Skip to main content
Journal of Virology logoLink to Journal of Virology
. 1997 May;71(5):3466–3473. doi: 10.1128/jvi.71.5.3466-3473.1997

RNA-protein interactions: involvement of NS3, NS5, and 3' noncoding regions of Japanese encephalitis virus genomic RNA.

C J Chen 1, M D Kuo 1, L J Chien 1, S L Hsu 1, Y M Wang 1, J H Lin 1
PMCID: PMC191493  PMID: 9094618

Abstract

The mechanism of replication of the flavivirus Japanese encephalitis virus (JEV) is not well known. The structures at the 3' end of the viral genome are highly conserved among divergent flaviviruses, suggesting that they may function as cis-acting signals for RNA replication and, as such, might specifically bind to cellular or viral proteins. UV cross-linking experiments were performed to identify the proteins that bind with the JEV plus-strand 3' noncoding region (NCR). Two proteins, p71 and p110, from JEV-infected but not from uninfected cell extracts were shown to bind specifically to the plus-strand 3' NCR. The quantities of these binding proteins increased during the course of JEV infection and correlated with the levels of JEV RNA synthesis in cell extracts. UV cross-linking coupled with Western blot and immunoprecipitation analysis showed that the p110 and p71 proteins were JEV NS5 and NS3, respectively, which are proposed as components of the RNA replicase. The putative stem-loop structure present within the plus-strand 3' NCR was required for the binding of these proteins. Furthermore, both proteins could interact with each other and form a protein-protein complex in vivo. These findings suggest that the 3' NCR of JEV genomic RNA may form a replication complex together with NS3 and NS5; this complex may be involved in JEV minus-strand RNA synthesis.

Full Text

The Full Text of this article is available as a PDF (1.2 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Andino R., Rieckhof G. E., Baltimore D. A functional ribonucleoprotein complex forms around the 5' end of poliovirus RNA. Cell. 1990 Oct 19;63(2):369–380. doi: 10.1016/0092-8674(90)90170-j. [DOI] [PubMed] [Google Scholar]
  2. Bartholomeusz A. I., Wright P. J. Synthesis of dengue virus RNA in vitro: initiation and the involvement of proteins NS3 and NS5. Arch Virol. 1993;128(1-2):111–121. doi: 10.1007/BF01309792. [DOI] [PubMed] [Google Scholar]
  3. Barton D. J., Sawicki S. G., Sawicki D. L. Solubilization and immunoprecipitation of alphavirus replication complexes. J Virol. 1991 Mar;65(3):1496–1506. doi: 10.1128/jvi.65.3.1496-1506.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Behrens S. E., Tomei L., De Francesco R. Identification and properties of the RNA-dependent RNA polymerase of hepatitis C virus. EMBO J. 1996 Jan 2;15(1):12–22. [PMC free article] [PubMed] [Google Scholar]
  5. Blackwell J. L., Brinton M. A. BHK cell proteins that bind to the 3' stem-loop structure of the West Nile virus genome RNA. J Virol. 1995 Sep;69(9):5650–5658. doi: 10.1128/jvi.69.9.5650-5658.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Blumenthal T. Qbeta RNA replicase and protein synthesis elongation factors EF-Tu and EF-Ts. Methods Enzymol. 1979;60:628–638. doi: 10.1016/s0076-6879(79)60059-9. [DOI] [PubMed] [Google Scholar]
  7. Brinton M. A., Dispoto J. H. Sequence and secondary structure analysis of the 5'-terminal region of flavivirus genome RNA. Virology. 1988 Feb;162(2):290–299. doi: 10.1016/0042-6822(88)90468-0. [DOI] [PubMed] [Google Scholar]
