跳到主要內容

臺灣博碩士論文加值系統

(18.97.14.91) 您好!臺灣時間:2025/01/16 21:21
字體大小: 字級放大   字級縮小   預設字形  
回查詢結果 :::

詳目顯示

我願授權國圖
: 
twitterline
研究生:劉宛菁
研究生(外文):Wang-Jing Liu
論文名稱:蝦白點症病毒極早期基因ie1之研究
論文名稱(外文):Studies on shrimp white spot syndrome virus(WSSV) immediate-early gene ie1
指導教授:羅竹芳羅竹芳引用關係郭光雄
指導教授(外文):Chu-Fang LoGuang-Hsiung Kou
學位類別:博士
校院名稱:國立臺灣大學
系所名稱:動物學研究研究所
學門:生命科學學門
學類:生物學類
論文種類:學術論文
論文出版年:2007
畢業學年度:95
語文別:中文
論文頁數:94
中文關鍵詞:放線菌酮白點症病毒極早期基因
外文關鍵詞:cycloheximidewhite spot syndrome virusimmediate early gene
相關次數:
  • 被引用被引用:0
  • 點閱點閱:496
  • 評分評分:
  • 下載下載:0
  • 收藏至我的研究室書目清單書目收藏:0
本研究首度成功的應用放線菌酮(cycloheximide)抑制了白點症病毒(white spot syndrome virus)感染細胞後病毒新生蛋白質的合成,再結合白點症病毒開放譯讀區(open reading frame)微陣列進行病毒基因表現整體分析,篩選出六十個候選的極早期(immediate early, IE)基因,進一步藉由反轉錄-聚合酶鏈反應(reverse transcriptase-polymerase chain reaction),確認出此六十個基因中在白點症病毒台灣分離株基因體上編號分別為126、242和418號的開放譯讀區,其基因表現確實不受到放線菌酮處理影響,將此三個基因分別命名為ie1, ie2和ie3。這三個基因的序列同樣也出現在其他的白點症病毒分離株,在中國分離株基因體上三個基因均可分別對應到其所預測的開放譯讀區,但在泰國分離株則僅有相對於ie1的序列被預測為是一個開放譯讀區。另外在秋夜盜蛾(Spodoptera frugiperda)細胞株Sf9中,以增強型綠螢光蛋白(enhanced green fluorescence protein)基因為報導基因進行啟動子(promoter)活性分析顯示,白點症病毒ie1的啟動子展現為一個極強勢的啟動子,其在此昆蟲細胞內所啟動增強型綠螢光蛋白表現量,甚而還高過昆蟲病毒–花旗松毒蛾核多角體病毒(Orgyia pseudotsugata multicapsid nucleopolyhedrovirus)極早期基因ie2啟動子所啟動的基因表現。在節肢動物例如果蠅中,Janus kinase-signal transducer and activator of transcription (JAK-STAT)訊息傳導路徑是其對抗病毒感染的機制上重要的角色,但在本研究中發現白點症病毒卻是可以利用草蝦的STAT作為一個轉錄因子來促進病毒基因ie1在感染細胞中的表現。由於白點症病毒ie1的啟動子不僅可在蝦細胞也可在昆蟲細胞中被活化,我們將ie1啟動子區域核苷酸序列進行其可能的功能預測,並在Sf9昆蟲細胞中對此啟動子區域進行一系列的核苷酸序列刪除及突變分析,發現此啟動子的區域中包含了一個STAT結合的位置,而同時也證實此結合位對於此一啟動子的整體活性是非常重要的。另外,利用Sf9昆蟲細胞以32P標定的白點症病毒ie1的啟動子中與STAT結合區域的DNA片段當作探針進行電泳流動性轉移分析(electrophoresis mobility shift assay),可偵測到一個特殊的蛋白質-DNA複合體的存在;將重組草蝦STAT在Sf9昆蟲細胞中進行大量表現,經電泳流動性轉移分析後再利用專一性抗體反應,證實了此一複合物中的蛋白質為STAT;另外的電泳流動性轉移分析也顯示,白點症病毒感染後的草蝦細胞內被活化的STAT的量多於未被病毒感染的草蝦。活化作用(transactivation)的分析顯示,STAT的劑量與ie1啟動子活性具有正相關性,當昆蟲細胞內重組草蝦STAT蛋白的表現量增加時,白點症病毒ie1的啟動子的活性也跟著增加。這些結果顯示STAT能夠直接活化白點症病毒ie1的表現,同時也顯示STAT在ie1啟動子呈現為一個強勢啟動子上扮演重要的角色,由此推論白點症病毒可以成功的利用一個可能是宿主的防禦機制,來加強病毒極早期基因的表現。
Here we report for the first time the successful use of cycloheximide (CHX) as an inhibitor to block de novo viral protein synthesis during white spot syndrome virus (WSSV) infection. Sixty candidate immediate early (IE) genes were identified using a global analysis microarray technique. RT-PCR showed that the genes corresponding to ORF126, ORF242 and ORF418 in the Taiwan isolate were consistently CHX-insensitive, and these genes were designated ie1, ie2 and ie3, respectively. The sequences for these IE genes also appear in the two other WSSV isolates that have been sequenced. Three corresponding ORFs were identified in the China WSSV isolate, but only an ORF corresponding to ie1 was predicted in the Thailand isolate. In a promoter activity assay in Sf9 insect cells using enhanced green fluorescence protein (EGFP) as a reporter, ie1 showed very strong promoter activity, producing higher EGFP signals than the insect Orgyia pseudotsugata multicapsid nucleopolyhedrovirus ie2 promoter. Although the Janus kinase-signal transducer and activator of transcription (JAK-STAT) signaling pathway is part of the