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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 金洛仁 | |
dc.contributor.author | SHWETA AJIT YEKONDI | en |
dc.contributor.author | 施妲 | zh_TW |
dc.date.accessioned | 2021-07-11T14:37:05Z | - |
dc.date.available | 2022-08-20 | |
dc.date.copyright | 2017-08-31 | |
dc.date.issued | 2017 | |
dc.date.submitted | 2017-08-14 | |
dc.identifier.citation | Biswa R Acharya, Byeong Wook Jeon, Wei Zhang, and Sarah M Assmann. Open stomata 1(ost1) is limiting in abscisic acid responses of arabidopsis guard cells. New Phytologist, 200(4):1049{1063, 2013.
GN Agrios. Plant pathology{ fth edition (2005). University of Florida, 1964.Shakoor Ahmad, RUTH GORDON-WEEKS, John Pickett, and Jurriaan Ton. Natural variationin priming of basal resistance: from evolutionary origin to agricultural exploitation.Molecular plant pathology, 11(6):817{827, 2010. Il-Pyung Ahn, Soonok Kim, Yong-Hwan Lee, and Seok-Cheol Suh. Vitamin b1-induced primingis dependent on hydrogen peroxide and the npr1 gene in arabidopsis. Plant physiology,143(2):838{848, 2007. Markus Albert, Anna K Jehle, Martin Lipschis, Katharina Mueller, Yi Zeng, and GeorgFelix. Regulation of cell behaviour by plant receptor kinases: pattern recognition receptorsas prototypical models. European journal of cell biology, 89(2):200{207, 2010. Jonathan P Anderson, Ellet Badruzsaufari, Peer M Schenk, John M Manners, Olivia JDesmond, Christina Ehlert, Donald J Maclean, Paul R Ebert, and Kemal Kazan. Antagonisticinteraction between abscisic acid and jasmonate-ethylene signaling pathways modulatesdefense gene expression and disease resistance in arabidopsis. The Plant Cell, 16(12):3460{3479, 2004. Tsuneaki Asai, Guillaume Tena, Joulia Plotnikova, Matthew R Willmann, Wan-Ling Chiu,Lourdes Gomez-Gomez, Thomas Boller, Frederick M Ausubel, and Jen Sheen. Map kinasesignalling cascade in arabidopsis innate immunity. Nature, 415(6875):977{983, 2002. Bob Asselbergh, David De Vleesschauwer, and Monica H ofte. Global switches and netuningabamodulates plant pathogen defense. Molecular Plant-Microbe Interactions, 21(6):709{719, 2008. Nicky J Atkinson and Peter E Urwin. The interaction of plant biotic and abiotic stresses:from genes to the eld. Journal of experimental botany, 63(10):3523{3543, 2012. Kris Audenaert, Geert B De Meyer, and Monica M H ofte. Abscisic acid determines basalsusceptibility of tomato tobotrytis cinerea and suppresses salicylic acid-dependent signalingmechanisms. Plant Physiology, 128(2):491{501, 2002. A Ayers, J Ebel, N Finelli, N Berger, and P Albersheim. Quantitative assay of elicitoractivity and characteristics of the elicitor present in the extracellular medium of culturesof phytophthora megasperma var. sojae. Plant Physiol, 57:751{759, 1976. Zabihollah Azami-Sardooei, Soraya C Fran ca, David De Vleesschauwer, and Monica H ofte.Riboflavin induces resistance against botrytis cinerea in bean, but not in tomato, by primingfor a hydrogen peroxide-fueled resistance response. Physiological and Molecular PlantPathology, 75(1):23{29, 2010. Zsuzsa Bauer, Lourdes G omez-G omez, Thomas Boller, and Georg Felix. Sensitivity of different ecotypes and mutants ofarabidopsis thaliana toward the bacterial elicitor agellin correlateswith the presence of receptor-binding sites. Journal of Biological Chemistry, 276(49):45669{45676, 2001. Gwyn A Beattie and Steven E Lindow. The secret life of foliar bacterial pathogens on leaves.Annual review of phytopathology, 33(1):145{172, 1995. Alexandre Berr, Rozenn M enard, Thierry Heitz, and Wen-Hui Shen. Chromatin modi cation and remodelling: a regulatory landscape for the control of arabidopsis defence responsesupon pathogen attack. Cellular microbiology, 14(6):829{839, 2012. MV Bhaskara Reddy, Joseph Arul, Paul Angers, and Luc Couture. Chitosan treatment of wheat seeds induces resistance to fusarium graminearum and improves seed quality. Journal of Agricultural and Food chemistry, 47(3):1208{1216, 1999. Thomas Boller and Georg Felix. A renaissance of elicitors: perception of microbe-associated molecular patterns and danger signals by pattern-recognition receptors. Annual review of plant biology, 60:379{406, 2009. Lorenza Bordoli, Marco Netsch, Urs L uthi, Werner Lutz, and Richard Eckner. Plant orthologs of p300/cbp: conservation of a core domain in metazoan p300/cbp acetyltransferase-related proteins. Nucleic acids research, 29(3):589{597, 2001. Marie Boudsocq, Matthew R Willmann, Matthew McCormack, Horim Lee, Libo Shan, Ping He, Jenifer Bush, Shu-Hua Cheng, and Jen Sheen. Di erential innate immune signalling via ca2+ sensor protein kinases. Nature, 464(7287):418, 2010. Klaas Bouwmeester and Francine Govers. Arabidopsis l-type lectin receptor kinases: phylogeny, classi cation, and expression pro les. Journal of Experimental Botany, 60(15): 4383{4396, 2009. Klaas Bouwmeester, Mara De Sain, Rob Weide, Anne Gouget, So eke Klamer, Herve Canut, and Francine Govers. The lectin receptor kinase lecrk-i. 9 is a novel phytophthora resistance component and a potential host target for a rxlr e ector. PLoS pathogens, 7(3):e1001327, 2011. Chris Bowler and Robert Fluhr. The role of calcium and activated oxygens as signals for controlling cross-tolerance. Trends in plant science, 5(6):241{246, 2000. David M Brooks, Gustavo Hern andez-Guzm an, Andrew P Kloek, Francisco Alarc on-Chaidez,Aswathy Sreedharan, Vidhya Rangaswamy, Alejandro Pe~naloza-V azquez, Carol L Bender, and Barbara N