Abstract
Rice diseases such as blast (Magnaporthe oryzae), sheath blight (Rhizoctonia solani) and bacterial blight (Xanthomonas oryzae pv oryzae) are a major obstacle to achieving optimal yields. To complement conventional breeding method, molecular and transgenic method represents an increasingly important approach for genetic improvement of disease resistance and reduction of pesticide usage. During the past two decades, a wide variety of genes and mechanisms involved in rice defense response have been identified and elucidated. These include components of pathogen recognition, signal transduction, downstream defense-related proteins, and crosstalk among different signaling pathways. In addition, various molecular strategies including use of specialized promoters, modification of target protein structures have been studied and proposed to improve the effectiveness of transgenes. While genetically improving rice for enhanced disease resistance, it is important to consider potential effects of the transgene on rice yield, tolerance to abiotic stresses, and defense against other pathogens.
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References
Skamnioti P, Gurr SJ (2009) Against the grain: safeguarding rice from blast disease. Trends Biotechnol 27:141–150
Wilson RA, Talbot NJ (2009) Under pressure: investigating the biology of plant infection by Magnaporthe oryzae. Nat Rev 7:185–195
Banniza S, Holderness M (2001) Pathogen biology and diversity. In: Sreenivasaprasad S, Johnson R (eds) Major fungal diseases of rice: recent advances. Kluwer Academic Publishers, The Netherlands. pp 201–211
Ou SH (1972) Rice diseases. Commonwealth Mycological Institute, Kew, Surrey, England
Niño-Liu DO, Ronald PC, Bogdanove AJ (2006) Xanthomonas oryzae pathovars: model pathogen of a model crop. Mol Plant Pathol 7:303–324
Baulcombe D (2004) RNA silencing in plants. Nature 431:356–363
Gust AA, Brunner F, Nürnberger T (2010) Biotechnological concepts for improving plant innate immunity. Curr Opin Biotechnol 21:204–210
Kou Y, Wang S (2010) Broad-spectrum and durability: understanding of quantitative disease resistance. Curr Opin Plant Biol 13:181–185
Fukuoka S, Saka N, Koga H, Ono K, Shimizu T, Ebana K, Hayashi N, Takahashi A, Hirochika H, Okuno K, Yano M (2009) Loss of function of a proline-containing protein confers durable disease resistance in rice. Science 325:998–1001
Qu S, Liu G, Zhou B, Bellizzi M, Zeng L, Dai L, Han B, Wang G-L (2006) The broad-spectrum blast resistance gene Pi9 encodes a nucleotide-binding site leucine-rich repeat protein and is a member of a multigene family in rice. Genetics 172:1901–1914
Niks RE, Marcel TC (2009) Nonhost and basal resistance: how to explain specificity? New Phytol 182:817–828
Poland JA, Balint-Kurti PJ, Wisser RJ, Pratt RC, Nelson RJ (2008) Shades of gray: the world of quantitative disease resistance. Trends Plant Sci 14:21–29
Jones JDG, Dangl JL (2006) The plant immune system. Nature 444:323–329
Gomez-Gomez L, Boller T (2006) FLS2: an LRR receptor like kinase involved in the perception of the bacterial elicitor flagellin in Arabidopsis. Mol Cell 5:1003–1011
Göhre V, Spallek T, Haweker H, Mersmann S, Mentzel T, Boller T, de Torres M, Mansfield JW, Robatzke S (2008) Plant pattern-recognition receptor FLS2 is directed for degradation by the bacterial ubiquitin ligase AvrPtoB. Curr Biol 18:1824–1832
Li H, Zhou SY, Zhao WS, Su SC, Peng YL (2009) A novel wall-associated receptor-like kinase gene, OsWAK1, plays important roles in rice blast disease resistance. Plant Mol Biol 69:337–346
