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Identification, characterization and mapping of differentially expressed genes in a winter wheat cultivar (Centenaire) resistant to Fusarium graminearum infection.

  1. Bai Guihua, Shaner Gregory, MANAGEMENT AND RESISTANCE IN WHEAT AND BARLEY TO FUSARIUM HEAD BLIGHT, 10.1146/annurev.phyto.42.040803.140340
  2. Foroud Nora A., Eudes François, Trichothecenes in Cereal Grains, 10.3390/ijms10010147
  3. Boyacioǧlu D., Hettiarachchy N.S., Changes in some biochemical components of wheat grain that was infected with Fusarium graminearum, 10.1016/s0733-5210(95)80008-5
  4. Rocha O., Ansari K., Doohan F. M., Effects of trichothecene mycotoxins on eukaryotic cells: A review, 10.1080/02652030500058403
  5. Brown Neil A., Urban Martin, van de Meene Allison M.L., Hammond-Kosack Kim E., The infection biology of Fusarium graminearum: Defining the pathways of spikelet to spikelet colonisation in wheat ears, 10.1016/j.funbio.2010.04.006
  6. Schroeder HW, Christensen JJ (1963) Factors affecting resistance of wheat to scab caused by Gibberella zeae. Phytopathology 53:831–838
  7. Waldron B. L., Moreno-Sevilla B., Anderson J. A., Stack R. W., Frohberg R. C., RFLP Mapping of QTL for Fusarium Head Blight Resistance in Wheat, 10.2135/cropsci1999.0011183x003900030032x
  8. Buerstmayr H., Lemmens M., Hartl L., Doldi L., Steiner B., Stierschneider M., Ruckenbauer P., Molecular mapping of QTLs for Fusarium head blight resistance in spring wheat. I. Resistance to fungal spread (Type II resistance), 10.1007/s001220200009
  9. Zhou Wenchun, Kolb Frederic L, Bai Guihua, Shaner Gregory, Domier Leslie L, Genetic analysis of scab resistance QTL in wheat with microsatellite and AFLP markers, 10.1139/g02-034
  10. Zhou M. P., Hayden M. J., Zhang Z. Y., Lu W. Z., Ma H. -X., Saturation and mapping of a majorFusarium head blight resistance QTL on chromosome 3BS of Sumai 3 wheat, 10.1007/bf03195706
  11. Liu Sixin, Zhang Xiuling, Pumphrey Michael O., Stack Robert W., Gill Bikram S., Anderson James A., Complex microcolinearity among wheat, rice, and barley revealed by fine mapping of the genomic region harboring a major QTL for resistance to Fusarium head blight in wheat, 10.1007/s10142-005-0007-y
  12. Cuthbert Patricia A., Somers Daryl J., Thomas Julian, Cloutier Sylvie, Brulé-Babel Anita, Fine mapping Fhb1, a major gene controlling fusarium head blight resistance in bread wheat (Triticum aestivum L.), 10.1007/s00122-006-0249-7
  13. Liu S, Pumphrey M, Gill B, Trick H, Zhang J, Dolezel J, Chalhoub B, Anderson J (2008) Toward positional cloning of Fhb1, a major QTL for Fusarium head blight resistance in wheat. In: 3rd International FHB symposium book, pp 195–201
  14. Pritsch Clara, Muehlbauer Gary J., Bushnell William R., Somers David A., Vance Carroll P., Fungal Development and Induction of Defense Response Genes During Early Infection of Wheat Spikes byFusarium graminearum, 10.1094/mpmi.2000.13.2.159
  15. Zhou Wenchun, Kolb Frederic L, Riechers Dean E, Identification of proteins induced or upregulated by Fusarium head blight infection in the spikes of hexaploid wheat (Triticum aestivum), 10.1139/g05-041
  16. Bernardo Amy, Bai Guihua, Guo Peiguo, Xiao Kai, Guenzi Arron C., Ayoubi Patricia, Fusarium graminearum-induced changes in gene expression between Fusarium head blight-resistant and susceptible wheat cultivars, 10.1007/s10142-006-0028-1
