Identification and characterization of Singapore grouper iridovirus (SGIV) ORF162L, an immediate-early gene involved in cell growth control and viral replication

Virus Research

Volumn 147, Issue 1, 2010, Pages 30-39

  Xia, Liqun ^b   Liang, Haiying ^b   Huang, Youhua ^c   Ou Yang, Zhengliang ^c   Qin, Qiwei ^a  

^a SOUTH CHINA SEA INSTITUTE OF OCEANOLOGY   (China)

^b GUANGDONG OCEAN UNIVERSITY   (China)

^c SUN YAT SEN UNIVERSITY   (China)

Author keywords

Cell growth; ICP46; Iridovirus; SGIV; Structural protein; Viral replication

Indexed keywords

PROTEIN ICP46; UNCLASSIFIED DRUG; VIRUS PROTEIN;

ARTICLE; CELL GROWTH; CONTROLLED STUDY; GENE FUNCTION; GENE SEQUENCE; GENETIC ANALYSIS; GROWTH REGULATION; IRIDOVIRUS; NONHUMAN; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PRIORITY JOURNAL; PROTEIN LOCALIZATION; SINGAPORE GROUPER IRIDOVIRUS; VIRAL GENETICS; VIRUS REPLICATION;

AMINO ACID SEQUENCE; ANIMALS; BLOTTING, WESTERN; CELL CULTURE TECHNIQUES; CELL CYCLE; CYTOPLASM; FISHES; GENE EXPRESSION PROFILING; GENES, IMMEDIATE-EARLY; GENES, VIRAL; MOLECULAR SEQUENCE DATA; OPEN READING FRAMES; PHYLOGENY; RANAVIRUS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID; VIRAL PROTEINS; VIRUS REPLICATION;

EPINEPHELINAE; IRIDOVIRIDAE; IRIDOVIRUS; SINGAPORE GROUPER IRIDOVIRUS;

EID: 71149109522     PISSN: 01681702     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.virusres.2009.09.015     Document Type: Article

References (41)