anti-viral response in arthropods such as Drosophila, here we show that WSSV uses shrimp STAT as a transcription factor to enhance viral gene expression in host cells. In a series of deletion and mutation assays using the WSSV immediate early gene ie1 promoter, which is active in shrimp cells and also in insect Sf9 cells, an element containing a STAT binding motif was shown to be important for the overall level of WSSV ie1 promoter activity. In the Sf9 insect cell line, a specific protein-DNA complex was detected by using electrophoresis mobility shift assays (EMSA) with the 32P-labeled STAT binding motif of the WSSV ie1 promoter as the probe. When recombinant Penaeus monodon STAT (rPmSTAT) was overexpressed in Sf9 cells, EMSA with specific antibodies confirmed that the STAT was responsible for the formation of the specific protein-DNA complex. Another EMSA showed that in WSSV-infected P. monodon, levels of activated PmSTAT were higher than in WSSV-free P. monodon. A transactivation assay of the WSSV ie1 promoter demonstrated that increasing the level of rPmSTAT led to dose-dependent increases in ie1 promoter activity. These results show that STAT directly transactivates WSSV ie1 gene expression and contributes to its high promoter activity. We conclude that WSSV has successfully annexed a putative shrimp defense mechanism, which it now uses to enhance the expression of viral immediate early genes.
中文摘要……………………………………………………………… I
英文摘要………………………………………………………………III
前言…………………………………………………………………… 1
材料與方法…………………………………………………………… 8
結果……………………………………………………………………27
討論……………………………………………………………………40
參考文獻………………………………………………………………50
表………………………………………………………………………68
圖………………………………………………………………………72
本研究發表之相關論文………………………………………………94
Adams, M. D., S. E. Celniker, R. A. Holt, C. A. Evans, J. D. Gocayne, P. G. Amanatides, S. E. Scherer, P. W. Li, R. A. Hoskins, R. F. Galle, R. A. George, S. E. Lewis, S. Richards, M. Ashburner, S. N. Henderson, G. G. Sutton, J. R. Wortman, M. D. Yandell, Q. Zhang, L. X. Chen, R. C. Brandon, Y. H. Rogers, R. G. Blazej, M. Champe, B. D. Pfeiffer, K. H. Wan, C. Doyle, E. G. Baxter, G. Helt, C. R. Nelson, G. L. Gabor, J. F. Abril, A. Agbayani, H. J. An, C. Andrews-Pfannkoch, D. Baldwin, R. M. Ballew, A. Basu, J. Baxendale, L. Bayraktaroglu, E. M. Beasley, K. Y. Beeson, P. V. Benos, B. P. Berman, D. Bhandari, S. Bolshakov, D. Borkova, M. R. Botchan, J. Bouck, P. Brokstein, P. Brottier, K. C. Burtis, D. A. Busam, H. Butler, E. Cadieu, A. Center, I. Chandra, J. M. Cherry, S. Cawley, C. Dahlke, L. B. Davenport, P. Davies, B. de Pablos, A. Delcher, Z. Deng, A. D. Mays, I. Dew, S. M. Dietz, K. Dodson, L. E. Doup, M. Downes, S. Dugan-Rocha, B. C. Dunkov, P. Dunn, K. J. Durbin, C. C. Evangelista, C. Ferraz, S. Ferriera, W. Fleischmann, C. Fosler, A. E. Gabrielian, N. S. Garg, W. M. Gelbart, K. Glasser, A. Glodek, F. Gong, J. H. Gorrell, Z. Gu, P. Guan, M. Harris, N. L. Harris, D. Harvey, T. J. Heiman, J. R. Hernandez, J. Houck, D. Hostin, K. A. Houston, T. J. Howland, M. H. Wei, and C. Ibegwam. 2000. The genome sequence of Drosophila melanogaster. Science 287:2185-2195.