Kunkel. Identi cation and characterization of a well-de ned series of coronatine biosynthetic mutants of pseudomonas syringae pv. tomato dc3000. Molecular plant-microbe interactions, 17(2):162{174, 2004. David M Brooks, Carol L Bender, and Barbara N Kunkel. The pseudomonas syringae phytotoxin coronatine promotes virulence by overcoming salicylic acid-dependent defences in arabidopsis thaliana. Molecular plant pathology, 6(6):629{639, 2005. Alexandre Brutus, Francesca Sicilia, Alberto Macone, Felice Cervone, and Giulia De Lorenzo.A domain swap approach reveals a role of the plant wall-associated kinase 1 (wak1) as a receptor of oligogalacturonides. Proceedings of the National Academy of Sciences, 107(20): 9452{9457, 2010. Delphine Chinchilla, Zsuzsa Bauer, Martin Regenass, Thomas Boller, and Georg Felix. The arabidopsis receptor kinase s2 bindsg22 and determines the speci city of agellin perception. The Plant Cell, 18(2):465{476, 2006. Delphine Chinchilla, Cyril Zipfel, Silke Robatzek, Birgit Kemmerling, Thorsten N urnberger, Jonathan DG Jones, Georg Felix, and Thomas Boller. A agellin-induced complex of the receptor s2 and bak1 initiates plant defence. Nature, 448(7152):497, 2007. Stephen T Chisholm, Gitta Coaker, Brad Day, and Brian J Staskawicz. Host-microbe interactions: shaping the evolution of the plant immune response. Cell, 124(4):803{814, 2006. Jeongmin Choi, Kiwamu Tanaka, Yangrong Cao, Yue Qi, Jing Qiu, Yan Liang, Sang Yeol Lee, and Gary Stacey. Identi cation of a plant receptor for extracellular atp. Science, 343 (6168):290{294, 2014. Steven J Clough and Andrew F Bent. Floral dip: a simpli ed method foragrobacteriummediated transformation ofarabidopsis thaliana. The plant journal, 16(6):735{743, 1998. Uwe Conrath, Gerold JM Beckers, Victor Flors, Pilar Garc a-Agust n, G abor Jakab, Felix Mauch, Mari-Anne Newman, Corn e MJ Pieterse, Benoit Poinssot, Mar a J Pozo, et al. Priming: getting ready for battle. Molecular Plant-Microbe Interactions, 19(10):1062{1071, 2006. Peter A Crisp, Diep Ganguly, Steven R Eichten, Justin O Borevitz, and Barry J Pogson. Reconsidering plant memory: Intersections between stress recovery, rna turnover, and epigenetics. Science advances, 2(2):e1501340, 2016. Maria Suarez Cristina, Morten Petersen, and John Mundy. Mitogen-activated protein kinase signaling in plants. Annual review of plant biology, 61:621{649, 2010. Sean R Cutler, David W Ehrhardt, Joel S Gri tts, and Chris R Somerville. Random gfp cdna fusions enable visualization of subcellular structures in cells of arabidopsis at a high frequency. Proceedings of the National Academy of Sciences, 97(7):3718{3723, 2000. Chris Dardick, Benjamin Schwessinger, and Pamela Ronald. Non-arginine-aspartate (non-rd) kinases are associated with innate immune receptors that recognize conserved microbial signatures. Current opinion in plant biology, 15(4):358{366, 2012. D'Maris Amick Dempsey, Jyoti Shah, and Daniel F Klessig. Salicylic acid and disease resistance in plants. Critical Reviews in Plant Sciences, 18(4):547{575, 1999. Keqin Deng, Qiming Wang, Jianxin Zeng, Xinhong Guo, Xiaoying Zhao, Dongying Tang, and Xuanming Liu. A lectin receptor kinase positively regulates aba response during seed germination and is involved in salt and osmotic stress response. Journal of Plant Biology, 52(6):493, 2009. WeiWei Deng, ChunYan Liu, YanXi Pei, Xian Deng, LiFang Niu, and XiaoFeng Cao. Involvement of the histone acetyltransferase athac1 in the regulation of owering time via repression of owering locus c in arabidopsis. Plant physiology, 143(4):1660{1668, 2007. Marie Desclos-Theveniau, Dominique Arnaud, Ting-Yu Huang, Grace Jui-Chih Lin, Wei-Yen Chen, Yi-Chia Lin, and Laurent Zimmerli. The arabidopsis lectin receptor kinase lecrk-v.5 represses stomatal immunity induced by pseudomonas syringae pv. tomato dc3000. PLoS pathogens, 8(2):e1002513, 2012. Radhika Desikan, John T Hancock, Kazuya Ichimura, Kazuo Shinozaki, and Steven J Neill.Harpin induces activation of the arabidopsis mitogen-activated protein kinases atmpk4 and atmpk6. Plant Physiology, 126(4):1579{1587, 2001. Radhika Desikan, Jakub Hor ak, Christina Chaban, Virtudes Mira-Rodado, Janika Witth oft,Kirstin Elgass, Christopher Grefen, Man-Kim Cheung, Alfred J Meixner, Richard Hooley, et al. The histidine kinase ahk5 integrates endogenous and environmental signals in arabidopsis guard cells. PLoS One, 3(6):e2491, 2008. Peter N Dodds and John P Rathjen. Plant immunity: towards an integrated view of plantpathogen interactions. Nature reviews. Genetics, 11(8):539, 2010. Jixin Dong, Chunhong Chen, and Zhixiang Chen. Expression pro les of the arabidopsis wrky gene superfamily during plant defense response. Plant molecular biology, 51(1):21{37, 2003. Daolong Dou and Jian-Min Zhou. Phytopathogen e ectors subverting host immunity: different foes, similar battleground. Cell host & microbe, 12(4):484{495, 2012. Max Dow, Mari-Anne Newman, and Edda von Roepenack. The induction and modulation of plant defense responses by bacterial lipopolysaccharides. Annual review of phytopathology, 38(1):241{261, 2000. Ian A Dubery, Natasha M Sanabria, and Ju-Chi Huang. Nonself perception in plant innate immunity. In Self and Nonself, pages 79{107. Springer, 2012. Wendy E Durrant and Xinnian Dong. Systemic acquired resistance. Annu. Rev. Phytopathol., 42:185{209, 2004. Anton Eberharter and Peter B Becker. Histone acetylation: a switch between repressive and permissive chromatin. EMBO reports, 