1. Trang chủ
  2. » Giáo Dục - Đào Tạo

INVESTIGATION OF THE FUNCTIONS OF p23 AND COAT PROTEIN OF HIBISCUS CHLOROTIC RINGSPOT VIRU

223 1,5K 0

Đang tải... (xem toàn văn)

Tài liệu hạn chế xem trước, để xem đầy đủ mời bạn chọn Tải xuống

THÔNG TIN TÀI LIỆU

Thông tin cơ bản

Định dạng
Số trang 223
Dung lượng 3,24 MB

Nội dung

INVESTIGATION OF THE FUNCTIONS OF P23 AND COAT PROTEIN OF HIBISCUS CHLOROTIC RINGSPOT VIRUS GAO RUIMIN NATIONAL UNIVERSITY OF SINGAPORE 2013 INVESTIGATION OF THE FUNCTIONS OF P23 AND COAT PROTEIN OF HIBISCUS CHLOROTIC RINGSPOT VIRUS GAO RUIMIN (B.Sc., M.Sc., Henan Agricultural University, PRC) A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR OF PHILOSOPHY DEPARMENT OF BIOLOGICAL SCIENCES NATIONAL UNIVERSITY OF SINGAPORE 2013 ACKNOWLEDGEMENTS My heartiest thank first goes to my supervisor, Prof. Wong Sek Man for his excellent guidance, invaluable instructions, insightful advices and kind support throughout my PhD candidature. I really appreciate Prof. Wong providing me the opportunity to learn plenty of knowledge in the molecular plant virology lab. I have also learnt a lot from Prof. Wong about his wisdom and rich experiences in life which enlightened my life and made me avoiding mistakes. I am grateful of his brilliant minds and warm heart which help me during my hard time and guide me to discover more about my future career. My truthful thanks also go to my PhD quanlify examination committee members, Associate Professor He Yuehui, Dr. He Ying Xin, Cynthia and Dr. Lin Qingsong for their support and kind help during my PhD journey. My sincere thanks to all the members of the Plant Molecular Virology Lab: Dr. Niu Shengniao for her useful research suggestions and experienced technical help. I also thank the undergraduate students Ng Kai Lin Florence, Tan Jia Xin Danica, Wan Zi Yi and Tan Chee Leong Kelvin for helping me in some of the experiments. I also would like to thank my current lab members, Mr. Xie Zhicheng, Ms Wen Yi, Ms Guo Song and Ms Wu Chao and my former lab members Dr. Zhang Xin, Dr. Qiao Yan and Dr. Sunil Kumar Tewary for all of their help and precious friendships during my four years PhD study in the lab. Special thanks also go to all my friends from A/P Pan Shenquan’s lab and Dr. Xu’s lab for their informative discussions and timely help. Special thanks also go to Ms Tong Yan and Ms Foong Choy Mei for their help in my confocal laser microscopy study. I also would like to thank Mr. Chong PL and Madam Loy GL from DBS for their support with electron microscopy work. Last but not the least, I wish to express my deepest appreciations to my family for their encouragement throughout all these years. Special thanks to my husband i Liu Peng, for his continuous support and critical comments. Finally, grateful thanks go to the National University of Singapore for awarding me the NUS research scholarship. ii List of publications 1. Ruimin Gao, Florence Kai Lin Ng, Peng Liu, Sek-Man Wong. (2012) Hibiscus chlorotic ringspot virus coat protein upregulates sulfur metabolism genes for enhanced pathogen defence. Molecular Plant-Microbe Interaction 25: 15741583. 2. Ruimin Gao, Peng Liu, Sek-Man Wong. (2012) Identification of a plant viral RNA genome in the nucleus. PLOS ONE 7(11): e48736. doi:10.1371/journal.pone.0048736 3. Ruimin Gao and Sek-Man Wong. (2013) Basic amino acid mutations in the nuclear localization signal of Hibiscus chlorotic ringspot virus p23 inhibit virus long distance movement. PLOS ONE 8(9): e74000. doi:10.1371/journal.pone.0074000. 4. Ruimin Gao, Danica Jia Xin Tan, Sek-Man Wong. (2013) Upregulation of miR395 targets ATP sulfurylase and sulfate transporter facilitates sulfur enhanced defence after Hibiscus chlorotic ringspot virus infection. Plant Pathology Bulletin 22(2): 107-117 5. Ruimin Gao, Zi Yi Wan, Sek-Man Wong. (2013) Correlation of miRNA fluctuation to plant growth retardation after Hibiscus chlorotic ringspot virus infection (under review). iii Table of Contents ACKNOWLEDGEMENTS . i List of publications iii Summary xi List of Tables . xiii List of Figures xiv Chapter Literature Review . 1.1 Plant virus and its infection . 1.1.1 Plant virus pathogenesis 1.2 Host-virus interaction 1.3 Sulfur enhanced defense 1.4 MicroRNAs and viral microRNAs 1.5 Nuclear localization signal 1.6 Virus movement 1.7 MiRNA related plant development and gene silencing suppressor 1.8 Rationales and objectives of this thesis research 12 Chapter General Materials and methods 14 2.1 Media and buffers 14 2.2 Plant materials and inoculation . 14 2.2.1 Plant materials and growth conditions 14 2.2.2 Plant inoculation 14 2.3 Molecular cloning . 15 2.3.1 Polymerase chain reaction (PCR) .15 2.3.2 Purification of PCR fragments and DNA fragments from agarose gel15 2.3.3 Ligation of DNA inserts into plasmid vectors 15 2.3.4 Preparation of competent E. coli .15 2.3.5 Transformation of bacteria with plasmids .16 2.3.6 Plasmid purification from E. coli 16 2.3.7 DNA sequencing .16 iv 2.3.8 PCR-based mutagenesis 17 2.3.9 Electro-transformation for Agrobacterium 17 2.3.10 Agrobacterium-infiltration 17 2.3.11 TaqMan two-step RT-PCR 18 2.4 Analysis of DNA . 