Shiu S-H, Karlowski WM, Pan R, Tzeng Y-H, Mayer KFX, Li W-H (2004) Comparative analysis of the receptor-like kinase family in Arabidopsis and Rice. Plant Cell 16:1220–1234
Dangl JL, Jones JDG (2001) Plant pathogens and integrated defense responses to infection. Nature 411:826–833
Carole LB, Michael LN, Reuben AC, Mangalathu SR (2000) Alternative transcript initiation and novel post-transcriptional processing of a leucine-rich repeat receptor-like protein kinase gene that responds to short-day photoperiodic floral induction in morning glory (Ipomoea nil). Plant Mol Biol 43:43–58
Nishiguchi M, Yoshida K, Sumizono T, Tazaki K (2002) A receptor-like protein kinase with a lectin-like domain from lombardy poplar: gene expression in response to wounding and characterization of phosphorylation activity. Mol Genet Genomics 267:506–514
Hong SW, Jon JH, Kwak JM, Nam HG (1997) Identification of a receptor-like protein kinase gene rapidly induced by abscisic acid, dehydration, high salt, and cold treatments in Arabidopsis thaliana. Plant Physiol 113:1203–1212
Li J, Wen J, Lease KA, Doke JT, Tax FE, Walker JC (2002) BAK1, an Arabidopsis LRR receptor-like protein kinase, interacts with BRI1 and modulates brassinosteroid signaling. Cell 110:213–222
Xiong L, Lee MW, Qi M, Yang Y (2001) Identification of defense-related genes by suppression subtractive hybridization and differential screening. Mol Plant Microbe Interact 14:685–692
Hu H, Xiong L, Yang Y (2005) Rice SERK1 gene positively regulates somatic embryogenesis of cultured cell and host defense response against fungal infection. Planta 222:107–117
Song D, Li G, Song F, Zheng Z (2008) Molecular characterization and expression analysis of OsBISERK1, a gene encoding a leucine-rich repeat receptor-like kinase, during disease resistance responses in rice. Mol Biol Rep 35:275–283
Peng H, Zhang Z, Li Y, Lei C, Zhai Y, Sun X, Sun D, Sun Y, Lu T (2009) A putative leucine-rich repeat receptor kinase, OsBRR1, is involved in rice blast resistance. Planta 230:377–385
Song WY, Wang G-L, Chen LL, Kim HS, Pi LY, Holsten T, Wang B, Zhai WX, Zhu H, Fauquet C, Ronald PC (1995) A receptor kinase-like protein encoded by the rice disease resistance gene, Xa21. Science 270:1804–1806
Lee SW, Han SW, Sririyanum M, Park CJ, Seo YS, Ronald PC (2009) A type-I secreted, sulfated peptide triggers XA21-mediated innate immunity. Science 326:850–853
Wang G-L, Song WY, Ruan DL, Sideris S, Ronald PC (1996) The cloned gene, Xa21, confers resistance to multiple X. oryzae pv. oryzae isolates in transgenic plants. Mol. Plant-Microbe Interct 9:850–855
Ito Y, Kaku H, Shibuya N (2002) Identification of a high affinity binding protein for N-acetylchitooligosaccharide elicitor in the plasma membrane of suspension-cultured rice cells by affinity labeling. Plant J 12:347–356
Shimizu T, Nakano T, Takamizawa D, Desaki Y, Ishii-Minami N, Nishizawa Y, Minami E, Okada K, Yamane H, Kaku H, Shibuya N (2010) Two LysM receptor molecules, CEBiP and OsCERK1, cooperatively regulate chitin elicitor signaling in rice. Plant J 64:204–214
Kaku H, Nishizawa Y, Ishii-Minami N, Akimoto-Tomiyama C, Dohmae N, Takio K, Minami E, Shibuya N (2006) Plant cells recognize chitin fragments for defense signaling through a plasma membrane receptor. Proc Natl Acad Sci USA 103:11086–11091
Ballini E, Morel J-B, Droc G, Price A, Courtois B, Notteghem J-L, Tharreau D (2008) A genome-wide meta-analysis of rice blast resistance genes and quantitative trait loci provides new insights into partial and complete resistance. Mol Plant Microbe Interact 21:859–868