3(3):224{229, 2002. K Edwards, C Johnstone, and C1 Thompson. A simple and rapid method for the preparation of plant genomic dna for pcr analysis. Nucleic acids research, 19(6):1349, 1991. Abdelbasset El Hadrami, Lorne R Adam, Ismail El Hadrami, and Fouad Daayf. Chitosan in plant protection. Marine drugs, 8(4):968{987, 2010. Juergen Engelberth, Hans T Alborn, Eric A Schmelz, and James H Tumlinson. Airborne signals prime plants against insect herbivore attack. Proceedings of the National Academy of Sciences of the United States of America, 101(6):1781{1785, 2004. Gitte Erbs, Alba Silipo, Shazia Aslam, Cristina De Castro, Valeria Liparoti, Angela Flagiello,Pietro Pucci, Rosa Lanzetta, Michelangelo Parrilli, Antonio Molinaro, et al. Peptidoglycan and muropeptides from pathogens agrobacterium and xanthomonas elicit plant innate immunity: structure and activity. Chemistry & biology, 15(5):438{448, 2008. Georg Felix, Martin Regenass, and Thomas Boller. Speci c perception of subnanomolar concentrations of chitin fragments by tomato cells: induction of extracellular alkalinization, changes in protein phosphorylation, and establishment of a refractory state. The Plant Journal, 4(2):307{316, 1993. Georg Felix, Juliana D Duran, Sigrid Volko, and Thomas Boller. Plants have a sensitive perception system for the most conserved domain of bacterial agellin. The Plant Journal, 18(3):265{276, 1999. Simone Ferrari, Roberta Galletti, Carine Denoux, Giulia De Lorenzo, Frederick M Ausubel, and Julia Dewdney. Resistance to botrytis cinerea induced in arabidopsis by elicitors is independent of salicylic acid, ethylene, or jasmonate signaling but requires phytoalexin de cient3. Plant physiology, 144(1):367{379, 2007. Leslie Friedrich, Kay Lawton, Wilhelm Ruess, Peter Masner, Nicole Specker, Manuela Gut Rella, Beatrice Meier, Sandra Dincher, Theodor Staub, Scott Uknes, et al. A benzothiadiazole derivative induces systemic acquired resistance in tobacco. The Plant Journal, 10(1): 61{70, 1996. William Fry. Phytophthora infestans: the plant (and r gene) destroyer. Molecular plant pathology, 9(3):385{402, 2008. Catherine A Frye and Roger W Innes. An arabidopsis mutant with enhanced resistance to powdery mildew. The Plant Cell, 10(6):947{956, 1998. Miki Fujita, Yasunari Fujita, Yoshiteru Noutoshi, Fuminori Takahashi, Yoshihiro Narusaka,Kazuko Yamaguchi-Shinozaki, and Kazuo Shinozaki. Crosstalk between abiotic and biotic stress responses: a current view from the points of convergence in the stress signaling networks. Current opinion in plant biology, 9(4):436{442, 2006. CA Gehring, HR Irving, R McConchie, and RW Parish. Jasmonates induce intracellular alkalinization and closure of paphiopedilum guard cells. Annals of Botany, 80(4):485{489, 1997. Paola A Gilardoni, Christian Hettenhausen, Ian T Baldwin, and Gustavo Bonaventure. Nicotiana attenuata lectin receptor kinase1 suppresses the insect-mediated inhibition of induced defense responses during manduca sexta herbivory. The Plant Cell, 23(9):3512{3532, 2011. Jane Glazebrook. Contrasting mechanisms of defense against biotrophic and necrotrophic pathogens. Annu. Rev. Phytopathol., 43:205{227, 2005. Lourdes G omez-G omez and Thomas Boller. Fls2: an lrr receptor{like kinase involved in the perception of the bacterial elicitor agellin in arabidopsis. Molecular cell, 5(6):1003{1011, 2000. Lourdes G omez-G omez, Georg Felix, and Thomas Boller. A single locus determines sensitivity to bacterial agellin in arabidopsis thaliana. The Plant Journal, 18(3):277{284, 1999. Lourdes G omez-G omez, Zsuzsa Bauer, and Thomas Boller. Both the extracellular leucine-rich repeat domain and the kinase activity of s2 are required for agellin binding and signaling in arabidopsis. The Plant Cell, 13(5):1155{1163, 2001. Xiaoping Gou, Kai He, Hui Yang, Tong Yuan, Honghui Lin, Steven D Clouse, and Jia Li. Genome-wide cloning and sequence analysis of leucine-rich repeat receptor-like protein kinase genes in arabidopsis thaliana. BMC genomics, 11(1):19, 2010. Anne Gouget, Virginie Senchou, Francine Govers, Arnaud Sanson, Annick Barre, Pierre Roug e, Rafael Pont-Lezica, and Herv e Canut. Lectin receptor kinases participate in proteinprotein interactions to mediate plasma membrane-cell wall adhesions in arabidopsis. Plant physiology, 140(1):81{90, 2006. Andrea A Gust, Raja Biswas, Heike D Lenz, Thomas Rauhut, Stefanie Ranf, Birgit Kemmerling, Friedrich G otz, Erich Glawischnig, Justin Lee, Georg Felix, et al. Bacteria-derived peptidoglycans constitute pathogen-associated molecular patterns triggering innate immunity in arabidopsis. Journal of Biological Chemistry, 282(44):32338{32348, 2007. Thierry Halter, Julia Imkampe, Sara Mazzotta, Michael Wierzba, Sandra Postel, Christoph B ucherl, Christian Kiefer, Mark Stahl, Delphine Chinchilla, Xiaofeng Wang, et al. The leucine-rich repeat receptor kinase bir2 is a negative regulator of bak1 in plant immunity. Current biology, 24(2):134{143, 2014. Soon-Ki Han, Ju-Dong Song, Yoo-Sun Noh, and Bosl Noh. Role of plant cbp/p300-like genes in the regulation of owering time. The Plant Journal, 49(1):103{114, 2007. Antje Heese, Dagmar R Hann, Selena Gimenez-Ibanez, Alexandra ME Jones, Kai He, Jia Li,Julian I Schroeder, Scott C Peck, and John P Rathjen. The receptor-like kinase serk3/bak1 is a central regulator of innate immunity in plants. Proceedings of the National Academy of Sciences, 104(29):12217{12222, 2007. Susan S Hirano and Christen D Upper. Population