Cloning and characterization of a caspase gene from black tiger shrimp (Penaeus monodon)-infected with white spot syndrome virus (WSSV)

Journal of Biotechnology

Volumn 131, Issue 1, 2007, Pages 9-19

  Wongprasert, Kanokpan ^a   Sangsuriya, Pakkakul ^a   Phongdara, Amornrat ^b   Senapin, Saengchan ^a,c  

^a MAHIDOL UNIVERSITY   (Thailand)

^b PRINCE OF SONGKLA UNIVERSITY   (Thailand)

^c NATIONAL SCIENCE AND TECHNOLOGY DEVELOPMENT AGENCY   (Thailand)

Author keywords

Apoptosis; Caspase; ICE; Penaeus monodon; Shrimp; WSSV

Indexed keywords

CASPASE; PENAEUS MONODON; SHRIMP; WSSV;

AMINO ACIDS; CELL DEATH; GENES; IMMUNOLOGY; PROTEINS; VIRUSES;

GENETIC ENGINEERING;

CASPASE; RECOMBINANT PROTEIN;

APOPTOSIS; ARTICLE; BLOOD CELL; CYTOPLASM; ENZYME ACTIVE SITE; ENZYME ACTIVITY; ESCHERICHIA COLI; GENE EXPRESSION; GILL; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PENAEUS MONODON; PLASMID; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SHRIMP; UPREGULATION; VIRUS INFECTION; WESTERN BLOTTING; WHITE SPOT SYNDROME VIRUS;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CASPASE 3; CLONING, MOLECULAR; GENE EXPRESSION REGULATION, ENZYMOLOGIC; GILLS; IMMUNOHISTOCHEMISTRY; MOLECULAR SEQUENCE DATA; PENAEIDAE; PHYLOGENY; PROTEIN TRANSPORT; RECOMBINANT PROTEINS; RNA, MESSENGER; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, DNA; WHITE SPOT SYNDROME VIRUS 1;

DECAPODA (CRUSTACEA); DROSOPHILA MELANOGASTER; ESCHERICHIA COLI; FENNEROPENAEUS MERGUIENSIS; ORYCTOLAGUS CUNICULUS; PENAEUS MONODON; SHRIMP WHITE SPOT SYNDROME VIRUS;

EID: 34447266005     PISSN: 01681656     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jbiotec.2007.05.032     Document Type: Article

References (33)

