Skip to main content
Springer Nature - PMC COVID-19 Collection logoLink to Springer Nature - PMC COVID-19 Collection
. 2005;287:57–94. doi: 10.1007/3-540-26765-4_3

The Coronavirus Replicase

J Ziebuhr 2
Editor: Luis Enjuanes1
PMCID: PMC7121973  PMID: 15609509

Abstract

Coronavirus genome replication and transcription take place at cytoplasmic membranes and involve coordinated processes of both continuous and discontinuous RNA synthesis that are mediated by the viral replicase, a huge protein complex encoded by the 20-kb replicase gene. The replicase complex is believed to be comprised of up to 16 viral subunits and a number of cellular proteins. Besides RNA-dependent RNA polymerase, RNA helicase, and protease activities, which are common to RNA viruses, the coronavirus replicase was recently predicted to employ a variety of RNA processing enzymes that are not (or extremely rarely) found in other RNA viruses and include putative sequence-specific endoribonuclease, 3′-to-5′ exoribonuclease, 2′-O-ribose methyltransferase, ADP ribose 1′-phosphatase and, in a subset of group 2 coronaviruses, cyclic phosphodiesterase activities. This chapter reviews (1) the organization of the coronavirus replicase gene, (2) the proteolytic processing of the replicase by viral proteases, (3) the available functional and structural information on individual subunits of the replicase, such as proteases, RNA helicase, and the RNA-dependent RNA polymerase, and (4) the subcellular localization of coronavirus proteins involved in RNA synthesis. Although many molecular details of the coronavirus life cycle remain to be investigated, the available information suggests that these viruses and their distant nidovirus relatives employ a unique collection of enzymatic activities and other protein functions to synthesize a set of 5′-leader-containing subgenomic mRNAs and to replicate the largest RNA virus genomes currently known.

Keywords: Severe Acute Respiratory Syndrome, Porcine Epidemic Diarrhea Virus, Infectious Bronchitis Virus, Mouse Hepatitis Virus, Severe Acute Respiratory Syndrome Coronavirus

Contributor Information

Luis Enjuanes, Email: L.Enjuanes@cnb.uam.es.

J. Ziebuhr, Email: j.ziebuhr@mail.uni-wuerzburg.de

References

  1. Allaire M., Chernaia M.M., Malcolm B.A., James M.N. Picornaviral 3C cysteine proteinases have a fold similar to chymotrypsin-like serine proteinases. Nature. 1994;369:72–76. doi: 10.1038/369072a0. [DOI] [PubMed] [Google Scholar]
  2. Almazán F., González J.M., Pénzes Z., Izeta A., Calvo E., Plana-Durán J., Enjuanes L. Engineering the largest RNA virus genome as an infectious bacterial artificial chromosome. Proc Natl Acad Sci USA. 2000;97:5516–5521. doi: 10.1073/pnas.97.10.5516. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Anand K., Palm G.J., Mesters J.R., Siddell S.G., Ziebuhr J., Hilgenfeld R. Structure of coronavirus main proteinase reveals combination of a chymotrypsin fold with an extra alpha-helical domain. EMBO J. 2002;21:3213–3224. doi: 10.1093/emboj/cdf327. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Anand K., Ziebuhr J., Wadhwani P., Mesters J.R., Hilgenfeld R. Coronavirus main proteinase (3CLpro) structure: basis for design of anti-SARS drugs. Science. 2003;300:1763–1767. doi: 10.1126/science.1085658. [DOI] [PubMed] [Google Scholar]
  5. Baker S.C., Shieh C.K., Soe L.H., Chang M.F., Vannier D.M., Lai M.M. Identification of a domain required for autoproteolytic cleavage of murine coronavirus gene A polyprotein. J Virol. 1989;63:3693–3699. doi: 10.1128/jvi.63.9.3693-3699.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Baker S.C., Yokomori K., Dong S., Carlisle R., Gorbalenya A.E., Koonin E.V., Lai M.M. Identification of the catalytic sites of a papain-like cysteine proteinase of murine coronavirus. J Virol. 1993;67:6056–6063. doi: 10.1128/jvi.67.10.6056-6063.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Baric R.S., Nelson G.W., Fleming J.O., Deans R.J., Keck J.G., Casteel N., Stohlman S.A. Interactions between coronavirus nucleocapsid protein and viral RNAs: implications for viral transcription. J Virol. 1988;62:4280–4287. doi: 10.1128/jvi.62.11.4280-4287.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Barrette-Ng I.H., Ng K.K., Mark B.L., Van Aken D., Cherney M.M., Garen C., Kolodenko Y., Gorbalenya A.E., Snijder E.J., James M.N. Structure of arterivirus nsp4. The smallest chymotrypsin-like proteinase with an alpha/beta C-terminal extension and alternate conformations of the oxyanion hole. J Biol Chem. 2002;277:39960–39966. doi: 10.1074/jbc.M206978200. [DOI] [PubMed] [Google Scholar]
  9. Bautista E.M., Faaberg K.S., Mickelson D., McGruder E.D. Functional properties of the predicted helicase of porcine reproductive and respiratory syndrome virus. Virology. 2002;298:258–270. doi: 10.1006/viro.2002.1495. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Bergmann E.M., Mosimann S.C., Chernaia M.M., Malcolm B.A., James M.N. The refined crystal structure of the 3C gene product from hepatitis A virus: specific proteinase activity and RNA recognition. J Virol. 1997;71:2436–2448. doi: 10.1128/jvi.71.3.2436-2448.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Bi W., Piñon J.D., Hughes S., Bonilla P.J., Holmes K.V., Weiss S.R., Leibowitz J.L. Localization of mouse hepatitis virus open reading frame 1A derived proteins. J Neurovirol. 1998;4:594–605. doi: 10.3109/13550289809114226. [DOI] [PubMed] [Google Scholar]