biology and epidemiology of pseudomonas syringae. Annual review of phytopathology, 28(1):155{177, 1990. Jarmo K Holopainen and Jonathan Gershenzon. Multiple stress factors and the emission of plant vocs. Trends in plant science, 15(3):176{184, 2010. Gregg A Howe and Georg Jander. Plant immunity to insect herbivores. Annu. Rev. Plant Biol., 59:41{66, 2008. Deping Hua, Cun Wang, Junna He, Hui Liao, Ying Duan, Ziqiang Zhu, Yan Guo, Zhizhong Chen, and Zhizhong Gong. A plasma membrane receptor kinase, ghr1, mediates abscisic acid-and hydrogen peroxide-regulated stomatal movement in arabidopsis. The Plant Cell Online, 24(6):2546{2561, 2012. Pin-Yao Huang, Yu-Hung Yeh, An-Chi Liu, Chiu-Ping Cheng, and Laurent Zimmerli. The arabidopsis lecrk-vi. 2 associates with the pattern-recognition receptor s2 and primes nicotiana benthamiana pattern-triggered immunity. The Plant Journal, 79(2):243{255, 2014. Ping Huang, Hyun-Woo Ju, Ji-Hee Min, Xia Zhang, Su-Hyun Kim, Kwang-Yeol Yang, and Cheol Soo Kim. Overexpression of l-type lectin-like protein kinase 1 confers pathogen resistance and regulates salinity response in arabidopsis thaliana. Plant science, 203:98{ 106, 2013. Tania V Humphrey, Dario T Bonetta, and Daphne R Goring. Sentinels at the wall: cell wall receptors and sensors. New Phytologist, 176(1):7{21, 2007. Marcello Iriti, Giulia Castorina, Sara Vitalini, Ilaria Mignani, Carlo Soave, Gelsomina Fico, and Franco Faoro. Chitosan-induced ethylene-independent resistance does not reduce crop yield in bean. Biological Control, 54(3):241{247, 2010. Gabor Jakab, Jurriaan Ton, Victor Flors, Laurent Zimmerli, Jean-Pierre M etraux, and Brigitte Mauch-Mani. Enhancing arabidopsis salt and drought stress tolerance by chemical priming for its abscisic acid responses. Plant Physiology, 139(1):267{274, 2005. Fabien Jammes, Xiaohua Yang, Shunyuan Xiao, and June M Kwak. Two arabidopsis guard cell-preferential mapk genes, mpk9 and mpk12, function in biotic stress response. Plant signaling & behavior, 6(11):1875{1877, 2011. Arif Tasleem Jan, Mudsser Azam, Arif Ali, and Qazi Mohd Rizwanul Haq. Novel approaches of bene cial pseudomonas in mitigation of plant diseases{an appraisal. Journal of plant interactions, 6(4):195{205, 2011. Michal Jaskiewicz, Uwe Conrath, and Christoph Peterh ansel. Chromatin modi cation acts as a memory for systemic acquired resistance in the plant stress response. EMBO reports,12(1):50{55, 2011. Christopher E Je ree. The ne structure of the plant cuticle. Biology of the plant cuticle, 23: 11{125, 2006. Zhenhua Jia, Baohong Zou, Xiaomeng Wang, Jian Qiu, Hong Ma, Zhenhua Gou, Shuishan Song, and Hansong Dong. Quercetin-induced h 2 o 2 mediates the pathogen resistance against pseudomonas syringae pv. tomato dc3000 in arabidopsis thaliana. Biochemical and biophysical research communications, 396(2):522{527, 2010. Louise N Johnson, Martin EM Noble, and David J Owen. Active and inactive protein kinases: structural basis for regulation. Cell, 85(2):149{158, 1996. Jonathan DG Jones and Je ery L Dangl. The plant immune system. Nature, 444(7117):323, 2006. Yasuhiro Kadota, Jan Sklenar, Paul Derbyshire, Lena Stransfeld, Shuta Asai, Vardis Ntoukakis, Jonathan DG Jones, Ken Shirasu, Frank Menke, Alexandra Jones, et al. Direct regulation of the nadph oxidase rbohd by the prr-associated kinase bik1 during plant immunity. Molecular cell, 54(1):43{55, 2014. Hanae Kaku, Yoko Nishizawa, Naoko Ishii-Minami, Chiharu Akimoto-Tomiyama, Naoshi Dohmae, Koji Takio, Eiichi Minami, and Naoto Shibuya. Plant cells recognize chitin fragments for defense signaling through a plasma membrane receptor. Proceedings of the National Academy of Sciences, 103(29):11086{11091, 2006. Leron Katsir, Anthony L Schilmiller, Paul E Staswick, Sheng Yang He, and Gregg A Howe. Coi1 is a critical component of a receptor for jasmonate and the bacterial virulence factor coronatine. Proceedings of the National Academy of Sciences, 105(19):7100{7105, 2008. L Dale Keppler, C Jacyn Baker, and Merelee M Atkinson. Active oxygen production during a bacteria-induced hypersensitive reaction in tobacco suspension cells. Phytopathology, 79 (9):974{978, 1989. MD Khokon, EIJI Okuma, Mohammad Anowar Hossain, Shintaro Munemasa, Misugi Uraji, Yoshimasa Nakamura, Izumi C Mori, and Yoshiyuki Murata. Involvement of extracellular oxidative burst in salicylic acid-induced stomatal closure in arabidopsis. Plant, cell & environment, 34(3):434{443, 2011. Md AR Khokon, MA Salam, F Jammes, W Ye, MA Hossain, M Uraji, Y Nakamura, IC Mori, JM Kwak, and Y Murata. Two guard cell mitogen-activated protein kinases, mpk9 and mpk12, function in methyl jasmonate-induced stomatal closure in arabidopsis thaliana. Plant Biology, 17(5):946{952, 2015. Md Atiqur Rahman Khokon, Misugi Uraji, Shintaro Munemasa, Eiji Okuma, Yoshimasa Nakamura, Izumi C Mori, and Yoshiyuki Murata. Chitosan-induced stomatal closure accompanied by peroxidase-mediated reactive oxygen species production in arabidopsis. Bio- science, biotechnology, and biochemistry, 74(11):2313{2315, 2010. Hyun-Jin Kim, Feng Chen, Xi Wang, and Nihal C Rajapakse. E ect of chitosan on the biological properties of sweet basil (ocimum basilicum l.). Journal of Agricultural and Food Chemistry, 53(9):3696{3701, 2005. Jong-Myong Kim, Taiko Kim To, Junko Ishida, Taeko Morosawa, Makiko Kawashima, Akihiro Matsui, Tetsuro Toyoda, Hiroshi Kimura, Kazuo Shinozaki, and Motoaki Seki. Alterations of lysine modi cations on the histone h3 n-tail