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| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 劉瑞芬(Ruey-Fen Liou) | |
| dc.contributor.author | Kuo-Hsin Wang | en |
| dc.contributor.author | 王國馨 | zh_TW |
| dc.date.accessioned | 2021-06-15T06:59:34Z | - |
| dc.date.available | 2021-01-25 | |
| dc.date.copyright | 2011-02-09 | |
| dc.date.issued | 2011 | |
| dc.date.submitted | 2011-01-25 | |
| dc.identifier.citation | 安寶貞 (2001) 植物病害的非農藥防治品-亞磷酸. 植物病理學會刊 10: 147-164
安寶貞, 謝廷芳 蔡, 王姻婷, 林俊義 (2000) 亞磷酸之簡便使用方法與防病範圍. 植物病理學會會刊 9: 179 Arce DP, Tonon C, Zanetti ME, Godoy AV, Hirose S, Casalongue CA (2006) The potato transcriptional co-activator StMBF1 is up-regulated in response to oxidative stress and interacts with the TATA-box binding protein. J Biochem Mol Biol 39: 355-360 Godoy AV, Zanetti ME, San Segundo B, Casalongue CA (2001) Identification of a putative Solanum tuberosum transcriptional coactivator up-regulated in potato tubers by Fusarium solani f. sp. eumartii infection and wounding. Physiol Plant 112: 217-222 Liu Y, Schiff M, Dinesh-Kumar SP (2002) Virus-induced gene silencing in tomato. Plant J 31: 777-786 Mariotti M, De Benedictis L, Avon E, Maier JA (2000) Interaction between endothelial differentiation-related factor-1 and calmodulin in vitro and in vivo. J Biol Chem 275: 24047-24051 Matsushita Y, Miyakawa O, Deguchi M, Nishiguchi M, Nyunoya H (2002) Cloning of a tobacco cDNA coding for a putative transcriptional coactivator MBF1 that interacts with the tomato mosaic virus movement protein. J Exp Bot 53: 1531-1532 Sugikawa Y, Ebihara S, Tsuda K, Niwa Y, Yamazaki K (2005) Transcriptional coactivator MBF1s from Arabidopsis predominantly localize in nucleolus. J Plant Res 118: 431-437 Suzuki N, Bajad S, Shuman J, Shulaev V, Mittler R (2008) The transcriptional co-activator MBF1c is a key regulator of thermotolerance in Arabidopsis thaliana. J Biol Chem 283: 9269-9275 Suzuki N, Rizhsky L, Liang H, Shuman J, Shulaev V, Mittler R (2005) Enhanced tolerance to environmental stress in transgenic plants expressing the transcriptional coactivator multiprotein bridging factor 1c. Plant Physiol 139: 1313-1322 Takemaru K, Li FQ, Ueda H, Hirose S (1997) Multiprotein bridging factor 1 (MBF1) is an evolutionarily conserved transcriptional coactivator that connects a regulatory factor and TATA element-binding protein. Proc Natl Acad Sci U S A 94: 7251-7256 Tao Y, Xie Z, Chen W, Glazebrook J, Chang HS, Han B, Zhu T, Zou G, Katagiri F (2003) Quantitative nature of Arabidopsis responses during compatible and incompatible interactions with the bacterial pathogen Pseudomonas syringae. Plant Cell 15: 317-330 Thomma BP, Penninckx IA, Broekaert WF, Cammue BP (2001) The complexity of disease signaling in Arabidopsis. Curr Opin Immunol 13: 63-68 Ton J, Van Pelt JA, Van Loon LC, Pieterse CM (2002) Differential effectiveness of salicylate-dependent and jasmonate/ethylene-dependent induced resistance in Arabidopsis. Mol Plant Microbe Interact 15: 27-34 Torres MA, Jones JDG, Dangl JL (2006) Reactive oxygen species signaling in response to pathogens. Plant Physiol. 141: 373-378 Tsuda K, Tsuji T, Hirose S, Yamazaki K (2004) Three Arabidopsis MBF1 homologs with distinct expression profiles play roles as transcriptional co-activators. Plant Cell Physiol 45: 225-231 Tsuda K, Yamazaki K (2004) Structure and expression analysis of three subtypes of Arabidopsis MBF1 genes. Biochim Biophys Acta 1680: 1-10 Van Loon LC, Rep M, Pieterse CMJ (2006) Significance of inducible defense-related proteins in infected plants. Annual Review of Phytopathology 44: 135-162 Vleeshouwers VG, van Dooijeweert W, Govers F, Kamoun S, Colon LT (2000) The hypersensitive response is associated with host and nonhost resistance to Phytophthora infestans. Planta 210: 853-864 Ward EW, Cahill DM, Bhattacharyya MK (1989) Abscisic acid suppression of phenylalanine ammonia-lyase activity and mRNA, and resistance of soybeans to Phytophthora megasperma f.sp. glycinea. Plant Physiol 91: 23-27 Way HM, Kazan K, Mitter N, Goulter KC, Birch RG, Manners JM (2002) Constitutive expression of a phenylalanine ammonia-lyase gene from Stylosanthes humilis in transgenic tobacco leads to enhanced disease resistance but impaired plant growth. Physiological and Molecular Plant Pathology 60: 275-282 Wicks TJ, Magarey PA, Wachtel MF, Frensham AB (1991) Effect of postinfection application of phosphorous (phosphonic) acid on the indidence and sporulation of Plasmopara viticola on grapevine. Plant Disease 75: 40-43 Yan HZ, Liou RF (2005) Cloning and analysis of pppg1, an inducible endopolygalacturonase gene from the oomycete plant pathogen Phytophthora parasitica. Fungal Genet Biol 42: 339-350 Yu D, Liu Y, Fan B, Klessig DF, Chen Z (1997) Is the high basal level of salicylic acid important for disease resistance in potato? Plant Physiol 115: 343-349 Zanetti ME, Blanco FA, Daleo GR, Casalongue CA (2003) Phosphorylation of a member of the MBF1 transcriptional co-activator family, StMBF1, is stimulated in potato cell suspensions upon fungal elicitor challenge. J Exp Bot 54: 623-632 Zegzouti H, Jones B, Frasse P, Marty C, Maitre B, Latch A, Pech JC, Bouzayen M (1999) Ethylene-regulated gene expression in tomato fruit: characterization of novel ethylene-responsive and ripening-related genes isolated by differential display. Plant J 18: 589-600 安寶貞（2001）植物病害的非農藥防治品-亞磷酸．植物病理學會刊10:147-164 安寶貞，謝廷芳 蔡，王姻婷，林俊義（2000）亞磷酸之簡便使用方法與防病範圍．植物病理學會會刊9:179 林筑蘋（2009）亞磷酸誘導植物抗病機制之初探．國立台灣大學植物病理與微生物學系碩士論文．70頁． | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/48504 | - |
