User menu

Identification and differential induction of ABCG transporter genes in wheat cultivars challenged by a deoxynivalenol-producing Fusarium graminearum strain.

Bibliographic reference Muhovski, Yordan ; Jacquemin, Jean-Marie ; Batoko, Henri. Identification and differential induction of ABCG transporter genes in wheat cultivars challenged by a deoxynivalenol-producing Fusarium graminearum strain.. In: Molecular Biology Reports : an international journal on molecular and cellular biology, Vol. 41, no.9, p. 6181-6194 (2014)
Permanent URL
  1. KAZAN KEMAL, GARDINER DONALD M., MANNERS JOHN M., On the trail of a cereal killer: recent advances in Fusarium graminearum pathogenomics and host resistance : Recent advances in Fusarium-cereal interactions, 10.1111/j.1364-3703.2011.00762.x
  2. Bai Guihua, Shaner Gregory, MANAGEMENT AND RESISTANCE IN WHEAT AND BARLEY TO FUSARIUM HEAD BLIGHT, 10.1146/annurev.phyto.42.040803.140340
  3. Foroud Nora A., Eudes François, Trichothecenes in Cereal Grains, 10.3390/ijms10010147
  4. 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
  5. Jansen C., von Wettstein D., Schafer W., Kogel K.-H., Felk A., Maier F. J., Infection patterns in barley and wheat spikes inoculated with wild-type and trichodiene synthase gene disrupted Fusarium graminearum, 10.1073/pnas.0508467102
  6. Rocha O., Ansari K., Doohan F. M., Effects of trichothecene mycotoxins on eukaryotic cells: A review, 10.1080/02652030500058403
  7. Masuda D., Ishida M., Yamaguchi K., Yamaguchi I., Kimura M., Nishiuchi T., Phytotoxic effects of trichothecenes on the growth and morphology of Arabidopsis thaliana, 10.1093/jxb/erl298
  8. DESMOND OLIVIA J., MANNERS JOHN M., STEPHENS AMBER E., MACLEAN DONALD J., SCHENK PEER M., GARDINER DONALD M., MUNN ALAN L., KAZAN KEMAL, TheFusariummycotoxin deoxynivalenol elicits hydrogen peroxide production, programmed cell death and defence responses in wheat, 10.1111/j.1364-3703.2008.00475.x
  9. Li Guangle, Yen Yang, Jasmonate and Ethylene Signaling Pathway May Mediate Fusarium Head Blight Resistance in Wheat, 10.2135/cropsci2008.02.0097
  10. 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
  11. 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
  12. 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
  13. Schroeder HW, Christensen JJ (1963) Factors affecting resistance of wheat to scab caused by Gibberella zeae. Phytopathology 53:831–838
  14. Mesterhazy A., Types and components of resistance to Fusarium head blight of wheat, 10.1111/j.1439-0523.1995.tb00816.x
  15. Arumuganathan K., Earle E. D., Nuclear DNA content of some important plant species, 10.1007/bf02672069
  16. Kruger Warren M., Pritsch Clara, Chao Shiaoman, Muehlbauer Gary J., Functional and Comparative Bioinformatic Analysis of Expressed Genes from Wheat Spikes Infected withFusarium graminearum, 10.1094/mpmi.2002.15.5.445
  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. 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
  19. 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
  20. 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
  21. Lulin Ma, Yi Shang, Aizhong Cao, Zengjun Qi, Liping Xing, Peidu Chen, Dajun Liu, Xiu-e Wang, Molecular cloning and characterization of an up-regulated UDP-glucosyltransferase gene induced by DON from Triticum aestivum L. cv. Wangshuibai, 10.1007/s11033-009-9606-3
  22. Lucyshyn Doris, Busch Bernhard L., Abolmaali Shamsozoha, Steiner Barbara, Chandler Elizabeth, Sanjarian Forough, Mousavi Amir, Nicholson Paul, Buerstmayr Hermann, Adam Gerhard, Cloning and characterization of the ribosomal protein L3 (RPL3) gene family from Triticum aestivum, 10.1007/s00438-006-0201-1
  23. 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
