Peanut genes identified during initial phase of Cercosporidium personatum infection

Plant Science

Volumn 174, Issue 1, 2008, Pages 78-87

  Nobile, Paula Macedo ^a,b   Lopes, Catalina Romero ^b   Barsalobres Cavallari, Carla ^b   Quecini, Vera ^a   Coutinho, Luiz L ^d   Hoshino, Andrea Akemi ^b   Gimenes, Marcos A ^b,c  

^a INSTITUTO AGRONÔMICO   (Brazil)

^b SÃO PAULO STATE UNIVERSITY UNESP   (Brazil)

^c EMBRAPA RECURSOS GENÉTICOS E BIOTECNOLOGIA   (Brazil)

^d UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Host defense response; Late leaf spot; O Methyltransferase; Peanut; Suppression subtractive hybridization (SSH)

Indexed keywords

ARACHIS HYPOGAEA; CERCOSPORIDIUM PERSONATUM; FUNGI;

EID: 36048934067     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2007.09.009     Document Type: Article

References (48)

1. S.A Moraes, I.J. Godoy, Amendoim (Arachis hypogaea L.) Controle e Doenças, in: F.X.R. do Vale, L. Zambolim (Eds.), Controle de Doenças de Plantas: Grandes Cultivares, vol. 1, Viçosa, MG, UFV, 1997, pp. 1-49.
2. Shokes F.M., and Culbreath A.K. Early and late leaf spots. In: Kokalis-Burelle N., Porter D.M., Rodríguez-Kábana R., Smith D.H., and Subrahmanyam P. (Eds). Compendium of Peanut Diseases. 2nd ed. (1997), St. Paul The American Phytopathological Society, APS Press pp. 1-17-20
3. Orlandi E.W., Hutcheson S.W., and Baker C.J. Early physiological responses associated with race-specific recognition in soybean leaf tissue and cell suspensions treated with Pseudomonas syringae pv. Glycinea. Physiol. Mol. Plant Pathol. 40 (1992) 173-180
4. Baker J.C., Mock N., Glazener J., and Orlandi E. Recognition responses in pathogen/non-host and race/cultivar interactions involving soybean (Glycine max) and Pseudomonas syringae pathovars. Physiol. Mol. Plant Pathol. 43 (1993) 81-94
5. Moraes S.A., Godoy I.J., and Veiga R.F.A. Variabilidade do germoplasma de Arachis hypogaea para resistência a doenças foliares. Fitopatol. Bras. 20 (1995) 297
6. Dwivedi S.L., Pande S., Rao J.N., and Nigam S.N. Components of resistance to late leaf spot and rust among interspecific derivates and their significance in a foliar disease resistance breeding in groundnut (Arachis hypogaea L.). Euphytica 125 (2002) 81-88
7. Moraes S.A., Godoy I.J., Gerin M.A.N., Pedro M.J., and Pereira J.C.V.N.A. Epidemiologia de Cercosporidium personatum em genótipos de amendoim. Fitopatol. Bras. 13 (1988) 255-260
8. Dangl J.L., Dietrich R.A., and Richberg M.H. Death don't have no mercy: cell death programs in plant-microbe interactions. Plant Cell 8 (1996) 1793-1807
9. Diantchenko L., Lau Y.-F., Campbell A.P., Chenchik A., Moqadam J., Huang B., Lukyanov S., Lukyanov K., Guskaya N., Sverdlov E.D., and Siebert P.D. Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries. Proc. Natl. Acad. Sci. U.S.A. 93 (1996) 6025-6030
10. S.A. Moraes, Técnica de folhas destacadas para testar reações de cultivares de amendoim (Arachis hypogaea L.) aos fungos Cercospora arachidicola Hori e Cercospora personata (Berk. & Curt.) Ell. & Everh., Piracicaba, 1981, Thesis (Philosophical Doctor), ESALQ, Escola Superior de Agricultura Luiz de Queiroz, Universidade de São Paulo, p. 107.
11. Huang X., and Madan A. CAP3: a DNA sequence assembly program. Genome Res. 9 (1999) 868-877
12. Altschul S.F., Madden T.L., Schaffer A.A., Zhang J., Miller W., and Lipman D.J. Gapped blast and Psi-blast: a new generation of protein database search programs. Nucleic Acids Res. 25 (1997) 3389-3402
13. Sambrook J., Fritsch E.F., and Maniatis T. Molecular Cloning: A Laboratory Manual (1989), Cold Spring Harbor Laboratory, NY p. 1659
14. Barsalobres-Cavallari C., De Rosa Júnior V., Nogueira F., Ferro J., Di Mauro S., Menossi M., Ulian E., and Silva-Filho M. A novel system for large-scale gene expression analysis: bacterial colonies array. Appl. Microbiol. Biotechnol. 71 (2006) 963-969