Liu J, Wang X, Mitchell T, Hu Y, Liu X, Dai L, Wang G-L (2010) Recent progress and understanding of the molecular mechanisms of the rice-Magnaporthe oryzae interaction. Mol Plant Pathol 11:419–427
Delteil A, Zhang J, Lessard P, Morel JB (2010) Potential candidate genes for improving rice disease resistance. Rice 3:56–71
Zhao J, Fu J, Li X, Xu C, Wang S (2009) Dissection of the factors affecting development-controlled and race-specific disease resistance conferred by leucine-rich repeat receptor kinase-type R genes in rice. Theor Appl Genet 119:231–239
Century KS, Lagman RA, Adkisson M, Morlan J, Tobias R, Schwartz K, Smith A, Love J, Ronald PC, Whalen MC (1999) Developmental control of Xa21- mediated disease resistance in rice. Plant J 20:231–236
Cao Y, Ding X, Cai M, Zhao J, In Y, Li X, Xu C, Wang S (2007) Expression pattern of a rice disease resistance gene Xa3/Xa26 is differentially regulated by the genetic backgrounds and developmental stages that influence its function. Genetics 177:523–533
Sun X, Cao Y, Yang Z, Xu C, Li X, Wang S, Zhang Q (2004) Xa26, a gene conferring resistance to Xanthomonas oryzae pv. oryzae in rice, encodes an LRR receptor kinase-like protein. Plant J 37:517–527
Hittalmani S, Parco A, Mew TV, Zeigler RS, Huang N (2000) Fine mapping and DNA marker-assisted pyramiding of the three major genes for blast resistance in rice. Theor Appl Genet 100:1121–1128
Koide Y, Kawasaki A, Telebanco-Yanoria MJ, Hairmansis A, Nguyen NTM, Bigirimana J, Fujita D, Kobayashi N, Fukuta Y (2010) Development of pyramided lines with two resistance genes, Pish and Pib, for blast disease (Magnaporthe oryzae B.Couch) in rice (Oryza sativa L.). Plant Breed 129:670–675
Farnham G, Baulcombe DC (2006) Artificial evolution extends the spectrum of viruses that are targeted by a disease-resistance gene from potato. Proc Natl Acad Sci USA 103:18828–18833
Foreman J, Demidchik V, Bothwell JHF, Mylona P, Miedema H, Torres MA, Linstead P, Costa S, Brownlee C, Jones JDG, Davies JM, Dolan L (2003) Reactive oxygen species produced by NADPH oxidase regulate plant cell growth. Nature 422:422–426
Levine A, Tenhaken R, Dixon R, Lamb C (1994) H2O2 from the oxidative burst orchestrates the plant hypersensitive disease resistance response. Cell 79:583–593
Wong HL, Pinontoan R, Hayashi K, Tabata R, Yaeno T, Hasegawa K, Kojima C, Yoshioka H, Iba K, Kawasaki T, Shimamoto K (2007) Regulation of rice NADPH oxidase by binding of Rac GTPase to its N-terminal extension. Plant Cell 19:4022–4034
Kawasaki T, Henmi K, Ono E, Hatakeyama S, Iwamo M, Satoh H, Shimamoto K (1999) The small GTP-binding protein Rac is a regulator of cell death in plants. Plant Cell 14:763–776
Ono E, Wong HL, Kawasaki T, Hasegawa M, Kodama O, Shimamoto K (2001) Essential role of the small GTPase Rac in disease resistance of rice. Proc Natl Acad Sci USA 98:759–764
Godfrey D, Able A, Dry I (2007) Induction of a grapevine germin-like protein (HvGLP3) gene is closely linked to the site of Erysiphe necator infection: a possible role in defense? Mol Plant Microbe Interact 20:1112–1125
Manosalva PM, Davidson RM, Liu B, Zhu X, Hulbert SH, Leung H, Leach JE (2009) A germin-like protein gene family functions as a complex quantitative trait locus conferring broad-spectrum disease resistance in rice. Plant Physiol 149:286–296
Rohila JS, Yang Y (2007) Rice mitogen-activated protein kinase gene family and its role in biotic and abiotic stress response. J Integr Plant Biol 49:751–759