under drought stress conditions in arabidopsis thaliana. Plant and Cell Physiology, 49(10):1580{1588, 2008. Andrew P Kloek, Michelle L Verbsky, Shashi B Sharma, James E Schoelz, John Vogel, Daniel F Klessig, and Barbara N Kunkel. Resistance to pseudomonas syringae conferred by an arabidopsis thaliana coronatine-insensitive (coi1) mutation occurs through two distinct mechanisms. The Plant Journal, 26(5):509{522, 2001. Birgit Kl usener, Jared J Young, Yoshiyuki Murata, Gethyn J Allen, Izumi C Mori, Veronique Hugouvieux, and Julian I Schroeder. Convergence of calcium signaling pathways of pathogenic elicitors and abscisic acid in arabidopsis guard cells. Plant physiology, 130 (4):2152{2163, 2002. Annegret Kohler, Sandra Schwindling, and Uwe Conrath. Benzothiadiazole-induced priming for potentiated responses to pathogen infection, wounding, and in ltration of water into leaves requires the npr1/nim1 gene in arabidopsis. Plant Physiology, 128(3):1046{1056, 2002. June M Kwak, Izumi C Mori, Zhen-Ming Pei, Nathalie Leonhardt, Miguel Angel Torres, Jeffery L Dangl, Rachel E Bloom, Sara Bodde, Jonathan DG Jones, and Julian I Schroeder. Nadph oxidase atrbohd and atrbohf genes function in ros-dependent aba signaling in arabidopsis. The EMBO journal, 22(11):2623{2633, 2003. Ulrich K Laemmli. Cleavage of structural proteins during the assembly of the head of bacteriophage t4. nature, 227(5259):680{685, 1970. Lan-Ying Lee and Stanton B Gelvin. Bimolecular uorescence complementation for imaging protein interactions in plant hosts of microbial pathogens. Host-Bacteria Interactions: Methods and Protocols, pages 185{208, 2014. Sumin Lee, Hyunjung Choi, SuJeoung Suh, In-Suk Doo, Ki-Young Oh, Eun Jeong Choi, Ann T Schroeder Taylor, Philip S Low, and Youngsook Lee. Oligogalacturonic acid and chitosan reduce stomatal aperture by inducing the evolution of reactive oxygen species from guard cells of tomato and commelina communis. Plant physiology, 121(1):147{152, 1999. Sung Chul Lee and Sheng Luan. Aba signal transduction at the crossroad of biotic and abiotic stress responses. Plant, Cell & Environment, 35(1):53{60, 2012. Jennifer D Lewis, David S Guttman, and Darrell Desveaux. The targeting of plant cellular systems by injected type iii e ector proteins. In Seminars in cell & developmental biology, volume 20, pages 1055{1063. Elsevier, 2009. Jianming Li and Joanne Chory. A putative leucine-rich repeat receptor kinase involved in brassinosteroid signal transduction. Cell, 90(5):929{938, 1997. Jing Li, G unter Brader, and E Tapio Palva. The wrky70 transcription factor: a node of convergence for jasmonate-mediated and salicylate-mediated signals in plant defense. The Plant Cell, 16(2):319{331, 2004. Lei Li, Meng Li, Liping Yu, Zhaoyang Zhou, Xiangxiu Liang, Zixu Liu, Gaihong Cai, Liyan Gao, Xiaojuan Zhang, Yingchun Wang, et al. The s2-associated kinase bik1 directly phosphorylates the nadph oxidase rbohd to control plant immunity. Cell host & microbe, 15(3):329{338, 2014. Chunyan Liu, Falong Lu, Xia Cui, and Xiaofeng Cao. Histone methylation in higher plants. Annual review of plant biology, 61:395{420, 2010a. Yu-Kun Liu, Yu-Bo Liu, Mao-Ying Zhang, and De-Quan Li. Stomatal development and movement: the roles of mapk signaling. Plant signaling & behavior, 5(10):1176{1180, 2010b. Zixu Liu, Ying Wu, Fan Yang, Yiyue Zhang, She Chen, Qi Xie, Xingjun Tian, and Jian-Min Zhou. Bik1 interacts with peprs to mediate ethylene-induced immunity. Proceedings of the National Academy of Sciences, 110(15):6205{6210, 2013. Dongping Lu, Shujing Wu, Xiquan Gao, Yulan Zhang, Libo Shan, and Ping He. A receptorlike cytoplasmic kinase, bik1, associates with a agellin receptor complex to initiate plant innate immunity. Proceedings of the National Academy of Sciences, 107(1):496{501, 2010. Karolin Luger, Armin W Mader, Robin K Richmond, David F Sargent, and Timothy J Richmond. Crystal structure of the nucleosome core particle at 2.8 angstrom resolution. Nature, 389(6648):251, 1997. Estrella Luna, Toby JA Bruce, Michael R Roberts, Victor Flors, and Jurriaan Ton. Nextgeneration systemic acquired resistance. Plant physiology, 158(2):844{853, 2012. Alexandra Lusser. Acetylated, methylated, remodeled: chromatin states for gene regulation. Current opinion in plant biology, 5(5):437{443, 2002. Andreas Madlung and Luca Comai. The e ect of stress on genome regulation and structure.Annals of botany, 94(4):481{495, 2004. Klaus Maleck, Aaron Levine, Thomas Eulgem, Allen Morgan, J urg Schmid, Kay A Lawton,Je ery L Dangl, and Robert A Dietrich. The transcriptome of arabidopsis thaliana during systemic acquired resistance. Nature genetics, 26(4):403, 2000. Maeli Melotto, William Underwood, Jessica Koczan, Kinya Nomura, and Sheng Yang He. Plant stomata function in innate immunity against bacterial invasion. Cell, 126(5):969{ 980, 2006. Maeli Melotto, William Underwood, and Sheng Yang He. Role of stomata in plant innate immunity and foliar bacterial diseases. Annu. Rev. Phytopathol., 46:101{122, 2008. Xiangzong Meng and Shuqun Zhang. Mapk cascades in plant disease resistance signaling. Annual review of phytopathology, 51:245{266, 2013. Sophia Mersmann, Gildas Bourdais, Ste en Rietz, and Silke Robatzek. Ethylene signaling regulates accumulation of the s2 receptor and is required for the oxidative burst contributing to plant immunity. Plant physiology, 154(1):391{400, 2010. Tatiana E Mishina and J urgen Zeier. Pathogen-associated molecular pattern recognition