  24. Balzi E, Wang M, Leterme S, Van Dyck L, Goffeau A (1994) PDR5, a novel yeast multidrug resistance conferring transporter controlled by the transcriptional regulator PDR1. J Biol Chem 269:2206–2214
  25. Muhitch Michael J, McCormick Susan P, Alexander Nancy J, Hohn Thomas M, Transgenic expression of the TRI101 or PDR5 gene increases resistance of tobacco to the phytotoxic effects of the trichothecene 4,15-diacetoxyscirpenol, 10.1016/s0168-9452(00)00282-x
  26. Mitterbauer Rudolf, Adam Gerhard, 10.1023/a:1020666627267
  27. Rea Philip A., Plant ATP-Binding Cassette Transporters, 10.1146/annurev.arplant.57.032905.105406
  28. Jasinski Michal, Banasiak Joanna, Radom Marcin, Kalitkiewicz Anna, Figlerowicz Marek, Full-Size ABC Transporters from the ABCG Subfamily inMedicago truncatula, 10.1094/mpmi-22-8-0921
  29. Verrier Paul J., Bird David, Burla Bo, Dassa Elie, Forestier Cyrille, Geisler Markus, Klein Markus, Kolukisaoglu Üner, Lee Youngsook, Martinoia Enrico, Murphy Angus, Rea Philip A., Samuels Lacey, Schulz Burkhard, Spalding Edgar P., Yazaki Kazufumi, Theodoulou Frederica L., Plant ABC proteins – a unified nomenclature and updated inventory, 10.1016/j.tplants.2008.02.001
  30. Crouzet Jérôme, Trombik Tomasz, Fraysse Å. Staffan, Boutry Marc, Organization and function of the plant pleiotropic drug resistance ABC transporter family, 10.1016/j.febslet.2005.12.043
  31. Lamping Erwin, Baret Philippe V., Holmes Ann R., Monk Brian C., Goffeau Andre, Cannon Richard D., Fungal PDR transporters: Phylogeny, topology, motifs and function, 10.1016/j.fgb.2009.10.007
  32. Moons Ann, Transcriptional profiling of the PDR gene family in rice roots in response to plant growth regulators, redox perturbations and weak organic acid stresses, 10.1007/s00425-008-0810-5
  33. Ruocco Michelina, Ambrosino Patrizia, Lanzuise Stefania, Woo Sheridan Lois, Lorito Matteo, Scala Felice, Four potato (Solanum tuberosum) ABCG transporters and their expression in response to abiotic factors and Phytophthora infestans infection, 10.1016/j.jplph.2011.07.008
  34. Migocka M., Papierniak A., Warzybok A., Kłobus G., CsPDR8 and CsPDR12, two of the 16 pleiotropic drug resistance genes in cucumber, are transcriptionally regulated by phytohormones and auxin herbicide in roots, 10.1007/s10725-012-9674-6
  35. Zhang Ling, Lu Xu, Shen Qian, Chen Yunfei, Wang Tao, Zhang Fangyuan, Wu Shaoyan, Jiang Weimin, Liu Pin, Zhang Lida, Wang Yueyue, Tang Kexuan, Identification of Putative Artemisia annua ABCG Transporter Unigenes Related to Artemisinin Yield Following Expression Analysis in Different Plant Tissues and in Response to Methyl Jasmonate and Abscisic Acid Treatments, 10.1007/s11105-011-0400-8
  36. Stukkens Y., NpPDR1, a Pleiotropic Drug Resistance-Type ATP-Binding Cassette Transporter from Nicotiana plumbaginifolia, Plays a Major Role in Plant Pathogen Defense, 10.1104/pp.105.062372
  37. BULTREYS ALAIN, TROMBIK TOMASZ, DROZAK ANNA, BOUTRY MARC, Nicotiana plumbaginifoliaplants silenced for the ATP-binding cassette transporter geneNpPDR1show increased susceptibility to a group of fungal and oomycete pathogens, 10.1111/j.1364-3703.2009.00562.x
  38. Jasinski M., A Plant Plasma Membrane ATP Binding Cassette-Type Transporter Is Involved in Antifungal Terpenoid Secretion, 10.1105/tpc.13.5.1095
  39. Sasabe Michiko, Toyoda Kazuhiro, Shiraishi Tomonori, Inagaki Yoshishige, Ichinose Yuki, cDNA cloning and characterization of tobacco ABC transporter:NtPDR1is a novel elicitor-responsive gene1, 10.1016/s0014-5793(02)02697-2
  40. Campbell E. J., Pathogen-Responsive Expression of a Putative ATP-Binding Cassette Transporter Gene Conferring Resistance to the Diterpenoid Sclareol Is Regulated by Multiple Defense Signaling Pathways in Arabidopsis, 10.1104/pp.103.024182