19 2.4.1 Plant genomic DNA extraction .19 2.4.2 Southern blot .20 2.5 Analysis of RNA . 25 2.5.1 Total RNA extraction using TRIZOL reagent 25 2.5.2 Protocol for separating LMW RNAs 26 2.5.3 Detection of Small RNAs by Northern Blot .27 2.6 Analysis of protein 29 2.6.1 Protein extraction from plants .29 2.6.2 Protein expression and extraction from E.coli 29 2.6.3 Enzyme-linked immuno sorbent assay (ELISA) for plant viral proteins30 2.6.4 Western blot 30 2.7 Isolation and transfection of kenaf protoplasts and isolation of HCRSVinfected kenaf cells 31 2.7.1 Isolation of kenaf protoplasts following previous published protocol (Liang et al., 2002a) .31 2.7.2 PEG transfection of protoplasts .32 2.7.3 Isolation of fixed plant cells 33 2.8 Fluorescent in situ hybridization . 34 2.8.1 The fixed cells were attached to coverslips .34 2.8.2 Hybridization .35 2.9 RNA-chromotin-immunoprecipitation (RNA-CHIP) . 36 2.9.1 Tissue collection and nuclear fixation with formaldehyde .36 2.9.2 Sonication 38 2.9.3 Pre-clearing .38 2.9.4 Immunprecipitation .39 2.9.5 RNA analyses 40 v Chapter Nuclear localization of p23 and identification of HCRSV genome in the nucleus where viral miRNAs are produced 42 3.1 Introduction . 42 3.2 Materials and methods 45 3.2.1 Plant materials, plasmid construction and generation of transgenic Arabidopsis .45 3.2.2 Verification of putative transgenic Arabidopsis plants using Southern blot 46 3.2.3 Construction of artificial vir-miRNA Hcrsv-miR-H1-5p 46 3.2.4 Agrobacterium tumefaciens–mediated transient expression .46 3.2.5 Co-immunoprecipitation assay 47 3.2.6 RNA-CHIP analysis 47 3.2.7 Preparation of plant cells and protoplasts for fluorescent in situ hybridization (FISH) and silver/DAPI staining .50 3.2.8 Isolation and verification of highly purified kenaf nuclei and detection of HCRSV RNA .50 3.2.9 Preparation of Total RNA, reverse transcriptase and real-time PCR 51 3.2.10 Prediction and detection of vir-miRNAs .51 3.3 Results . 52 3.3.1 A novel NLS was detected in the p23 .52 3.3.2 Localization of HCRSV RNA in nucleus using fluorescent in situ hybridization (FISH) and highly purified nuclei 59 3.3.3 The NLS of p23 facilitates the entry of HCRSV RNA into nucleus through its binding to impotin α. 63 3.3.4 Prediction and detection of vir-miRNA in total RNA extracted from highly purified kenaf nuclei of HCRSV-infected and agro-infiltrated leaves65 3.4 Discussion . 68 3.4.1 Vir-miRNA Hcrsv-Mir-H1-5p targets the p23 gene of HCRSV 68 3.4.2 The NLS of p23 facilitates Importin α and HCRSV RNA to enter nucleus 70 3.4.3 The presence of viral RNA in the nucleus may unravel novel funcitons in gene regulation .73 vi Chapter Basic amino acid mutations in the nuclear localization signal of Hibiscus chlorotic ringspot virus p23 inhibit virus long distance movement 74 4.1. Introduction 74 4.2 Materials and methods 77 4.2.1 Plant materials and plasmid construction 77 4.2.2 Plant inoculation with in vitro transcripts of p223 and its two mutants79 4.2.3 Preparation of kenaf protoplasts for fluorescent in situ hybridization (FISH) .79 4.2.4 RNA extraction and cDNA synthesis for RT-PCR and qRT-PCR .80 4.2.5 Western blot analysis of HCRSV CP 80 4.2.6 Agrobacterium tumefaciens-mediated transient expression of amiRp23 and amiRSO .81 4.2.7 Inoculation of amiRp23 and amiRSO into apical meristems of HCRSV-infected kenaf leaves .81 4.3. Results 82 4.3.1 Viral replication was unaffected in the two HCRSV mutants 82 4.3.2 Symptoms were only observed in HCRSV wt-inoculated kenaf leaves at 19 dpi 85 4.3.3 Detection of p23 and CP transcript level in the newly emerged leaves of kenaf plants inoculated with wt HCRSV and its two mutants at 19 dpi 87 4.3.4 Less severe symptoms in pGreen-amiRp23-inoculated kenaf plants pre-inoculated with HCRSV 89 4.4. Discussion 91 Chapter Hibiscus chlorotic ringspot virus coat protein upregulates sulfur metabolism genes for enhanced pathogen defence . 94 5.1 Introduction . 94 5.2 Materials and methods 97 5.2.1 Plant materials and preparation of sulfur solution 97 5.2.2 Virus inoculation .97 5.2.3 GSH treatment on HCRSV-inoculated kenaf plants .98 5.2.4 Construction of plasmids and detection of HCRSV-CP-GFP in agroinfiltrated leaves .98 vii Khraiwesh, B., Zhu, J.K., and Zhu, J. 2012. Role of miRNAs and siRNAs in biotic and abiotic stress responses of plants. Biochem. Biophys. Acta. 1819:137-148. Kidner, C.A., and Martienssen, R.A. 2005. The developmental role of microRNA in plants. Curr. Opin. Plant. Biol. 8:38-44. Kim, S.W., Li, Z., Moore, P.S., Monaghan, A.P., Chang, Y., et al. 2010. A sensitive non-radioactive northern blot method to detect small RNAs. Nucleic Acids Res. 38:e98. Kiraly, L., Cole, A.B., Bourque, J.E., and Schoelz, J.E. 1999. Systemic cell death is elicited by the interaction of a single gene in Nicotiana clevelandii and gene VI of cauliflower mosaic virus. Mol. Plant Microbe Interact. 12:919925. Kiraly, L., Kunstler, A., Holler, K., Fattinger, M., Juhasz, C., et al. 2011. Sulfate supply influences compartment specific glutathione metabolism and confers enhanced resistance to Tobacco mosaic virus during a hypersensitive response. Plant Physiol. Biochem. 