virus: variation of gene expression with temperature. Virology. 1984 Dec;139(2):366–374. doi: 10.1016/0042-6822(84)90382-9. [DOI] [PubMed] [Google Scholar]
  11. Graham F. L., van der Eb A. J. A new technique for the assay of infectivity of human adenovirus 5 DNA. Virology. 1973 Apr;52(2):456–467. doi: 10.1016/0042-6822(73)90341-3. [DOI] [PubMed] [Google Scholar]
  12. Hamelin R., Brizzard B. L., Nash M. A., Murphy E. C., Jr, Arlinghaus R. B. Temperature-sensitive viral RNA expression in Moloney murine sarcoma virus ts110-infected cells. J Virol. 1985 Feb;53(2):616–623. doi: 10.1128/jvi.53.2.616-623.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hamelin R., Kabat K., Blair D., Arlinghaus R. B. Temperature-sensitive splicing defect of ts110 Moloney murine sarcoma virus is virus encoded. J Virol. 1986 Jan;57(1):301–309. doi: 10.1128/jvi.57.1.301-309.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Horn J. P., Wood T. G., Murphy E. C., Jr, Blair D. G., Arlinghaus R. B. A selective temperature-sensitive defect in viral RNA expression in cells infected with a ts transformation mutant of murine sarcoma virus. Cell. 1981 Jul;25(1):37–46. doi: 10.1016/0092-8674(81)90229-4. [DOI] [PubMed] [Google Scholar]
  15. Hwang L. H., Gilboa E. Expression of genes introduced into cells by retroviral infection is more efficient than that of genes introduced into cells by DNA transfection. J Virol. 1984 May;50(2):417–424. doi: 10.1128/jvi.50.2.417-424.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Junghans R. P., Murphy E. C., Jr, Arlinghaus R. B. Electron microscopic analysis of ts1 10 Moloney mouse sarcoma virus, a variant of wild-type virus with two RNAs containing large deletions. J Mol Biol. 1982 Oct 25;161(2):229–250. doi: 10.1016/0022-2836(82)90150-4. [DOI] [PubMed] [Google Scholar]
  17. Kloetzer W. S., Maxwell S. A., Arlinghaus R. B. Further characterization of the P85gag-mos -associated protein kinase activity. Virology. 1984 Oct 15;138(1):143–155. doi: 10.1016/0042-6822(84)90154-5. [DOI] [PubMed] [Google Scholar]
  18. Kloetzer W. S., Maxwell S. A., Arlinghaus R. B. P85gag-mos encoded by ts110 Moloney murine sarcoma virus has an associated protein kinase activity. Proc Natl Acad Sci U S A. 1983 Jan;80(2):412–416. doi: 10.1073/pnas.80.2.412. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Lazo P. A., Prasad V., Tsichlis P. N. Splice acceptor site for the env message of Moloney murine leukemia virus. J Virol. 1987 Jun;61(6):2038–2041. doi: 10.1128/jvi.61.6.2038-2041.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Mann R., Baltimore D. Varying the position of a retrovirus packaging sequence results in the encapsidation of both unspliced and spliced RNAs. J Virol. 1985 May;54(2):401–407. doi: 10.1128/jvi.54.2.401-407.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Mann R., Mulligan R. C., Baltimore D. Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus. Cell. 1983 May;33(1):153–159. doi: 10.1016/0092-8674(83)90344-6. [DOI] [PubMed] [Google Scholar]
  22. Maxwell S. A., Arlinghaus R. B. Use of site-specific antipeptide antibodies to perturb the serine kinase catalytic activity of p37mos. J Virol. 1985 Sep;55(3):874–876. doi: 10.1128/jvi.55.3.874-876.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Nash M., Brown N. V., Wong J. L., Arlinghaus R. B., Murphy E. C., Jr S1 nuclease mapping of viral RNAs from a temperature-sensitive transformation mutant of murine sarcoma virus. J Virol. 1984 May;50(2):478–488. doi: 10.1128/jvi.50.2.478-488.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Padgett R. A., Grabowski P. J., Konarska M. M., Seiler S., Sharp P. A. Splicing of messenger RNA precursors. Annu Rev Biochem. 1986;55:1119–1150. doi: 10.1146/annurev.bi.55.070186.005351. [DOI] [PubMed] [Google Scholar]
  25. Rao R. N., Rogers S. G. Plasmid pKC7: a vector containing ten restriction endonuclease sites suitable for cloning DNA segments. Gene. 1979 Sep;7(1):79–82. doi: 10.1016/0378-1119(79)90044-1. [DOI] [PubMed] [Google Scholar]
  26. Singh L., Jones K. W. The use of heparin as a simple cost-effective means of controlling background in nucleic acid hybridization procedures. Nucleic Acids Res. 1984 Jul 25;12(14):5627–5638. doi: 10.1093/nar/12.14.5627. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
  28. Van Beveren C., van Straaten F., Galleshaw J. A., Verma I. M. Nucleotide sequence of the genome of a murine sarcoma virus. Cell. 1981 Nov;27(1 Pt 2):97–108. doi: 10.1016/0092-8674(81)90364-0. [DOI] [PubMed] [Google Scholar]

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