  12. Blom N., Hansen J., Blaas D., Brunak S. Cleavage site analysis in picornaviral polyproteins: discovering cellular targets by neural networks. Protein Sci. 1996;5:2203–2216. doi: 10.1002/pro.5560051107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Bonilla P.J., Gorbalenya A.E., Weiss S.R. Mouse hepatitis virus strain A59 RNA polymerase gene ORF 1a: heterogeneity among MHV strains. Virology. 1994;198:736–740. doi: 10.1006/viro.1994.1088. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Bonilla P.J., Hughes S.A., Weiss S.R. Characterization of a second cleavage site and demonstration of activity in trans by the papain-like proteinase of the murine coronavirus mouse hepatitis virus strain A59. J Virol. 1997;71:900–909. doi: 10.1128/jvi.71.2.900-909.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Bost A.G., Carnahan R.H., Lu X.T., Denison M.R. Four proteins processed from the replicase gene polyprotein of mouse hepatitis virus colocalize in the cell periphery and adjacent to sites of virion assembly. J Virol. 2000;74:3379–3387. doi: 10.1128/JVI.74.7.3379-3387.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Bost A.G., Prentice E., Denison M.R. Mouse hepatitis virus replicase protein complexes are translocated to sites of M protein accumulation in the ERGIC at late times of infection. Virology. 2001;285:21–29. doi: 10.1006/viro.2001.0932. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Boursnell M.E., Brown T.D., Foulds I.J., Green P.F., Tomley F.M., Binns M.M. Completion of the sequence of the genome of the coronavirus avian infectious bronchitis virus. J Gen Virol. 1987;68:57–77. doi: 10.1099/0022-1317-68-1-57. [DOI] [PubMed] [Google Scholar]
  18. Bredenbeek P.J., Pachuk C.J., Noten A.F., Charite J., Luytjes W., Weiss S.R., Spaan W.J. The primary structure and expression of the second open reading frame of the polymerase gene of the coronavirus MHV-A59; a highly conserved polymerase is expressed by an efficient ribosomal frameshifting mechanism. Nucleic Acids Res. 1990;18:1825–1832. doi: 10.1093/nar/18.7.1825. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Brierley I., Boursnell M.E., Binns M.M., Bilimoria B., Blok V.C., Brown T.D., Inglis S.C. An efficient ribosomal frame-shifting signal in the polymerase-encoding region of the coronavirus IBV. EMBO J. 1987;6:3779–3785. doi: 10.1002/j.1460-2075.1987.tb02713.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Brierley I., Digard P., Inglis S.C. Characterization of an efficient coronavirus ribosomal frameshifting signal: requirement for an RNA pseudoknot. Cell. 1989;57:537–547. doi: 10.1016/0092-8674(89)90124-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Brockway S.M., Clay C.T., Lu X.T., Denison M.R. Characterization of the expression, intracellular localization, and replication complex association of the putative mouse hepatitis virus RNA-dependent RNA polymerase. J Virol. 2003;77:10515–10527. doi: 10.1128/JVI.77.19.10515-10527.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Buck K.W. Comparison of the replication of positive-stranded RNA viruses of plants and animals. Adv Virus Res. 1996;47:159–251. doi: 10.1016/S0065-3527(08)60736-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Bügl H., Fauman E.B., Staker B.L., Zheng F., Kushner S.R., Saper M.A., Bardwell J.C., Jakob U. RNA methylation under heat shock control. Mol Cell. 2000;6:349–360. doi: 10.1016/S1097-2765(00)00035-6. [DOI] [PubMed] [Google Scholar]
  24. Burns C.C., Lawson M.A., Semler B.L., Ehrenfeld E. Effects of mutations in poliovirus 3Dpol on RNA polymerase activity and on polyprotein cleavage. J Virol. 1989;63:4866–4874. doi: 10.1128/jvi.63.11.4866-4874.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Casais R., Thiel V., Siddell S.G., Cavanagh D., Britton P. Reverse genetics system for the avian coronavirus infectious bronchitis virus. J Virol. 2001;75:12359–12369. doi: 10.1128/JVI.75.24.12359-12369.2001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Cavanagh D. Nidovirales: a new order comprising Coronaviridae and Arteriviridae. Arch Virol. 1997;142:629–633. [PubMed] [Google Scholar]
  27. Cho M.W., Teterina N., Egger D., Bienz K., Ehrenfeld E. Membrane rearrangement and vesicle induction by recombinant poliovirus 2C and 2BC in human cells. Virology. 1994;202:129–145. doi: 10.1006/viro.1994.1329. [DOI] [PubMed] [Google Scholar]
  28. Chouljenko V.N., Lin X.Q., Storz J., Kousoulas K.G., Gorbalenya A.E. Comparison of genomic and predicted amino acid sequences of respiratory and enteric bovine coronaviruses isolated from the same animal with fatal shipping pneumonia. J Gen Virol. 2001;82:2927–2933. doi: 10.1099/0022-1317-82-12-2927. [DOI] [PubMed] [Google Scholar]
  29. Compton S.R., Rogers D.B., Holmes K.V., Fertsch D., Remenick J., McGowan J.J. In vitro replication of mouse hepatitis virus strain A59. J Virol. 1987;61:1814–1820. doi: 10.1128/jvi.61.6.1814-1820.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Cowley J.A., Dimmock C.M., Spann K.M., Walker P.J. Gill-associated virus of Penaeus monodon prawns: an invertebrate virus with ORF1a and ORF1b genes related to arteri-and coronaviruses. J Gen Virol. 2000;81:1473–1484. doi: 10.1099/0022-1317-81-6-1473. [DOI] [PubMed] [Google Scholar]
  31. Culver G.M., Consaul S.A., Tycowski K.T., Filipowicz W., Phizicky E.M. tRNA splicing in yeast and wheat germ. A cyclic phosphodiesterase implicated in the metabolism of ADP-ribose 1″,2″-cyclic phosphate. J Biol Chem. 1994;269:24928–24934. [PubMed] [Google Scholar]
  32. Datta U., Dasgupta A. Expression and subcellular localization of poliovirus VPg-precursor protein 3AB in eukaryotic cells: evidence for glycosylation in vitro. J Virol. 1994;68:4468–4477. doi: 10.1128/jvi.68.7.4468-4477.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. De Graaff M., Coscoy L., Jaspars E.M. Localization and biochemical characterization of alfalfa mosaic virus replication complexes. Virology. 1993;194:878–881. doi: 10.1006/viro.1993.1335. [DOI] [PubMed] [Google Scholar]
  34. de Vries A.A.F., Horzinek M.C., Rottier P.J.M., de Groot R.J. The genome organization of the Nidovirales: similarities and differences between arteri-, toro-, and coronaviruses. Sem Virol. 1997;8:33–47. doi: 10.1006/smvy.1997.0104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. den Boon J.A., Snijder E.J., Chirnside E.D., de Vries A.A., Horzinek M.C., Spaan W.J. Equine arteritis virus is not a togavirus but belongs to the coronaviruslike superfamily. J Virol. 1991;65:2910–2920. doi: 10.1128/jvi.65.6.2910-2920.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Denison M.R., Hughes S.A., Weiss S.R. Identification and characterization of a 65-kDa protein processed from the gene 1 polyprotein of the murine coronavirus MHV-A59. Virology. 1995;207:316–320. doi: 10.1006/viro.1995.1085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Denison M.R., Spaan W.J., van der Meer Y., Gibson C.A., Sims A.C., Prentice E., Lu X.T. The putative helicase of the coronavirus mouse hepatitis virus is processed from the replicase gene polyprotein and localizes in complexes that are active in viral RNA synthesis. J Virol. 