59:44-54. Knauer, S., Holt, A.L., Rubio-Somoza, I., Tucker, E.J., Hinze, A., et al. 2013. A protodermal miR394 signal defines a region of stem cell competence in the Arabidopsis shoot meristem. Deve. Cell 24:125-132. Kohm, B.A., Goulden, M.G., Gilbert, J.E., Kavanagh, T.A., and Baulcombe, D.C. 1993. A Potato virus X resistance gene mediates an induced, nonspecific resistance in protoplasts. Plant Cell 5:913-920. Kojima, M., Arai, Y., Iwase, N., Shirotori, K., Shioiri, H., et al. 2000. Development of a simple and efficient method for transformation of buckwheat plants (Fagopyrum esculentum) using Agrobacterium tumefaciens. Biosci. Biotechnol. Biochem. 64:845-847. Kojima, M., Shioiri, H., Nogawa, M., Nozue, M., Matsumoto, D., et al. 2004. In planta transformation of kenaf plants (Hibiscus cannabinus var. aokawa No. 3) by Agrobacterium tumefaciens. J. Biosci. Bioeng. 98:136-139. 184 Koonin, E.V., Senkevich, T.G., and Dolja, V.V. 2006. The ancient virus world and evolution of cells. Biol. Direct. 1:29. Kopriva, S. 2006. Regulation of sulfate assimilation in Arabidopsis and beyond. Ann. Bot. 97:479-495. Kopriva, S., Mugford, S.G., Matthewman, C., and Koprivova, A. 2009. Plant sulfate assimilation genes: redundancy versus specialization. Plant Cell Rep. 28:1769-1780. Koprivova, A., Mugford, S.T., and Kopriva, S. 2010. Arabidopsis root growth dependence on glutathione is linked to auxin transport. Plant Cell Rep. 29:1157-1167. Kumaran, S., Yi, H., Krishnan, H.B., and Jez, J.M. 2009. Assembly of the cysteine synthase complex and the regulatory role of protein-protein interactions. J. Biol. Chem. 284:10268-10275. Lakatos, L., Csorba, T., Pantaleo, V., Chapman, E.J., Carrington, J.C., et al. 2006. Small RNA binding is a common strategy to suppress RNA silencing by several viral suppressors. EMBO J. 25:2768-2780. Laliberte, J.F., and Sanfacon, H. 2010. Cellular remodeling during plant virus infection. Annu. Rev. Phytopathol. 48:69-91. Landgraf, P., Rusu, M., Sheridan, R., Sewer, A., Iovino, N., et al. 2007. A mammalian microRNA expression atlas based on small RNA library sequencing. Cell 129:1401-1414. Lanford, R.E., and Butel, J.S. 1984. Construction and characterization of an Sv40 mutant defective in nuclear transport of T-antigen. Cell 37:801-813. Lee, J.Y., Wang, X., Cui, W., Sager, R., Modla, S., et al. 2011. A plasmodesmatalocalized protein mediates crosstalk between cell-to-cell communication and innate immunity in Arabidopsis. Plant Cell 23:3353-3373. 185 Leustek, T., Martin, M.N., Bick, J.A., and Davies, J.P. 2000. Pathways and regulation of sulfur metabolism revealed through molecular and genetic studies. Annu. Rev. Plant Physiol. Plant Mol. Biol. 51:141-165. Li, H.W., Lucy, A.P., Guo, H.S., Li, W.X., Ji, L.H., et al. 1999. Strong host resistance targeted against a viral suppressor of the plant gene silencing defence mechanism. EMBO J. 18:2683-2691. Li, S.C., and Chang, Y.C. 2002. First report of Hibiscus chlorotic ringspot virus in Taiwan. Plant Pathology 51:803. Li, S.C., Pan, C.Y., and Lin, W.C. 2006. Bioinformatic discovery of microRNA precursors from human ESTs and introns. BMC Genomics 7:164. Li, S.C., Shiau, C.K., and Lin, W.C. 2008. Vir-Mir db: prediction of viral microRNA candidate hairpins. Nucleic Acids Res. 36:D184-189. Li, V.Z., Qu, F., and Morris, T.J. 1998. Cell-to-cell movement of Turnip crinkle virus is controlled by two small open reading frames that function in trans. Virology 244:405-416. Li, Y., Zhao, L., Wang, S., Xing, J., and Zheng, C. 2012. Identification of a novel NLS of Herpes simplex virus type (HSV-1) VP19C and its nuclear localization is required for efficient production of HSV-1. J. Gen. Virol. 93:1869-1875. Liang, G., Yang, F., and Yu, D. 2010. MicroRNA395 mediates regulation of sulfate accumulation and allocation in Arabidopsis thaliana. Plant J. 62:1046-1057. Liang, X.Z., Ding, S.W., and Wong, S.M. 2002a. Development of a kenaf (Hibiscus cannabinus L.) protoplast system for a replication study of Hibiscus chlorotic ringspot virus. Plant Cell Rep. 20:982-986. Liang, X.Z., Lucy, A.P., Ding, S.W., and Wong, S.M. 2002b. The p23 protein of Hibiscus chlorotic ringspot virus is indispensable for host-specific replication. J. Virol. 76:12312-12319. 186 Llave, C., Xie, Z., Kasschau, K.D., and Carrington, J.C. 2002. Cleavage of Scarecrow-like mRNA targets directed by a class of Arabidopsis miRNA. Science 297:2053-2056. Lo, A.K., To, K.F., Lo, K.W., Lung, R.W., Hui, J.W., et al. 2007. Modulation of LMP1 protein expression by EBV-encoded microRNAs. Proc. Natl. Acad. Sci. U S A 104:16164-16169. Lough, T.J., Shash, K., Xoconostle-Cazares, B., Hofstra, K.R., Beck, D.L., et al. 1998. Molecular dissection of the mechanism by which potexvirus triple gene block proteins mediate cell-to-cell transport of infectious RNA. Mol. Plant Microbe Interact. 11:801-814. Lough, T.J., Netzler, N.E., Emerson, S.J., Sutherland, P., Carr, F., et al. 2000. Cell-to-cell movement of potexviruses: Evidence for a ribonucleoprotein complex involving the coat protein and first triple gene block protein. Mol. Plant Microbe Interact. 