Agaisse, H., and N. Perrimon. 2004. The roles of JAK/STAT signaling in Drosophila immune responses. Immunol. Rev. 198:72-82.
Agaisse, H., U. M. Petersen, M. Boutros, B. Mathey-Prevot, and N. Perrimon. 2003. Signaling role of hemocytes in Drosophila JAK/STAT-dependent response to septic injury. Dev. Cell. 5:441-450.
Antonucci, T. K., and W. J. Rutter. 1989. Hepatitis B virus (HBV) promoters are regulated by the HBV enhancer in a tissue-specific manner. J. Virol. 63:579-583.
Aubert, M., and J. A. Blaho. 1999. The Herpes Simplex Virus Type 1 Regulatory Protein ICP27 Is Required for the Prevention of Apoptosis in Infected Human Cells. J. Virol. 73:2803-2813.
Barillas-Mury, C., Y.-S. Han, D. Seeley, and F. C. Kafatos. 1999. Anopheles gambiae Ag-STAT, a new insect member of the STAT family, is activated in response to bacterial infection. EMBO J. 18:959-967.
Caenorhabditis elegans Sequencing Consortium. 1998. Genome sequence of the nematode Caenorhabditis elegans: a platform for investigating biology. Science 282:2012-2018.
Carson, D. D., M. D. Summers, and L. A. Guarino. 1991. Transient expression of the Autographa californica nuclear polyhedrosis virus immediate-early gene, IE-N, is regulated by three viral elements. J. Virol. 65:945-951.
Chen, L.-L., H.-C. Wang, C.-J. Huang, S.-E. Peng, Y.-G. Chen, S.-J. Lin, W.-Y. Chen, C.-F. Dai, H.-T. Yu, C.-H. Wang, C.-F. Lo, and G.-H. Kou. 2002. Transcriptional analysis of the DNA polymerase gene of shrimp white spot syndrome virus. Virology 301:136-147.
Cherbas, L., and P. Cherbas. 1993. The arthropod initiator: the capsite consensus plays an important role in transcription. Insect Biochem. Mol. Biol. 23:81-90.
Chou, H.-Y., C.-Y. Huang, C.-H. Wang, H.-C. Chiang, and C.-F. Lo. 1995. Pathogenicity of a baculovirus infection causing white spot syndrome in cultured penaeid shrimp in Taiwan. Dis. Aquat. Org. 23:165-173.
Darnell, J. E., Jr., I. M. Kerr, and G. M. Stark. 1994. Jak-STAT pathways and transcriptional activation in response to IFNs and other extracellular signaling proteins. Science 264:1415-1421.
Dehal, P., Y. Satou, R. K. Campbell, J. Chapman, B. Degnan, A. De Tomaso, B. Davidson, A. Di Gregorio, M. Gelpke, D. M. Goodstein, N. Harafuji, K. E. Hastings, I. Ho, K. Hotta, W. Huang, T. Kawashima, P. Lemaire, D. Martinez, I. A. Meinertzhagen, S. Necula, M. Nonaka, N. Putnam, S. Rash, H. Saiga, M. Satake, A. Terry, L. Yamada, H. G. Wang, S. Awazu, K. Azumi, J. Boore, M. Branno, S. Chin-Bow, R. DeSantis, S. Doyle, P. Francino, D. N. Keys, S. Haga, H. Hayashi, K. Hino, K. S. Imai, K. Inaba, S. Kano, K. Kobayashi, M. Kobayashi, B. I. Lee, K. W. Makabe, C. Manohar, G. Matassi, M. Medina, Y. Mochizuki, S. Mount, T. Morishita, S. Miura, A. Nakayama, S. Nishizaka, H. Nomoto, F. Ohta, K. Oishi, I. Rigoutsos, M. Sano, A. Sasaki, Y. Sasakura, E. Shoguchi, T. Shin-i, A. Spagnuolo, D. Stainier, M. M. Suzuki, O. Tassy, N. Takatori, M. Tokuoka, K. Yagi, F. Yoshizaki, S. Wada, C. Zhang, P. D. Hyatt, F. Larimer, C. Detter, N. Doggett, T. Glavina, T. Hawkins, P. Richardson, S. Lucas, Y. Kohara, M. Levine, N. Satoh, and D. S. Rokhsar. 2002. The draft genome of Ciona intestinalis: insights into chordate and vertebrate origins. Science 298:2157-2167.
Dickson, J. A., and P. D. Friesen. 1991. Identification of upstream promoter elements mediating early transcription from the 35,000-molecular-weight protein gene of Autographa californica nuclear polyhedrosis virus. J. Virol. 65:4006-4016.