  17. Somers Daryl, Kong Lingrang, Ohm Herbert W., Anderson Joseph M., Expression analysis of defense-related genes in wheat in response to infection byFusarium graminearumContribution from Purdue University Agricultural Research Programs as journal article No. 2007-18090., 10.1139/g07-085
  18. Golkari Saber, Gilbert Jeannie, Prashar Suvira, Procunier J. Douglas, Microarray analysis of Fusarium graminearum-induced wheat genes: identification of organ-specific and differentially expressed genes, 10.1111/j.1467-7652.2006.00213.x
  19. Belzile Francois, Golkari Saber, Gilbert Jeannie, Ban Tomohiro, Procunier J. Douglas, QTL-specific microarray gene expression analysis of wheat resistance to Fusarium head blight in Sumai-3 and two susceptible NILs, 10.1139/g09-018
  20. Walter Stephanie, Brennan Josephine M., Arunachalam Chanemougasoundharam, Ansari Khairul I., Hu Xuejun, Khan Mojibur R., Trognitz Friederike, Trognitz Bodo, Leonard Gerald, Egan Damian, Doohan Fiona M., Components of the gene network associated with genotype-dependent response of wheat to the Fusarium mycotoxin deoxynivalenol, 10.1007/s10142-008-0089-4
  21. Jia Haiyan, Cho Seungho, Muehlbauer Gary J., Transcriptome Analysis of a Wheat Near-Isogenic Line Pair Carrying Fusarium Head Blight–Resistant and –Susceptible Alleles, 10.1094/mpmi-22-11-1366
  22. Steiner Barbara, Kurz Harald, Lemmens Marc, Buerstmayr Hermann, Differential gene expression of related wheat lines with contrasting levels of head blight resistance after Fusarium graminearum inoculation, 10.1007/s00122-008-0935-8
  23. Walter Stephanie, Nicholson Paul, Doohan Fiona M., Action and reaction of host and pathogen during Fusarium head blight disease, 10.1111/j.1469-8137.2009.03041.x
  24. Ansari Khairul I., Walter Stephanie, Brennan Josephine M., Lemmens Marc, Kessans Sarah, McGahern Angela, Egan Damian, Doohan Fiona M., Retrotransposon and gene activation in wheat in response to mycotoxigenic and non-mycotoxigenic-associated Fusarium stress, 10.1007/s00122-006-0490-0
  25. Schweiger Wolfgang, Boddu Jayanand, Shin Sanghyun, Poppenberger Brigitte, Berthiller Franz, Lemmens Marc, Muehlbauer Gary J., Adam Gerhard, Validation of a Candidate Deoxynivalenol-Inactivating UDP-Glucosyltransferase from Barley by Heterologous Expression in Yeast, 10.1094/mpmi-23-7-0977
  26. Gardiner Stephanie A., Boddu Jayanand, Berthiller Franz, Hametner Christian, Stupar Robert M., Adam Gerhard, Muehlbauer Gary J., Transcriptome Analysis of the Barley–Deoxynivalenol Interaction: Evidence for a Role of Glutathione in Deoxynivalenol Detoxification, 10.1094/mpmi-23-7-0962
  27. Anand A., Zhou T., Trick H. N., Gill B. S., Bockus W. W., Muthukrishnan S., Greenhouse and field testing of transgenic wheat plants stably expressing genes for thaumatin-like protein, chitinase and glucanase against Fusarium graminearum, 10.1093/jxb/erg110
  28. Shin S., Mackintosh C. A., Lewis J., Heinen S. J., Radmer L., Dill-Macky R., Baldridge G. D., Zeyen R. J., Muehlbauer G. J., Transgenic wheat expressing a barley class II chitinase gene has enhanced resistance against Fusarium graminearum, 10.1093/jxb/ern103
  29. Makandar Ragiba, Essig Juliane S., Schapaugh Melissa A., Trick Harold N., Shah Jyoti, Genetically Engineered Resistance to Fusarium Head Blight in Wheat by Expression ofArabidopsis NPR1, 10.1094/mpmi-19-0123