  8. Brinton M. A., Fernandez A. V., Dispoto J. H. The 3'-nucleotides of flavivirus genomic RNA form a conserved secondary structure. Virology. 1986 Aug;153(1):113–121. doi: 10.1016/0042-6822(86)90012-7. [DOI] [PubMed] [Google Scholar]
  9. Cardiff R. D., Dalrymple J. M., Russell P. K. RNA polymerase in group B arbovirus (dengue-2) infected cells. Brief report. Arch Gesamte Virusforsch. 1973;40(3):392–396. doi: 10.1007/BF01242561. [DOI] [PubMed] [Google Scholar]
  10. Chambers T. J., Hahn C. S., Galler R., Rice C. M. Flavivirus genome organization, expression, and replication. Annu Rev Microbiol. 1990;44:649–688. doi: 10.1146/annurev.mi.44.100190.003245. [DOI] [PubMed] [Google Scholar]
  11. Chang M. F., Chen C. H., Lin S. L., Chen C. J., Chang S. C. Functional domains of delta antigens and viral RNA required for RNA packaging of hepatitis delta virus. J Virol. 1995 Apr;69(4):2508–2514. doi: 10.1128/jvi.69.4.2508-2514.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Chang M. F., Chen C. J., Chang S. C. Mutational analysis of delta antigen: effect on assembly and replication of hepatitis delta virus. J Virol. 1994 Feb;68(2):646–653. doi: 10.1128/jvi.68.2.646-653.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Chang M. F., Sun C. Y., Chen C. J., Chang S. C. Functional motifs of delta antigen essential for RNA binding and replication of hepatitis delta virus. J Virol. 1993 May;67(5):2529–2536. doi: 10.1128/jvi.67.5.2529-2536.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Chu P. W., Westaway E. G. Characterization of Kunjin virus RNA-dependent RNA polymerase: reinitiation of synthesis in vitro. Virology. 1987 Apr;157(2):330–337. doi: 10.1016/0042-6822(87)90275-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Chu P. W., Westaway E. G. Replication strategy of Kunjin virus: evidence for recycling role of replicative form RNA as template in semiconservative and asymmetric replication. Virology. 1985 Jan 15;140(1):68–79. doi: 10.1016/0042-6822(85)90446-5. [DOI] [PubMed] [Google Scholar]
  16. Cianci C., Tiley L., Krystal M. Differential activation of the influenza virus polymerase via template RNA binding. J Virol. 1995 Jul;69(7):3995–3999. doi: 10.1128/jvi.69.7.3995-3999.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Cleaves G. R., Ryan T. E., Schlesinger R. W. Identification and characterization of type 2 dengue virus replicative intermediate and replicative form RNAs. Virology. 1981 May;111(1):73–83. doi: 10.1016/0042-6822(81)90654-1. [DOI] [PubMed] [Google Scholar]
  18. Cui T., Sankar S., Porter A. G. Binding of encephalomyocarditis virus RNA polymerase to the 3'-noncoding region of the viral RNA is specific and requires the 3'-poly(A) tail. J Biol Chem. 1993 Dec 15;268(35):26093–26098. [PubMed] [Google Scholar]
  19. Cullen B. R. The HIV-1 Tat protein: an RNA sequence-specific processivity factor? Cell. 1990 Nov 16;63(4):655–657. doi: 10.1016/0092-8674(90)90129-3. [DOI] [PubMed] [Google Scholar]
  20. Dam E., Pleij K., Draper D. Structural and functional aspects of RNA pseudoknots. Biochemistry. 1992 Dec 1;31(47):11665–11676. doi: 10.1021/bi00162a001. [DOI] [PubMed] [Google Scholar]
  21. Dasgupta A. Purification of host factor required for in vitro transcription of poliovirus RNA. Virology. 1983 Jul 15;128(1):245–251. doi: 10.1016/0042-6822(83)90335-5. [DOI] [PubMed] [Google Scholar]
