Differentially expressed proteins in suspension culture of rice induced by blast disease

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Research Paper 01/11/2013
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Differentially expressed proteins in suspension culture of rice induced by blast disease

A. Kahe1, M. Toorchi, E. Dorani1, S. Aharizad, M. Arzanlo
Int. J. Biosci.3( 11), 189-197, November 2013.
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Abstract

Rice (Oryza sativa L.) is an important cereal for more than half of the human population in the world. Magnaporthe grisea is the agent of the most important rice fungus diseases in the world. This experiment was conducted to investigate the effect of blast fungus on expression of proteins in suspension culture of rice. Suspension culture of rice inoculated with conidial suspension (1105 conidia/mL) races of M. grisea for 48 hours. For identification of proteins involved in resistance to magnaporth disease, proteins profile of suspension culture was investigated after inoculation. Comparing proteome pattern of susceptible rice cultivar, Tarom, under control and stress conditions lead to classification differentially expressed proteins into two functional categories, defense and metabolism/biosynthesis. Metabolism and biosantesis related proteins include triose phosphate isomerase, Isoflavone reductase and Transketolase were as the most important defense protein was pathogen related protein.

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Afroz A, Ali GM, Mir A, Komatsu S. 2011. Application of proteomics to investigate stress-induced proteins for improvement in crop protection. Plant Cell Repeat 30, 745-763. http://dx.doi.org/10.1007/s00299-010-0982-x

Agrios  GN.  2005.  Plant  Pathology.  5th  Edition. Elsevier-Academic Press. San Diego, CA.

Bantignies B, Seguin J, Muzac I, Dedaldechamp F, Gulick P, Ibrahim R. 2000. Direct evidence for ribonucleolytic activity of a PR-10 like protein from white lupin roots. Plant Molecular Biology 42, 871-881.

Casasoli M, Spadoni S, Lilley KS, Cervone F, De Lorenzo G, Mattei B. 2008. Identification by 2-D DIGE of apoplastic proteins regulated by oligogalacturonides in Arabidopsis thaliana. Proteomics 8, 1042-1054. http://dx.doi.org/10.1002/pmic.200700523

Chao L, DongZhi L, Yan Jun D, ShengHai, YE, XiaoMing Z. 2010. Genetic analysis and mapping of a thermo-sensitive white stripe-leaf mutant at seedling stage in rice (Oryza sativa). Rice Science 17, 276-281.

Cluzet S, Torregrosa C, Jacquet C, Lafitte C. 2004. Gene expression profiling and protection of Medicago truncatula against a fungal infection in response to an elicitor from green algaeUlva spp. Plant Cell Environment 27, 917-928.

Curto M, Camafeita E, Lopez JA, Maldonado AM, Rubiales D, Jorrın JV. 2006. A proteomic approach  to study pea  (Pisum sativum) responses topowdery mildew (Erysiphe pisi). Proteomics  6, 163-174. http://dx.doi.org/10.1002/pmic.200500396

Dorion S, Jeukens J, Matton DP, Rivoal J. 2005.  Cloning  and  characterization  of  a  cytosolic isoform of triosephosphate isomerase developmentally regulated in potato leaves. Plant Science 168, 183-194.

Ebbole DJ. 2007. Magnaporthe as a model for understandinghost-pathogen interactions. Annual Review of Phytopathology 45, 437-456. http://dx.doi.org/10.1146/annurev.phyto.45.062806 .094346

Juhnke H, Krems B, Kötter P, Entian KD. 1996. Mutants that show increased sensitivity to hydrogen peroxide reveal an important role for the pentose phosphate pathway in protection of yeast against oxidative stress. Molecular and General Genetics 252, 456-464. http://dx.doi.org/10.1007/BF02173011

Jwa NS, Agrawalb Gk, Tamogamic S, Yonekurad M, Hane O, Iwahashif H, Rakwalb R. 2006. Role of defense/stress-related marker genes proteins and secondary metabolites in defining rice self-defense mechanisms. Plant Physiology and Biochemistry 44, 261-273.

Kim ST, Cho KS, Yu S, Kim SG, Hong JC, Han CD, Bae DW, Nam MH, Kang KY. 2003. Proteomic analysis of differentially expressed protein induced by rice blast fungus and elicitor in suspension-cultured rice cells. Proteomics 3, 2368-2378. http://dx.doi.org/10.1002/pmic.200300577

Kim ST, Kang YH, Wang Y, Wu J, Park ZY, Rakwal R, Agrawal GK, Lee SY, Kang KY. 2009. Secretome analysis of differentially induced proteins in rice suspension-cultured cells triggered by rice blast fungus and elicitor. Proteomics 9, 1302-1313.

Kim ST, Kim SG, Hwang DH, Kang SY, Kim HJ, Lee BH, Lee JJ, Kang KY. 2004. Proteomic analysis of pathogen-responsive proteins from rice leaves induced by rice blast fungus, Magnaporthe grisea. Proteomics 4, 3569-3578. http://dx.doi.org/10.1002/pmic.200400999

Konishi H, Ishiguro K, Komatsu K. 2001. A proteomics approach towards understanding blast fungus infection of rice grown under different levels of nitrogen fertilization. Proteomics 1, 1162-1171.