  30. Di Rong, Blechl Ann, Dill-Macky Ruth, Tortora Andrew, Tumer Nilgun E., Expression of a truncated form of yeast ribosomal protein L3 in transgenic wheat improves resistance to Fusarium head blight, 10.1016/j.plantsci.2010.02.003
  31. Li Zhao, Zhou Miaoping, Zhang Zengyan, Ren Lijuan, Du Lipu, Zhang Boqiao, Xu Huijun, Xin Zhiyong, Expression of a radish defensin in transgenic wheat confers increased resistance to Fusarium graminearum and Rhizoctonia cerealis, 10.1007/s10142-011-0211-x
  32. Wang Yun, Yang Liming, Xu Haibin, Li Qifu, Ma Zhengqiang, Chu Chenggen, Differential proteomic analysis of proteins in wheat spikes induced by Fusarium graminearum, 10.1002/pmic.200401317
  33. Dornez Emmie, Croes Evi, Gebruers Kurt, Carpentier Sebastien, Swennen Rony, Laukens Kris, Witters Erwin, Urban Martin, Delcour Jan A., Courtin Christophe M., 2-D DIGE reveals changes in wheat xylanase inhibitor protein families due to Fusarium graminearum ΔTri5 infection and grain development, 10.1002/pmic.200900493
  34. Geddes Jennifer, Eudes François, Laroche André, Selinger L. Brent, Differential expression of proteins in response to the interaction between the pathogenFusarium graminearum and its host,Hordeum vulgare, 10.1002/pmic.200700115
  35. MALLARD STÉPHANIE, NÈGRE SYLVIE, POUYA SHALA, GAUDET DENIS, LU ZHEN-XIANG, DEDRYVER FRANÇOISE, Adult plant resistance-related gene expression in ‘Camp Remy’ wheat inoculated with Puccinia striiformis, 10.1111/j.1364-3703.2007.00459.x
  36. Han F P, Fedak G, Ouellet T, Dan H, Somers D J, Mapping of genes expressed inFusarium graminearum-infected heads of wheat cultivar 'Frontana', 10.1139/g04-098
  37. Yu Xiumei, Wang Xiaojie, Wang Chenfang, Chen Xianming, Qu Zhipeng, Yu Xiudao, Han Qingmei, Zhao Jie, Guo Jun, Huang Lili, Kang Zhensheng, Wheat defense genes in fungal (Puccinia striiformis) infection, 10.1007/s10142-010-0161-8
  38. Zhang Hong, Hu Yingang, Wang Changyou, Ji Wanquan, Gene Expression in Wheat Induced by Inoculation with Puccinia striiformis West, 10.1007/s11105-010-0245-6
  39. Diatchenko L., Lau Y. F., Campbell A. P., Chenchik A., Moqadam F., Huang B., Lukyanov S., Lukyanov K., Gurskaya N., Sverdlov E. D., Siebert P. D., Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries., 10.1073/pnas.93.12.6025
  40. Duvick JP, Rood T, Rao AG, Marshak DR (1992) Purification and characterization of a novel antimicrobial peptide from maize (Zea mays L.) kernels. J Biol Chem 267:18814–18820
  41. Livak Kenneth J., Schmittgen Thomas D., Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method, 10.1006/meth.2001.1262
  42. Endo T. R., Gill B. S., The Deletion Stocks of Common Wheat, 10.1093/oxfordjournals.jhered.a023003
  43. Prasad M, Varshney RK, Roy JK, Balyan HS, Gupta PK (2000) The use of microsatellite for detecting DNA polymorphism genotype identification and genetic diversity in wheat. Theor Appl Genet 100:584–592
  44. Liu Bao, Segal Gregorio, Vega Juan Manuel, Feldman Moshe, Abbo Shahal, Isolation and characterization of chromosome-specific DNA sequences from a chromosome arm genomic library of common wheat, 10.1046/j.1365-313x.1997.11050959.x
  45. Somers Daryl, Bilgic Hatice, Cho Seungho, Garvin David F., Muehlbauer Gary J., Mapping barley genes to chromosome arms by transcript profiling of wheat–barley ditelosomic chromosome addition lines, 10.1139/g07-059
  46. Miftahudin, Analysis of Expressed Sequence Tag Loci on Wheat Chromosome Group 4, 10.1534/genetics.104.034827