15. - Δ Δ Ct method. Methods 25 (2001) 402-408
16. Luo M., Dang P., Bausher M.G., Holbrook C.C., Lee R.D., Lynch R.E., and Guo B.Z. Identification of transcripts involved in resistance responses to leaf spot disease caused by Cercosporidium personatum in peanut (Arachis hypogaea). Phytopathology 95 (2005) 381-387
17. Kellmann J.W., Kleinow T., Engelhardt K., Philipp C., Wegener D., Schel J., and Schreier P.H. Characterization of two class II chitinase genes from peanut and expression studies in transgenic tobacco plants. Plant Mol. Biol. 30 (1996) 351-358
18. Thompson J.D., Gibson T.J., Plewniak F., Jeanmougin F., and Higgins D.G. The ClustalX windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 24 (1997) 4876-4882
19. Kumar S., Tamura K., and Nei M. MEGA3: integrated software for molecular evolutionary genetics analysis and sequence alignment. Brief. Bioinform. 5 (2004) 150-163
20. Nicholson R.L., and Epstein L. Adhesion of fungi to the plant surface: prerequisite for pathogenesis. In: Cole G.T., and Hoch H.C. (Eds). The Funga1 Spore and Disease Initiation in Plants and Animals (1991), Plenum Press, New York 3-23
21. R. Gopalakrishna, M. Udayakumar, M.K. Mathew, Arachis hypogaea putative caffeic acid methyl transferase (Gsi-75) mRNA, partial cds. AF479308. Identification and characterization of stress responsive genes from groundnut (Arachis hypogaea L.), a moisture stress tolerant crop, 2003. Available in: http://www.ncbi.nlm.nih.gov/entrez/viewer.fcgi?db=nucleotideandval=28194656 (accessed August 30, 2005).
22. Van Loon L.C., and Van Strien L.A. The families of pathogenesis related proteins, their activities, and comparative analysis of PR-1 type proteins. Physiol. Mol. Plant Pathol. 55 (1999) 85-97
23. Chen Z., Silva H., and Klessig D.F. Active oxygen species in the induction of plant systemic acquired resistance by salicylic acid. Science 262 (1993) 1883-1886
24. Heo W.D., Lee S.H., Kim M.C., Kim J.C., Chung W.S., Chun H.J.K.J., Lee C.Y., Park Y.C., Choi J.Y., and Cho M.J. Involvement of specific calmodulin isoforms in salicylic acid-independent activation of plant disease resistance responses. Proc. Natl. Acad. Sci. U.S.A. 96 (1999) 766-771
25. Kawalleck P., Plesch G., Hahlbrock K., and Somssich I.E. Induction by fungal elicitor of S-adenosyl-l-methionine synthetase and S-adenosyl-l-homocysteine hydrolase mRNAs in cultured cells and leaves of Petroselinum crispur. Proc. Natl. Acad. Sci. U.S.A. 89 (1992) 4713-4717
26. Iturriaga E.A., Leech M.J., Barratt D.H., and Wang T.L. Two ABA-responsive proteins from pea (Pisum sativum L.) are closely related to intracellular pathogenesis-related proteins. Plant Mol. Biol. 24 (1994) 235-240
27. Ibrahim R.K., Bruneauand A., and Bantignies B. Plant O-methyltransferases: molecular analysis, common signature and classification. Plant Mol. Biol. 36 (1998) 1-10
28. Gowri G., Bugos R.C., Campbell W.H., Maxwell C.A., and Dixon R.A. Stress responses in alfalfa (Medicago sativa L.): X. molecular cloning and expression of S-adenosyl-l-methionine:caffeic acid 3-O-methyltransferase, a key enzyme of lignin biosynthesis. Plant Physiol. 97 (1991) 7-14
29. Toquin V., Grausem B., Geoffroy P., and Legrand M. Structrure of the tobacco caffeic acid O-methyltransferase (COMT) II gene: identification of promoter sequences involved in gene inducibility by various stimuli. Plant Mol. Biol. 52 (2003) 495-509
30. Wu S., Watanabe N., Mita S., Ueda Y., Shibuya M., and Ebizuka Y. Two O-methyltransferases isolated from flower petals of Rosa chinensis var. spontanea involved in scent biosynthesis. J. Biosci. Bioeng. 96 (2003) 119-128
31. Ounaroon A., Decker G., Schmidt J., Lottspeich F., and Kutchan T.M. (R,S)-Reticuline 7-O-methyltransferase and (R,S)-norcoclaurine 6-O-methyltransferase of Papaver somniferum-cDNA cloning and characterization of methyl transfer enzymes of alkaloid biosynthesis in opium poppy. Plant J. 36 (2003) 808-819