rather than development of tissue necrosis contributes to bacterial induction of systemic acquired resistance in arabidopsis. The Plant Journal, 50(3):500{513, 2007. Ayako Miya, Premkumar Albert, Tomonori Shinya, Yoshitake Desaki, Kazuya Ichimura, Ken Shirasu, Yoshihiro Narusaka, Naoto Kawakami, Hanae Kaku, and Naoto Shibuya. Cerk1, a lysm receptor kinase, is essential for chitin elicitor signaling in arabidopsis. Proceedingsof the National Academy of Sciences, 104(49):19613{19618, 2007. Jean-Luc Montillet, Nathalie Leonhardt, Samuel Mondy, Sylvain Tranchimand, Dominique Rumeau, Marie Boudsocq, Ana Victoria Garcia, Thierry Douki, Jean Bigeard, Christiane Lauri ere, et al. An abscisic acid-independent oxylipin pathway controls stomatal closure and immune defense in arabidopsis. PLoS biology, 11(3):e1001513, 2013. Izumi C Mori, Reinhard Pinontoan, Tomonori Kawano, and Shoshi Muto. Involvement of superoxide generation in salicylic acid-induced stomatal closure in vicia faba. Plant and Cell Physiology, 42(12):1383{1388, 2001. Izumi C Mori, Yoshiyuki Murata, Yingzhen Yang, Shintaro Munemasa, Yong-FeiWang, Shannon Andreoli, Herv e Tiriac, Jose M Alonso, Je ery F Harper, Joseph R Ecker, et al. Cdpkscpk6 and cpk3 function in aba regulation of guard cell s-type anion-and ca2+-permeable channels and stomatal closure. PLoS biology, 4(10):e327, 2006. Izumi C Mori, Yoshiyuki Murata, and Misugi Uraji. Integration of ros and hormone signaling.In Reactive Oxygen Species in Plant Signaling, pages 25{42. Springer, 2009. Rebecca A Mosher, Wendy E Durrant, Dong Wang, Junqi Song, and Xinnian Dong. A comprehensive structure{function analysis of arabidopsis sni1 de nes essential regions and transcriptional repressor activity. The Plant Cell, 18(7):1750{1765, 2006. Stephen Mosher, Wolfgang Moeder, Noriyuki Nishimura, Yusuke Jikumaru, Se-Hwan Joo, William Urquhart, Daniel F Klessig, Seong-Ki Kim, Eiji Nambara, and Keiko Yoshioka.The lesion-mimic mutant cpr22 shows alterations in abscisic acid signaling and abscisic acid insensitivity in a salicylic acid-dependent manner. Plant Physiology, 152(4):1901{1913, 2010. Keith A Mott and Jon Y Takemoto. Syringomycin, a bacterial phytotoxin, closes stomata. Plant physiology, 90(4):1435{1439, 1989. Khaled Moustafa, Synan AbuQamar, Mohammad Jarrar, Abdul Jabbar Al-Rajab, and JocelyneTr emouillaux-Guiller. Mapk cascades and major abiotic stresses. Plant cell reports, 33 (8):1217{1225, 2014. Shintaro Munemasa, Kenji Oda, Megumi Watanabe-Sugimoto, Yoshimasa Nakamura, Yasuaki Shimoishi, and Yoshiyuki Murata. The coronatine-insensitive 1 mutation reveals the hormonal signaling interaction between abscisic acid and methyl jasmonate in arabidopsis guard cells. speci c impairment of ion channel activation and second messenger production. Plant physiology, 143(3):1398{1407, 2007. Shintaro Munemasa, Mohammad Anowar Hossain, Yoshimasa Nakamura, Izumi C Mori, and Yoshiyuki Murata. The arabidopsis calcium-dependent protein kinase, cpk6, functions as a positive regulator of methyl jasmonate signaling in guard cells. Plant physiology, 155(1): 553{561, 2011. Luis AJ Mur, Grant Naylor, Simon AJ Warner, Jane M Sugars, Ray F White, and John Draper. Salicylic acid potentiates defence gene expression in tissue exhibiting acquired resistance to pathogen attack. The Plant Journal, 9(4):559{571, 1996. Yoshiyuki Murata, Zhen-Ming Pei, Izumi C Mori, and Julian Schroeder. Abscisic acid activation of plasma membrane ca2+ channels in guard cells requires cytosolic nad (p) h and is di erentially disrupted upstream and downstream of reactive oxygen species production in abi1-1 and abi2-1 protein phosphatase 2c mutants. The Plant Cell, 13(11):2513{2523, 2001. Anna-Chiara Mustilli, Sylvain Merlot, Alain Vavasseur, Francesca Fenzi, and J er^ome Giraudat.Arabidopsis ost1 protein kinase mediates the regulation of stomatal aperture by abscisic acid and acts upstream of reactive oxygen species production. The Plant Cell, 14 (12):3089{3099, 2002. Sushma Naithani, Thanat Chookajorn, Daniel R Ripoll, and June B Nasrallah. Structural modules for receptor dimerization in the s-locus receptor kinase extracellular domain. Pro-ceedings of the National Academy of Sciences, 104(29):12211{12216, 2007. Steven Neill, Raimundo Barros, Jo Bright, Radhika Desikan, John Hancock, Judith Harrison, Peter Morris, Dimas Ribeiro, and Ian Wilson. Nitric oxide, stomatal closure, and abiotic stress. Journal of experimental botany, 59(2):165{176, 2008. Brook K Nelson, Xue Cai, and Andreas Nebenf uhr. A multicolored set of in vivo organelle markers for co-localization studies in arabidopsis and other plants. The Plant Journal, 51 (6):1126{1136, 2007. Valerie Nicaise, Milena Roux, and Cyril Zipfel. Recent advances in pamp-triggered im | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/77904 | - |
dc.description.abstract | 在自然中,植物氣孔常被做為病原細菌入侵的入口。然而,植物可藉由透過膜受體來感知病原細菌並誘導氣孔之關閉。其中,大多數凝集素受器激(LecRKs) 會受病原菌及病原菌相關分子模式所啟動(PAMPs)。在本研究中,我們發現lecrk-V.2 及lecrk-VII.1 突變株之氣孔關閉對於細菌行斑點病(Pst DC3000) 及病原細菌鞭毛(flg22) 受損。除此之外,增量表現之LecRK-V.2 及LecRK-VII.1 之氣孔關閉對於Flg22 較為敏感、並延緩受Pst DC3000造成的氣孔重新開啟。在lecrk-V.2 及lecrk-VII.1 的突變株之氣孔關閉能力,對於甲基茉莉酸(MeJA) 較為不敏感。在雙分子螢光互補(BiFC) 及免疫共沉澱(CoIP) 中發現LecRK-V.2及LecRK-VII.1 會和細菌鞭毛受體(FLS2) 結合。本研究表明LecRK-V.2 and LecRK-VII.1 參與氣孔免疫並且參與在鞭毛受體及共受體FLS2-BAK1 複合體中。
除此之外,本研究也發現阿拉伯芥如何因非生物逆境影響,而調控對於細菌行斑點病之致病性。受過7 天之鹽、熱、寒害逆境之阿拉伯芥能提高對於細菌病害之感染。並發現逆境下提升抗性之阿拉伯芥之原因是和預先準備免疫有所關聯,並且預先準備先天免疫之啟動是透過RNAPII 調控之轉錄影響。除此,阿拉伯芥在此逆境下會提升免疫相關基因之組蛋白H3K4之二甲基及三甲基化的能力。進一步研究發現,在乙烯基轉移(hac1-1 ) 突變株中並無法誘導,表明預先準備免疫和組蛋白之轉錄後修飾之關聯性。在本次研究中結果表明,植物中的組蛋白修飾和預先準備免疫之間的運作方式。 | zh_TW |