13:962-974. Lu, C., and Fedoroff, N. 2000. A mutation in the Arabidopsis HYL1 gene encoding a dsRNA binding protein affects responses to abscisic acid, auxin, and cytokinin. Plant Cell 12:2351-2366. Lu, Y.D., Gan, Q.H., Chi, X.Y., and Qin, S. 2008. Roles of microRNA in plant defense and virus offense interaction. Plant Cell Rep. 27:1571-1579. Ma, H., Zhu, J., Maronski, M., Kotzbauer, P.T., Lee, V.M., et al. 2002. Nonclassical nuclear localization signal peptides for high efficiency lipofection of primary neurons and neuronal cell lines. Neuroscience 112:1-5. Marty, L., Siala, W., Schwarzlander, M., Fricker, M.D., Wirtz, M., et al. 2009. The NADPH-dependent thioredoxin system constitutes a functional backup for cytosolic glutathione reductase in Arabidopsis. Proc. Natl. Acad. Sci. U S A 106:9109-9114. Mas, P., and Beachy, R.N. 2000. Role of microtubules in the intracellular distribution of Tobacco mosaic virus movement protein. Proc. Natl. Acad. Sci. U S A 97:12345-12349. 187 McConnell, J.R., and Barton, M.K. 1998. Leaf polarity and meristem formation in Arabidopsis. Development 125:2935-2942. McConnell, J.R., Emery, J., Eshed, Y., Bao, N., Bowman, J., et al. 2001. Role of PHABULOSA and PHAVOLUTA in determining radial patterning in shoots. Nature 411:709-713. McLean, B.G., Hempel, F.D., and Zambryski, P.C. 1997. Plant intercellular communication via plasmodesmata. Plant Cell 9:1043-1054. Meng, C., Chen, J., Peng, J., and Wong, S.M. 2006. Host-induced avirulence of Hibiscus chlorotic ringspot virus mutants correlates with reduced genesilencing suppression activity. J. Gen. Virol. 87:451-459. Meng, C.Y., Chen, J., Din, S.W., Peng, J.R., and Wong, S.M. 2008. Hibiscus chlorotic ringspot virus coat protein inhibits trans-acting small interfering RNA biogenesis in Arabidopsis. J. Gen. Virol. 89:2349-2358. Mink, G.I. 1993. Pollen-transmitted and seed-transmitted viruses and viroids. Annu. Rev. Phytopathol. 31:375-402. Mlotshwa, S., Pruss, G.J., and Vance, V. 2008. Small RNAs in viral infection and host defense. Trends Plant Sci. 13:375-382. Moissiard, G., and Voinnet, O. 2006. RNA silencing of host transcripts by Cauliflower mosaic virus requires coordinated action of the four Arabidopsis Dicer-like proteins. Proc. Natl. Acad. Sci. U S A 103:1959319598. Morel, J.B., Godon, C., Mourrain, P., Beclin, C., Boutet, S., et al. 2002. Fertile hypomorphic ARGONAUTE (ago1) mutants impaired in posttranscriptional gene silencing and virus resistance. Plant Cell 14:629-639. Mosammaparast, N., and Pemberton, L.F. 2004. Karyopherins: from nucleartransport mediators to nuclear-function regulators. Trends in Cell Biol. 14:547-556. 188 Mugford, S.G., Yoshimoto, N., Reichelt, M., Wirtz, M., Hill, L., et al. 2009. Disruption of adenosine-5'-phosphosulfate kinase in Arabidopsis reduces levels of sulfated secondary metabolites. Plant Cell 21:910-927. Nagy, P.D. 2008. Yeast as a model host to explore plant virus-host interactions. Annu. Rev. Phytopathol. 46:217-242. Navarro, L., Dunoyer, P., Jay, F., Arnold, B., Dharmasiri, N., et al. 2006. A plant miRNA contributes to antibacterial resistance by repressing auxin signaling. Science 312:436-439. Navratil, V., de Chassey, B., Combe, C.R., and Lotteau, V. 2011. When the human viral infectome and diseasome networks collide: towards a systems biology platform for the aetiology of human diseases. BMC Systems Biol. 5:13. Nikiforova, V.J., Bielecka, M., Gakiere, B., Krueger, S., Rinder, J., et al. 2006. Effect of sulfur availability on the integrity of amino acid biosynthesis in plants. Amino Acids 30:173-183. Noctor, G., Gomez, L., Vanacker, H., and Foyer, C.H. 2002. Interactions between biosynthesis, compartmentation and transport in the control of glutathione homeostasis and signalling. J. Exp. Bot. 53:1283-1304. Nowak, K., Luniak, N., Witt, C., Wustefeld, Y., Wachter, A., et al. 2004. Peroxisomal localization of sulfite oxidase separates it from chloroplastbased sulfur assimilation. Plant Cell Physiol. 45:1889-1894. Pagan, I., Fraile, A., Fernandez-Fueyo, E., Montes, N., Alonso-Blanco, C., et al. 2010. Arabidopsis thaliana as a model for the study of plant-virus coevolution. Philosophi. Transac. Royal Soci. B-Biol. Sci. 365:1983-1995. Palatnik, J.F., Allen, E., Wu, X., Schommer, C., Schwab, R., et al. 2003. Control of leaf morphogenesis by microRNAs. Nature 425:257-263. Pallas, V., and Garcia, J.A. 2011. How plant viruses induce disease? Interactions and interference with host components. J. Gen. Virol. 92:2691-2705. 189 Parmar, S., Buchner, P., and Hawkesford, M.J. 2007. Leaf developmental stage affects sulfate depletion and specific sulfate transporter expression during sulfur deprivation in Brassica napus L. Plant Biol. 9:647-653. Pfeffer, S., Zavolan, M., Grasser, F.A., Chien, M., Russo, J.J., et al. 2004. Identification of virus-encoded microRNAs. Science 304:734-736. Pouwels, J., Kornet, N., van Bers, N., Guighelaar, T., van Lent, J., et al. 2003. Identification of distinct steps during tubule formation by the movement protein of Cowpea mosaic virus. J Gen. Virol. 