1999;73:6862–6871. doi: 10.1128/jvi.73.8.6862-6871.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Dong S., Baker S.C. Determinants of the p28 cleavage site recognized by the first papain-like cysteine proteinase of murine coronavirus. Virology. 1994;204:541–549. doi: 10.1006/viro.1994.1567. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Dougherty W.G., Semler B.L. Expression of virus-encoded proteinases: functional and structural similarities with cellular enzymes. Microbiol Rev. 1993;57:781–822. doi: 10.1128/mr.57.4.781-822.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Egger D., Wölk B., Gosert R., Bianchi L., Blum H.E., Moradpour D., Bienz K. Expression of hepatitis C virus proteins induces distinct membrane alterations including a candidate viral replication complex. J Virol. 2002;76:5974–5984. doi: 10.1128/JVI.76.12.5974-5984.2002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Eleouet J.F., Rasschaert D., Lambert P., Levy L., Vende P., Laude H. Complete sequence (20 kilobases) of the polyprotein-encoding gene 1 of transmissible gastroenteritis virus. Virology. 1995;206:817–822. doi: 10.1006/viro.1995.1004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Fan K., Wei P., Feng Q., Chen S., Huang C., Ma L., Lai B., Pei J., Liu Y., Chen J., Lai L. Biosynthesis, purification, and substrate specificity of severe acute respiratory syndrome coronavirus 3C-like proteinase. J Biol Chem. 2003;279:1637–1642. doi: 10.1074/jbc.M310875200. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Filipowicz W., Pogacic V. Biogenesis of small nucleolar ribonucleoproteins. Curr Opin Cell Biol. 2002;14:319–327. doi: 10.1016/S0955-0674(02)00334-4. [DOI] [PubMed] [Google Scholar]
  44. Froshauer S., Kartenbeck J., Helenius A. Alphavirus RNA replicase is located on the cytoplasmic surface of endosomes and lysosomes. J Cell Biol. 1988;107:2075–2086. doi: 10.1083/jcb.107.6.2075. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Gallagher T.M. Murine coronavirus membrane fusion is blocked by modification of thiols buried within the spike protein. J Virol. 1996;70:4683–4690. doi: 10.1128/jvi.70.7.4683-4690.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Goldbach R. Genome similarities between plant and animal RNA viruses. Microbiol Sci. 1987;4:197–202. [PubMed] [Google Scholar]
  47. Gorbalenya A.E., Donchenko A.P., Blinov V.M., Koonin E.V. Cysteine proteases of positive strand RNA viruses and chymotrypsin-like serine proteases. A distinct protein superfamily with a common structural fold. FEBS Lett. 1989;243:103–114. doi: 10.1016/0014-5793(89)80109-7. [DOI] [PubMed] [Google Scholar]
  48. Gorbalenya A.E., Koonin E.V., Donchenko A.P., Blinov V.M. Two related superfamilies of putative helicases involved in replication, recombination, repair and expression of DNA and RNA genomes. Nucleic Acids Res. 1989;17:4713–4730. doi: 10.1093/nar/17.12.4713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Gorbalenya A.E., Koonin E.V., Donchenko A.P., Blinov V.M. Coronavirus genome: prediction of putative functional domains in the non-structural polyprotein by comparative amino acid sequence analysis. Nucleic Acids Res. 1989;17:4847–4861. doi: 10.1093/nar/17.12.4847. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Gorbalenya A.E., Koonin E.V., Lai M.M. Putative papain-related thiol proteases of positive-strand RNA viruses. Identification of rubi-and aphthovirus proteases and delineation of a novel conserved domain associated with proteases of rubi-, alpha-and coronaviruses. FEBS Lett. 1991;288:201–205. doi: 10.1016/0014-5793(91)81034-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Gorbalenya A.E., Koonin E.V. Helicases: amino acid sequence comparisons and structure-function relationships. Curr Opin Struct Biol. 1993;3:419–429. doi: 10.1016/S0959-440X(05)80116-2. [DOI] [Google Scholar]
  52. Gorbalenya A.E., Snijder E.J. Viral cysteine proteinases. Persp Drug Discov Des. 1996;6:64–86. doi: 10.1007/BF02174046. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Gorbalenya A.E. Big nidovirus genome. When count and order of domains matter. Adv Exp Med Biol. 2001;494:1–17. [PubMed] [Google Scholar]
  54. Gosert R., Kanjanahaluethai A., Egger D., Bienz K., Baker S.C. RNA replication of mouse hepatitis virus takes place at double-membrane vesicles. J Virol. 2002;76:3697–3708. doi: 10.1128/JVI.76.8.3697-3708.2002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  55. Grötzinger C., Heusipp G., Ziebuhr J., Harms U., Süss J., Siddell S.G. Characterization of a 105-kDa polypeptide encoded in gene 1 of the human coronavirus HCV 229E. Virology. 1996;222:227–235. doi: 10.1006/viro.1996.0413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Guarné A., Tormo J., Kirchweger R., Pfistermueller D., Fita I., Skern T. Structure of the foot-and-mouth disease virus leader protease: a papain-like fold adapted for self-processing and eIF4G recognition. EMBO J. 1998;17:7469–7479. doi: 10.1093/emboj/17.24.7469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  57. Guarné A., Hampoelz B., Glaser W., Carpena X., Tormo J., Fita I., Skern T. Structural and biochemical features distinguish the foot-and-mouth disease virus leader proteinase from other papain-like enzymes. J Mol Biol. 2000;302:1227–240. doi: 10.1006/jmbi.2000.4115. [DOI] [PubMed] [Google Scholar]
  58. Hansen J.L., Long A.M., Schultz S.C. Structure of the RNA-dependent RNA polymerase of poliovirus. Structure. 1997;5:1109–1122. doi: 10.1016/S0969-2126(97)00261-X. [DOI] [PubMed] [Google Scholar]
  59. Hegyi A., Friebe A., Gorbalenya A.E., Ziebuhr J. Mutational analysis of the active centre of coronavirus 3C-like proteases. J Gen Virol. 2002;83:581–593. doi: 10.1099/0022-1317-83-3-581. [DOI] [PubMed] [Google Scholar]
  60. Hegyi A., Ziebuhr J. Conservation of substrate specificities among coronavirus main proteases. J Gen Virol. 2002;83:595–599. doi: 10.1099/0022-1317-83-3-595. [DOI] [PubMed] [Google Scholar]