1. Ahne W.H.J., Schlotfeldt H.J., and Thomsen I. Fish viruses: isolation of an icosahedral cytoplasmic deoxyribovirus from sheatfish (Silurus glanis). J. Vet. Med. 36 (1989) 333-336
2. Beckman W., Tham T.N., Aubertin A.M., and Willis D.B. Structure and regulation of the immediate-early frog virus3 gene that encodes ICR489. J. Virol. 62 (1988) 1271-1277
3. Castillo J.P., and Kowalik T.F. Human cytomegalovirus immediate early proteins and cell growth control. Gene 290 (2002) 19-34
4. Chinchar V.G., Essbauer S., He J.G., Hyatt A., Miyazaki T., Seligy D., and Williams T. In: Fauqet C.M., Mayo M.A., Maniloff J., Desselberger U., and Ball L.A. (Eds). Iridovirade. Virus Taxonomy, VIIIth Report of the International Committee on Taxonomy of Viruses (2005), Academic Press, London 163-175
5. Deng M., He J.G., Weng S.P., Lü L., and He H.H. Characterization of the ICR489 gene of infectious spleen and kidney necrosis virus of Siniperca chuatsi. Acta Sci. Nat. Univ. Sunyatseni 41 (2002) 64-67 (in Chinese with English abstract)
6. Eaton H.E., Metcalf J., Penny E., Tcherepanov V., Upton C., and Brunetti C.R. Comparative genomic analysis of the family Iridoviridae: re-annotating and defining the core set of iridovirus genes. Virol. J. 19 (2007) 4-11
7. Elliott G., Hafezi W., Whiteley A., and Bernard E. Deletion of the herpes simplex virus VP22-encoding gene (UL49) alters the expression, localization, and virion incorporation of ICP0. J. Virol. 79 (2005) 9735-9745
8. Everett R.D. The regulation of transcription of viral and cellular genes by herpesvirus immediate-early gene products. Anticancer Res. 7 (1987) 589-604
9. Everett R.D. ICP0, a regulator of herpes simplex virus during lytic and latent infection. Bioessays 22 (2000) 761-770
10. Heppell J., and Berthiaume L. Ultrastructure of lymphocystis disease virus (LDV) as compared to frog virus 3 (FV3) and chilo iridescent virus (CIV): effects of enzymatic digestions and detergent degradations. Arch. Virol. 125 (1992) 215-226
11. Hobbs W.E., and DeLuca N.A. Perturbation of cell cycle progression and cellular gene expression as a function of herpes simplex virus ICP0. J. Virol. 73 (1999) 8245-8255
12. Hyatt A.D., Gould A.R., Zupanovic Z., Cummingham A.A., Hengstberger S., Whittington R.J., Kattenbelt J., and Coupar B.E.H. Comparative studies of piscine and amphibian iridoviruses. Arch. Virol. 145 (2000) 301-331
13. Kalejta R.F. Tegument proteins of human cytomegalovirus. Microbiol. Mol. Biol. Rev. 72 (2008) 249-265
14. Kinchington P.R., Fite K., Seman A., and Turse S.E. Virion association of IE62, the varicella-zoster virus (VZV) major transcriptional regulatory protein, requires expression of the VZV open reading frame 66 protein kinase. J. Virol. 75 (2001) 9106-9113
15. Kinchington P.R., Hougland J.K., Arvin A.M., Ruyechan W.T., and Hay J. The varicella-zoster virus immediate-early protein IE62 is a major component of virus particles. J. Virol. 66 (1992) 359-366
16. Lua D.T., Yasuike M., Hirono I., and Aoki T. Transcription program of red sea bream iridovirus as revealed by DNA microarrays. J. Virol. 79 (2005) 15151-15164
17. Moss B., and Shisler J.L. Immunology 101 at poxvirus U: immune evasion genes. Semin. Immunol. 13 (2001) 59-66
18. Pallister J., Goldie S., Coupar B., and Hyatt A. Promoter activity in the 5′ flanking regions of the Bohle iridovirus ICP 18, ICP 46 and major capsid protein genes. Arch. Virol. 150 (2005) 1911-1919
19. Petrik D.T., Schmitt K.P., and Stinski M.F. Inhibition of cellular DNA synthesis by the human cytomegalovirus IE86 protein is necessary for efficient virus replication. J. Virol. 80 (2006) 3872-3883
20. Piaskoski T.O., and Plumb J.A. Characterization of the largemouth bass virus in cell culture. J. Aquat. Anim. Health 11 (1999) 45-51
21. Qin Q.W., Chang S.F., Ngoh-Lim G.H., Gibson-Kueh S., Shi C., and Lam T.J. Characterization of a novel ranavirus isolated from grouper Epinephelus tauvina. Dis. Aquat. Organ. 53 (2003) 1-9
22. Qin Q.W., Lam T.J., Sin Y.M., Shen H., Chang S.F., Ngoh G.H., and Chen C.L. Electron microscopic observations of a marine fish iridovirus isolated from brown-spotted grouper, Epinepheous tauvina. J. Virol. Methods 98 (2001) 17-24
23. Reed L.J., and Muench H. A simple method of estimating fifty per cent endpoints. Am. J. Epidemiol. 27 (1938) 493-497
24. Romanowski M.J., and Shenk T. Characterization of the human cytomegalovirus irs1 and trs1 genes: a second immediate-early transcription unit within irs1 whose product antagonizes transcriptional activation. J. Virol. 71 (1997) 1485-1496
25. Samaniego L.A., Neiderhiser L., and DeLuca N.A. Persistence and expression of the herpes simplex virus genome in the absence of immediate-early proteins. J. Virol. 72 (1998) 3307-3320
26. Sedlackova L., and Rice S.A. Herpes simplex virus type 1 immediate-early protein ICP27 is required for efficient incorporation of ICP0 and ICP4 into virions. J. Virol. 82 (2008) 268-277
27. Song W.J., Lin Q., Joshi S.B., Lim T.K., and Hew C.L. Proteomic studies of the Singapore grouper iridovirus. Mol. Cell Proteomics 5 (2006) 256-264
28. Song W.J., Qin Q.W., Qiu J., Huang C.H., Wang F., and Hew C.L. Functional genomics analysis of Singapore grouper iridovirus: complete sequence determination and proteomic analysis. J. Virol. 78 (2004) 12576-12590
29. Stinski M.F., and Petrik D.T. Functional roles of the human cytomegalovirus essential IE86 protein. Curr. Top. Microbiol. Immunol. 325 (2008) 133-152
30. Teng Y., Hou Z., Gong J., Liu H., Xie X., Zhang L., Chen X.H., and Qin Q.W. Whole-genome transcriptional profiles of a novel marine fish iridovirus, Singapore grouper iridovirus (SGIV) in virus-infected grouper spleen cell cultures and in orange-spotted grouper, Epinephulus coioides. Virology 377 (2008) 39-48
31. Varnum S.M., Streblow D.N., Monroe M.E., Smith P., Auberry K.J., Pasa-Tolic L., Wang D., Camp D.G., Rodland K., Wiley S., Britt W., Shenk T., Smith R.D., and Nelson J. Identification of proteins in human cytomegalovirus (HCMV) particles: the HCMV proteome. J. Virol. 78 (2004) 10960-10966
32. Wang Y.Q., Lu L., Weng S.P., Huang J.N., Chan S.M., and He J.G. Molecular epidemiology and phylogenetic analysis of a marine fish infectious spleen and kidney necrosis virus-like (ISKNV-like) virus. Arch. Virol. 152 (2007) 763-773
33. Wiebusch L., Neuwirth A., Grabenhenrich L., Voigt S., and Hagemeier C. Cell cycle-independent expression of immediate-early gene 3 results in G1 and G2 arrest in murine cytomegalovirus-infected cells. J. Virol. 82 (2008) 10188-10198
34. Williams T. The iridoviruses. Adv. Virus Res. 46 (1996) 347-412
35. Williams T., Barbosa-Solomieu V., and Chinchar V.G. A decade of advances in iridovirus research. Adv. Virus Res. 65 (2005) 173-248
36. Willis D.B., Goorha R., Miles M., and Granoff A. Macromolecular synthesis in cells infected by frog virus 3. VII. Transcriptional and post-transcriptional regulation of virus gene expression. J. Virol. 24 (1977) 326-342
37. Willis D.B., and Granoff A. Macromolecular synthesis in cells infected by frog virus 3. IX. Two temporal classes of early viral RNA. Virology 86 (1978) 443-453
38. Xia L.Q., Cao J.H., Huang X.H., and Qin Q.W. Characterization of the Singapore grouper iridovirus (SGIV) ORF086R, a putative homolog of ICP18 involved in cell growth control and virus replication. Arch. Virol. 154 (2009) 1409-1416
39. Yao F., and Courtney R.J. A major transcriptional regulatory protein (ICP4) of herpes simplex virus type 1 is associated with purified virions. J. Virol. 63 (1989) 3338-3344
40. Yao F., and Courtney R.J. Association of ICP0 but not ICP27 with purified virions of herpes simplex virus type 1. J. Virol. 66 (1992) 2709-2716
41. Zhou Y.F., Yu Z.X., Wanishsawad C., Shou M., and Epstein S.E. The immediate early gene products of human cytomegalovirus increase vascular smooth muscle cell migration, proliferation, and expression of PDGF β-receptor. Biochem. Biophys. Res. Commun. 256 (1999) 608-613