84:3485-3494. Pouwels, J., van der Velden, T., Willemse, J., Borst, J.W., van Lent, J., et al. 2004. Studies on the origin and structure of tubules made by the movement protein of Cowpea mosaic virus. J. Gen. Virol. 85:3787-3796. Pruss, G.J., Lawrence, C.B., Bass, T., Li, Q.Q., Bowman, L.H., et al. 2004. The potyviral suppressor of RNA silencing confers enhanced resistance to multiple pathogens. Virology 320:107-120. Rajendran, K.S., Pogany, J., and Nagy, P.D. 2002. Comparison of Turnip crinkle virus RNA-dependent RNA polymerase preparations expressed in Escherichia coli or derived from infected plants. J. Virol. 76:1707-1717. Rausch, T., and Wachter, A. 2005. Sulfur metabolism: a versatile platform for launching defence operations. Trends Plant Sci. 10:503-509. Renosto, F., Patel, H.C., Martin, R.L., Thomassian, C., Zimmerman, G., et al. 1993. ATP sulfurylase from higher plants: kinetic and structural characterization of the chloroplast and cytosol enzymes from spinach leaf. Arch. Biochem. Biophys. 307:272-285. Rhoades, M.W., Reinhart, B.J., Lim, L.P., Burge, C.B., Bartel, B., et al. 2002. Prediction of plant microRNA targets. Cell 110:513-520. Riviere, C.J., and Rochon, D.M. 1990. Nucleotide sequence and genomic organization of Melon necrotic spot virus. J. Gen. Virol. 71:1887-1896. 190 Robbins, J., Dilworth, S.M., Laskey, R.A., and Dingwall, C. 1991. Two interdependent basic domains in nucleoplasmin nuclear targeting sequence: identification of a class of bipartite nuclear targeting sequence. Cell 64:615-623. Rouached, H., Berthomieu, P., El Kassis, E., Cathala, N., Catherinot, V., et al. 2005. Structural and functional analysis of the C-terminal STAS (sulfate transporter and anti-sigma antagonist) domain of the Arabidopsis thaliana sulfate transporter SULTR1.2. J. Biol. Chem. 280:15976-15983. Saito, K. 2004. Sulfur assimilatory metabolism. The long and smelling road. Plant Physiol. 136:2443-2450. Samols, M.A., Skalsky, R.L., Maldonado, A.M., Riva, A., Lopez, M.C., et al. 2007. Identification of cellular genes targeted by KSHV-encoded microRNAs. PLoS Pathog. 3:e65. Schauer, S.E., Jacobsen, S.E., Meinke, D.W., and Ray, A. 2002. DICER-LIKE1: blind men and elephants in Arabidopsis development. Trends Plant Sci. 7:487-491. Schnug, E., Haneklaus, S., Borchers, A., and Polle, A. 1995. Relations between sulfur supply and glutathione and ascorbate concentrations in Brassicanapus. Z. Pflanz. Bodenkunde 158:67-69. Schoelz, J.E., Harries, P.A., and Nelson, R.S. 2011. Intracellular transport of plant viruses: finding the door out of the cell. Mol. Plant 4:813-831. Scholthof, K.B., Scholthof, H.B., and Jackson, A.O. 1995. The Tomato bushy stunt virus replicase proteins are coordinately expressed and membrane associated. Virology 208:365-369. Schwab, R., Palatnik, J.F., Riester, M., Schommer, C., Schmid, M., et al. 2005. Specific effects of microRNAs on the plant transcriptome. Dev. Cell 8:517-527. Schwartz, M., Chen, J., Lee, W.M., Janda, M., and Ahlquist, P. 2004. Alternate, virus-induced membrane rearrangements support positive-strand RNA virus genome replication. Proc. Natl. Acad. Sci. U S A 101:11263-11268. 191 Shimura, H., Pantaleo, V., Ishihara, T., Myojo, N., Inaba, J., et al. 2011. A viral satellite RNA induces yellow symptoms on tobacco by targeting a gene involved in chlorophyll biosynthesis using the RNA silencing machinery. PLoS Pathog. 7:e1002021. Silver, P.A. 1991. How Proteins Enter the Nucleus. Cell 64:489-497. Simon-Mateo, C., and Garcia, J.A. 2006. MicroRNA-Guided processing impairs Plum pox virus replication, but the virus readily evolves to escape this silencing mechanism. J. Virol. 80:2429-2436. Smith, F.W., Ealing, P.M., Hawkesford, M.J., and Clarkson, D.T. 1995. Plant members of a family of sulfate transporters reveal functional subtypes. Proc. Natl. Acad. Sci. U S A 92:9373-9377. Smith, N.A., Eamens, A.L., and Wang, M.B. 2011. Viral small interfering RNAs target host genes to mediate disease symptoms in plants. PLoS Pathog. 7:e1002022. Suel, K.E., and Chook, Y.M. 2009. Kap104p imports the PY-NLS-containing transcription factor Tfg2p into the nucleus. J. Biol. Chem. 284:1541615424. Sullivan, C.S., and Ganem, D. 2005. MicroRNAs and viral infection. Mol. Cell 20:3-7. Sullivan, C.S., Grundhoff, A.T., Tevethia, S., Pipas, J.M., and Ganem, D. 2005. SV40-encoded microRNAs regulate viral gene expression and reduce susceptibility to cytotoxic T cells. Nature 435:682-686. Takahashi, H. 2010. Regulation of sulfate transport and assimilation in plants. Inter. Rev. Cell. Mol. Biol. 281:129-159. Takahashi, H., Kopriva, S., Giordano, M., Saito, K., and Hell, R. 2011. Sulfur assimilation in photosynthetic organisms: molecular functions and regulations of transporters and assimilatory enzymes. Annu. Rev. Plant. Biol. 62:157-184. 192 Takahashi, H., Watanabe-Takahashi, A., Smith, F.W., Blake-Kalff, M., Hawkesford, M.J., et al. 2000. The roles of three functional sulphate transporters involved in uptake and translocation of sulphate in Arabidopsis thaliana. Plant J. 23:171-182. Takahashi, H., Yamazaki, M., Sasakura, N., Watanabe, A., Leustek, T., et al. 1997. Regulation of sulfur assimilation in higher plants: a sulfate transporter induced in sulfate-starved roots plays a central role in Arabidopsis thaliana. Proc. Natl. Acad. Sci. U S A 94:11102-11107. Taliansky, M.E., Brown, J.W., Rajamaki, M.L., Valkonen, J.P., and Kalinina, N.O. 2010. Involvement of the plant nucleolus in virus and viroid infections: parallels with animal pathosystems. Adv. Virus Res. 77:119-158. Tan, S.L., Ganji, G., Paeper, B., Proll, S., and Katze, M.G. 2007. Systems biology and the host response to viral infection. Nat. Biotechnol. 25:1383-1389. Tang, J., Elliott, D.R., Quinn, B.D., Clover, G.R.G., and Alexander, B.J.R. 2008a. Occurrence of Hibiscus chlorotic ringspot virus in Hibiscus spp. in new Zealand. Plant Disease 92:1367-1367. Tang, S., Bertke, A.S., Patel, A., Wang, K., Cohen, J.I., et al. 2008b. An acutely and latently expressed Herpes simplex virus viral microRNA inhibits expression of ICP34.5, a viral neurovirulence factor. Proc. Natl. Acad. Sci. U S A 105:10931-10936. Telfer, A., and Poethig, R.S. 1998. HASTY: a gene that regulates the timing of shoot maturation in Arabidopsis thaliana. Development 125:1889-1898. Truant, R., and Cullen, B.R. 1999. The arginine-rich domains present in Human immunodeficiency virus type Tat and Rev function as direct importin beta-dependent nuclear localization signals. Mol. Cell Biol. 19:1210-1217. Tsang, C.K., Bertram, P.G., Ai, W., Drenan, R., and Zheng, X.F. 2003. Chromatin-mediated regulation of nucleolar structure and RNA Pol I localization by TOR. EMBO J. 22:6045-6056. 193 Uetz, P., Dong, Y.A., Zeretzke, C., Atzler, C., Baiker, A., et al. 2006. Herpesviral protein networks and their interaction with the human proteome. Science 311:239-242. Umbach, J.L., Kramer, M.F., Jurak, I., Karnowski, H.W., Coen, D.M., et al. 2008. MicroRNAs expressed by Herpes simplex virus during latent infection regulate viral mRNAs. Nature 454:780-783. Vanlent, J., Storms, M., Vandermeer, F., Wellink, J., and Goldbach, R. 1991. Tubular structures involved in movement of Cowpea mosaic Virus are also formed in infected cowpea protoplasts. J. Gen. Virol. 72:2615-2623. Varble, A., Chua, M.A., Perez, J.T., Manicassamy, B., Garcia-Sastre, A., et al. 2010. Engineered RNA viral synthesis of microRNAs. Proc. Natl. Acad. Sci. U S A 107:11519-11524. Vargason, J.M., Szittya, G., Burgyan, J., and Hall, T.M. 2003. Size selective recognition of siRNA by an RNA silencing suppressor. Cell 115:799-811. Varkonyi-Gasic, E., Wu, R., Wood, M., Walton, E.F., and Hellens, R.P. 2007. Protocol: a highly sensitive RT-PCR method for detection and quantification of microRNAs. Plant Methods 3:12. Vaucheret, H., Mallory, A.C., and Bartel, D.P. 2006. AGO1 homeostasis entails coexpression of MIR168 and AGO1 and preferential stabilization of miR168 by AGO1. Mol. Cell 22:129-136. Vaucheret, H., Vazquez, F., Crete, P., and Bartel, D.P. 2004. The action of ARGONAUTE1 in the miRNA pathway and its regulation by the miRNA pathway are crucial for plant development. Genes Dev. 18:1187-1197. Vazquez, F., Gasciolli, V., Crete, P., and Vaucheret, H. 2004. The nuclear dsRNA binding protein HYL1 is required for microRNA accumulation and plant development, but not posttranscriptional transgene silencing. Curr. Biol. 14:346-351. Wachter, A., Wolf, S., Steininger, H., Bogs, J., and Rausch, T. 2005. Differential targeting of GSH1 and GSH2 is achieved by multiple transcription 194 initiation: implications for the compartmentation biosynthesis in the Brassicaceae. Plant J. 41:15-30. of glutathione Watanabe, M., Hubberten, H.M., Saito, K., and Hoefgen, R. 2010. General regulatory patterns of plant mineral nutrient depletion as revealed by serat quadruple mutants disturbed in cysteine synthesis. Mol. Plant 3:438-466. Waterworth, H.E. 1980. Hibiscus chlorotic ringspot virus CMI/AAB descriptions of plant viruses. Associ. Aplied Biol. UK No. 227. Waterworth, H.E., Lawson, R.H., and Monroe, R.L. 1976. Purification and properties of Hibiscus chlorotic ringspot virus. Phytopathology 66:570575. Weis, K. 2003. Regulating access to the genome: nucleocytoplasmic transport throughout the cell cycle. Cell 112:441-451. Weng, Z., and Xiong, Z. 1997. Genome organization and gene expression of Saguaro cactus carmovirus. J. Gen. Virol. 78:525-534. White, K.A., Skuzeski, J.M., Li, W., Wei, N., and Morris, T.J. 1995. Immunodetection, expression strategy and complementation of Turnip crinkle virus p28 and p88 replication components. Virology 211:525-534. Whitham, S., McCormick, S., and Baker, B. 1996. The N gene of tobacco confers resistance to Tobacco mosaic virus in transgenic tomato. Proc. Natl. Acad. Sci. U S A 93:8776-8781. Whitham, S.A., and Wang, Y. 2004. Roles for host factors in plant viral pathogenicity. Curr. Opin. Plant Biol. 7:365-371. Wirtz, M., and Hell, R. 2007. Dominant-negative modification reveals the regulatory function of the multimeric cysteine synthase protein complex in transgenic tobacco. Plant Cell 19:625-639. Wolf, S., Deom, C.M., Beachy, R.N., and Lucas, W.J. 1989. Movement protein of Tobacco mosaic virus modifies plasmodesmatal size exclusion limit. Science 246:377-379. 