  61. Herold J., Raabe T., Schelle-Prinz B., Siddell S.G. Nucleotide sequence of the human coronavirus 229E RNA polymerase locus. Virology. 1993;195:680–691. doi: 10.1006/viro.1993.1419. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. Herold J., Siddell S.G. An ‘elaborated’ pseudoknot is required for high frequency frameshifting during translation of HCV 229E polymerase mRNA. Nucleic Acids Res. 1993;21:5838–5842. doi: 10.1093/nar/21.25.5838. [DOI] [PMC free article] [PubMed] [Google Scholar]
  63. Herold J., Gorbalenya A.E., Thiel V., Schelle B., Siddell S.G. Proteolytic processing at the amino terminus of human coronavirus 229E gene 1-encoded polyproteins: identification of a papain-like proteinase and its substrate. J Virol. 1998;72:910–918. doi: 10.1128/jvi.72.2.910-918.1998. [DOI] [PMC free article] [PubMed] [Google Scholar]
  64. Herold J., Siddell S.G., Gorbalenya A.E. A human RNA viral cysteine proteinase that depends upon a unique Zn2+-binding finger connecting the two domains of a papain-like fold. J Biol Chem. 1999;274:14918–14925. doi: 10.1074/jbc.274.21.14918. [DOI] [PMC free article] [PubMed] [Google Scholar]
  65. Heusipp G., Grötzinger C., Herold J., Siddell S.G., Ziebuhr J. Identification and subcellular localization of a 41 kDa, polyprotein 1ab processing product in human coronavirus 229E-infected cells. J Gen Virol. 1997;78:2789–2794. doi: 10.1099/0022-1317-78-11-2789. [DOI] [PubMed] [Google Scholar]
  66. Heusipp G., Harms U., Siddell S.G., Ziebuhr J. Identification of an ATPase activity associated with a 71-kilodalton polypeptide encoded in gene 1 of the human coronavirus 229E. J Virol. 1997;71:5631–5634. doi: 10.1128/jvi.71.7.5631-5634.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  67. Hughes S.A., Bonilla P.J., Weiss S.R. Identification of the murine coronavirus p28 cleavage site. J Virol. 1995;69:809–813. doi: 10.1128/jvi.69.2.809-813.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Ivanov K.A., Thiel V., Dobbe J.C., van der Meer Y., Snijder E.J., Ziebuhr J. Multiple enzymatic activities associated with severe acute respiratory syndrome coronavirus helicase. J Virol. 2004;78:5619–5632. doi: 10.1128/JVI.78.11.5619-5632.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Ivanov K.A., Ziebuhr J. Human coronavirus nonstructural protein 13: characterization of duplex-unwinding, (deoxy)nucleoside triphosphatase, and RNA 50-triphosphatase activities. J Virol. 2004;78:7833–7838. doi: 10.1128/JVI.78.14.7833-7838.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  70. Kadaré G., Haenni A.L. Virus-encoded RNA helicases. J Virol. 1997;71:2583–2590. doi: 10.1128/jvi.71.4.2583-2590.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  71. Kanjanahaluethai A., Baker S.C. Identification of mouse hepatitis virus papain-like proteinase 2 activity. J Virol. 2000;74:7911–7921. doi: 10.1128/JVI.74.17.7911-7921.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  72. Kanjanahaluethai A., Jukneliene D., Baker S.C. Identification of the murine coronavirus MP1 cleavage site recognized by papain-like proteinase 2. J Virol. 2003;77:7376–7382. doi: 10.1128/JVI.77.13.7376-7382.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  73. Khan A.R., Khazanovich-Bernstein N., Bergmann E.M., James M.N. Structural aspects of activation pathways of aspartic protease zymogens and viral 3C protease precursors. Proc Natl Acad Sci USA. 1999;96:10968–10975. doi: 10.1073/pnas.96.20.10968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  74. Kim J.C., Spence R.A., Currier P.F., Lu X., Denison M.R. Coronavirus protein processing and RNA synthesis is inhibited by the cysteine proteinase inhibitor E64d. Virology. 1995;208:1–8. doi: 10.1006/viro.1995.1123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  75. Kiss T. Small nucleolar RNA-guided post-transcriptional modification of cellular RNAs. EMBO J. 2001;20:3617–3622. doi: 10.1093/emboj/20.14.3617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  76. Kocherhans R., Bridgen A., Ackermann M., Tobler K. Completion of the porcine epidemic diarrhoea coronavirus (PEDV) genome sequence. Virus Genes. 2001;23:137–144. doi: 10.1023/A:1011831902219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  77. Koonin E.V. The phylogeny of RNA-dependent RNA polymerases of positive-strand RNA viruses. J Gen Virol. 1991;72:2197–2206. doi: 10.1099/0022-1317-72-9-2197. [DOI] [PubMed] [Google Scholar]
  78. Koonin E.V., Dolja V.V. Evolution and taxonomy of positive-strand RNA viruses: implications of comparative analysis of amino acid sequences. Crit Rev Biochem Mol Biol. 1993;28:375–430. doi: 10.3109/10409239309078440. [DOI] [PubMed] [Google Scholar]
  79. Kräusslich H.G., Wimmer E. Viral proteinases. Annu Rev Biochem. 1988;57:701–754. doi: 10.1146/annurev.bi.57.070188.003413. [DOI] [PubMed] [Google Scholar]
  80. Kujala P., Ikäheimonen A., Ehsani N., Vihinen H., Auvinen P., Kääriäinen L. Biogenesis of the Semliki Forest virus RNA replication complex. J Virol. 2001;75:3873–3884. doi: 10.1128/JVI.75.8.3873-3884.2001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  81. Kwong A.D., Kim J.L., Lin C. Structure and function of hepatitis C virus NS3 helicase. Curr Top Microbiol Immunol. 2000;242:171–196. doi: 10.1007/978-3-642-59605-6_9. [DOI] [PubMed] [Google Scholar]
  82. Laakkonen P., Ahola T., Kääriäinen L. The effects of palmitoylation on membrane association of Semliki forest virus RNA capping enzyme. J Biol Chem. 1996;271:28567–28571. doi: 10.1074/jbc.271.45.28567. [DOI] [PubMed] [Google Scholar]
  83. Lai M.M., Patton C.D., Baric R.S., Stohlman S.A. Presence of leader sequences in the mRNA of mouse hepatitis virus. J Virol. 1983;46:1027–1033. doi: 10.1128/jvi.46.3.1027-1033.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  84. Lai M.M., Cavanagh D. The molecular biology of coronaviruses. Adv Virus Res. 1997;48:1–10. doi: 10.1016/S0168-1702(96)01421-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  85. Laneve P., Altieri F., Fiori M.E., Scaloni A., Bozzoni I., Caffarelli E. Purification, cloning, and characterization of XendoU, a novel endoribonuclease involved in processing of intron-encoded small nucleolar RNAs in Xenopus laevis. J Biol Chem. 2003;278:13026–13032. doi: 10.1074/jbc.M211937200. [DOI] [PubMed] [Google Scholar]
  86. Lee H.J., Shieh C.K., Gorbalenya A.E., Koonin E.V., La Monica N., Tuler J., Bagdzhadzhyan A., Lai M.M. The complete sequence (22 kilobases) of murine coronavirus gene 1 encoding the putative proteases and RNA polymerase. Virology. 1991;180:567–582. doi: 10.1016/0042-6822(91)90071-I. [DOI] [PMC free article] [PubMed] [Google Scholar]