1. Altschul S.F., Gish W., Miller W., Myers E.W., and Lipman D.J. Basic local alignment search tool. J. Mol. Biol. 215 (1990) 403-410
2. Bell T., and Lightner D. Handbook of Normal Penaeid Shrimp Histology (1988), The World Aquaculture Society, Louisiana, USA
3. Bushell M., Stonely M., Sarnow P., and Willis A.E. Translation inhibition during the induction of apoptosis: RNA or protein degradation?. Biochem. Soc. Trans. 32 (2004) 606-610
4. Cohen G.M. Caspases: the executioners of apoptosis. Biochem. J. 326 (1997) 1-6
5. Denault J., and Salvesen G. Caspases: keys in the ignition of cell death. Chem. Rev. 102 (2002) 4489-4500
6. Flegel T.W. Update on viral accommodation, a model for host-viral interaction in shrimp and other arthropods. Dev. Comp. Immunol. 31 (2007) 217-231
7. Flegel T.W., and Pasharawipas T. Active viral accommodation:a new concept for crustacean response to viral pathogens. In: Flegel T.W. (Ed). Advances in Shrimp Biotechnology (1998), National Center for Genetic Engineering and Biotechnology, Bangkok 245-250
8. Fraser A.G., and Evan G.I. Identification of a Drosophila melanogaster ICE/CED-3-related protease, drICE. EMBO J. 16 (1997) 2805-2813
9. Grutter M.G. Caspases: key players in programmed cell death. Curr. Opin. Struct. Biol. 10 (2000) 649-655
10. Hengartner M.O. The biochemistry of apoptosis. Nature 407 (2000) 770-776
11. Johansson M., Keyser P., Sritunyalucksana K., and Soderhall K. Crustacean haemocytes and haematopoiesis. Aquaculture 191 (2000) 45-52
12. Khanobdee K., Soowannayan C., Flegel T.W., Ubol S., and Withyachumnarnkul B. Evidence for apoptosis correlated with mortality in the giant black tiger shrimp Penaeus monodon infected with yellow head virus. Dis. Aquat. Organ. 48 (2002) 79-90
13. Krajewska M., Wang H.G., Krajewski S., Zapata J.M., Shabaik A., Gascoyne R., and Reed J.C. Immunohistochemical analysis of in vivo patterns of expression of CPP32 (caspase-3), a cell death protease. Cancer Res. 57 (1997) 1605-1613
14. Marchler-Bauer A., Anderson J.B., Cherukuri P.F., DeWeese-Scott C., Geer L.Y., Gwadz M., He S., Hurwitz D.I., Jackson J.D., Ke Z., Lanczycki C.J., Liebert C.A., Liu C., Lu F., Marchler G.H., Mullokandov M., Shoemaker B.A., Simonyan V., Song J.S., Thiessen P.A., Yamashita R.A., Yin J.J., Zhang D., and Bryant S.H. CDD: a Conserved Domain Database for protein classification. Nucleic Acids Res. 33 (2005) D192-D196
15. Nagata S., Nagase H., Kawane K., Mukae N., and Fuguyama H. Degradation of chromosomal DNA during apoptosis. Cell Death Differ. 10 (2003) 108-116
16. Nicholson D.W., and Thornberry N.A. Caspases: killer proteases. Trends Biochem. Sci. 22 (1997) 299-306
17. Paterson W.D., and Stewart J.E. In vitro phagocytosis of the American lobster (Homarus americanus). J. Fish Res. Board. Can. 31 (1974) 1051-1056
18. Phongdara A., Wanna W., and Chotigeat W. Molecular cloning and expression of caspase from white shrimp Penaeus merguiensis. Aquaculture 252 (2006) 114-120
19. Sambrook J., and Russell D.W. Molecular Cloning: A Laboratory Manual. 3th ed. (2001), Cold Spring Harbor, NY
20. Shi Y. Mechanisms of caspase activation and inhibition during apoptosis. Mol. Cell 9 (2002) 459-470
21. Soderhall K., and Smith V.J. Separation of the hemocyte populations of Carcinus maenas and other marine decapods, and prophenoloxidase distribution. Dev. Comp. Immunol. 7 (1983) 229-239
22. Song Z., McCall K., and Steller H. DCP-1, a Drosophila cell death protease essential for development. Science 275 (1997) 536-540
23. Thompson J.D., Higgins D.G., and Gibson T.J. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 22 (1994) 4673-4680
24. Thornberry N.A., and Lazebnik Y. Caspases: enemies within. Science 281 (1998) 1312-1316
25. 1/2 mouse embryonic cells: evidence for internucleosomal DNA modification in the absence of double strand cleavage. Proc. Natl. Acad. Sci. U.S.A. 90 (1993) 853-857
26. Tonganunt M., Phongdara A., Chotigeat W., and Fujise K. Identification and characterization of syntenin binding protein in the black tiger shrimp Penaeus monodon. J. Biotechnol. 120 (2005) 135-145
27. van de Braak, K., 2002. Haemocytic defence in black tiger shrimp (Penaeus monodon). PhD Thesis. Wageningen University.
28. Villa P., Kaufmann S.H., and Earnshaw W.C. Caspases and caspase inhibitors. TIBS 22 (1997) 388-393
29. Wang X., Zelenski N.G., Yang J., Sakai J., Brown M.S., and Goldstein J.L. Cleavage of sterol regulatory element binding proteins (SREBPs) by CPP32 during apoptosis. EMBO J. 15 (1996) 1012-1020
30. Wolf B.B., and Green D.R. Suicidal tendencies: apoptotic cell death by caspase family proteinases. J. Biol. Chem. 274 (1999) 20049-20052
31. Wongprasert K., Khanobdee K., Glunukarn S.S., Meeratana P., and Withyachumnarnkul B. Time-course and levels of apoptosis in various tissues of black tiger shrimp Penaeus monodon infected with white-spot syndrome virus. Dis. Aquat. Organ. 55 (2003) 3-10
32. Wongteerasupaya C., Vickers J.E., Sriurairatana S., Nash G.L., Akarajamon A., Boonsaeng V., Panyim S., Tasanakajorn A., Withyachamnarnkul B., and Flegel T.W. A non-occluded systemic baculovirus that occurs in cell of ectodermal and mesodermal origin and cause high mortality in the black tiger prawn Penaeus monodon. Dis. Aquat. Organ. 21 (1995) 69-77
33. Wu J.L., and Muroga K. Apoptosis does not play an important role in the resistance of 'immune' Penaeus japonicus against white spot syndrome virus. J. Fish Dis. 27 (2004) 15-21