Reyna NS, Yang Y (2006) Molecular analysis of the rice MAP kinase gene family in relation to Magnaporthe grisea infection. Mol Plant Microbe Interact 19:530–540
Lieberherr D, Thao NP, Nakashima A, Umemura K, Kawasaki T, Shimamoto K (2005) A sphingolipid elicitor-inducible mitogen-activated protein kinase is regulated by the small GTPase OsRac1 and heterotrimeric G-protein in rice. Plant Physiol 138:1644–1652
Cheong YH, Moon BC, Kim JK, Kim CY, Kim MC, Park CY, Kim JC, Park BO, Koo SC, Yoon HW, Chung WS, Lim CO, Lee SY, Cho MJ (2003) BWMK1, a rice mitogen-activated protein kinase, locates in the nucleus and mediates pathogenesis-related gene expression by activation of a transcription factor. Plant Physiol 132:1961–1972
He C, Fong SH, Yang D, Wang GL (1999) BWMK1, a novel MAP kinase induced by fungal infection and mechanical wounding in rice. Mol Plant Microbe Interact 12:1064–1073
Xiong L, Yang Y (2003) Disease resistance and abiotic stress tolerance in rice are inversely modulated by an abscisic acid-inducible mitogen-activated protein kinase. Plant Cell 15:745–759
Vleesschauwer D, Yang Y, Vera Cruz C, Höfte M (2010) Abscisic acid-induced resistance against the brown spot pathogen Cochliobolus miyabeanus in rice involves MAP kinase-mediated repression of ethylene signaling. Plant Physiol 152:2036–2052
Yuan B, Shen X, Li X, Xu C, Wang S (2007) Mitogen-activated protein kinase OsMPK6 negatively regulates rice disease resistance to bacterial pathogens. Planta 226:953–960
Kishi-Kaboshi M, Okada K, Kurimoto L, Murakami S, Umezawa T, Shibuya N, Yamane H, Miyao A, Takatsuji H, Takahashi A, Hirochika H (2010) A rice fungal MAMP-responsive MAPK cascade regulates metabolic flow to antimicrobial metabolite synthesis. Plant J 63:599–612
Silverman P, Seskar M, Kanter D, Schweizer P, Métraux J-P, Raskin I (1995) Salicylic acid in rice: biosynthesis, conjugation, and possible role. Plant Physiol 108:633–639
Yang Y, Qi M, Mei C (2004) Endogenous salicylic acid protects rice plants from oxidative damage caused by aging as well as biotic and abiotic stress. Plant J 40:909–919
Mou Z, Fan W, Dong X (2003) Inducers of plant systemic acquired resistance regulate NPR1 function through redox changes. Cell 113:935–944
Chern MS, Fitzgerald HA, Yadav RC, Canlas PE, Dong X, Ronald PC (2001) Evidence for a disease-resistance pathway in rice similar to the NPR1-mediated signaling pathway in Arabidopsis. Plant J 27:101–113
Chern MS, Fitzgerald HA, Canlas PE, Navarre DA, Ronald PC (2005) Overexpression of a rice NPR1 homolog leads to constitutive activation of defense response and hypersensitivity to light. Mol Plant Microbe Interact 18:511–526
Jiang C-J, Shimono M, Maeda S, Inoue H, Mori M, Hasegawa M, Sugano S, Takasuji H (2009) Suppression of the rice fatty-acid desaturase gene OsSSI2 enhances resistance to blast and leaf blight diseases in rice. Mol Plant Microbe Interact 22:820–829
Iwai T, Seo S, Mitsuhara I, Ohashi Y (2007) Probenazole-induced accumulation of salicylic acid confers resistance to Magnaporthe grisea in adult rice plants. Plant Cell Physiol 48:915–924
Umemura K, Satou J, Iwata M, Uozumi N, Koga J, Kawano T, Koshiba T, Anzai H, Mitomi M (2009) Contribution of salicylic acid glucosyltransferase, OsSGT1, to chemically induced disease resistance in rice plants. Plant J 57:463–472
Seo S, Ishizuka K, Ohashi Y (1995) Induction of salicylic acid β-glucosidase in tobacco leaves by exogenous salicylic acid. Plant Cell Physiol 36:447–453