Dostert, C., E. Jouanguy, P. Irving, L. Troxler, D. Galiana-Arnoux, C. Hetru, J. A. Hoffmann, and J. L. Imler. 2005. The Jak-STAT signaling pathway is required but not sufficient for the antiviral response of drosophila. Nat. Immunol. 6:946-953.
Durand, S., D. V. Lightner, R. M. Redman, J. R. Bonami. 1997. Ultrastructure and morphogenesis of White Spot Syndrome Baculovirus (WSSV). Dis. Aquat. Org. 29:205-211.
Edwards, D. R., and L. C. Mahadevan. 1992. Protein synthesis inhibitors differentially superinduce c-fos and c-jun by three distinct mechanisms: lack of evidence for labile repressors. EMBO J. 11:2415-2424.
Flegel, T. W. 1997. Special topic review: major viral disease of the black tiger prawn (Penaeus monodon) in Thailand. World J. Microbiol. Biotech. 13:433-442.
Frech, B., and E. Peterhans. 1994. RT-PCR: ‘background priming’ during reverse transcription. Nucleic Acids Res. 22:4342-4343.
Friesen, P. D. 1997. Regulation of baculovirus early gene expression, p. 141-170. In L. K. Miller (ed.), The baculoviruses. Plenum Publishing Corporation, New York, N.Y.
Friesen, P. D., and L. K. Miller. 1986. The regulation of baculovirus gene expression. Curr. Top. Microbiol. Immunol. 131:31-49.
Greenberg, M. E., A. L. Hermanowski, and E. B. Ziff. 1986. Effect of Protein Synthesis Inhibitors on Growth Factor Activation of c-fos, c-myc, and Actin Gene Transcription. 6:1050-1057.
Guarino, L. A., and M. D. Summers. 1986. Functional mapping of a trans-activating gene required for expression of a baculovirus delayed-early gene. J. Virol. 57: 563-571.
Guarino, L. A., and M. W. Smith. 1992. Regulation of delayed-early gene transcription by dual TATA boxes. J. Virol. 66:3733-3739.
Gwack, Y., S. Hwang, C. Lim, Y. S. Won, C. H. Lee, and J. Choe. 2002. Kaposi’s sarcoma-associated herpesvirus open reading frame 50 stimulates the transcriptional activity of STAT3. J. Biol. Chem. 277:6438-6442.
Halford, W. P., and P. A. Schaffer. 2001. ICP0 is required for efficient reactivation of herpes simplex virus type 1 from neuronal latency.J. Virol. 75:3240-3249.
Harrison, R. L., and B. C. Bonning. 2003. Comparative analysis of the genomes of Rachiplusia ou and Autographa californica multiple nucleopolyhedroviruses. J. Gen. Virol. 84:1827-1842.
He, N., Q. Qin, and X. Xu. 2005. Differential profile of genes expressed in hemocytes of White Spot Syndrome Virus-resistant shrimp (Penaeus japonicus) by combining suppression subtractive hybridization and differential hybridization. Antiviral Res. 66:39-45.
Hegedus, D. D., T. A. Pfeifer, J. Hendry, D. A. Theilmann, and T. A. Grigliatti. 1998. A series of broad host range shuttle vectors for constitutive and inducible expression of heterologous proteins in insect cell lines. Gene 207:241-249.
Holt, R. A., G. M. Subramanian, A. Halpern, G. G. Sutton, R. Charlab, D. R. Nusskern, P. Wincker, A. G. Clark, J. M. Ribeiro, R. Wides, S. L. Salzberg, B. Loftus, M. Yandell, W. H. Majoros, D. B. Rusch, Z. Lai, C. L. Kraft, J. F. Abril, V. Anthouard, P. Arensburger, P. W. Atkinson, H. Baden, V. de Berardinis, D. Baldwin, V. Benes, J. Biedler, C. Blass, R. Bolanos, D. Boscus, M. Barnstead, S. Cai, A. Center, K. Chatuverdi, G. K. Christophides, M. A. Chrystal, M. Clamp, A. Cravchik, V. Curwen, A. Dana, A. Delcher, I. Dew, C. A. Evans, M. Flanigan, A. Grundschober-Freimoser, L. Friedli, Z. Gu, P. Guan, R. Guigo, M. E. Hillenmeyer, S. L. Hladun, J. R. Hogan, Y. S. Hong, J. Hoover, O. Jaillon, Z. Ke, C. Kodira, E. Kokoza, A. Koutsos, I. Letunic, A. Levitsky, Y. Liang, J. J. Lin, N. F. Lobo, J. R. Lopez, J. A. Malek, T. C. McIntosh, S. Meister, J. Miller, C. Mobarry, E. Mongin, S. D. Murphy, D. A. O''Brochta, C. Pfannkoch, R. Qi, M. A. Regier, K. Remington, H. Shao, M. V. Sharakhova, C. D. Sitter, J. Shetty, T. J. Smith, R. Strong, J. Sun, D. Thomasova, L. Q. Ton, P. Topalis, Z. Tu, M. F. Unger, B. Walenz, A. Wang, J. Wang, M. Wang, X. Wang, K. J. Woodford, J. R. Wortman, M. Wu, A. Yao, E. M. Zdobnov, H. Zhang, and Q. Zhao. 2002. The genome sequence of the malaria mosquito Anopheles gambiae. Science 298:129-149.