32. Cursino-Santos J.R., Defina T.P., and Martinez-Rossi N.M. Os Segredos das Plantas e de Seus Patógenos na Era Molecular. 1st ed. (2003), Sociedade Brasileira de Genética (SBG), Ribeirão Preto p. 45
33. Pyee J., Yu H., and Kolattukudy P.E. Identification of a lipid transfer protein as the major protein in the suface, wax of broccoli (Brassica oleracea) leaves. Arch. Biochem. Biophys. 311 (1994) 460-468
34. Cammue B.P.A., Thevissen K., Hendriks M., Eggermont K., Goderis I.J., Proost P., Van Damme J., Osborn R.W., Guerbette F., Kader J.-C., and Broekaert W.F. A potent antimicrobial protein from onion seeds showing sequence homology to plant lipid transfer proteins. Plant Physiol. 109 (1995) 445-1445
35. Buhot N., Gomès E., Milat M.-L., Ponchet M., Marion D., Lequeu J., Detrot S., Coutos-Thévenot P., and Blein J.-P. Modulation of the biological activity of a tobacco Ltp1 by lipid complexation. Mol. Biol. Cell. 15 (2004) 5047-5052
36. Blein J.-P., Coutos-Thévenot P., Marion D., and Ponchet M. From elicitins lipid-transfer proteins: a new insight in cell signaling involved in plant defence mechanisms. Trends Plant Sci. 7 (2002) 293-295
37. Missotten M., Nichols A., Rieger K., and Sadoul R. Alix, a novel mouse protein undergoing calcium-dependent interaction with the apoptosis-linked-gene 2 (ALG-2) protein. Cell Death Differ. 6 (1999) 124-129
38. Wada Y., Miyamoto K., Kusano T., and Sano H. Association between up-regulation of stress-responsive genes and hypomethylation of genomic DNA in tobacco plants. Mol. Genet. Genomics 271 (2004) 658-666
39. Swidzinski J.A., Sweetlove L.J., and Leaver C.J. A custom microarray analysis of gene expression during programmed cell death in Arabidopsis thaliana. Plant J. 30 (2002) 431-446
40. Takahashi A.C., Asais C., Ichimura K., and Shirasu K. HSP90 interacts with RAR1 and SGT1 and is essential for RPS2-mediated disease resistance in Arabidopsis. Proc. Natl. Acad. Sci. U.S.A. 100 (2003) 11777-11782
41. Legrand M., Fritig B., and Hirth L. O-Diphenol O-methyltransferases of healthy and tobacco-mosaic-virus-infected hypersensitive tobacco. Planta 144 (1978) 101-108
42. Hermann C., Legrand M., Geoffroy P., and Fritig B. Enzymatic synthesis of lignin: purification to homogeneity of the three O-methyltransferases of tobacco and production of specific antibodies. Arch. Biochem. Biophys. 253 (1987) 367-376
43. Jaeck E., Dumas B., Geoffroy P., Favet N., Inze D., Van Montagu M., Fritig B., and Legrand M. Regulation of enzymes involved in lignin biosynthesis: induction of O-methyltransferase mRNAs during the hypersensitive reaction of tobacco to tobacco mosaic virus. Mol. Plant Microbe Interact. 5 (1992) 294-300
44. Jaeck E., Martz F., Stiefel V., Fritig B., and Legrand M. Expression of class I O-methyltransferase in healthy and TMV-infected tobacco. Mol. Plant Microbe Interact. 9 (1996) 681-688
45. Pellegrini L., Geoffroy P., Fritig B., and Legrand M. Molecular cloning and expression of a new class of ortho-diphenol-O-methyltransferases induced in tobacco (Nicotiana tabacum L.) leaves by infection or elicitor treatment. Plant Physiol. 103 (1993) 509-517
46. Inoue K., Sewalt V.J.H., Balance G.M., Ni W., Sturzer C., and Dixon R.A. Developmental expression and substrate specificities of alfalfa caffeic acid 3-O-methyltransferase in relation to lignification. Plant Physiol. 117 (1998) 761-770
47. Zubieta C., Kota P., Ferrer J.-L., Dixon R.A., and Noel J.P. Structural basis for the modulation of lignin monomer methylation by caffeic acid/5-hydroxyferulic acid 3/5-O-methyltransferase. Plant Cell 14 (2002) 1265-1277
48. Albrecht K.A., Wedin W.F., and Buxton D.R. Cell-wall composition and digestibility of alfalfa stems and leaves. Crop Sci. 27 (1987) 735-741