  22. Dildine S. L., Semler B. L. Conservation of RNA-protein interactions among picornaviruses. J Virol. 1992 Jul;66(7):4364–4376. doi: 10.1128/jvi.66.7.4364-4376.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Duke G. M., Hoffman M. A., Palmenberg A. C. Sequence and structural elements that contribute to efficient encephalomyocarditis virus RNA translation. J Virol. 1992 Mar;66(3):1602–1609. doi: 10.1128/jvi.66.3.1602-1609.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Furuya T., Lai M. M. Three different cellular proteins bind to complementary sites on the 5'-end-positive and 3'-end-negative strands of mouse hepatitis virus RNA. J Virol. 1993 Dec;67(12):7215–7222. doi: 10.1128/jvi.67.12.7215-7222.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Gorbalenya A. E., Donchenko A. P., Koonin E. V., Blinov V. M. N-terminal domains of putative helicases of flavi- and pestiviruses may be serine proteases. Nucleic Acids Res. 1989 May 25;17(10):3889–3897. doi: 10.1093/nar/17.10.3889. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Grun J. B., Brinton M. A. Characterization of West Nile virus RNA-dependent RNA polymerase and cellular terminal adenylyl and uridylyl transferases in cell-free extracts. J Virol. 1986 Dec;60(3):1113–1124. doi: 10.1128/jvi.60.3.1113-1124.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Haller A. A., Semler B. L. Linker scanning mutagenesis of the internal ribosome entry site of poliovirus RNA. J Virol. 1992 Aug;66(8):5075–5086. doi: 10.1128/jvi.66.8.5075-5086.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Hayes R. J., Buck K. W. Complete replication of a eukaryotic virus RNA in vitro by a purified RNA-dependent RNA polymerase. Cell. 1990 Oct 19;63(2):363–368. doi: 10.1016/0092-8674(90)90169-f. [DOI] [PubMed] [Google Scholar]
  29. Jacobson S. J., Konings D. A., Sarnow P. Biochemical and genetic evidence for a pseudoknot structure at the 3' terminus of the poliovirus RNA genome and its role in viral RNA amplification. J Virol. 1993 Jun;67(6):2961–2971. doi: 10.1128/jvi.67.6.2961-2971.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Janda M., Ahlquist P. RNA-dependent replication, transcription, and persistence of brome mosaic virus RNA replicons in S. cerevisiae. Cell. 1993 Mar 26;72(6):961–970. doi: 10.1016/0092-8674(93)90584-d. [DOI] [PubMed] [Google Scholar]
  31. Jang S. K., Wimmer E. Cap-independent translation of encephalomyocarditis virus RNA: structural elements of the internal ribosomal entry site and involvement of a cellular 57-kD RNA-binding protein. Genes Dev. 1990 Sep;4(9):1560–1572. doi: 10.1101/gad.4.9.1560. [DOI] [PubMed] [Google Scholar]
  32. Kapoor M., Zhang L., Ramachandra M., Kusukawa J., Ebner K. E., Padmanabhan R. Association between NS3 and NS5 proteins of dengue virus type 2 in the putative RNA replicase is linked to differential phosphorylation of NS5. J Biol Chem. 1995 Aug 11;270(32):19100–19106. doi: 10.1074/jbc.270.32.19100. [DOI] [PubMed] [Google Scholar]
  33. Landers T. A., Blumenthal T., Weber K. Function and structure in ribonucleic acid phage Q beta ribonucleic acid replicase. The roles of the different subunits in transcription of synthetic templates. J Biol Chem. 1974 Sep 25;249(18):5801–5808. [PubMed] [Google Scholar]
  34. Lee C. Z., Lin J. H., Chao M., McKnight K., Lai M. M. RNA-binding activity of hepatitis delta antigen involves two arginine-rich motifs and is required for hepatitis delta virus RNA replication. J Virol. 1993 Apr;67(4):2221–2227. doi: 10.1128/jvi.67.4.2221-2227.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Leopardi R., Hukkanen V., Vainionpä R., Salmi A. A. Cell proteins bind to sites within the 3' noncoding region and the positive-strand leader sequence of measles virus RNA. J Virol. 1993 Feb;67(2):785–790. doi: 10.1128/jvi.67.2.785-790.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Lin J. H., Chang M. F., Baker S. C., Govindarajan S., Lai M. M. Characterization of hepatitis delta antigen: specific binding to hepatitis delta virus RNA. J Virol. 1990 Sep;64(9):4051–4058. doi: 10.1128/jvi.64.9.4051-4058.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Mattaj I. W. RNA recognition: a family matter? Cell. 1993 Jun 4;73(5):837–840. doi: 10.1016/0092-8674(93)90265-r. [DOI] [PubMed] [Google Scholar]