Honess, R. W., and B. Roizman. 1974. Regulation of herpesvirus macromolecular synthesis. I. Cascade regulation of the synthesis of three groups of viral proteins. J. Virol. 14:8-19.
Honigwachs, J., O. Faktor, R. Dikstein, Y. Shaul, and O. Laub. 1989. Liver-specific expression of hepatitis B virus is determined by the combined action of the core gene promoter and the enhancer. J. Virol. 63:919-924.
Horvath, C. M., Z. Wen, and J. E. Darnell, Jr. 1995. A STAT protein domain that determines DNA sequence recognition suggests a novel DNA-binding domain. Genes Dev. 9:984-994.
Hossain, M. S., S. Khadijah, and J. Kwang. 2004. Characterization of ORF89- a latency-related gene of white spot syndrome virus. Virology. 325:106-115.
Huang, J., X. L. Song, J. Yu, and C. H. Yang. 1995. Baculoviral hypodermal and hematopoietic necrosis-study on the pathogen and pathology of the explosive epidemic disease of shrimp. Marine Fish. Res. 16:1-10.
Jameel, S., and A. Siddiqui. 1986. The human hepatitis B virus enhancer requires trans-acting cellular factor(s) for activity. Mol. Cell. Biol. 6:710-715.
Khadijah, S., S. Y. Neo, M. S. Hossain, L. D. Miller, S. Mathavan, and J. Kwang. 2003. Identification of white spot syndrome virus latency-related genes in specific-pathogen-free shrimps by use of a microarray. J. Virol. 77:10162-10167.
Kisseleva, T., S. Bhattacharya, J. Braunstein, and C. W. Schindler. 2002. Signaling through the JAK/STAT pathway, recent advances and future challenges. Gene. 285:1-24.
Kogan, P. H., and G. W. Blissard. 1994. A baculovirus gp64 early promoter is activated by host transcription factor binding to CACGTG and GATA elements. J. Virol. 68:813-822.
Komatsu, T., K. Takeuchi, J. Yokoo, Y. Tanaka, and B. Gotoh. 2000. Sendai virus blocks alpha interferon signaling to signal transducers and activators of transcription. J Virol. 74:2477-2480.
Kou, G.-H., S.-E. Peng, Y.-L. Chiu, and C.-F. Lo. 1998. Tissue distribution of white spot syndrome virus (WSSV) in shrimp and crabs. In Felgel TW (ed) Advances in shrimp biotechnology. National Center for Genetic Engineering and Biotechnology, Bangkok. pp267-271.
Kovacs, G. R., J. Choi, L. A. Guarino, and M. D. Summers. 1992. Functional dissection of the Autographa californica nuclear polyhedrosis virus immediate-early 1 transcriptional regulatory protein. J. Virol. 66:7429-7437.
Kovacs, G. R., L. A. Guarino, and M. D. Summers. 1991. Novel regulatory properties of the IE1 and IE0 transactivators encoded by the baculovirus Autographa californica multicapsid nuclear polyhedrosis virus. J. Virol. 65:5281-5288.
Kwon, E. J., H. S. Park, Y. S. Kim, E. J. Oh, Y. Nishida, A. Matsukage, M. A. Yoo, and M. Yamaguchi. 2000. Transcriptional regulation of the Drosophila raf proto-oncogene by Drosophila STAT during development and in immune response. J. Biol. Chem. 275:19824-19830.
Lahiri, D. K., and Y.-W. Ge. 2000. Electrophoretic mobility shift assay for the detection of specific DNA-protein complex in nuclear extracts from the cultured cells and frozen autopsy human brain tissue. Brain Res. Protoc. 5:257-265.
Leu, J.-H., J.-M. Tsai, H.-C. Wang, A.-H. Wang, C.-H. Wang, G.-H. Kou, and C.-F. Lo. 2005. The unique stacked rings in the nucleocapsid of the white spot syndrome virus virion are formed by the major structural protein VP664, the largest viral structural protein ever found. J. Virol. 79:140-149.