  87. Lemm J.A., Rümenapf T., Strauss E.G., Strauss J.H., Rice C.M. Polypeptide requirements for assembly of functional Sindbis virus replication complexes: a model for the temporal regulation of minus-and plus-strand RNA synthesis. EMBO J. 1994;13:2925–2934. doi: 10.1002/j.1460-2075.1994.tb06587.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  88. Lim K.P., Liu D.X. Characterization of the two overlapping papain-like proteinase domains encoded in gene 1 of the coronavirus infectious bronchitis virus and determination of the C-terminal cleavage site of an 87-kDa protein. Virology. 1998;245:303–312. doi: 10.1006/viro.1998.9164. [DOI] [PMC free article] [PubMed] [Google Scholar]
  89. Lim K.P., Ng L.F., Liu D.X. Identification of a novel cleavage activity of the first papain-like proteinase domain encoded by open reading frame 1a of the coronavirus avian infectious bronchitis virus and characterization of the cleavage products. J Virol. 2000;74:1674–1685. doi: 10.1128/JVI.74.4.1674-1685.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  90. Liu C., Xu H.Y., Liu D.X. Induction of caspase-dependent apoptosis in cultured cells by the avian coronavirus infectious bronchitis virus. J Virol. 2001;75:6402–6409. doi: 10.1128/JVI.75.14.6402-6409.2001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  91. Liu D.X., Brown T.D. Characterisation and mutational analysis of an ORF 1a-encoding proteinase domain responsible for proteolytic processing of the infectious bronchitis virus 1a/1b polyprotein. Virology. 1995;209:420–427. doi: 10.1006/viro.1995.1274. [DOI] [PMC free article] [PubMed] [Google Scholar]
  92. Lu X., Lu Y., Denison M.R. Intracellular and in vitro-translated 27-kDa proteins contain the 3C-like proteinase activity of the coronavirus MHV-A59. Virology. 1996;222:375–382. doi: 10.1006/viro.1996.0434. [DOI] [PMC free article] [PubMed] [Google Scholar]
  93. Lu Y., Denison M.R. Determinants of mouse hepatitis virus 3C-like proteinase activity. Virology. 1997;230:335–342. doi: 10.1006/viro.1997.8479. [DOI] [PMC free article] [PubMed] [Google Scholar]
  94. Mackenzie J.M., Jones M.K., Westaway E.G. Markers for trans-Golgi membranes and the intermediate compartment localize to induced membranes with distinct replication functions in flavivirus-infected cells. J Virol. 1999;73:9555–9567. doi: 10.1128/jvi.73.11.9555-9567.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  95. Marra M.A., Jones S.J., Astell C.R., Holt R.A., Brooks-Wilson A., Butterfield Y.S., Khattra J., Asano J.K., Barber S.A., Chan S.Y., Cloutier A., Coughlin S.M., Freeman D., Girn N., Griffith O.L., Leach S.R., Mayo M., McDonald H., Montgomery S.B., Pandoh P.K., Petrescu A.S., Robertson A.G., Schein J.E., Siddiqui A., Smailus D.E., Stott J.M., Yang G.S., Plummer F., Andonov A., Artsob H., Bastien N., Bernard K., Booth T.F., Bowness D., Czub M., Drebot M., Fernando L., Flick R., Garbutt M., Gray M., Grolla A., Jones S., Feldmann H., Meyers A., Kabani A., Li Y., Normand S., Stroher U., Tipples G.A., Tyler S., Vogrig R., Ward D., Watson B., Brunham R.C., Krajden M., Petric M., Skowronski D.M., Upton C., Roper R.L. The genome sequence of the SARS-associated coronavirus. Science. 2003;300:1399–1404. doi: 10.1126/science.1085953. [DOI] [PubMed] [Google Scholar]
  96. Martzen M.R., McCraith S.M., Spinelli S.L., Torres F.M., Fields S., Grayhack E.J., Phizicky E.M. A biochemical genomics approach for identifying genes by the activity of their products. Science. 1999;286:1153–1155. doi: 10.1126/science.286.5442.1153. [DOI] [PubMed] [Google Scholar]
  97. Matthews D.A., Smith W.W., Ferre R.A., Condon B., Budahazi G., Sisson W., Villafranca J.E., Janson C.A., McElroy H.E., Gribskov C.L., et al. Structure of human rhinovirus 3C protease reveals a trypsin-like polypeptide fold, RNA-binding site, and means for cleaving precursor polyprotein. Cell. 1994;77:761–771. doi: 10.1016/0092-8674(94)90059-0. [DOI] [PubMed] [Google Scholar]
  98. Miller D.J., Schwartz M.D., Ahlquist P. Flock house virus RNA replicates on outer mitochondrial membranes in Drosophila cells. J Virol. 2001;75:11664–11676. doi: 10.1128/JVI.75.23.11664-11676.2001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  99. Mills D.R., Priano C., DiMauro P., Binderow B.D. Q beta replicase: mapping the functional domains of an RNA-dependent RNA polymerase. J Mol Biol. 1989;205:751–764. doi: 10.1016/0022-2836(89)90319-7. [DOI] [PubMed] [Google Scholar]
  100. Mosimann S.C., Cherney M.M., Sia S., Plotch S., James M.N. Refined X-ray crystallographic structure of the poliovirus 3C gene product. J Mol Biol. 1997;273:1032–1047. doi: 10.1006/jmbi.1997.1306. [DOI] [PubMed] [Google Scholar]
  101. Nasr F., Filipowicz W. Characterization of the Saccharomyces cerevisiae cyclic nucleotide phosphodiesterase involved in the metabolism of ADP-ribose 1″,2″-cyclic phosphate. Nucleic Acids Res. 2000;28:1676–1683. doi: 10.1093/nar/28.8.1676. [DOI] [PMC free article] [PubMed] [Google Scholar]
  102. Ng L.F., Liu D.X. Further characterization of the coronavirus infectious bronchitis virus 3C-like proteinase and determination of a new cleavage site. Virology. 2000;272:27–39. doi: 10.1006/viro.2000.0330. [DOI] [PMC free article] [PubMed] [Google Scholar]
  103. Ng L.F., Liu D.X. Membrane association and dimerization of a cysteine-rich, 16-kilodalton polypeptide released from the C-terminal region of the coronavirus infectious bronchitis virus 1a polyprotein. J Virol. 2002;76:6257–6267. doi: 10.1128/JVI.76.12.6257-6267.2002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  104. Pang P.S., Jankowsky E., Planet P.J., Pyle A.M. The hepatitis C viral NS3 protein is a processive DNA helicase with cofactor enhanced RNA unwinding. EMBO J. 2002;21:1168–1176. doi: 10.1093/emboj/21.5.1168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  105. Pedersen K.W., van der Meer Y., Roos N., Snijder E.J. Open reading frame 1a-encoded subunits of the arterivirus replicase induce endoplasmic reticulum-derived double-membrane vesicles which carry the viral replication complex. J Virol. 1999;73:2016–2026. doi: 10.1128/jvi.73.3.2016-2026.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  106. Penzes Z., González J.M., Calvo E., Izeta A., Smerdou C., Mendez A., Sánchez C.M., Sola I., Almazán F., Enjuanes L. Complete genome sequence of transmissible gastroenteritis coronavirus PUR46-MAD clone and evolution of the Purdue virus cluster. Virus Genes. 2001;23:105–118. doi: 10.1023/A:1011147832586. [DOI] [PMC free article] [PubMed] [Google Scholar]
