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PMID: 12829829 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Transmissible gastroenteritis coronavirus packaging signal is located at the 5' end of the virus genome.

Journal of virology ·Vol. 77 ·No. 14 ·2003-07-00 ·Pages 7890-902

Escors D, Izeta A, Capiscol C, Enjuanes L

Abstract

To locate the transmissible gastroenteritis coronavirus (TGEV) packaging signal, the incorporation of TGEV subgenomic mRNAs (sgmRNAs) into virions was first addressed. TGEV virions were purified by three different techniques, including an immunopurification using an M protein-specific monoclonal antibody. Detection of sgmRNAs in virions by specific reverse transcription-PCRs (RT-PCRs) was related to the purity of virus preparations. Interestingly, virus mRNAs were detected in partially purified virus but not in virus immunopurified using stringent conditions. Analyses by quantitative RT-PCR confirmed that virus mRNAs were not present in highly purified preparations. Lack of sgmRNA encapsidation was probably due to the absence of a packaging signal (Psi) within these mRNAs. This information plus that from the encapsidation of a collection of TGEV-derived minigenomes suggested that Psi is located at the 5' end of the genome. To confirm that this was the case, a set of minigenomes was expressed that included an expression cassette for an mRNA including the beta-glucuronidase gene (GUS) plus variable sequence fragments from the 5' end of the virus genome potentially including Psi. Insertion of the first 649 nucleotides (nt) of the TGEV genome led to the specific encapsidation of the mRNA, indicating that a Psi was located within this region which was absent from all of the other virus mRNAs. The presence of this packaging signal was further confirmed by showing the expression and rescue of the mRNA including the first 649 nt of the TGEV genome under control of the cytomegalovirus promoter in TGEV-infected cells. This mRNA was successfully amplified and encapsidated, indicating that the first 649 nt of TGEV genome also contained the 5' cis-acting replication signals. The encapsidation efficiency of this mRNA was about 30-fold higher than the genome encapsidation efficiency, as estimated by quantitative RT-PCR. In contrast, viral mRNAs presented significantly lower encapsidation efficiencies (about 100-fold) than those of the virus genome, strongly suggesting that TGEV mRNAs in fact lacked an alternative TGEV Psi.

MeSH Terms
5' Untranslated Regions/chemistry,genetics Animals Base Sequence Capsid/metabolism Cell Line Genome, Viral Molecular Sequence Data RNA, Messenger/metabolism RNA, Viral/metabolism Reverse Transcriptase Polymerase Chain Reaction Signal Transduction Swine Transmissible gastroenteritis virus/genetics,metabolism Virion/metabolism Virus Assembly Virus Replication
Chemicals
5' Untranslated Regions RNA, Messenger RNA, Viral
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Escors David
Department of Molecular and Cell Biology, Centro Nacional de Biotecnología, CSIC, Campus Universidad Autónoma, Cantoblanco, 28049 Madrid, Spain.
Izeta Ander
Capiscol Carmen
Enjuanes Luis
References (74)
74 references, click to expand
  1. Replication of murine coronavirus defective interfering RNA from negative-strand transcripts.
    J Virol. 1996 Sep;70(9):5769-76 PMID: 8709192
  2. cis-active structural motifs involved in specific encapsidation of Moloney murine leukemia virus RNA.
    J Virol. 1996 Aug;70(8):5043-50 PMID: 8764011
  3. Murine coronavirus packaging signal confers packaging to nonviral RNA.
    J Virol. 1997 Jan;71(1):824-7 PMID: 8985424
  4. A subgenomic mRNA transcript of the coronavirus mouse hepatitis virus strain A59 defective interfering (DI) RNA is packaged when it contains the DI packaging signal.
    J Virol. 1997 Jul;71(7):5684-7 PMID: 9188649
  5. Heterogeneous nuclear ribonucleoprotein A1 binds to the transcription-regulatory region of mouse hepatitis virus RNA.
    Proc Natl Acad Sci U S A. 1997 Sep 2;94(18):9544-9 PMID: 9275159
  6. A role for two hairpin structures as a core RNA encapsidation signal in murine leukemia virus virions.
    J Virol. 1997 Oct;71(10):8061-5 PMID: 9311905
  7. Protein interactions during coronavirus assembly.
    J Virol. 1997 Dec;71(12):9278-84 PMID: 9371586
  8. Identification of a region of the rabies virus N protein involved in direct binding to the viral RNA.
    J Gen Virol. 1998 May;79 ( Pt 5):1005-13 PMID: 9603315
  9. Encapsidation of the flavivirus kunjin replicon RNA by using a complementation system providing Kunjin virus structural proteins in trans.