  38. Meerovitch K., Nicholson R., Sonenberg N. In vitro mutational analysis of cis-acting RNA translational elements within the poliovirus type 2 5' untranslated region. J Virol. 1991 Nov;65(11):5895–5901. doi: 10.1128/jvi.65.11.5895-5901.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Meerovitch K., Pelletier J., Sonenberg N. A cellular protein that binds to the 5'-noncoding region of poliovirus RNA: implications for internal translation initiation. Genes Dev. 1989 Jul;3(7):1026–1034. doi: 10.1101/gad.3.7.1026. [DOI] [PubMed] [Google Scholar]
  40. Meerovitch K., Svitkin Y. V., Lee H. S., Lejbkowicz F., Kenan D. J., Chan E. K., Agol V. I., Keene J. D., Sonenberg N. La autoantigen enhances and corrects aberrant translation of poliovirus RNA in reticulocyte lysate. J Virol. 1993 Jul;67(7):3798–3807. doi: 10.1128/jvi.67.7.3798-3807.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Najita L., Sarnow P. Oxidation-reduction sensitive interaction of a cellular 50-kDa protein with an RNA hairpin in the 5' noncoding region of the poliovirus genome. Proc Natl Acad Sci U S A. 1990 Aug;87(15):5846–5850. doi: 10.1073/pnas.87.15.5846. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Nakhasi H. L., Cao X. Q., Rouault T. A., Liu T. Y. Specific binding of host cell proteins to the 3'-terminal stem-loop structure of rubella virus negative-strand RNA. J Virol. 1991 Nov;65(11):5961–5967. doi: 10.1128/jvi.65.11.5961-5967.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Nakhasi H. L., Rouault T. A., Haile D. J., Liu T. Y., Klausner R. D. Specific high-affinity binding of host cell proteins to the 3' region of rubella virus RNA. New Biol. 1990 Mar;2(3):255–264. [PubMed] [Google Scholar]
  44. O'Neill R. E., Palese P. Cis-acting signals and trans-acting factors involved in influenza virus RNA synthesis. Infect Agents Dis. 1994 Apr-Jun;3(2-3):77–84. [PubMed] [Google Scholar]
  45. Pardigon N., Lenches E., Strauss J. H. Multiple binding sites for cellular proteins in the 3' end of Sindbis alphavirus minus-sense RNA. J Virol. 1993 Aug;67(8):5003–5011. doi: 10.1128/jvi.67.8.5003-5011.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Pardigon N., Strauss J. H. Cellular proteins bind to the 3' end of Sindbis virus minus-strand RNA. J Virol. 1992 Feb;66(2):1007–1015. doi: 10.1128/jvi.66.2.1007-1015.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Pogue G. P., Hall T. C. The requirement for a 5' stem-loop structure in brome mosaic virus replication supports a new model for viral positive-strand RNA initiation. J Virol. 1992 Feb;66(2):674–684. doi: 10.1128/jvi.66.2.674-684.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Quadt R., Jaspars E. M. Purification and characterization of brome mosaic virus RNA-dependent RNA polymerase. Virology. 1990 Sep;178(1):189–194. doi: 10.1016/0042-6822(90)90393-6. [DOI] [PubMed] [Google Scholar]