  41. Eichhorn H., Isolation of a novel ABC-transporter gene from soybean induced by salicylic acid, 10.1093/jxb/erj179
  42. Stein M., Arabidopsis PEN3/PDR8, an ATP Binding Cassette Transporter, Contributes to Nonhost Resistance to Inappropriate Pathogens That Enter by Direct Penetration, 10.1105/tpc.105.038372
  43. KANG Z, BUCHENAUER H, Immunocytochemical localization of fusarium toxins in infected wheat spikes by Fusarium culmorum, 10.1006/pmpp.1999.0233
  44. Smart Cheryl C., Fleming Andrew J., Hormonal and Environmental Regulation of a Plant PDR5-like ABC Transporter, 10.1074/jbc.271.32.19351
  45. Ducos Eric, Fraysse Å Staffan, Boutry Marc, NtPDR3, an iron-deficiency inducible ABC transporter inNicotiana tabacum, 10.1016/j.febslet.2005.11.014
  46. Lee M., AtPDR12 Contributes to Lead Resistance in Arabidopsis, 10.1104/pp.104.058107
  47. Kim Do-Young, Bovet Lucien, Maeshima Masayoshi, Martinoia Enrico, Lee Youngsook, The ABC transporter AtPDR8 is a cadmium extrusion pump conferring heavy metal resistance : Role of AtPDR8 in cadmium resistance, 10.1111/j.1365-313x.2007.03044.x
  48. Krattinger S. G., Lagudah E. S., Spielmeyer W., Singh R. P., Huerta-Espino J., McFadden H., Bossolini E., Selter L. L., Keller B., A Putative ABC Transporter Confers Durable Resistance to Multiple Fungal Pathogens in Wheat, 10.1126/science.1166453
  49. Shang Yi, Xiao Jin, Ma LuLin, Wang HaiYan, Qi ZengJun, Chen PeiDu, Liu DaJun, Wang XiuE, Characterization of a PDR type ABC transporter gene from wheat (Triticum aestivum L.), 10.1007/s11434-009-0553-0
  50. Chen G., Komatsuda T., Ma J. F., Nawrath C., Pourkheirandish M., Tagiri A., Hu Y.-G., Sameri M., Li X., Zhao X., Liu Y., Li C., Ma X., Wang A., Nair S., Wang N., Miyao A., Sakuma S., Yamaji N., Zheng X., Nevo E., An ATP-binding cassette subfamily G full transporter is essential for the retention of leaf water in both wild barley and rice, 10.1073/pnas.1108444108
  51. 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
  52. 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
  53. 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
  54. Sambrook J, Russell DW (2001) Molecular cloning: a laboratory manual, 3rd edn. New Age International Pvt Ltd, New Delhi
  55. Tamura K., Peterson D., Peterson N., Stecher G., Nei M., Kumar S., MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods, 10.1093/molbev/msr121
  56. 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
  57. Kang Joohyun, Park Jiyoung, Choi Hyunju, Burla Bo, Kretzschmar Tobias, Lee Youngsook, Martinoia Enrico, Plant ABC Transporters, 10.1199/tab.0153
  58. Boutigny Anne-Laure, Richard-Forget Florence, Barreau Christian, Natural mechanisms for cereal resistance to the accumulation of Fusarium trichothecenes, 10.1007/s10658-007-9266-x
  59. Poppenberger Brigitte, Berthiller Franz, Lucyshyn Doris, Sieberer Tobias, Schuhmacher Rainer, Krska Rudolf, Kuchler Karl, Glössl Josef, Luschnig Christian, Adam Gerhard, Detoxification of theFusariumMycotoxin Deoxynivalenol by a UDP-glucosyltransferase fromArabidopsis thaliana, 10.1074/jbc.m307552200
  60. Moons Ann, Ospdr9, which encodes a PDR-type ABC transporter, is induced by heavy metals, hypoxic stress and redox perturbations in rice roots1, 10.1016/s0014-5793(03)01060-3
  61. van den Brûle Sybille, Smart Cheryl, The plant PDR family of ABC transporters, 10.1007/s00425-002-0889-z
  62. Bienert Manuela D., Siegmund Stephanie E. G., Drozak Anna, Trombik Tomasz, Bultreys Alain, Baldwin Ian T., Boutry Marc, A pleiotropic drug resistance transporter inNicotiana tabacumis involved in defense against the herbivoreManduca sexta : ABCG5/PDR5 is involved in herbivore resistance, 10.1111/j.1365-313x.2012.05108.x
  63. 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
  64. 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