Langvad F. 1980. A simple and rapid method for qualitative and quantitative study of the fungal flora of leaves. Canadian Journal of Microbiology 26, 666-670.

Lee DG, Ahsan N, Lee SH, Kang KY, Bahk JD, Lee  IJ,  Lee  BH.  2007.  Proteomic  approach  in analyzing heat-responsive proteins in rice leaves. Proteomics 7, 3369-3383.

Liao M, Li Y, Wang Z. 2009. Identification of elicitor-responsive protein in rice leave by a proteomics approach. Proteomics 9, 2809-2819. http://dx.doi.org/10.1002/pmic.200800192

Mahmood T, Jan A, Kakishima M, Komatsu S. 2006. Proteomic analysis of bacterial-blight defense responsive proteins in rice leaf blades. Proteomics 6, 6053-6065.

Meyers BC, Kaushik S, Nandety RS. 2005. Evolving disease resistance genes. Current Opinion in Plant Biology 8, 129-134.

Panstruga R. 2003. Establishing compatibility between plants and obligate biotrophic pathogens. Current Opinion in Plant Biology l6, 320-326.

Quirino BF, Candido ES, Campo PF, Franco OL, Kruger RH. 2010. Proteomic approaches to study plant-pathogen interaction. Phytochemistry 71, 351-362.

Rakwal R, Agrawal, GK. 2003. Rice proteomics: current status and future perspectives. Electrophoresis 24, 3378-3389

Rakwal R, Komatsu S. 2000. Role of jasmonate in the rice (Oryza sativa L.) self-defense mechanism using proteome analysis. Electrophoresis 21, 2492-2500.

RiceEvans C, Miller N, Paganga G. 1997. Antioxidant properties of phenolic compounds. Trend in Plant Science 2, 152-159.

Ryals JA, NeuenschwanderUH, Willits MG, Molina A, Steiner HY, Hunt MD. 1996. Systemic acquired resistance. The Plant Cell 8, 1809-1819

Ryu HS, Song MY, Kim CY, Han M, Lee SK, Ryoo N, Cho JI, Hahn TR, Jeon J. S. 2009. Proteomic  analysis  of  rice  mutants  susceptible  to Magnaporthe  Oryzae.  Plant  Biotechnol  Report  3, 167-174. http://dx.doi.org/10.1007/s11816-009-0087-6

Salekdeh GH, Siopongco J, Wade LJ, Ghareyazie B, Bennett J. 2002. Proteomic analysis of rice leaves during drought stress and recovery. Proteomics 2, 1131-1145.

Schenk PM, Kazan K, Wilson I, Anderson JP, Richmond T, Somerville SC, Segarra G, Casanova E, Bellido D, Odena MA, Oliveira E. 2007.  Proteome,  salicylic  acid,  and  jasmonic  acid changes in cucumber plants inoculated with Trichoderma asperellum strain T34. Proteomics 7, 3943-3952. http://dx.doi.org/10.1002/pmic.200700173

Skamnioti P, Gurr SJ. 2009. Against the grain: safeguarding rice from rice blast disease. Trends in Biotechnology 27, 141-50.

Sticher L, MauchMani B, Metraux JP. 1997. Systemic acquired resistance. Annual Review of Phytopathology 35, 235-270. http://dx.doi.org/10.1146/annurev.phyto.35.1.235

Stefan H, Uwe S, Ralf B, Ralf F, Mark S. 2001. A small decrease of plastid transketolase activity in antisense tobacco transformants has dramatic effects on photosynthesis and phenylpropanoid has dramatic effects on photosynthesis and phenylpropanoid metabolism. Plant Cell 13, 535-540.

Thurstona G, Reganb S, Rampitschc C, Xinga T. 2005. Proteomic and phosphoproteomic approaches to understand plant-pathogen interaction. Physiological and Molecular Plant Pathology 66, 3-11

Van Loon LC. 1985. Pathogenesis-related proteins. Plant Moecularl Biology 4, 111-116. http://dx.doi.org/10.1007/BF02418757

Van Loon LC, Van Kammen A. 1970. Polyacrylamide disc electrophoresis of the soluble leaf proteins from Nicotiana tabacum var. ‘‘Smsun’’ and ‘‘Samsun NN’’ II Changes in protein constitution after infection with tobacco mosaic virus. Virology 40, 199-206.

Velazhahan  R,  ChenCole  K,  Anuratha  CS, Muthukrishnan S. 1998. Induction of thaumatin- like protein (TLPs) in rhizoctonia solania infected rice and characterization of two new cDNA clone. Physiologia Plantarum 102, 21-28.

Yang P, Chen H, Liang Y, Shen S. 2007. Proteomic analysis of de-etiolated rice seedlings upon exposure to light. Proteomics 7, 2459-2468. http://dx.doi.org/10.1002/pmic.200600215