  49. Quadt R., Kao C. C., Browning K. S., Hershberger R. P., Ahlquist P. Characterization of a host protein associated with brome mosaic virus RNA-dependent RNA polymerase. Proc Natl Acad Sci U S A. 1993 Feb 15;90(4):1498–1502. doi: 10.1073/pnas.90.4.1498. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Qureshi A. A., Trent D. W. Saint Louis encephalitis viral ribonucleic acid replication complex. J Virol. 1972 Apr;9(4):565–573. doi: 10.1128/jvi.9.4.565-573.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Rice C. M., Lenches E. M., Eddy S. R., Shin S. J., Sheets R. L., Strauss J. H. Nucleotide sequence of yellow fever virus: implications for flavivirus gene expression and evolution. Science. 1985 Aug 23;229(4715):726–733. doi: 10.1126/science.4023707. [DOI] [PubMed] [Google Scholar]
  52. Richards O. C., Ehrenfeld E. Poliovirus RNA replication. Curr Top Microbiol Immunol. 1990;161:89–119. doi: 10.1007/978-3-642-75602-3_4. [DOI] [PubMed] [Google Scholar]
  53. Romaniuk P. J., Lowary P., Wu H. N., Stormo G., Uhlenbeck O. C. RNA binding site of R17 coat protein. Biochemistry. 1987 Mar 24;26(6):1563–1568. doi: 10.1021/bi00380a011. [DOI] [PubMed] [Google Scholar]
  54. Simoes E. A., Sarnow P. An RNA hairpin at the extreme 5' end of the poliovirus RNA genome modulates viral translation in human cells. J Virol. 1991 Feb;65(2):913–921. doi: 10.1128/jvi.65.2.913-921.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Sumiyoshi H., Mori C., Fuke I., Morita K., Kuhara S., Kondou J., Kikuchi Y., Nagamatu H., Igarashi A. Complete nucleotide sequence of the Japanese encephalitis virus genome RNA. Virology. 1987 Dec;161(2):497–510. doi: 10.1016/0042-6822(87)90144-9. [DOI] [PubMed] [Google Scholar]
  56. Takeda H., Oya A., Hashimoto K., Yasuda T., Yamada M. A. Association of virus specific replicative ribonucleic acid with nuclear membrane in chick embryo cells infected with japanese encephalitis virus. J Gen Virol. 1978 Feb;38(2):281–291. doi: 10.1099/0022-1317-38-2-281. [DOI] [PubMed] [Google Scholar]
  57. Takegami T., Washizu M., Yasui K. Nucleotide sequence at the 3' end of Japanese encephalitis virus genomic RNA. Virology. 1986 Jul 30;152(2):483–486. doi: 10.1016/0042-6822(86)90152-2. [DOI] [PubMed] [Google Scholar]
  58. Tan B. H., Fu J., Sugrue R. J., Yap E. H., Chan Y. C., Tan Y. H. Recombinant dengue type 1 virus NS5 protein expressed in Escherichia coli exhibits RNA-dependent RNA polymerase activity. Virology. 1996 Feb 15;216(2):317–325. doi: 10.1006/viro.1996.0067. [DOI] [PubMed] [Google Scholar]
  59. Wengler G., Wengler G. Terminal sequences of the genome and replicative-from RNA of the flavivirus West Nile virus: absence of poly(A) and possible role in RNA replication. Virology. 1981 Sep;113(2):544–555. doi: 10.1016/0042-6822(81)90182-3. [DOI] [PubMed] [Google Scholar]
  60. Yen J. H., Chang S. C., Hu C. R., Chu S. C., Lin S. S., Hsieh Y. S., Chang M. F. Cellular proteins specifically bind to the 5'-noncoding region of hepatitis C virus RNA. Virology. 1995 Apr 20;208(2):723–732. doi: 10.1006/viro.1995.1204. [DOI] [PubMed] [Google Scholar]
  61. Zebovitz E., Leong J. K., Doughty S. C. Involvement of the host cell nuclear envelope membranes in the replication of Japanese encephalitis virus. Infect Immun. 1974 Jul;10(1):204–211. doi: 10.1128/iai.10.1.204-211.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. del Angel R. M., Papavassiliou A. G., Fernández-Tomás C., Silverstein S. J., Racaniello V. R. Cell proteins bind to multiple sites within the 5' untranslated region of poliovirus RNA. Proc Natl Acad Sci U S A. 1989 Nov;86(21):8299–8303. doi: 10.1073/pnas.86.21.8299. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Virology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES