Functional analysis of cis- and trans-acting replication factors of porcine circovirus type 1

Journal of Virology

Volumn 81, Issue 11, 2007, Pages 5696-5704

  Steinfeldt, Tobias ^b   Finsterbusch, Tim ^a   Mankertz, Annette ^a  

^a ROBERT KOCH INSTITUTE   (Germany)

^b UNIVERSITY OF COLOGNE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

HELICASE; VIRUS DNA;

AMINO ACID SEQUENCE; ARTICLE; CIRCOVIRIDAE; ENERGY CONSERVATION; GENE AMPLIFICATION; IN VITRO STUDY; INVERTED REPEAT; NONHUMAN; PRIORITY JOURNAL; PROTEIN MOTIF; ROLLING CIRCLE REPLICATION; VIRUS MUTATION; VIRUS REPLICATION;

ANIMALS; CELLS, CULTURED; CIRCOVIRUS; GENE EXPRESSION REGULATION, VIRAL; MUTATION; REPLICATION ORIGIN; SWINE; TRANS-ACTIVATION (GENETICS); TRANS-ACTIVATORS; VIRAL PROTEINS; VIRUS REPLICATION;

PORCINE CIRCOVIRUS 1;

EID: 34249802636     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/JVI.02420-06     Document Type: Article

References (32)

1. Bassami, M. R., D. Berryman, G. E. Wilcox, and S. R. Raidal. 1998. Psittacine beak and feather disease virus nucleotide sequence analysis and its relationship to porcine circovirus, plant circoviruses, and chicken anaemia virus. Virology 249:453-459.
2. Cheung, A. K. 2005. Mutational analysis of the direct tandem repeat sequences at the origin of DNA replication of porcine circovirus type I. Virology 339:192-199.
3. Danen-Van Oorschot, A. A., D. F. Fischer, J. M. Grimhergen, B. Klein, S. Zhuang, J. H. Falkenhurg, C. Backendorf, P. H. Quax, A. J. Van der Eh, and M. H. Notehorn. 1997. Apoptin induces apoptosis in human transformed and malignant cells but not in normal cells. Proc. Natl. Acad. Sci. USA 94:5843-5847.
4. Darwich, L., J. Segales, and E. Mateu. 2004. Pathogenesis of postweaning multisystcmic wasting syndrome caused by porcine circovirus 2: an immune riddle. Arch. Virol. 149:857-874. [Epub ahead of print.]
5. del Solar, G., R. Giraldo, M. J. Ruiz-Echevarria, M. Espinosa, and R. Diaz-Orejas. 1998. Replication and control of circular bacterial plasmids. Microbiol. Mol. Biol. Rev. 62:434-464.
6. Ellis, J., S. Krakowka, M. Lairmore, D. Haines, A. Bratanich, E. Clark, G. Allan, C. Konohy, L. Hassard, B. Meehan, K. Martin, J. Harding, S. Kennedy, and F. McNeilly. 1999. Reproduction of lesions of postweaning multisystcmic wasting syndrome in gnotohiotic piglets. J. Vet. Diagn. Investig. 11:3-14.
7. Gilhert, W., and D. Dressler. 1968. DNA replication: the rolling circle model. Cold Spring Harb. Symp. Quant. Biol. 33:473-484.
8. Hafner, G. J., M. R. Stafford, L. C. Wolter, R. M. Harding, and J. L. Dale. 1997. Nicking and joining activity of banana bunchy top virus replication protein in vitro. J. Gen. Virol. 78:1795-1799.
9. Hamel, A. L., L. L. Lin, and G. P. Nayar. 1998. Nucleotide sequence of porcine circovirus associated with postweaning multisystcmic wasting syndrome in pigs. J. Virol. 72:5262-5267.
10. Heyraud-Nitschke, F., S. Schumacher, J. Laufs, S. Schaefer, J. Schell, and B. Gronenhorn. 1995. Determination of the origin cleavage and joining domain of geminivirus Rep proteins. Nucleic Acids Res. 23:910-916.
11. Ilyina, T. V., and E. V. Koonin. 1992. Conserved sequence motifs in the initiator proteins for rolling circle DNA replication encoded by diverse replicons from eubacteria, eucaryotes and archaebacteria. Nucleic Acids Res. 20:3279-3285.
12. Koonin, E. V., and T. V. Ilyina. 1992. Geminivirus replication proteins are related to prokaryotic plasmid rolling circle DNA replication initiator proteins. J. Gen. Virol. 73:2763-2766.
13. Krakowka, S., J. Ellis, F. McNeilly, C. Waldner, and G. Allan. 2005. Features of porcine circovirus-2 disease: correlations between lesions, amount and distribution of virus, and clinical outcome. J. Vet. Diagn. Investig. 17:213-222.
14. Laufs, J., S. Schumacher, N. Geisler, I. Jupin, and B. Gronenborn. 1995. Identification of the nicking tyrosine of geminivirus Rep protein. FEBS Lett. 377:258-262.
15. Laufs, J., W. Traut, F. Heyraud, V. Matzeit, S. G. Rogers, J. Schell, and B. Gronenborn. 1995. In vitro cleavage and joining at the viral origin of replication hy the replication initiator protein of tomato yellow leaf curl virus. Proc. Natl. Acad. Sci. USA 92:3879-3883.
16. Liu, J., I. Chen, and J. Kwang. 2005. Characterization of a previously unidentified viral protein in porcine circovirus type 2-infected cells and its role in virus-induced apoptosis. J. Virol. 79:8262-8274.
17. Mankertz, A., R. Caliskan, K. Hattermann, B. Hillenbrand, P. Kurzendoerfer, B. Mueller, C. Schmitt, T. Steinfeldt, and T. Finsterbusch. 2004. Molecular biology of porcine circovirus: analyses of gene expression and viral replication. Vet. Microbiol. 98:81-88.
18. Mankertz, A., K. Hattermann, B. Ehlers, and D. Soike. 2000. Cloning and sequencing of columbid circovirus (CoCV), a new circovirus from pigeons. Arch. Virol. 145:2469-2480.
19. Mankertz, A., and B. Hillenbrand. 2002. Analysis of transcription of porcine circovirus type 1. J. Gen. Virol. 83:2743-2751.
20. Mankertz, A., and B. Hillenbrand. 2001. Replication of porcine circovirus type 1 requires two proteins encoded by the viral rep gene. Virology 279: 429-438.
21. Mankertz, A., B. Mueller, T. Steinfeldt, C. Schmitt, and T. Finsterbusch. 2003. New reporter gene-based replication assay reveals exchangeability of replication factors of porcine circovirus types 1 and 2. J. Virol. 77:9885-9893.
22. Mankertz, A., F. Persson, J. Mankertz, G. Blaess, and H. J. Buhk. 1997. Mapping and characterization of the origin of DNA replication of porcine circovirus. J. Virol. 71:2562-2566.
23. Newman, B. J., and N. D. Grindley. 1984. Mutants of the gamma delta resolvase: a genetic analysis of the recombination function. Cell 38:463-469.
24. Noirot, P., J. Bargonetti, and R. P. Novick. 1990. Initiation of rolling-circle replication in pT181 plasmid: initiator protein enhances cruciform extrusion at the origin. Proc. Natl. Acad. Sci. USA 87:8560-8564.
25. Phenix, K. V., J. H. Weston, I. Ypelaar, A. Lavazza, J. A. Smyth, D. Todd, G. E. Wilcox, and S. R. Raidal. 2001. Nucleotide sequence analysis of a novel circovirus of canaries and its relationship to other members of the genus Circovirus of the family Circoviridae. J. Gen. Virol. 82:2805-2809.
26. Reed, R. R., and C. D. Moser. 1984. Resolvase-mediated recombination intermediates contain a serine residue covalently linked to DNA. Cold Spring Harb. Symp. Quant. Biol. 49:245-249.
27. Steinfeldt, T., T. Finsterbusch, and A. Mankertz. 2006. Demonstration of nicking/joining activity at the origin of DNA replication associated with the Rep and Rep' proteins of porcine circovirus type 1. J. Virol. 80:6225-6234.
28. Steinfeldt, T., T. Finsterbusch, and A. Mankertz. 2001. Rep and Rep' protein of porcine circovirus type 1 bind to the origin of replication in vitro. Virology 291:152-160.
29. Timchenko, T., F. de Kouchkovsky, L. Katul, C. David, H. J. Vetten, and B. Gronenborn. 1999. A single Rep protein initiates replication of multiple genome components of faba bean necrotic yellows virus, a single-stranded DNA virus of plants. J. Virol. 73:10173-10182.
30. Todd, D., J. H. Weston, D. Soike, and J. A. Smyth. 2001. Genome sequence determinations and analyses of novel circoviruses from goose and pigeon. Virology 286:354-362.
31. Vega-Rocha. S., I. J. Byeon, B. Gronenborn, A. M. Gronenborn, and R. Campos-Olivas. 2007. Solution structure, divalent metal and DNA binding of the endonuclease domain from the replication initiation protein from porcine circovirus 2. J. Mol. Biol. 9:9.
32. Walker, J. E., M. Saraste, M. J. Runswick, and N. J. Gay. 1982. Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold. EMBO J. 1:945-951.