    J Virol. 1998 Jul;72(7):5967-77 PMID: 9621059
  10. Importance of the positive-strand RNA secondary structure of a murine coronavirus defective interfering RNA internal replication signal in positive-strand RNA synthesis.
    J Virol. 1998 Oct;72(10):7926-33 PMID: 9733830
  11. Aura alphavirus subgenomic RNA is packaged into virions of two sizes.
    J Virol. 1995 Mar;69(3):1741-6 PMID: 7853512
  12. cis Requirement for N-specific protein sequence in bovine coronavirus defective interfering RNA replication.
    J Virol. 1996 Apr;70(4):2201-7 PMID: 8642643
  13. The membrane M protein carboxy terminus binds to transmissible gastroenteritis coronavirus core and contributes to core stability.
    J Virol. 2001 Feb;75(3):1312-24 PMID: 11152504
  14. cis-Acting signals in encapsidation of Hantaan virus S-segment viral genomic RNA by its N protein.
    J Virol. 2001 Mar;75(6):2646-52 PMID: 11222687
  15. Coupling between replication and packaging of flavivirus RNA: evidence derived from the use of DNA-based full-length cDNA clones of Kunjin virus.
    J Virol. 2001 May;75(10):4633-40 PMID: 11312333
  16. RNA is a structural element in retrovirus particles.
    Proc Natl Acad Sci U S A. 2001 Apr 24;98(9):5246-51 PMID: 11320254
  17. Heterogeneous nuclear ribonucleoprotein a1 binds to the 3'-untranslated region and mediates potential 5'-3'-end cross talks of mouse hepatitis virus RNA.
    J Virol. 2001 Jun;75(11):5009-17 PMID: 11333880
  18. Infectious RNA transcribed in vitro from a cDNA copy of the human coronavirus genome cloned in vaccinia virus.
    J Gen Virol. 2001 Jun;82(Pt 6):1273-81 PMID: 11369870
  19. Cooperation of an RNA packaging signal and a viral envelope protein in coronavirus RNA packaging.
    J Virol. 2001 Oct;75(19):9059-67 PMID: 11533169
  20. Complete genome sequence of transmissible gastroenteritis coronavirus PUR46-MAD clone and evolution of the purdue virus cluster.
    Virus Genes. 2001;23(1):105-18 PMID: 11556396
  21. The major human immunodeficiency virus type 2 (HIV-2) packaging signal is present on all HIV-2 RNA species: cotranslational RNA encapsidation and limitation of Gag protein confer specificity.
    J Virol. 2001 Dec;75(24):12058-69 PMID: 11711596
  22. Organization of two transmissible gastroenteritis coronavirus membrane protein topologies within the virion and core.
    J Virol. 2001 Dec;75(24):12228-40 PMID: 11711614
  23. Reverse genetics system for the avian coronavirus infectious bronchitis virus.
    J Virol. 2001 Dec;75(24):12359-69 PMID: 11711626
  24. Transcription regulatory sequences and mRNA expression levels in the coronavirus transmissible gastroenteritis virus.
    J Virol. 2002 Feb;76(3):1293-308 PMID: 11773405
  25. Structure elucidation of the hepatitis B virus encapsidation signal by NMR on selectively labeled RNAs.
    J Biomol Struct Dyn. 2002 Feb;19(4):627-36 PMID: 11843624
  26. Positional effect of deletions on viability, especially on encapsidation, of Brome mosaic virus D-RNA in barley protoplasts.
    Virology. 2002 Feb 15;293(2):314-9 PMID: 11886251
  27. Stabilization of a full-length infectious cDNA clone of transmissible gastroenteritis coronavirus by insertion of an intron.
