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Journal of Virology logoLink to Journal of Virology
. 1997 Feb;71(2):1635–1639. doi: 10.1128/jvi.71.2.1635-1639.1997

Expression and maturation of human foamy virus Gag precursor polypeptides.

M L Giron 1, S Colas 1, J Wybier 1, F Rozain 1, R Emanoil-Ravier 1
PMCID: PMC191222  PMID: 8995691

Abstract

In this report, we address the processing of the Gag polypeptides of human foamy virus previously reported to be atypical. In the cytoplasm or the nucleus of infected cells as well as in free virus particles, two Gag precursor polypeptides were identified at approximately 72 and 68 kDa, p72 giving rise to p68 by a maturation process. Efficient maturation of Gag precursors was observed only in two situations: (i) during the early steps of virus adsorption and (ii) under experimental conditions, including treatment with DNase I, known to dissociate actin polymers associated with high ionic strength and ionic detergents. Rather than being a defective viral protease function, an association of Gag precursors with a cytoskeleton network might be responsible for the low rate of Gag protein maturation through inhibition of their cleavage by the protease.

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Selected References

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  1. Achong B. G., Mansell P. W., Epstein M. A., Clifford P. An unusual virus in cultures from a human nasopharyngeal carcinoma. J Natl Cancer Inst. 1971 Feb;46(2):299–307. [PubMed] [Google Scholar]
  2. Aguzzi A., Wagner E. F., Netzer K. O., Bothe K., Anhauser I., Rethwilm A. Human foamy virus proteins accumulate in neurons and induce multinucleated giant cells in the brain of transgenic mice. Am J Pathol. 1993 Apr;142(4):1061–1071. [PMC free article] [PubMed] [Google Scholar]
  3. Bartholomä A., Muranyi W., Flügel R. M. Bacterial expression of the capsid antigen domain and identification of native gag proteins in spumavirus-infected cells. Virus Res. 1992 Apr;23(1-2):27–38. doi: 10.1016/0168-1702(92)90065-h. [DOI] [PubMed] [Google Scholar]
  4. Ben-Ze'ev A., Horowitz M., Skolnik H., Abulafia R., Laub O., Aloni Y. The metabolism of SV40 RNA is associated with the cytoskeletal framework. Virology. 1981 Jun;111(2):475–487. doi: 10.1016/0042-6822(81)90350-0. [DOI] [PubMed] [Google Scholar]
  5. Bukrinsky M. I., Haggerty S., Dempsey M. P., Sharova N., Adzhubel A., Spitz L., Lewis P., Goldfarb D., Emerman M., Stevenson M. A nuclear localization signal within HIV-1 matrix protein that governs infection of non-dividing cells. Nature. 1993 Oct 14;365(6447):666–669. doi: 10.1038/365666a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bukrinsky M. I., Sharova N., Dempsey M. P., Stanwick T. L., Bukrinskaya A. G., Haggerty S., Stevenson M. Active nuclear import of human immunodeficiency virus type 1 preintegration complexes. Proc Natl Acad Sci U S A. 1992 Jul 15;89(14):6580–6584. doi: 10.1073/pnas.89.14.6580. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gallay P., Swingler S., Aiken C., Trono D. HIV-1 infection of nondividing cells: C-terminal tyrosine phosphorylation of the viral matrix protein is a key regulator. Cell. 1995 Feb 10;80(3):379–388. doi: 10.1016/0092-8674(95)90488-3. [DOI] [PubMed] [Google Scholar]
  8. Giron M. L., Rozain F., Debons-Guillemin M. C., Canivet M., Peries J., Emanoil-Ravier R. Human foamy virus polypeptides: identification of env and bel gene products. J Virol. 1993 Jun;67(6):3596–3600. doi: 10.1128/jvi.67.6.3596-3600.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hiller G., Weber K., Schneider L., Parajsz C., Jungwirth C. Interaction of assembled progeny pox viruses with the cellular cytoskeleton. Virology. 1979 Oct 15;98(1):142–153. doi: 10.1016/0042-6822(79)90533-6. [DOI] [PubMed] [Google Scholar]
  10. Hooks J. J., Gibbs C. J., Jr The foamy viruses. Bacteriol Rev. 1975 Sep;39(3):169–185. doi: 10.1128/br.39.3.169-185.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Höner B., Shoeman R. L., Traub P. Human immunodeficiency virus type 1 protease microinjected into cultured human skin fibroblasts cleaves vimentin and affects cytoskeletal and nuclear architecture. J Cell Sci. 1991 Dec;100(Pt 4):799–807. doi: 10.1242/jcs.100.4.799. [DOI] [PubMed] [Google Scholar]
  12. Keller A., Garrett E. D., Cullen B. R. The Bel-1 protein of human foamy virus activates human immunodeficiency virus type 1 gene expression via a novel DNA target site. J Virol. 1992 Jun;66(6):3946–3949. doi: 10.1128/jvi.66.6.3946-3949.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Keller A., Partin K. M., Löchelt M., Bannert H., Flügel R. M., Cullen B. R. Characterization of the transcriptional trans activator of human foamy retrovirus. J Virol. 1991 May;65(5):2589–2594. doi: 10.1128/jvi.65.5.2589-2594.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Konvalinka J., Löchelt M., Zentgraf H., Flügel R. M., Kräusslich H. G. Active foamy virus proteinase is essential for virus infectivity but not for formation of a Pol polyprotein. J Virol. 1995 Nov;69(11):7264–7268. doi: 10.1128/jvi.69.11.7264-7268.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Kögel D., Aboud M., Flügel R. M. Mutational analysis of the reverse transcriptase and ribonuclease H domains of the human foamy virus. Nucleic Acids Res. 1995 Jul 25;23(14):2621–2625. doi: 10.1093/nar/23.14.2621. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Lee A. H., Lee K. J., Kim S., Sung Y. C. Transactivation of human immunodeficiency virus type 1 long terminal repeat-directed gene expression by the human foamy virus bel1 protein requires a specific DNA sequence. J Virol. 1992 May;66(5):3236–3240. doi: 10.1128/jvi.66.5.3236-3240.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Luftig R. B., Lupo L. D. Viral interactions with the host-cell cytoskeleton: the role of retroviral proteases. Trends Microbiol. 1994 May;2(5):178–182. doi: 10.1016/0966-842x(94)90669-6. [DOI] [PubMed] [Google Scholar]
  18. Löchelt M., Muranyi W., Flügel R. M. Human foamy virus genome possesses an internal, Bel-1-dependent and functional promoter. Proc Natl Acad Sci U S A. 1993 Aug 1;90(15):7317–7321. doi: 10.1073/pnas.90.15.7317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Löchelt M., Zentgraf H., Flügel R. M. Construction of an infectious DNA clone of the full-length human spumaretrovirus genome and mutagenesis of the bel 1 gene. Virology. 1991 Sep;184(1):43–54. doi: 10.1016/0042-6822(91)90820-2. [DOI] [PubMed] [Google Scholar]
  20. Mannherz H. G., Leigh J. B., Leberman R., Pfrang H. A specific 1:1 G-actin:DNAase i complex formed by the action of DNAase I on F-actin. FEBS Lett. 1975 Dec 1;60(1):34–38. doi: 10.1016/0014-5793(75)80412-1. [DOI] [PubMed] [Google Scholar]
  21. Melki R., Gaudin Y., Blondel D. Interaction between tubulin and the viral matrix protein of vesicular stomatitis virus: possible implications in the viral cytopathic effect. Virology. 1994 Jul;202(1):339–347. doi: 10.1006/viro.1994.1350. [DOI] [PubMed] [Google Scholar]
  22. Muranyi W., Flügel R. M. Analysis of splicing patterns of human spumaretrovirus by polymerase chain reaction reveals complex RNA structures. J Virol. 1991 Feb;65(2):727–735. doi: 10.1128/jvi.65.2.727-735.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Netzer K. O., Rethwilm A., Maurer B., ter Meulen V. Identification of the major immunogenic structural proteins of human foamy virus. J Gen Virol. 1990 May;71(Pt 5):1237–1241. doi: 10.1099/0022-1317-71-5-1237. [DOI] [PubMed] [Google Scholar]
  24. Netzer K. O., Schliephake A., Maurer B., Watanabe R., Aguzzi A., Rethwilm A. Identification of pol-related gene products of human foamy virus. Virology. 1993 Jan;192(1):336–338. doi: 10.1006/viro.1993.1039. [DOI] [PubMed] [Google Scholar]
  25. Oroszlan S., Luftig R. B. Retroviral proteinases. Curr Top Microbiol Immunol. 1990;157:153–185. doi: 10.1007/978-3-642-75218-6_6. [DOI] [PubMed] [Google Scholar]
  26. Pahl A., Flügel R. M. Endonucleolytic cleavages and DNA-joining activities of the integration protein of human foamy virus. J Virol. 1993 Sep;67(9):5426–5434. doi: 10.1128/jvi.67.9.5426-5434.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Pollard T. D., Cooper J. A. Actin and actin-binding proteins. A critical evaluation of mechanisms and functions. Annu Rev Biochem. 1986;55:987–1035. doi: 10.1146/annurev.bi.55.070186.005011. [DOI] [PubMed] [Google Scholar]
  28. Rethwilm A., Mori K., Maurer B., ter Meulen V. Transacting transcriptional activation of human spumaretrovirus LTR in infected cells. Virology. 1990 Apr;175(2):568–571. doi: 10.1016/0042-6822(90)90442-t. [DOI] [PubMed] [Google Scholar]
  29. Schliephake A. W., Rethwilm A. Nuclear localization of foamy virus Gag precursor protein. J Virol. 1994 Aug;68(8):4946–4954. doi: 10.1128/jvi.68.8.4946-4954.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Sen A., Todaro G. J. A murine sarcoma virus-associated protein kinase: interaction with actin and microtubular protein. Cell. 1979 Jun;17(2):347–356. doi: 10.1016/0092-8674(79)90161-2. [DOI] [PubMed] [Google Scholar]
  31. Sharova N., Bukrinskaya A. p17 and p17-containing gag precursors of input human immunodeficiency virus are transported into the nuclei of infected cells. AIDS Res Hum Retroviruses. 1991 Mar;7(3):303–306. doi: 10.1089/aid.1991.7.303. [DOI] [PubMed] [Google Scholar]
  32. Shoeman R. L., Höner B., Mothes E., Traub P. Potential role of the viral protease in human immunodeficiency virus type 1 associated pathogenesis. Med Hypotheses. 1992 Mar;37(3):137–150. doi: 10.1016/0306-9877(92)90071-j. [DOI] [PubMed] [Google Scholar]
  33. Shoeman R. L., Sachse C., Höner B., Mothes E., Kaufmann M., Traub P. Cleavage of human and mouse cytoskeletal and sarcomeric proteins by human immunodeficiency virus type 1 protease. Actin, desmin, myosin, and tropomyosin. Am J Pathol. 1993 Jan;142(1):221–230. [PMC free article] [PubMed] [Google Scholar]
  34. Tomasselli A. G., Hui J. O., Adams L., Chosay J., Lowery D., Greenberg B., Yem A., Deibel M. R., Zürcher-Neely H., Heinrikson R. L. Actin, troponin C, Alzheimer amyloid precursor protein and pro-interleukin 1 beta as substrates of the protease from human immunodeficiency virus. J Biol Chem. 1991 Aug 5;266(22):14548–14553. [PubMed] [Google Scholar]
  35. Venkatesh L. K., Yang C., Theodorakis P. A., Chinnadurai G. Functional dissection of the human spumaretrovirus transactivator identifies distinct classes of dominant-negative mutants. J Virol. 1993 Jan;67(1):161–169. doi: 10.1128/jvi.67.1.161-169.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]

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