Chen Z, Malamy J, Henning J, Conrath U, Sanchez-Casas P, Silva H, Ricigliano J, Klessig K (1995) Induction, modification, and transduction of the salicylic acid signal in plant defense responses. Proc Natl Acad Sci USA 92:4134–4137
He Y, Fukushige H, Hildebrand DF, Gan S (2002) Evidence supporting a role of jasmonic acid in Arabidopsis leaf senescence. Plant Physiol 128:876–884
Tamogami S, Rakwal R, Kodama O (1997) Phytoalexin production elicited by exogenously applied jasmonic acid in rice leaves (Oryza sativa L.) is under the control of cytokinins and ascorbic acid. FEBS Lett 412:61–64
Schweizer P, Buchala A, Métraux J-P (1997) Gene-expression patterns and levels of jasmonic acid in rice treated with the resistance inducer 2, 6-dichloroisonicotinic acid. Plant Physiol 115:61–70
Mei C, Min Q, Sheng G, Yang Y (2006) Inducible overexpression of a rice allele oxide synthase gene increases the endogenous jasmonic acid level, PR gene expression and host resistance to fungal infection. Mol Plant Microbe Interact 19:1127–1137
Singh MP, Lee FN, Counce PA, Gibbons JH (2004) Mediation of partial resistance to rice blast through anaerobic induction of ethylene. Phytopathology 94:819–825
Iwai T, Miyasaka A, Seo S, Ohashi Y (2006) Contribution of ethylene biosynthesis for resistance to blast fungus infection in young rice plants. Plant Physiol 142:1202–1215
Seo S, Mitsuhara I, Feng J, Iwai T, Hasegawa M, Ohashi Y (2010) Cyanide, a coproduct of plant hormone ethylene biosynthesis, contributes to the resistance of rice to blast fungus. Plant Physiol 155:502–514
Bailey TA, Zhou X, Chen J, Yang Y (2009) Role of ethylene, abscisic acid and MAP kinase pathways in rice blast resistance. In: Wang G-L, Valent B (eds) Advances in genetics, genomics and control of rice blast disease. Springer pp 185–190
Mauch-Mani B, Mauch F (2005) The role of abscisic acid in plant-pathogen interactions. Curr Opin Plant Biol 8:409–414
Jiang C-J, Shimono M, Sugano S, Kojima M, Azawa K, Yoshida R, Inoue H, Hayashi N, Sakakibara H, Takatsuji H (2010) Abscisic acid interacts antagonistically with salicylic acid signaling pathway in rice-Magnaporthe grisea interaction. Mol Plant Microbe Interact 23:791–798
Kazan K, Manners JM (2009) Linking development to defense: auxin in plant- pathogen interactions. Trends Plant Sci 14:373–382
Shinshu H, Mohnen D, Meins F (1987) Regulation of a plant pathogenesis-related enzyme: inhibition of chitinase and chitinase mRNA accumulation in cultured tobacco tissues by auxin and cytokinin. Proc Natl Acad Sci USA 84:89–93
Abreu ME, Munne-Bosch S (2009) Salicylic acid deficiency in NahG transgenic lines and sid2 mutants increases seed yield in the annual plant Arabidopsis thaliana. J Exp Bot 60:1261–1271
Ding X, Cao Y, Huang L, Zhao J, Xu C, Li X, Wang S (2009) Activation of the indole-3-acetic acid-amido synthetase GH3. 8 suppresses expansin expression and promotes salicylate- and jasmonate-independent basal immunity in rice. Plant Cell 20:228–240
Domingo C, Andrés F, Tharreau D, Iglesias DJ, Talón M (2009) Constitutive expression of OsGH3.1 reduces auxin content and enhances defense response and resistance to a fungal pathogen in rice. Mol Plant Microbe Interact 22:201–210
Liu X, Bai X, Wang X, Chu C (2007) OsWRKY71, a rice transcription factor, is involved in rice defense response. J Plant Physiol 164:969–979
Hu K, Qiu D, Shen X, Li X, Wang S (2008) Isolation and manipulation of quantitative trait loci for disease resistance in rice using a candidate gene approach. Mol Plant Pathol 1:786–793