dc.description.abstract | Stomata act as natural ports for bacterial entry. However, plants can sense biotic invasion through plasma membrane localized receptors and stomatal closure is one of the first innate immunity responses activated upon bacterial infection. Most lectin receptor kinases (LecRKs) are induced in response to pathogens or pathogen-associated molecular patterns (PAMPs). Here, we observed impaired stomatal closure upon infection with bacteria Pst DC3000 or after treatment with the PAMP flg22 in lecrk-V.2 and lecrk-VII.1 mutants. In addition, stomata of transgenic lines over-expressing LecRK-V.2 and LecRK-VII.1 were hypersensitive to flg22 and showed delayed stomatal reopening upon Pst DC3000 inoculation. Stomata of mutants lecrk-V.2 and lecrk-VII.1 were also insensitive to MeJA. Furthermore, BiFC and CoIP data demonstrated association of LecRK-V.2 and LecRK-VII.1 with FLS2. Overall these data suggest that LecRK-V.2 and LecRK-VII.1 are involved in stomatal immunity and are part of the FLS2-BAK1 pattern-recognition receptor complex.
In addition, I also evaluated how mild abiotic stresses modulate Arabidopsis resistance to hemi-biotroph Pst DC3000. Arabidopsis exposed to salt, heat or cold stresses for 7 days were more resistant to bacteria infection. Enhanced resistance was correlated with a primed immunity in Arabidopsis exposed to stresses. Priming of innate immunity was associated with RNAPII mediated transcription. Furthermore, Arabidopsis exposed to recurrent stresses showed enrichment of H3K4 dimethylation and trimethylation at immunity-responsive genes. In addition, priming of immunity-responsive genes was not observed in histone acetyltrans-ferase 1-1 (hac1-1 ) mutants after repetitive abiotic stress treatments, further suggesting that primed immunity is related to post translational histone modification. Taken together this work suggests a mechanistic link between histone modifications and the primed state in plants. | en |
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dc.description.tableofcontents | List of Figures v
1 General Introduction 1 1.1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 1.2 Plant pathogen interaction and disease formation . . . . . . . . . . . . . . . . . 1 1.3 Plant innate immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 1.4 Pattern Recognition Receptors . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 1.4.1 Receptor like kinases . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 1.4.2 Potential PRRs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 1.4.3 FLS2- g22, a representative pair model . . . . . . . . . . . . . . . . . . 6 1.5 Role of PTI in plant defense . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 1.5.1 Activation of PRR complex upon ligand binding . . . . . . . . . . . . . 7 1.5.2 RLCKs as positive regulators of PRR complexes . . . . . . . . . . . . . 7 1.6 Pseudomonas syringae pv. tomato DC3000: A virulent pathogen model in stomatal immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 1.7 Role of stomata in innate immunity . . . . . . . . . . . . . . . . . . . . . . . . 8 1.7.1 Signaling cascades involved in PAMP induced stomatal closure . . . . . 9 1.7.2 ROS as secondary messenger in stomatal immunity . . . . . . . . . . . . 9 1.7.3 Role of the Protein Kinases MAPK and CDPK in Stomatal immunity . 9 1.7.4 Hormones involved in stomatal immunity . . . . . . . . . . . . . . . . . 10 2 Material and Methods 12 2.1 Plant growth conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 2.1.1 Seed Sterilization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 2.2 Nucleic acid Extraction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 2.2.1 Isolation of total RNA from Arabidopsis . . . . . . . . . . . . . . . . . . 12 2.2.2 cDNA Synthesis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12 2.2.3 Isolation of Genomic DNA from Arabidopsis . . . . . . . . . . . . . . . 13 2.3 PCR Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 2.3.1 Standard PCR Method . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 2.3.2 Hi-delity PCR . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 2.3.3 Quantitative Real-Time PCR (qPCR) . . . . . . . . . . . . . . . . . . . 14 2.4 Cloning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 2.4.1 TOPO TA Cloning Method . . . . . . . . . . . . . . . . . . . . . . . . . 14 2.4.2 Gateway LR reaction. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 2.4.3 Transformation of bacteria by heat-shock . . . . . . . . . . . . . . . . . 15 2.4.4 Plasmid miniprep . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 2.4.5 Transformation of bacteria by electroporation . . . . . . . . . . . . . . . 15 2.4.6 Stable transformation of A. thaliana by Floral Dipping Method . . . . . 15 2.5 Bacterial Growth and Infection . . . . . . . . . . . . . . . . . . . . . . . . . . . 16 2.5.1 Pseudomonas syringae DC3000 growth . . . . . . . . . . . . . . . . . . 16 2.5.2 Pseudomonas syringae DC3000 dip inoculation . . . . . . . . . . . . . . 16 2.5.3 Pseudomonas syringae DC3000 syringe inltration . . . . . . . . . . . . 16 2.6 Botrytis cinerea growth and infection . . . . . . . . . . . . . . . . . . . . . . . . 17 2.7 Stomatal Assay . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17 2.7.1 ROS Detection in Guard Cell . . . . . . . . . . . . . . . . . . . . . . . . 