Levy, D. E., and A. Garcia-Sastre. 2001. The virus battles: IFN induction of the antiviral state and mechanisms of viral evasion. Cytokine Growth Factor Rev. 12:143-156.
Lin, C.-C., C.-M. Chou, Y.-L. Hsu, J.-C. Lien, Y.-M. Wang, S.-T. Chen, S.-C. Tsai, P.-W. Hsiao, and C.-J. Huang. 2004. Characterization of two mosquito STATs, AaSTAT and CtSTAT. J. Biol. Chem. 279:3308-3317.
Liu, W.-J., H.-T. Yu, S.-E. Peng, Y.-S. Chang, H.-W. Pien, C.-J. Lin, C.-J. Huang,
Lo, C.-F., C.-H. Ho, C.-H. Chen, K.-F. Liu, Y.-L. Chiu, P.-Y. Yeh, S.-E. Peng, H.-C. Hsu, H.-C. Liu, C.-F. Chang, M.-S. Su, C.-H. Wang, and G.-H. Kou. 1997. Detection and tissue tropism of white spot syndrome baculovirus (WSBV) in captured brooders of Penaeus monodon with a special emphasis on reproductive organs. Dis. Aquat. Org. 30:53-72.
Lo, C.-F., C.-H. Ho, S.-E. Peng, C.-H. Chen, H.-C. Hsu, Y.-L. Chiu, C.-F. Chang, K.-F. Liu, M.-S. Su, C.-H. Wang, and G.-H. Kou. 1996. White spot syndrome baculovirus (WSBV) detected in cultured and captured shrimp, crabs and other arthropods. Dis. Aquat. Org. 27:215-225.
Lo, C.-F., S.-E. Peng, Y.-S. Chang, and G.-H. Kou. 2005 White spot syndrome-What we have learned about the virus and the disease. In Walker P, R. Lester, M. G. Bondad-Reantaso (eds). Diseases in Asian Aquaculture V, Fish Health Section, Asian Fisheries Society, Manila. pp 421-433.
Lo, C.-F., Y.-S. Chang, S.-E. Peng, and G.-H. Kou. 2003. Major viral disase of Penaeus monodon in Taiwan. J. Fish. Soc. Taiwan. 30: 1-13.
Lu, L., and J. Kwang. 2004. Identification of a novel shrimp protein phosphatase and its association with latency-related ORF427 of white spot syndrome virus. FEBS Lett. 577:141-146.
Lu, L., H. Wang, I. Manopo, L. Yu, and J. Kwang. 23 August 2005, posting date. Baculovirus-mediated promoter assay and transcriptional analysis of white spot syndrome virus orf427 gene. Virol. J. 2. http://www.virologyj.com/content/2/1/71.
M.-F. Tsai, C.-H. Wang, J.-Y. Lin, C.-F. Lo, and G.-H. Kou. 2001. Cloning, characterization, and phylogenetic analysis of a shrimp white spot syndrome virus gene that encodes a protein kinase. Virology 289:362-377.
Maeda, M., H. Saitoh, E. Mizuki, T. Itami, and M. Ohba. 2004. Replication of white spot syndrome virus in ovarian primary cultures from the kuruma shrimp, Marsupenaeus japonicus. J. Virol. Methods. 116:89-94.
Nakano, H., H. Koube, S. Umezawa, K. Momoyama, M. Hiraoka, K. Inouye, and N. Oseko. 1994. Mass mortalities of cultured kuruma shrimp, Penaeus japonicus, in Japan in 1993: Epizootiological survey and infection trails. Fish Pathol. 29:135-139.
O’ Hare P. 1993. The virion transactivator of herpes simplex virus. Semin. Virol. 4:145-155.
Olson, V. A., J. A. Wetter, and P. D. Friesen. 2001. Oligomerization mediated by a helix-loop-helix-like domain of baculovirus IE1 is required for early promoter transactivation. J. Virol. 75:6042-6051.
Passarelli, A. L., and L. K. Miller. 1993. Three baculovirus genes involved in late and very late gene expression: ie-1, ie-n, and lef-2. J. Virol. 67:2149-2158.
Preston, C. M., A. Rinaldi, and M. J. Nicholl. 1998. Herpes simplex virus type 1 immediate early gene expression is stimulated by inhibition of protein synthesis. J. Gen. Virol. 79:117-24.
Pullen, S. S., and P. D. Friesen. 1995. Early transcription of the ie-1 transregulator gene of Autographa californica nuclear polyhedrosis virus is regulated by DNA sequences within its 5'' noncoding leader region. J. Virol. 69:156-65.
Pullen, S. S., and P. D. Friesen. 1995. The CAGT motif functions as an initiator element during early transcription of the baculovirus transregulator ie-1. J. Virol. 69:3575-3583.