Wen N, Chu Z, Wang S (2003) Three types of defense-responsive genes are involved in resistance to bacterial blight and fungal blast diseases in rice. Mol Genet Genomics 269:331–339
Wang GL, Mackill DJ, Bonman M, McCouch SR, Champoux MC, Nelson RJ (1994) RFLP mapping of genes conferring complete and partial resistance to blast in a durably resistant rice cultivar. Genetics 136:1421–1434
Chen H, Wang S, Xing Y, Xu C, Hayes P, Zhang Q (2003) Comparative analyses of genomic locations and race specificities of loci for quantitative resistance to Pyricularia grisea in rice and barley. Proc Natl Acad Sci USA 100:2544–2549
Qiu D, Xiao J, Ding X, Xiong M, Cai M, Cao Y, Li X, Xu C, Wang S (2007) OsWRKY13 mediates rice disease resistance by regulating defense related genes in salicylate and jasmonate-dependent signaling. Mol Plant Microbe Interact 20:492–499
Shimono M, Sugano S, Nakayama A, Jiang CJ, Ono K, Toki S et al (2007) Rice WRKY45 plays a crucial role in benzothiadiazole-inducible blast resistance. Plant Cell 19:2064–2076
Ohnishi T, Sugahara S, Yamada T, Kikuchi K, Yoshiba Y, Hirano HY, Tsutsumi N (2005) OsNAC6, a member of the NAC gene family, is induced by various stresses in rice. Genes Genet Syst 80:135–139
Nakashima K, Tran L-SP, Nguyen DV, Fujita M, Maruyama K, Todaka D, Ito Y, Hayashi N, Shinozaki K, Yamaguchi-Shinozaki K (2007) Functional analysis of a NAC-type transcription factor OsNAC6 involved in abiotic and biotic stress-responsive gene expression in rice. Plant J 51:617–630
Tran L-SP, Nakashima K, Sakuma Y, Simpson SD, Fujita Y, Maruyama K, Fujita M, Seki M, Shinozaki K, Yamaguchi-Shinozaki K (2004) Isolation and functional analysis of Arabidopsis stress-inducible NAC transcription factors that bind to a drought-responsive cis-element in the early responsive to dehydration stress 1 promoter. Plant Cell 16:2481–2498
Fitzgerald HA, Canlas PE, Chern MS, Ronald PC (2005) Alteration of TGA factor activity in rice results in enhanced tolerance to Xanthomonas oryzae pv. oryzae. Plant J 43:335–347
van Loon LC, Rep M, Pieterse CMJ (2006) Significance of inducible defense-related proteins in infected plants. Annu Rev Phytopathol 44:1–28
Datta K, Baisakh N, Maung T, Thet KM, Tu J, Datta S (2002) Pyramiding transgenes for multiple resistance in rice against bacterial blight, yellow stem borer and sheath blight. Theor Appl Genet 106:1–8
Anžlovar S, Dermastia M (2003) The comparative analysis of osmotins and osmotin-like PR-5 proteins. Plant Biol 5:116–124
Datta K, Velazhahan R, Oliva N, Ona I, Mew T, Khush GS, Muthukrishnan S, Datta SK (1999) Over-expression of the cloned rice thaumatin-like protein (PR-5) gene in transgenic rice plants enhances environmental friendly resistance to Rhizoctonia solani causing sheath blight disease. Theor Appl Genet 98:1138–1145
Gomez-Ariza J, Campo S, Rufat M, Estopa M, Messeguer J, Segundo BS, Coca M (2007) Sucrose-mediated priming of plant defense responses and broad-spectrum disease resistance of the maize pathogenesis-related PRms protein in rice plants. Mol Plant Microbe Interact 20:832–842
Shimura K, Okada A, Okada K, Jikumaru Y, Ko K-W, Toyomasu T, Sassa T, Hasegawa M, Kodama O, Shibuya N, Koga J, Nojiri H, Yamane H (2007) Identification of a biosynthetic gene cluster in rice for momilactones. J Biol Chem 282:34013–34018
Okada A, Okada K, Miyamoto K, Koga J, Shibuya N, Nojiri H, Yamane H (2009) OsTGAP1, a bZIP transcription factor, coordinately regulates the inductive production of diterpenoid phytoalexins in rice. J Biol Chem 284:26510–26518