  47. Paillard S., Schnurbusch T., Tiwari R., Messmer M., Winzeler M., Keller B., Schachermayr G., QTL analysis of resistance to Fusarium head blight in Swiss winter wheat (Triticum aestivum L.), 10.1007/s00122-004-1628-6
  48. Schmolke M., Zimmermann G., Buerstmayr H., Schweizer G., Miedaner T., Korzun V., Ebmeyer E., Hartl L., Molecular mapping of Fusarium head blight resistance in the winter wheat population Dream/Lynx, 10.1007/s00122-005-2060-2
  49. Häberle Jennifer, Schmolke Michael, Schweizer Günther, Korzun Viktor, Ebmeyer Erhard, Zimmermann Gerhard, Hartl Lorenz, Effects of Two Major Fusarium Head Blight Resistance QTL Verified in a Winter Wheat Backcross Population, 10.2135/cropsci2006.12.0800
  50. Klahr Anja, Zimmermann Gerhard, Wenzel Gerhard, Mohler Volker, Effects of environment, disease progress, plant height and heading date on the detection of QTLs for resistance to Fusarium head blight in an European winter wheat cross, 10.1007/s10681-006-9264-7
  51. Gervais L., Dedryver F., Morlais J.-Y., Bodusseau V., Negre S., Bilous M., Groos C., Trottet M., Mapping of quantitative trait loci for field resistance to Fusarium head blight in an European winter wheat, 10.1007/s00122-002-1160-5
  52. Draeger R., Gosman N., Steed A., Chandler E., Thomsett M., Srinivasachary, Schondelmaier J., Buerstmayr H., Lemmens M., Schmolke M., Mesterhazy A., Nicholson P., Identification of QTLs for resistance to Fusarium head blight, DON accumulation and associated traits in the winter wheat variety Arina, 10.1007/s00122-007-0592-3
  53. Semagn Kassa, Skinnes Helge, Bjørnstad Åsmund, Marøy Anne Guri, Tarkegne Yalew, Quantitative Trait Loci Controlling Fusarium Head Blight Resistance and Low Deoxynivalenol Content in Hexaploid Wheat Population from ‘Arina’ and NK93604, 10.2135/cropsci2006.02.0095
  54. Gilsinger J., Kong L., Shen X., Ohm H., DNA markers associated with low Fusarium head blight incidence and narrow flower opening in wheat, 10.1007/s00122-005-1953-4
  55. Dangl Jeffery L., Jones Jonathan D. G., Plant pathogens and integrated defence responses to infection, 10.1038/35081161
  56. Dilbirligi Muharrem, Gill Kulvinder S., Identification and analysis of expressed resistance gene sequences in wheat, 10.1023/b:plan.0000023663.55701.5f
  57. Chang Ing-Feng, Curran Amy, Woolsey Rebekah, Quilici David, Cushman John C., Mittler Ron, Harmon Alice, Harper Jeffrey F., Proteomic profiling of tandem affinity purified 14-3-3 protein complexes inArabidopsis thaliana, 10.1002/pmic.200800445
  58. Roberts Michael R., Salinas Julio, Collinge David B., 10.1023/a:1021261614491
  59. Sun G, Xie F, Zhang B (2011) Transcriptome-wide identification and stress properties of the 14-3-3 gene family in cotton (Gossypium hirsutum L.). Funct Integr Genomics. doi: 10.1007/s10142-011-0242-3
  60. Brandt J, Thordal-Christensen H, Vad K, Gregersen PL, Collinge DB (1992) A pathogen-induced gene of barley encodes a protein showing high similarity to a protein kinase regulator. Plant J 2:815–820
  61. Li W. L., Liu D. J., Chen P. D., Gill B. S., Faris J. D., Candidate gene analysis of quantitative disease resistance in wheat, 10.1007/s001220051061
  62. Oh Chang-Sik, Martin Gregory B., Tomato 14-3-3 Protein TFT7 Interacts with a MAP Kinase Kinase to Regulate Immunity-associated Programmed Cell Death Mediated by Diverse Disease Resistance Proteins, 10.1074/jbc.m111.225086
  63. Campo Sonia, Peris-Peris Cristina, Montesinos Laura, Peñas Gisela, Messeguer Joaquima, San Segundo Blanca, Expression of the maize ZmGF14-6 gene in rice confers tolerance to drought stress while enhancing susceptibility to pathogen infection, 10.1093/jxb/err328
  64. Li Legong, He Zengyong, Pandey Girdhar K., Tsuchiya Tomofusa, Luan Sheng, Functional Cloning and Characterization of a Plant Efflux Carrier for Multidrug and Heavy Metal Detoxification, 10.1074/jbc.m108777200
  65. Morita M., Shitan N., Sawada K., Van Montagu M. C. E., Inze D., Rischer H., Goossens A., Oksman-Caldentey K.-M., Moriyama Y., Yazaki K., Vacuolar transport of nicotine is mediated by a multidrug and toxic compound extrusion (MATE) transporter in Nicotiana tabacum, 10.1073/pnas.0812512106
  66. Marinova Krasimira, Pourcel Lucille, Weder Barbara, Schwarz Michael, Barron Denis, Routaboul Jean-Marc, Debeaujon Isabelle, Klein Markus, The Arabidopsis MATE Transporter TT12 Acts as a Vacuolar Flavonoid/H + -Antiporter Active in Proanthocyanidin-Accumulating Cells of the Seed Coat , 10.1105/tpc.106.046029
  67. Maron Lyza G., Piñeros Miguel A., Guimarães Claudia T., Magalhaes Jurandir V., Pleiman Jennifer K., Mao Chuanzao, Shaff Jon, Belicuas Silvia N.J., Kochian Leon V., Two functionally distinct members of the MATE (multi-drug and toxic compound extrusion) family of transporters potentially underlie two major aluminum tolerance QTLs in maize, 10.1111/j.1365-313x.2009.04103.x
  68. Savitch Leonid V., Subramaniam Rajagopal, Allard Ghislaine C., Singh Jas, The GLK1 ‘regulon’ encodes disease defense related proteins and confers resistance to Fusarium graminearum in Arabidopsis, 10.1016/j.bbrc.2007.05.084
  69. Nawrath C., EDS5, an Essential Component of Salicylic Acid-Dependent Signaling for Disease Resistance in Arabidopsis, Is a Member of the MATE Transporter Family, 10.1105/tpc.010376
  70. Dixon Richard A., Achnine Lahoucine, Kota Parvathi, Liu Chang-Jun, Reddy M. S. Srinivasa, Wang Liangjiang, The phenylpropanoid pathway and plant defence-a genomics perspective, 10.1046/j.1364-3703.2002.00131.x
  71. Paranidharan V., Abu-Nada Y., Hamzehzarghani H., Kushalappa A. C., Mamer O., Dion Y., Rioux S., Comeau A., Choiniere L., Resistance-related metabolites in wheat againstFusarium graminearumand the virulence factor deoxynivalenol (DON), 10.1139/b08-052
  72. Bi Caili, Chen Fang, Jackson Lisa, Gill Bikram S., Li Wanlong, Expression of Lignin Biosynthetic Genes in Wheat during Development and upon Infection by Fungal Pathogens, 10.1007/s11105-010-0219-8
  73. Shah Jyoti, Lipids, Lipases, and Lipid-Modifying Enzymes in Plant Disease Resistance, 10.1146/annurev.phyto.43.040204.135951
  74. Falk A., Feys B. J., Frost L. N., Jones J. D. G., Daniels M. J., Parker J. E., EDS1, an essential component of R gene-mediated disease resistance in Arabidopsis has homology to eukaryotic lipases, 10.1073/pnas.96.6.3292
  75. Jirage D., Tootle T. L., Reuber T. L., Frost L. N., Feys B. J., Parker J. E., Ausubel F. M., Glazebrook J., Arabidopsis thaliana PAD4 encodes a lipase-like gene that is important for salicylic acid signaling, 10.1073/pnas.96.23.13583
  76. Lu Zhen-Xiang, Gaudet Denis A., Frick Michele, Puchalski Byron, Genswein Bernie, Laroche Andre, Identification and Characterization of Genes Differentially Expressed in the Resistance Reaction in Wheat Infected with Tilletia tritici, the Common Bunt Pathogen, 10.5483/bmbrep.2005.38.4.420
  77. Oh I. S., Secretome Analysis Reveals an Arabidopsis Lipase Involved in Defense against Alternaria brassicicola, 10.1105/tpc.105.034819
  78. Lee Dong Sook, Kim Bo Kyung, Kwon Sun Jae, Jin Hak Chul, Park Ohkmae K., Arabidopsis GDSL lipase 2 plays a role in pathogen defense via negative regulation of auxin signaling, 10.1016/j.bbrc.2009.01.006
  79. Mizutani Masaharu, Ohta Daisaku, Diversification of P450 Genes During Land Plant Evolution, 10.1146/annurev-arplant-042809-112305
  80. Kong Lingrang, Anderson Joseph M, Ohm Herbert W, Induction of wheat defense and stress-related genes in response toFusarium graminearum, 10.1139/g04-097
  81. Cantu Dario, Vanzetti Leonardo S, Sumner Adam, Dubcovsky Martin, Matvienko Marta, Distelfeld Assaf, Michelmore Richard W, Dubcovsky Jorge, Small RNAs, DNA methylation and transposable elements in wheat, 10.1186/1471-2164-11-408
  82. Kashkush Khalil, Feldman Moshe, Levy Avraham A., Transcriptional activation of retrotransposons alters the expression of adjacent genes in wheat, 10.1038/ng1063
  83. Ivashuta Sergey, Naumkina Marina, Gau Mitsuru, Uchiyama Kazuhiro, Isobe Sachiko, Mizukami Yuko, Shimamoto Yoshiya, Genotype-dependent transcriptional activation of novel repetitive elements during cold acclimation of alfalfa (Medicago sativa), 10.1046/j.1365-313x.2002.01383.x
  84. Berger Shelley L., The complex language of chromatin regulation during transcription, 10.1038/nature05915
  85. Ha M., Ng D. W.-K., Li W.-H., Chen Z. J., Coordinated histone modifications are associated with gene expression variation within and between species, 10.1101/gr.116467.110
  86. Coemans B, Takahashi Y, Berberich T, Ito A, Kanzaki H, Matsumura H, Saitoh H, Tsuda S, Kamoun S, Sagi L, Swennen R, Terauchi R (2008) High-throughput in planta expression screening identifies an ADP-ribosylation factor (ARF1) involved in non-host resistance and R gene-mediated resistance. Mol Plant Pathol 9:25–36
  87. Bhuiyan Nazmul H., Liu Weiping, Liu Guosheng, Selvaraj Gopalan, Wei Yangdou, King John, Transcriptional regulation of genes involved in the pathways of biosynthesis and supply of methyl units in response to powdery mildew attack and abiotic stresses in wheat, 10.1007/s11103-007-9155-x
  88. Sun Jin-Yue, Gaudet Denis A., Lu Zhen-Xiang, Frick Michele, Puchalski Byron, Laroche André, Characterization and Antifungal Properties of Wheat Nonspecific Lipid Transfer Proteins, 10.1094/mpmi-21-3-0346
  89. Buerstmayr H., Ban T., Anderson J. A., QTL mapping and marker-assisted selection forFusariumhead blight resistance in wheat: a review, 10.1111/j.1439-0523.2008.01550.x
  90. Liu Shuyu, Hall Marla D., Griffey Carl A., McKendry Anne L., Meta-Analysis of QTL Associated with Fusarium Head Blight Resistance in Wheat, 10.2135/cropsci2009.03.0115
  91. Zwart Rebecca S., Muylle Hilde, Van Bockstaele Erik, Roldán-Ruiz Isabel, Evaluation of genetic diversity of Fusarium head blight resistance in European winter wheat, 10.1007/s00122-008-0822-3
Bibliographic reference Muhovski, Yordan ; Batoko, Henri ; Jacquemin, Jean-Marie. Identification, characterization and mapping of differentially expressed genes in a winter wheat cultivar (Centenaire) resistant to Fusarium graminearum infection.. In: Molecular Biology Reports : an international journal on molecular and cellular biology, Vol. 39, no.10, p. 9583-600 (2012)
Permanent URL http://hdl.handle.net/2078.1/124605