195 Wu, W.W., and Pante, N. 2009. The directionality of the nuclear transport of the influenza A genome is driven by selective exposure of nuclear localization sequences on nucleoprotein. Virol. J. 6:68. Wykoff, D.D., Davies, J.P., Melis, A., and Grossman, A.R. 1998. The regulation of photosynthetic electron transport during nutrient deprivation in Chlamydomonas reinhardtii. Plant Physiol. 117:129-139. Xie, Z., Kasschau, K.D., and Carrington, J.C. 2003. Negative feedback regulation of Dicer-Like1 in Arabidopsis by microRNA-guided mRNA degradation. Curr. Biol. 13:784-789. Ye, K., and Patel, D.J. 2005. RNA silencing suppressor p21 of Beet yellows virus forms an RNA binding octameric ring structure. Structure 13:1375-1384. Ye, K., Malinina, L., and Patel, D.J. 2003. Recognition of small interfering RNA by a viral suppressor of RNA silencing. Nature 426:874-878. Yi, H., Galant, A., Ravilious, G.E., Preuss, M.L., and Jez, J.M. 2010. Sensing sulfur conditions: simple to complex protein regulatory mechanisms in plant thiol metabolism. Mol. Plant 3:269-279. Yonekura-Sakakibara, K., Ashikari, T., Tanaka, Y., Kusumi, T., and Hase, T. 1998. Molecular characterization of tobacco sulfite reductase: enzyme purification, gene cloning, and gene expression analysis. J. Biochem. 124:615-621. You, X.J., Kim, J.W., Stuart, G.W., and Bozarth, R.F. 1995. The nucleotide sequence of Cowpea mottle virus and its assignment to the genus Carmovirus. J. Gen. Virol. 76:2841-2845. Yu, H., Ito, T., Wellmer, F., and Meyerowitz, E.M. 2004. Repression of AGAMOUS-LIKE 24 is a crucial step in promoting flower development. Nature Genetics 36:157-161. Zaitlin, M. 1998. The discovery of the causal agent of the Tobacco mosaic disease. Discov. Plant Biol. Hong Kong: World Publishing Co. :105–110. 196 Zambryski, P. 1995. Plasmodesmata: plant channels for molecules on the move. Science 270:1943-1944. Zechmann, B., and Mueller, M. 2008. Effects of Zucchini yellow mosaic virus infection on the subcellular distribution of glutathione and its precursors in a highly tolerant Cucurbita pepo cultivar. Botany-Botanique 86:10921100. Zechmann, B., Zellnig, G., Urbanek-Krajnc, A., and Muller, M. 2007. Artificial elevation of glutathione affects symptom development in ZYMV-infected Cucurbita pepo L. plants. Arch. Virol. 152:747-762. Zechmann, B., Mauch, F., Sticher, L., and Muller, M. 2008. Subcellular immunocytochemical analysis detects the highest concentrations of glutathione in mitochondria and not in plastids. J. Exp. Bot. 59:4017-4027. Zenklusen, D., and Singer, R.H. 2010. Analyzing mRNA expression using single mRNA resolution fluorescent in situ hybridization. Methods in Enzymology, Vol 470: Guide to Yeast Genetics: 470:641-659. Zenklusen, D., Larson, D.R., and Singer, R.H. 2008. Single-RNA counting reveals alternative modes of gene expression in yeast. Nat. Struct. Mol. Biol. 15:1263-1271. Zhang, B., Pan, X., Cannon, C.H., Cobb, G.P., and Anderson, T.A. 2006a. Conservation and divergence of plant microRNA genes. Plant J. 46:243259. Zhang, J., Zeng, R., Chen, J., Liu, X., and Liao, Q. 2008. Identification of conserved microRNAs and their targets from Solanum lycopersicum Mill. Gene 423:1-7. Zhang, X., and Wong, S.M. 2009. Hibiscus chlorotic ringspot virus upregulates plant sulfite oxidase transcripts and increases sulfate levels in kenaf (Hibiscus cannabinus L.). J. Gen. Virol. 90:3042-3050. 197 Zhang, X., and Wong, S.M. 2011. Development of a cell sorting procedure to increase the sensitivity of detection of protein-protein interactions in plant protoplasts. J. Virol. Methods 173:347-352. Zhang, X.R., Henriques, R., Lin, S.S., Niu, Q.W., and Chua, N.H. 2006b. Agrobacterium-mediated transformation of Arabidopsis thaliana using the floral dip method. Nature Protocols 1:641-646. Zhang, X.R., Yuan, Y.R., Pei, Y., Lin, S.S., Tuschl, T., et al. 2006c. Cucumber mosaic virus-encoded 2b suppressor inhibits Arabidopsis Argonaute1 cleavage activity to counter plant defense. Genes Dev. 20:3255-3268. Zhang, Y., Zhang, X., Niu, S., Han, C., Yu, J., et al. 2011. Nuclear localization of Beet black scorch virus capsid protein and its interaction with importin alpha. Virus Res. 155:307-315. Zheng, H.Q., Wang, G.L., and Zhang, L. 1997. Alfalfa mosaic virus movement protein induces tubules in plant protoplasts. Mol. Plant Microbe Interact. 10:1010-1014. Zhong, R., and Ye, Z.H. 2004. Amphivasal vascular bundle 1, a gain-of-function mutation of the IFL1/REV gene, is associated with alterations in the polarity of leaves, stems and carpels. Plant Cell Physiol. 45:369-385. Zhou, T., Fan, Z.F., Li, H.F., and Wong, S.M. 2006. Hibiscus chlorotic ringspot virus p27 and its isoforms affect symptom expression and potentiate virus movement in kenaf (Hibiscus cannabinus L.). Mol. Plant Microbe Interact. 19:948-957. 