Eckhardt NA (2002) Plant disease susceptibility genes? Plant Cell 14:1983–1986
Pavan S, Jacobsen E, Visser RGF, Bai Y (2010) Loss of susceptibility as a novel breeding strategy for durable and broad-spectrum resistance. Mol Breed 25:1–12
Iyer AS, McCouch SR (2004) The rice bacterial blight resistance gene xa5 encodes a novel form of disease resistance. Mol Plant Microbe Interact 17:1348–1354
Chu Z, Yuan M, Yao J, Ge X, Yuan B, Xu C, Li X, Fu B, Li Z, Bennetzen JL, Zhang Q, Wang S (2006) Promoter mutations of an essential gene for pollen development result in disease resistance in rice. Genes Dev 20:1250–1255
Iyer-Pascuzzi AS, McCouch SR (2007) Recessive resistance genes and the Oryza sativa-Xanthomonas oryzae pv oryzae pathosystem. Mol Plant Microbe Interact 20:731–739
Fukuoka S, Okuno K (2001) QTL analysis and mapping of pi21, a recessive gene for field resistance to rice blast in Japanese upland rice. Theor Appl Genet 103:185–190
Brown JKM (2002) Yield penalties of disease resistance in crops. Curr Opin Plant Biol 5:1–6
Kim EH, Kim YS, Park S-H, Koo YJ, Choi YD, Chung Y-Y, Lee I-J, Kim J-K (2009) Methyl jasmonate reduces grain yield by mediating signals to alter spikelet development in rice. Plant Physiol 149:1751–1760
Potenza C, Aleman L, Sengupta-Gopalan C (2004) Targeting transgene expression in research, agricultural, and environmental applications: promoters used in plant transformation. In Vitro Cell Dev Biol 40:1–22
Liu Y, Zhang S (2004) Phosphorylation of 1-aminocyclopropane-1-carboxylic acid synthase by MPK6, a stress-responsive mitogen-activated protein kinase, induces ethylene biosynthesis in Arabidopsis. Plant Cell 16:3386–3399
Joo S, Liu Y, Lueth A, Zhang S (2008) MAPK phosphorylation-induced stabilization of ACS6 protein is mediated by the non-catalytic C-terminal domain, which also contains the cis-determinant for rapid degradation by the 26S proteasome pathway. Plant J 54:129–140
Salmeron JM, Oldroyd GED, Rommens CMT, Scofield SR, Kim H-S, Lavelle DT, Dahlbeck D, Staskawicz BJ (1996) Tomato Prf is a member of the leucine- rich repeat class of plant disease resistance genes and lies embedded within the Pto kinase gene cluster. Cell 86:123–133
Century KS, Shapiro AD, Repetti PP, Dahlbeck D, Holub E, Staskawicz BJ (1997) NDR1, a pathogen-induced component required for Arabidopsis disease resistance. Science 278:1963
Jia Y, Martin R (2008) Identification of a new locus, Ptr(t), required for rice blast resistance gene Pi-ta-mediated resistance. Mol Plant Microbe Interact 21:396–403
Lee S-K, Song M-Y, Seo Y-S, Kim H-K, Ko S, Cao P-J, Suh J-P, Yi G, Roh J-H, Lee S, An G, Hahn T-R, Wang G-L, Ronald P, Jeon J-S (2009) Rice Pi5-mediated resistance to Magnaporthe oryzae requires the presence of two coiled-coil-nucleotide-binding-leucine-rich-repeat genes. Genetics 181:1627–1638
Spoel SH, Johnson JS, Dong X (2007) Regulation of tradeoffs between plant defenses against pathogens with different lifestyles. Proc Natl Acad Sci USA 104:18842–18847
Acknowledgment
This work was supported by the grants from USDA/NRI (2008-35301-19028) and NSF Plant Genome Research Program (DBI-0605017 and DBI-0922747).
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Helliwell, E.E., Yang, Y. (2013). Molecular Strategies to Improve Rice Disease Resistance. In: Yang, Y. (eds) Rice Protocols. Methods in Molecular Biology, vol 956. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-62703-194-3_21
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