  107. Peränen J., Kääriäinen L. Biogenesis of type I cytopathic vacuoles in Semliki Forest virus-infected BHK cells. J Virol. 1991;65:1623–1627. doi: 10.1128/jvi.65.3.1623-1627.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  108. Peränen J., Laakkonen P., Hyvönen M., Kääriäinen L. The alphavirus replicase protein nsP1 is membrane-associated and has affinity to endocytic organelles. Virology. 1995;208:610–620. doi: 10.1006/viro.1995.1192. [DOI] [PubMed] [Google Scholar]
  109. Piñon J.D., Mayreddy R.R., Turner J.D., Khan F.S., Bonilla P.J., Weiss S.R. Efficient autoproteolytic processing of the MHV-A59 3C-like proteinase from the flanking hydrophobic domains requires membranes. Virology. 1997;230:309–322. doi: 10.1006/viro.1997.8503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  110. Piñon J.D., Teng H., Weiss S.R. Further requirements for cleavage by the murine coronavirus 3C-like proteinase: identification of a cleavage site within ORF1b. Virology. 1999;263:471–484. doi: 10.1006/viro.1999.9954. [DOI] [PMC free article] [PubMed] [Google Scholar]
  111. Plotch S.J., Palant O., Gluzman Y. Purification and properties of poliovirus RNA polymerase expressed in Escherichia coli. J Virol. 1989;63:216–225. doi: 10.1128/jvi.63.1.216-225.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  112. Restrepo-Hartwig M., Ahlquist P. Brome mosaic virus RNA replication proteins 1a and 2a colocalize and 1a independently localizes on the yeast endoplasmic reticulum. J Virol. 1999;73:10303–10309. doi: 10.1128/jvi.73.12.10303-10309.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  113. Restrepo-Hartwig M.A., Ahlquist P. Brome mosaic virus helicase-and polymerase-like proteins colocalize on the endoplasmic reticulum at sites of viral RNA synthesis. J Virol. 1996;70:8908–8916. doi: 10.1128/jvi.70.12.8908-8916.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  114. Rota P.A., Oberste M.S., Monroe S.S., Nix W.A., Campagnoli R., Icenogle J.P., Penaranda S., Bankamp B., Maher K., Chen M.H., Tong S., Tamin A., Lowe L., Frace M., DeRisi J.L., Chen Q., Wang D., Erdman D.D., Peret T.C., Burns C., Ksiazek T.G., Rollin P.E., Sanchez A., Liffick S., Holloway B., Limor J., McCaustland K., Olsen-Rasmussen M., Fouchier R., Gunther S., Osterhaus A.D., Drosten C., Pallansch M.A., Anderson L.J., Bellini W.J. Characterization of a novel coronavirus associated with severe acute respiratory syndrome. Science. 2003;300:1394–1399. doi: 10.1126/science.1085952. [DOI] [PubMed] [Google Scholar]
  115. Ruan Y.J., Wei C.L., Ee A.L., Vega V.B., Thoreau H., Su S.T., Chia J.M., Ng P., Chiu K.P., Lim L., Zhang T., Peng C.K., Lin E.O., Lee N.M., Yee S.L., Ng L.F., Chee R.E., Stanton L.W., Long P.M., Liu E.T. Comparative full-length genome sequence analysis of 14 SARS coronavirus isolates and common mutations associated with putative origins of infection. Lancet. 2003;361:1779–1785. doi: 10.1016/S0140-6736(03)13414-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  116. Russo M., Di Franco A., Martelli G.P. The fine structure of Cymbidium ringspot virus infections in host tissues. III. Role of peroxisomes in the genesis of multivesicular bodies. J Ultrastruct Res. 1983;82:52–63. doi: 10.1016/S0022-5320(83)90096-5. [DOI] [PubMed] [Google Scholar]
  117. Ryan M.D., Flint M. Virus-encoded proteinases of the picornavirus supergroup. J Gen Virol. 1997;78:699–723. doi: 10.1099/0022-1317-78-4-699. [DOI] [PubMed] [Google Scholar]
  118. Sawicki D., Wang T., Sawicki S. The RNA structures engaged in replication and transcription of the A59 strain of mouse hepatitis virus. J Gen Virol. 2001;82:385–396. doi: 10.1099/0022-1317-82-2-385. [DOI] [PubMed] [Google Scholar]
  119. Sawicki S.G., Sawicki D.L. Coronavirus transcription: subgenomic mouse hepatitis virus replicative intermediates function in RNA synthesis. J Virol. 1990;64:1050–1056. doi: 10.1128/jvi.64.3.1050-1056.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  120. Schaad M.C., Baric R.S. Genetics of mouse hepatitis virus transcription: evidence that subgenomic negative strands are functional templates. J Virol. 1994;68:8169–8179. doi: 10.1128/jvi.68.12.8169-8179.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  121. Schaad M.C., Jensen P.E., Carrington J.C. Formation of plant RNA virus replication complexes on membranes: role of an endoplasmic reticulum-targeted viral protein. EMBO J. 1997;16:4049–4059. doi: 10.1093/emboj/16.13.4049. [DOI] [PMC free article] [PubMed] [Google Scholar]
  122. Schiller J.J., Kanjanahaluethai A., Baker S.C. Processing of the coronavirus MHV-JHM polymerase polyprotein: identification of precursors and proteolytic products spanning 400 kilodaltons of ORF1a. Virology. 1998;242:288–302. doi: 10.1006/viro.1997.9010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  123. Schlegel A., Giddings T.H., Jr., Ladinsky M.S., Kirkegaard K. Cellular origin and ultrastructure of membranes induced during poliovirus infection. J Virol. 1996;70:6576–6588. doi: 10.1128/jvi.70.10.6576-6588.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  124. Schmidt-Mende J., Bieck E., Hügle T., Penin F., Rice C.M., Blum H.E., Moradpour D. Determinants for membrane association of the hepatitis C virus RNA-dependent RNA polymerase. J Biol Chem. 2001;276:44052–44063. doi: 10.1074/jbc.M103358200. [DOI] [PubMed] [Google Scholar]
  125. Schwartz M., Chen J., Janda M., Sullivan M., den Boon J., Ahlquist P. A positive-strand RNA virus replication complex parallels form and function of retrovirus capsids. Mol Cell. 2002;9:505–514. doi: 10.1016/S1097-2765(02)00474-4. [DOI] [PubMed] [Google Scholar]
  126. Seipelt J., Guarne A., Bergmann E., James M., Sommergruber W., Fita I., Skern T. The structures of picornaviral proteinases. Virus Res. 1999;62:159–168. doi: 10.1016/S0168-1702(99)00043-X. [DOI] [PubMed] [Google Scholar]
  127. Sethna P.B., Hung S.L., Brian D.A. Coronavirus subgenomic minus-strand RNAs and the potential for mRNA replicons. Proc Natl Acad Sci USA. 1989;86:5626–5630. doi: 10.1073/pnas.86.14.5626. [DOI] [PMC free article] [PubMed] [Google Scholar]
  128. Sethna P.B., Brian D.A. Coronavirus genomic and subgenomic minus-strand RNAs copartition in membrane-protected replication complexes. J Virol. 1997;71:7744–7749. doi: 10.1128/jvi.71.10.7744-7749.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  129. Seybert A., Hegyi A., Siddell S.G., Ziebuhr J. The human coronavirus 229E superfamily 1 helicase has RNA and DNA duplex-unwinding activities with 5′-to-3′ polarity. RNA. 2000;6:1056–1068. doi: 10.1017/S1355838200000728. [DOI] [PMC free article] [PubMed] [Google Scholar]
  130. Seybert A., van Dinten L.C., Snijder E.J., Ziebuhr J. Biochemical characterization of the equine arteritis virus helicase suggests a close functional relationship between arterivirus and coronavirus helicases. J Virol. 2000;74:9586–9593. doi: 10.1128/JVI.74.20.9586-9593.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  131. Seybert A., Ziebuhr J. Guanosine triphosphatase activity of the human coronavirus helicase. Adv Exp Med Biol. 2001;494:255–260. doi: 10.1007/978-1-4615-1325-4_40. [DOI] [PubMed] [Google Scholar]
  132. Shi S.T., Schiller J.J., Kanjanahaluethai A., Baker S.C., Oh J.W., Lai M.M. Colocalization and membrane association of murine hepatitis virus gene 1 products and de novo-synthesized viral RNA in infected cells. J Virol. 1999;73:5957–5969. doi: 10.1128/jvi.73.7.5957-5969.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  133. Siddell S., Sawicki D., Meyer Y., Thiel V., Sawicki S. Identification of the mutations responsible for the phenotype of three MHV RNA-negative ts mutants. Adv Exp Med Biol. 2001;494:453–458. doi: 10.1007/978-1-4615-1325-4_66. [DOI] [PubMed] [Google Scholar]
  134. Siddell S.G. The Coronaviridae: an introduction. In: Siddell S.G., editor. The Coronaviridae. New York: Plenum Press; 1995. pp. 1–10. [Google Scholar]
  135. Sims A.C., Ostermann J., Denison M.R. Mouse hepatitis virus replicase proteins associate with two distinct populations of intracellular membranes. J Virol. 2000;74:5647–5654. doi: 10.1128/JVI.74.12.5647-5654.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  136. Snijder E.J., den Boon J.A., Bredenbeek P.J., Horzinek M.C., Rijnbrand R., Spaan W.J. The carboxyl-terminal part of the putative Berne virus polymerase is expressed by ribosomal frameshifting and contains sequence motifs which indicate that toro-and coronaviruses are evolutionarily related. Nucleic Acids Res. 1990;18:4535–4542. doi: 10.1093/nar/18.15.4535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  137. Snijder E.J., Horzinek M.C. Toroviruses: replication, evolution and comparison with other members of the coronavirus-like superfamily. J Gen Virol. 1993;74:2305–2316. doi: 10.1099/0022-1317-74-11-2305. [DOI] [PubMed] [Google Scholar]
  138. Snijder E.J., Meulenberg J.J. The molecular biology of arteriviruses. J Gen Virol. 1998;79:961–979. doi: 10.1099/0022-1317-79-5-961. [DOI] [PubMed] [Google Scholar]
  139. Snijder E.J., van Tol H., Roos N., Pedersen K.W. Non-structural proteins 2 and 3 interact to modify host cell membranes during the formation of the arterivirus replication complex. J Gen Virol. 2001;82:985–994. doi: 10.1099/0022-1317-82-5-985. [DOI] [PubMed] [Google Scholar]
  140. Snijder E.J., Bredenbeek P.J., Dobbe J.C., Thiel V., Ziebuhr J., Poon L.L., Guan Y., Rozanov M., Spaan W.J., Gorbalenya A.E. Unique and conserved features of genome and proteome of SARS-coronavirus, an early split-off from the coronavirus group 2 lineage. J Mol Biol. 2003;331:991–1004. doi: 10.1016/S0022-2836(03)00865-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  141. Spaan W., Delius H., Skinner M., Armstrong J., Rottier P., Smeekens S., van der Zeijst B.A., Siddell S.G. Coronavirus mRNA synthesis involves fusion of non-contiguous sequences. EMBO J. 1983;2:1839–1844. doi: 10.1002/j.1460-2075.1983.tb01667.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  142. Stinchcombe J.C., Griffiths G.M. Regulated secretion from hemopoietic cells. J Cell Biol. 1999;147:1–6. doi: 10.1083/jcb.147.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  143. Strauss J.H., Strauss E.G. Evolution of RNA viruses. Annu Rev Microbiol. 1988;42:657–683. doi: 10.1146/annurev.mi.42.100188.003301. [DOI] [PubMed] [Google Scholar]
  144. Tanner J.A., Watt R.M., Chai Y.B., Lu L.Y., Lin M.C., Peiris J.S., Poon L.L., Kung H.F., Huang J.D. The severe acute respiratory syndrome (SARS) coronavirus NTPase/helicase belongs to a distinct class of 5′ to 3′ viral helicases. J Biol Chem. 2003;278:39578–39582. doi: 10.1074/jbc.C300328200. [DOI] [PMC free article] [PubMed] [Google Scholar]
  145. Teng H., Piñon J.D., Weiss S.R. Expression of murine coronavirus recombinant papain-like proteinase: efficient cleavage is dependent on the lengths of both the substrate and the proteinase polypeptides. J Virol. 1999;73:2658–2666. doi: 10.1128/jvi.73.4.2658-2666.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  146. Teterina N.L., Bienz K., Egger D., Gorbalenya A.E., Ehrenfeld E. Induction of intracellular membrane rearrangements by HAV proteins 2C and 2BC. Virology. 1997;237:66–77. doi: 10.1006/viro.1997.8775. [DOI] [PubMed] [Google Scholar]
  147. Thiel V., Herold J., Schelle B., Siddell S.G. Infectious RNA transcribed in vitro from a cDNA copy of the human coronavirus genome cloned in vaccinia virus. J Gen Virol. 2001;82:1273–1281. doi: 10.1099/0022-1317-82-6-1273. [DOI] [PubMed] [Google Scholar]
  148. Thiel V., Herold J., Schelle B., Siddell S.G. Viral replicase gene products suffice for coronavirus discontinuous transcription. J Virol. 2001;75:6676–6681. doi: 10.1128/JVI.75.14.6676-6681.2001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  149. Thiel V., Ivanov K.A., Putics A., Hertzig T., Schelle B., Bayer S., Weissbrich B., Snijder E.J., Rabenau H., Doerr H.W., Gorbalenya A.E., Ziebuhr J. Mechanisms and enzymes involved in SARS coronavirus genome expression. J Gen Virol. 2003;84:2305–2315. doi: 10.1099/vir.0.19424-0. [DOI] [PubMed] [Google Scholar]