| dc.description.abstract | The genus Phytophthora, which belong to Oomycetes, includes many devastating plant pathogens that can infect a wide variety of crop species. Neutralized phosphorous acid (NPA) is known to be an effective control of many plant diseases caused by Oomycetes including P. parasitica. Previously it has been shown by DNA array analysis that, in response to NPA treatment, some of the tomato genes are differentially expressed, especially those involved in the ethylene-signaling pathway including SlER24. This gene is predicted to encode an ethylene-responsive transcription coactivator. Induction of SlER24 in response to NPA was further confirmed by semi-quantitative reverse transcriptase-PCR. Southern hybridization revealed the presence of a single copy of SlER24 in the genome of tomato. Analysis of the deduced amino acid sequence indicated that SlER24 contain an MBF1 domain and a helix-turn-helix domain. Phylogenetic analysis indicated that SlER24 along with AtMBF1c and pNbER24 was clustered into a group which is distinct from other tomato genes of the MBF1 family. Analysis by semi-quantitative PCR indicated that, SlER24 was up-regulated in response to heat and NPA. Moreover, it was induced when the tomato plants were inoculated with either P. parasitica or Ralstonia solanacearum. When SlER24 was overexpressed, using Potato Virus X as a vector, the plant displayed enhanced resistance against R. solanacearum, although its resistance against P. parasitica was not affected. Virus-induced gene silencing by the use of Tobacco Rattle Virus (TRV), on the other hand, indicated that down-regulation of pNbER24 caused the tobacco more susceptible to P. parasitica. These results indicated SlER24 plays a key role in plant stress response, especially the abiotic stress. However, it will need more studies to prove the interaction between tomato and stress. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-15T06:59:34Z (GMT). No. of bitstreams: 1 ntu-100-R97633008-1.pdf: 2450844 bytes, checksum: d4d7afda7d1cbe30f342511968b25ae2 (MD5) Previous issue date: 2011 | en |
| dc.description.tableofcontents | Abstract...............................................................................................................................i
中文摘要...........................................................................................................................iii 壹、前人研究.....................................................................................................................1 貳、材料與方法...............................................................................................................15 參、結果...........................................................................................................................19 肆、討論...........................................................................................................................25 伍、參考文獻...................................................................................................................31 陸、附表...........................................................................................................................38 柒、附圖...........................................................................................................................39 | |
| dc.language.iso | zh-TW | |
| dc.subject | 疫病菌 | zh_TW |
| dc.subject | 植物逆境反應 | zh_TW |
| dc.subject | TRV | zh_TW |
| dc.subject | PVX | zh_TW |
| dc.subject | MBF1 | zh_TW |
| dc.subject | 番茄 | zh_TW |
| dc.subject | 亞磷酸化合物 | zh_TW |
| dc.subject | MBF1 | en |
| dc.subject | phosphonate | en |
| dc.subject | Phytophthora | en |
| dc.subject | Ralotonia solanacearum | en |
| dc.subject | tobacco rattle virus | en |
| dc.subject | potato virus X | en |
| dc.subject | plant stress | en |
| dc.title | 探討番茄SlER24基因在生物逆境之重要性 | zh_TW |
| dc.title | To study the role of SlER24 gene in the plant responses to biotic stress | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 99-1 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 安寶貞(Pao-jen Ann),張雅君(Ya-Chun Chang),葉信宏(Hsin-Hung Yeh),鄭秋萍(Chiu-Ping Cheng) | |
| dc.subject.keyword | 番茄,疫病菌,亞磷酸化合物,MBF1,PVX,TRV,植物逆境反應, | zh_TW |
| dc.subject.keyword | MBF1,phosphonate,Phytophthora,Ralotonia solanacearum,tobacco rattle virus,potato virus X,plant stress, | en |
| dc.relation.page | 54 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2011-01-25 | |
| dc.contributor.author-college | 生物資源暨農學院 | zh_TW |
| dc.contributor.author-dept | 植物病理與微生物學研究所 | zh_TW |
| 顯示於系所單位： | 植物病理與微生物學系 | |
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