198 Appendix I ® LB medium: 1% Bacto - tryptone, ® 0.5% Bacto - yeast extract, 0.5% NaCl, pH 7.5 LB agar: LB medium with ® 1.5% Bacto - agar, pH 7.5 TAE: 40 mM Tris-acetate, 20 mM sodium acetate, mM EDTA, pH 8.2 TBE: 89 mM Tris-borate, mM EDTA, pH 8.3 TE: 10 mM Tris-HCl, mM EDTA, pH 8.0 20 × SSC: M NaCl, 0.3 M Trisodium citrate Murashige and Skoog (MS) medium: 16 mg/L MnSO •H O, 8.6 mg/L ZnSO •7H O, 6.2 mg/L H BO , 0.83 mg/L KI, 0.25 mg/L, Na MoO , 0.025 mg/L CuSO •5H O, 0.025 mg/L CoCl •6H O 199 [...]... times and large population sizes of viruses impart them with a remarkable evolutionary potential The construction of a molecular model that confines physical interactions established between the components of the host cell and virus is the foundation of the emerging discipline of systems virology (Tan et al., 2007; Bailer and Haas, 2009) Using this model, we can understand how the virus manipulates the. .. p23 in HCRSV, which belongs to Family Tombusviridae Genus Carmovirus, is predicted to be a transcription factor that is indispensable for host-specific replication The overall aim of this study is to investigate the additional functions of p23 and CP of HCRSV The specific aims of this study include: (1) To determine and investigate the subcellular localization of p23 The presence of a positive-strand... Chook, 2009) At this point, Ran-GTP will bind to the importin -protein complex, and its binding will cause the importin to lose affinity for the protein The protein is released, and now the Ran-GTP/importin complex will move back out of the nucleus through the nuclear pore A GTPase activating protein (GAP) in the cytoplasm hydrolyzes the Ran-GTP to GDP, and this causes a conformational change in Ran,... 126 kDa and 183 kDa replicase proteins 7 of TMV (Derrick et al., 1997), helper component proteinase (HC-pro) protein of potyvirus (Cronin et al., 1995), the 2b protein of cucumber mosaic virus (CMV) (Ding et al., 1994) and p19 of tomato bushy stunt virus (TBSV) (Scholthof et al., 1995) have been shown to have specific functions in long-distance movement 1.7 MiRNA related plant development and gene... benefit, and what the actions it achieves for shunting host defenses (Whitham and Wang, 2004; Culver and Padmanabhan, 2007; Dodds and Rathjen, 2010; Elena et al., 2011) Furthermore, the own proteins and small RNAs of a virus interact and compete in replication cycle (Guo et al., 2001), and these interactions may create new paths to communicate separated cellular functions, leading to the appearance of novel... entry into the nucleus through the nuclear envelope, which consists of concentric membranes, the outer, the inner membrane, pores and large nuclear complexes These are the gateways to the nucleus A protein translated with a NLS will bind strongly to importin (aka karyopherin), and the complex will move through the nuclear pore (Fried and Kutay, 2003; Mosammaparast and Pemberton, 2004; Suel and Chook,... kinase (APK), sulfite oxidase (SO) and Hibiscus chlorotic ringspot virus coat protein (HCRSV-CP) gene transcripts in kenaf (Hibiscus cannabinus L.) leaves 10 days post inoculation (dpi) as determined by qRT-PCR 104 Figure 5.2 Gene transcript levels of sulfite reductase (SIR), APS kinase (APK), sulfite oxidase (SO) and Hibiscus chlorotic ringspot virus coat protein (HCRSV-CP) after CP gene was... 8 Conclusion and further work 168 8.1 Conclusion 168 8.2 Future work 171 x Summary Hibiscus cannabinus L (kenaf) was used as a host plant to study a plant virus Hibiscus chlorotic ringspot virus (HCRSV) The p23 is a novel open reading frame in the HCRSV which belongs to Family Tombusviridae Genus Carmovirus The p23 was found to localize in the nucleus and a novel nuclear... CHAPTER 7 147 xiii List of Figures Figure 3.1 Structural organization of HCRSV genomic RNA and its predicted virmiRNAs 43 Figure 3.2 Schematic representations of constructs of HCRSV p23 and its deletion mutants fused with GFP 53 Figure 3.3 Nuclear localization of the p23 protein of HCRSV 54 Figure 3.4 Localization of p23 of HCRSV in nucleus of transgenic Arabidopsis thaliana... countermeasure, viruses and bacteria have evolved VSRs and BSRs to suppress host RNAi machinery and compromise disease resistance in plants Many viruses encode specific proteins that suppress the host antiviral silencing response and thereby benefit viral infection It was reported that suppressor proteins can block host RNA silencing at various stages of the RNA silencing pathways and the molecular mechanisms of . INVESTIGATION OF THE FUNCTIONS OF P23 AND COAT PROTEIN OF HIBISCUS CHLOROTIC RINGSPOT VIRUS GAO RUIMIN NATIONAL UNIVERSITY OF SINGAPORE 2013 INVESTIGATION OF THE FUNCTIONS. FUNCTIONS OF P23 AND COAT PROTEIN OF HIBISCUS CHLOROTIC RINGSPOT VIRUS (B.Sc., M.Sc., Henan Agricultural University, PRC) GAO RUIMIN A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR OF. study a plant virus Hibiscus chlorotic ringspot virus (HCRSV). The p23 is a novel open reading frame in the HCRSV which belongs to Family Tombusviridae Genus Carmovirus. The p23 was found

Ngày đăng: 10/09/2015, 09:03

TỪ KHÓA LIÊN QUAN

TÀI LIỆU CÙNG NGƯỜI DÙNG

TÀI LIỆU LIÊN QUAN