    J Virol. 2002 May;76(9):4655-61 PMID: 11932433
  28. Coronavirus transcription early in infection.
    J Virol. 1998 Nov;72(11):8517-24 PMID: 9765389
  29. A new model for coronavirus transcription.
    Adv Exp Med Biol. 1998;440:215-9 PMID: 9782283
  30. Coronavirus nucleocapsid protein. RNA interactions.
    Adv Exp Med Biol. 1998;440:355-9 PMID: 9782303
  31. Replication and packaging of transmissible gastroenteritis coronavirus-derived synthetic minigenomes.
    J Virol. 1999 Feb;73(2):1535-45 PMID: 9882359
  32. Functional coupling between replication and packaging of poliovirus replicon RNA.
    J Virol. 1999 Jan;73(1):427-35 PMID: 9847348
  33. Presence of subgenomic mRNAs in virions of coronavirus IBV.
    Virology. 1993 Sep;196(1):172-8 PMID: 8395112
  34. Subgenomic mRNA of Aura alphavirus is packaged into virions.
    J Virol. 1994 Jan;68(1):56-62 PMID: 7902874
  35. Evidence for coronavirus discontinuous transcription.
    J Virol. 1994 Apr;68(4):2615-23 PMID: 8139040
  36. Specific binding of HIV-1 nucleocapsid protein to PSI RNA in vitro requires N-terminal zinc finger and flanking basic amino acid residues.
    EMBO J. 1994 Apr 1;13(7):1525-33 PMID: 8156990
  37. The proximate 5' and 3' ends of the 120-base viral RNA (pRNA) are crucial for the packaging of bacteriophage phi 29 DNA.
    Virology. 1994 May 15;201(1):77-85 PMID: 8178491
  38. Identification of a bovine coronavirus packaging signal.
    J Virol. 2000 Jan;74(1):580-3 PMID: 10590153
  39. The ends on herpesvirus DNA replicative concatemers contain pac2 cis cleavage/packaging elements and their formation is controlled by terminal cis sequences.
    J Virol. 2000 Feb;74(3):1587-92 PMID: 10627574
  40. Host protein interactions with the 3' end of bovine coronavirus RNA and the requirement of the poly(A) tail for coronavirus defective genome replication.
    J Virol. 2000 Jun;74(11):5053-65 PMID: 10799579
  41. Engineering the largest RNA virus genome as an infectious bacterial artificial chromosome.
    Proc Natl Acad Sci U S A. 2000 May 9;97(10):5516-21 PMID: 10805807
  42. RNA secondary structures of the bacteriophage phi6 packaging regions.
    RNA. 2000 Jun;6(6):880-9 PMID: 10864045
  43. In the beginning: genome recognition, RNA encapsidation and the initiation of complex retrovirus assembly.
    J Gen Virol. 2000 Aug;81(Pt 8):1889-99 PMID: 10900025
  44. Characterization of the coronavirus M protein and nucleocapsid interaction in infected cells.
    J Virol. 2000 Sep;74(17):8127-34 PMID: 10933723
  45. Heterogeneous nuclear ribonucleoprotein A1 regulates RNA synthesis of a cytoplasmic virus.
    EMBO J. 2000 Sep 1;19(17):4701-11 PMID: 10970862
  46. RNA binding properties of bunyamwera virus nucleocapsid protein and selective binding to an element in the 5' terminus of the negative-sense S segment.
    J Virol. 2000 Nov;74(21):9946-52 PMID: 11024122
  47. Strategy for systematic assembly of large RNA and DNA genomes: transmissible gastroenteritis virus model.
    J Virol. 2000 Nov;74(22):10600-11 PMID: 11044104
  48. Recognition of RNA encapsidation signal by the yeast L-A double-stranded RNA virus.
    J Biol Chem. 2000 Nov 24;275(47):37118-26 PMID: 10954712
  49. cis-acting sequences required for coronavirus infectious bronchitis virus defective-RNA replication and packaging.
    J Virol. 2001 Jan;75(1):125-33 PMID: 11119581
  50. Host cell proteins binding to the encapsidation signal epsilon in hepatitis B virus RNA.
    Arch Virol. 2002 Mar;147(3):471-91 PMID: 11958450
  51. Genetic evidence for a structural interaction between the carboxy termini of the membrane and nucleocapsid proteins of mouse hepatitis virus.