Rodems, S. M., S. S. Pullen, and P. D. Friesen. 1997. DNA-dependent transregulation by IE1 of Autographa californica nuclear polyhedrosis virus: IE1 domains required for transactivation and DNA binding. J. Virol.71:9270-9277.
Roizman, B., and A. E. Sears. 1996. Herpes simplex viruses and their replication, p. 1043-1107. In Fields, B. N., D. M. Knipe, and P. M. Howley (ed.). Fundamental virology, 3rd ed. Lippincott-Raven, Philadelphia, Pa.
Samuel, C. E. 2001. Antiviral actions of interferons. Clin. Microbiol. Rev. 14:778-809.
Sanfilippo, C. M., and J. A. Blaho. 2006. ICP0 Gene Expression Is a Herpes Simplex Virus Type 1 Apoptotic Trigger. J. Virol. 80:6810-6821.
Schindler, C., and J. E. Darnell, Jr. 1995. Transcriptional responses to polypeptide ligands: the JAK-STAT pathway. Annu. Rev. Biochem. 64:621-651.
Slack, J. M., and G. W. Blissard. 1997. Identification of two independent transcriptional activation domains in the Autographa californica multicapsid nuclear polyhedrosis virus IE1 protein. J. Virol. 71:9579-9587.
Sliva, D., and L.-A. Haldosen. 1996. STAT-like DNA-binding activity in Spodoptera frugiperda cells. Biochem. Biophysic. Res. Com. 225:562-569.
Sliva, D., T. J. Wood, C. Schindler, P. E. Lobie, and G. Norstedt. 1994. Growth hormone specifically regulates serine protease inhibitor gene transcription via gamma-activated sequence-like DNA elements. J. Biol. Chem. 269:26208-26214.
Stewart, T. M., I. Huijskens, L. G. Willis, and D. A. Theilmann. 2005. The Autographa californica Multiple Nucleopolyhedrovirus ie0-ie1 Gene Complex Is Essential for Wild-Type Virus Replication, but either IE0 or IE1 Can Support Virus Growth. J. Virol. 79:4619-4629.
Takaoka, A., and H. Yanai. 2006. Interferon signalling network in innate defence. Cell Microbiol. 8:907-22.
Torok, I., and F. Karch. 1980 Nucleotide sequences of heat shock activated genes in Drosophila melanogaster. I. Sequences in the regions of the 5’ and 3’ ends of the hsp 70 gene in the hybrid plasmid 56H8. Nucleic Acids Res. 8:3105-3123.
Tsai, J.-M., H.-C. Wang, J.-H. Leu, A. H. Wang, Y. Zhung, P. J. Walker, G.-H. Kou, and C.-F. Lo. 2006. Identification of the nucleocapsid, tegument, and envelope proteins of the shrimp white spot syndrome virus virion. J. Virol. 80:3021-3029.
Tsai, J.-M., H.-C. Wang, J.-H. Leu, H.-H. Hsiao, A. H. Wang, G.-H. Kou, and C.-F. Lo. 2004. Genomic and proteomic analysis of thirty-nine structural proteins of shrimp white spot syndrome virus. J. Virol. 78:11360-11370.
Tsai, M.-F., C.-F. Lo, M. C. W. van Hulten, H.-F. Tzeng, C.-M. Chou, C.-J. Huang, C.-H. Wang, J.-Y. Lin, J. M. Vlak, and G.-H. Kou. 2000a. Transcriptional analysis of the ribonucleotide reductase genes of shrimp white spot syndrome virus. Virology 277:92-99.
Tsai, M.-F., G.-H. Kou, H.-C. Liu, K.-F. Liu, C.-F. Chang, S.-E. Peng, H.-C. Hsu, C.-H. Wang, and C.-F. Lo. 1999. Long-term presence of white spot syndrome virus (WSSV) in a cultivated shrimp population without disease outbreaks. Dis. Aquat. Org. 38:107-114.
Tsai, M.-F., H.-T. Yu, H.-F. Tzeng, J.-H. Leu, C.-M. Chou, C.-J. Huang, C.-H. Wang, J.-Y. Lin, G.-H. Kou, and C.-F. Lo. 2000b. Identification and characterization of a shrimp white spot syndrome virus (WSSV) gene that encodes a novel chimeric polypeptide of cellular-type thymidine kinase and thymidylate kinase. Virology 277:100-110.
van Hulten, M. C. W., J. Witteveldt, S. Peters, N. Kloosterboer, R. Tarchini, M. Fiers, H. Sandbrink, R. K. Lankhorst, and J. M. Vlak. 2001. The white spot syndrome virus DNA genome sequence. Virology 286:7-22.
van Hulten, M. C. W., M. Reijus, A. M. G. Vermeesch, F. Zandbergen, and J. M. Vlak. 2002 . Identification of VP19 and VP15 of white spot syndrome virus (WSSV) and glycosylation of the WSSV major structural proteins. J. Gen. Virol. 83:257-265.
van Hulten, M. C., M. Westenberg, S. D. Goodall, and J. M. Vlak. 2000. Identification of two major virion protein genes of white spot syndrome virus of shrimp. Virology 266:227-236.