17 2.8 Apoplastic PTI Assay . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18 2.8.1 Apoplastic FRK1 Expression . . . . . . . . . . . . . . . . . . . . . . . . 18 2.8.2 Analysis of Pst hrcC -mediated callose deposition . . . . . . . . . . . . 18 2.8.3 Detection of H2O2 in Leaf Tissues . . . . . . . . . . . . . . . . . . . . . 18 2.9 Analysis of seedling roots and shoots growth . . . . . . . . . . . . . . . . . . . 18 2.10 Isolation and Transformation of Protoplast from Arabidopsis . . . . . . . . . . 19 2.10.1 Protoplast Isolation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 2.10.2 Protoplast Transfection . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 2.10.3 GFP Localization in Arabidopsis Protoplast . . . . . . . . . . . . . . . . 20 2.11 GUS Promoter Activity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20 2.12 General Protein Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20 2.12.1 SDS-polyacrylamide gel electrophoresis . . . . . . . . . . . . . . . . . . 20 2.12.2 Western Blot . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20 2.12.3 Immunoblotting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 2.13 Protein Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 2.13.1 Co-Immunoprecipitation Assay in Arabidopsis Protoplasts . . . . . . . 21 2.13.2 Bimolecular uorescence complementation (BiFC) Assay . . . . . . . . . 22 2.14 Biological Materials, Growth Conditions, and Environmental Stress Treatments 22 2.14.1 ChIP Assay . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23 3 LecRK-V.2 and LecRK-VII.1 are part of the FLS2-BAK1 PRR complex and positively regulates stomatal immunity 26 3.1 Abstract . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26 3.2 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27 3.3 L-type Lectin receptor kinase (LecRK) . . . . . . . . . . . . . . . . . . . . . . . 27 3.4 Objective . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29 3.5 Results . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30 3.5.1 Preliminary Screening to identify LecRKs involved in PTI response . . . 30 3.5.2 Role of LecRK-V.2 and LecRK-VII.1 in stomatal immunity . . . . . . . 37 3.5.3 Role of LecRK-V.2 and LecRK-VII.1 in FLS2 complex . . . . . . . . . 44 3.5.4 LecRK-V.2 and LecRK-VII.1 are involved in stomatal immunity through methyl jasmonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50 3.6 Discussion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58 4 Environmental History Modulates Arabidopsis Pattern-Triggered Immu- nity in a HISTONE ACETYLTRANSFERASE1-Dependent Manner 62 4.1 Abstract . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63 4.2 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64 4.2.1 Priming or stress memory . . . . . . . . . . . . . . . . . . . . . . . . . . 64 4.2.2 Priming by natural compounds . . . . . . . . . . . . . . . . . . . . . . . 65 4.2.3 Priming by pathogens . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66 4.2.4 Priming induced by BABA in Arabidopsis . . . . . . . . . . . . . . . . 66 4.2.5 Systemic acquired resistance (SAR) and priming . . . . . . . . . . . . . 66 4.2.6 Priming during induced resistance . . . . . . . . . . . . . . . . . . . . . 67 4.2.7 Priming is linked to chromatin modication . . . . . . . . . . . . . . . . 67 4.2.8 Histone modication in SAR . . . . . . . . . . . . . . . . . . . . . . . . 68 4.3 Objective . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70 4.4 Results . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71 4.4.1 Environmentally challenged Arabidopsis plants are resistance to virulent bacterial pathogens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71 4.4.2 Enhanced resistance after repetitive stress is lost after seven day of recovery period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 73 4.4.3 Arabidopsis exposed to seven times repetitive environmental stress shows enhanced PTI response . . . . . . . . . . . . . . . . . . . . . . . . . . . 73 4.4.4 Seven day stress treatments is necessary for priming and lasts for seven days recovery period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76 4.4.5 Chromatin modications in Arabidopsis exposed to recurrent stress treatments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79 4.4.6 RNAPII enrichment status in Arabidopsis exposed to repetitive environmental challenges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82 4.4.7 Role of HAC1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84 References 110 Appendices 131 A List of homozygotic T-DNA insertion lines 132 B Primers used in Section 4.4 133 C Gene-specic primer pairs for quantitative RT-PCR and for ChIP assays 135 | |
dc.language.iso | en | |
dc.title | 凝集素受體激 LecRK-V.2 和 LecRK-VII.1 參與氣孔免疫及非生物逆境透過組蛋白乙醯轉移1敏化阿拉伯芥模式誘發免疫之研究 | zh_TW |
dc.title | Role of LecRK-V.2 and LecRK-VII.1 in stomatal immunity and
Abiotic stress primes PTI responses in a HISTONE ACETYLTRANSFERASE1-Dependent manner in Arabidopsis | en |
dc.type | Thesis | |
dc.date.schoolyear | 105-2 | |
dc.description.degree | 博士 | |
dc.contributor.oralexamcommittee | 鄭石通,謝旭亮,鄭秋萍,張英?,林乃君 | |
dc.subject.keyword | LecRKs, | zh_TW |
dc.relation.page | 166 | |
dc.identifier.doi | 10.6342/NTU201703256 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2017-08-14 | |
dc.contributor.author-college | 生命科學院 | zh_TW |
dc.contributor.author-dept | 植物科學研究所 | zh_TW |
顯示於系所單位: | 植物科學研究所 |
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