    J Virol. 2002 May;76(10):4987-99 PMID: 11967315
  52. Evidence for segment-nonspecific packaging of the influenza a virus genome.
    J Virol. 2002 Jul;76(14):7133-9 PMID: 12072513
  53. Systematic assembly of a full-length infectious cDNA of mouse hepatitis virus strain A59.
    J Virol. 2002 Nov;76(21):11065-78 PMID: 12368349
  54. Generation of a replication-competent, propagation-deficient virus vector based on the transmissible gastroenteritis coronavirus genome.
    J Virol. 2002 Nov;76(22):11518-29 PMID: 12388713
  55. Nucleocapsid-independent specific viral RNA packaging via viral envelope protein and viral RNA signal.
    J Virol. 2003 Mar;77(5):2922-7 PMID: 12584316
  56. Studies on transmissible gastroenteritis of swine. II. Selected characteristics of a cytopathogenic virus common to five isolates from transmissible gastroenteritis.
    Can J Comp Med Vet Sci. 1966 Jul;30(7):190-8 PMID: 4224292
  57. Selective packaging of host tRNA's by murine leukemia virus particles does not require genomic RNA.
    J Virol. 1979 Jan;29(1):328-35 PMID: 219227
  58. Isolation of coronavirus envelope glycoproteins and interaction with the viral nucleocapsid.
    J Virol. 1980 Jan;33(1):449-62 PMID: 6245243
  59. Reverse transcriptase as the major determinant for selective packaging of tRNA's into Avian sarcoma virus particles.
    J Virol. 1980 Dec;36(3):692-700 PMID: 6162035
  60. Identification of a packaged cellular mRNA in virions of rous sarcoma virus.
    J Virol. 1981 Aug;39(2):471-80 PMID: 6268836
  61. Critical epitopes in transmissible gastroenteritis virus neutralization.
    J Virol. 1986 Oct;60(1):131-9 PMID: 2427744
  62. Induction of alpha interferon by transmissible gastroenteritis coronavirus: role of transmembrane glycoprotein E1.
    J Virol. 1988 Jan;62(1):8-11 PMID: 2824858
  63. Coronavirus subgenomic minus-strand RNAs and the potential for mRNA replicons.
    Proc Natl Acad Sci U S A. 1989 Jul;86(14):5626-30 PMID: 2546161
  64. Antigenic homology among coronaviruses related to transmissible gastroenteritis virus.
    Virology. 1990 Feb;174(2):410-7 PMID: 1689525
  65. Bovine coronavirus mRNA replication continues throughout persistent infection in cell culture.
    J Virol. 1990 Sep;64(9):4108-14 PMID: 2384915
  66. Portable encapsidation signal of the L-A double-stranded RNA virus of S. cerevisiae.
    Cell. 1990 Aug 24;62(4):819-28 PMID: 2117501
  67. Minus-strand copies of replicating coronavirus mRNAs contain antileaders.
    J Virol. 1991 Jan;65(1):320-5 PMID: 1985203
  68. A domain at the 3' end of the polymerase gene is essential for encapsidation of coronavirus defective interfering RNAs.
    J Virol. 1991 Jun;65(6):3219-26 PMID: 2033672
  69. Residues involved in the antigenic sites of transmissible gastroenteritis coronavirus S glycoprotein.
    Virology. 1991 Jul;183(1):225-38 PMID: 1711257
  70. Single amino acid changes in the viral glycoprotein M affect induction of alpha interferon by the coronavirus transmissible gastroenteritis virus.
    J Virol. 1992 Feb;66(2):743-9 PMID: 1309909
  71. Identification and characterization of a coronavirus packaging signal.
    J Virol. 1992 Jun;66(6):3522-30 PMID: 1316465
  72. Porcine respiratory coronavirus: molecular features and virus-host interactions.
    Vet Res. 1993;24(2):125-50 PMID: 8393722
  73. Replication of synthetic defective interfering RNAs derived from coronavirus mouse hepatitis virus-A59.
    Virology. 1996 Feb 1;216(1):174-83 PMID: 8614984
  74. The transmissible gastroenteritis coronavirus contains a spherical core shell consisting of M and N proteins.
    J Virol. 1996 Jul;70(7):4773-7 PMID: 8676505
Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
2003-07-00
Pages
7890-902
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC161917
Subset
IM
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