Vlak, J. M., J. R. Bonami, T. W. Flegel, G. H. Kou, D. V. Lightner, C.-F. Lo, P. C. Loh, and P. W. Walker. 2004. Nimaviridae, p. 187-192. In Fauquet, C. M., M. A. Mayo, J. Maniloff, U. Desselberger, and L. A. Ball (ed.). VIIIth Report of the International Committee on Taxonomy of Viruses. Elsevier.
Wang, C.-H., C.-F. Lo, J.-H. Leu, C.-M. Chou, P.-Y. Yeh, H.-Y. Chou, M.-C. Tung, C.-F. Chang, M.-S. Su, and G.-H. Kou. 1995. Purification and genomic analysis of baculovirus associated with white spot syndrome (WSBV) of Penaeus monodon. Dis. Aquat. Org. 23:239-242.
Wang, H.-C., A.-T. Lin, D.-M. Yii, Y.-S. Chang, G.-H. Kou, and C.-F. Lo. 2004. DNA microarrays of the white spot syndrome virus genome: genes expressed in the gills of infected shrimp. Mar. Biotechnol. 6:S106-S111.
Wang, Z., L. Hu, G. Yi, H. Xu, Y. Qi, and L. Yao. 2004. ORF390 of white spot syndrome virus genome is identified as a novel anti-apoptosis gene. Biochem. Biophys. Res. Commun. 325:899-907.
Waris, G., and A. Siddiqui. 2002. Interaction between STAT-3 and HNF-3 leads to the activation of liver-specific hepatitis B virus enhancer 1 function. J. Virol. 76:2721-27299.
Watson, R. J., and J. B. Clements. 1980. A herpes simplex virus type 1 function continuously required for early and late virus RNA synthesis. Nature 285:329-330.
Weir, J. P. 2001. Regulation of herpes simplex virus gene expression. Gene 271:117-130.
Wongteerasupaya, C., J. E. Vickers, S. Sriurairatana, G. L. Nash, A. Akarajamorn, V. Boonsaeng, S. Panyim, A. Tassanakajon, B. Withyachumnarnkul, and T. W. Flegel. 1995. A non-occluded, systemic baculovirus that occurs in the cells of ectodermal and mesodermal origin and causes high mortality in the black tiger prawn Penaeus monodon. Dis. Aquat. Org. 21:69-77.
Xu, X., Y. L. Sun, and T. Hoey. 1996. Cooperative DNA binding and sequence-selection recognition conferred by the STAT amino-terminal domain. Science 273:794-797.
Yang, F., J. He, X. Lin, Q. Li, D. Pan, X. Zhang, and X. Xu. 2001. Complete genome sequence of the shrimp white spot bacilliform virus. J. Virol. 75:11811-11820.
Yokosawa, N., T. Kubota, and N. Fujii. 1998. Poor induction of interferon-induced 2’, 5’-oligoadenylate synthetase (2-5 AS) in cells persistently infected with mumps virus is caused by decrease of STAT-1 alpha. Arch. Virol. 143: 1985-1992.
York, I., C. Roop, D. W. Andrews, S. R. Riddel, F. L. Graham, and D. C. Johnson. 1994. A cytosolic herpes simplex virus protein inhibits antigen presentation to CD82 T lymphocytes. Cell 77:525-535.
Zhang, X., C. Huang, X Tang, Y. Zhuang, and C. L. Hew. 2004. Identification of structural proteins from shrimp white spot syndrome virus (WSSV) by 2DE-MS. Proteins. 55:229-235.
Zhao, Y. G., and P. Eggleston. 1999. Comparative analysis of promoters for transient gene expression in cultured mosquito cells. Insect Mol. Biol. 8:31-38.
Zinck, R., M. A. Cahill, M. Kracht, C. Sachsenmaier, R. A. Hipskind, and A. Nordheim. 1995. Protein synthesis inhibitors reveal differential regulation of mitogen-activated protein kinase and stress-activated protein kinase pathways that converge on Elk-1. Mol. Cell. Biol. 15:4930-4938.
QRCODE
 
 
 
 
 
                                                                                                                                                                                                                                                                                                                                                                                                               
第一頁 上一頁 下一頁 最後一頁 top