  150. Tibbles K.W., Brierley I., Cavanagh D., Brown T.D. Characterization in vitro of an autocatalytic processing activity associated with the predicted 3C-like proteinase domain of the coronavirus avian infectious bronchitis virus. J Virol. 1996;70:1923–1930. doi: 10.1128/jvi.70.3.1923-1930.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  151. Tibbles K.W., Cavanagh D., Brown T.D. Activity of a purified His-tagged 3C-like proteinase from the coronavirus infectious bronchitis virus. Virus Res. 1999;60:137–145. doi: 10.1016/S0168-1702(99)00011-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  152. Tijms M.A., van Dinten L.C., Gorbalenya A.E., Snijder E.J. A zinc finger-containing papain-like protease couples subgenomic mRNA synthesis to genome translation in a positive-stranded RNA virus. Proc Natl Acad Sci USA. 2001;98:1889–1894. doi: 10.1073/pnas.041390398. [DOI] [PMC free article] [PubMed] [Google Scholar]
  153. van der Meer Y., van Tol H., Krijnse Locker J., Snijder E.J. ORF1a-encoded replicase subunits are involved in the membrane association of the arterivirus replication complex. J Virol. 1998;72:6689–6698. doi: 10.1128/jvi.72.8.6689-6698.1998. [DOI] [PMC free article] [PubMed] [Google Scholar]
  154. van der Meer Y., Snijder E.J., Dobbe J.C., Schleich S., Denison M.R., Spaan W.J., Krijnse Locker J. Localization of mouse hepatitis virus nonstructural proteins and RNA synthesis indicates a role for late endosomes in viral replication. J Virol. 1999;73:7641–7657. doi: 10.1128/jvi.73.9.7641-7657.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  155. van Dinten L.C., Rensen S., Gorbalenya A.E., Snijder E.J. Proteolytic processing of the open reading frame 1b-encoded part of arterivirus replicase is mediated by nsp4 serine protease and Is essential for virus replication. J Virol. 1999;73:2027–2037. doi: 10.1128/jvi.73.3.2027-2037.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  156. van Dinten L.C., van Tol H., Gorbalenya A.E., Snijder E.J. The predicted metal-binding region of the arterivirus helicase protein is involved in subgenomic mRNA synthesis, genome replication, and virion biogenesis. J Virol. 2000;74:5213–5223. doi: 10.1128/JVI.74.11.5213-5223.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  157. van Kuppeveld F.J., Galama J.M., Zoll J., Melchers W.J. Genetic analysis of a hydrophobic domain of coxsackie B3 virus protein 2B: a moderate degree of hydrophobicity is required for a cis-acting function in viral RNA synthesis. J Virol. 1995;69:7782–7790. doi: 10.1128/jvi.69.12.7782-7790.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  158. Vasiljeva L., Merits A., Golubtsov A., Sizemskaja V., Kaariainen L., Ahola T. Regulation of the sequential processing of Semliki Forest virus replicase polyprotein. J Biol Chem. 2003;278:41636–41645. doi: 10.1074/jbc.M307481200. [DOI] [PubMed] [Google Scholar]
  159. Wang T., Sawicki S.G. Mouse hepatitis virus minus-strand templates are unstable and turnover during viral replication. Adv Exp Med Biol. 2001;494:491–497. doi: 10.1007/978-1-4615-1325-4_71. [DOI] [PubMed] [Google Scholar]
  160. Xu H.Y., Lim K.P., Shen S., Liu D.X. Further identification and characterization of novel intermediate and mature cleavage products released from the ORF 1b region of the avian coronavirus infectious bronchitis virus 1a/1b polyprotein. Virology. 2001;288:212–222. doi: 10.1006/viro.2001.1098. [DOI] [PMC free article] [PubMed] [Google Scholar]
  161. Yount B., Curtis K.M., Baric R.S. Strategy for systematic assembly of large RNA and DNA genomes: transmissible gastroenteritis virus model. J Virol. 2000;74:10600–10611. doi: 10.1128/JVI.74.22.10600-10611.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  162. Yount B., Denison M.R., Weiss S.R., Baric R.S. Systematic assembly of a full-length infectious cDNA of mouse hepatitis virus strain A59. J Virol. 2002;76:11065–11078. doi: 10.1128/JVI.76.21.11065-11078.2002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  163. Yount B., Curtis K.M., Fritz E.A., Hensley L.E., Jahrling P.B., Prentice E., Denison M.R., Geisbert T.W., Baric R.S. Reverse genetics with a full-length infectious cDNA of severe acute respiratory syndrome coronavirus. Proc Natl Acad Sci USA. 2003;100:12995–13000. doi: 10.1073/pnas.1735582100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  164. Ziebuhr J., Herold J., Siddell S.G. Characterization of a human coronavirus (strain 229E) 3C-like proteinase activity. J Virol. 1995;69:4331–4338. doi: 10.1128/jvi.69.7.4331-4338.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  165. Ziebuhr J., Heusipp G., Siddell S.G. Biosynthesis, purification, and characterization of the human coronavirus 229E 3C-like proteinase. J Virol. 1997;71:3992–3997. doi: 10.1128/jvi.71.5.3992-3997.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  166. Ziebuhr J., Siddell S.G. Processing of the human coronavirus 229E replicase polyproteins by the virus-encoded 3C-like proteinase: identification of proteolytic products and cleavage sites common to pp1a and pp1ab. J Virol. 1999;73:177–185. doi: 10.1128/jvi.73.1.177-185.1999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  167. Ziebuhr J., Snijder E.J., Gorbalenya A.E. Virus-encoded proteinases and proteolytic processing in the Nidovirales. J Gen Virol. 2000;81:853–879. doi: 10.1099/0022-1317-81-4-853. [DOI] [PubMed] [Google Scholar]
  168. Ziebuhr J., Thiel V., Gorbalenya A.E. The autocatalytic release of a putative RNA virus transcription factor from its polyprotein precursor involves two paralogous papain-like proteases that cleave the same peptide bond. J Biol Chem. 2001;276:33220–33232. doi: 10.1074/jbc.M104097200. [DOI] [PMC free article] [PubMed] [Google Scholar]
  169. Ziebuhr J., Bayer S., Cowley J.A., Gorbalenya A.E. The 3C-like proteinase of an invertebrate nidovirus links coronavirus and potyvirus homologs. J Virol. 2003;77:1415–1426. doi: 10.1128/JVI.77.2.1415-1426.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  170. Zuo Y., Deutscher M.P. Exoribonuclease superfamilies: structural analysis and phylogenetic distribution. Nucleic Acids Res. 2001;29:1017–1026. doi: 10.1093/nar/29.5.1017. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Coronavirus Replication and Reverse Genetics are provided here courtesy of Nature Publishing Group

RESOURCES