作物学报 ›› 2016, Vol. 42 ›› Issue (08): 1122-1133.doi: 10.3724/SP.J.1006.2016.01122
刘永杰,马传禹,马雪娜,徐明良*
LIU Yong-Jie,MA Chuan-Yu,MA Xue-Na,XU Ming-Liang*
摘要:
赤霉菌茎腐病是由禾谷镰刀菌(Fusarium graminearum,有性态,Gibberella zeae)引起的一类土传性病害,严重危害玉米的产量和品质。本研究依据玉米第10和第1染色体上的2个抗茎腐病QTL,qRfg1和qRfg2,培育近等基因系NIL-R (2个QTL位点均为抗病等位基因)和NIL-S (2个QTL均为感病等位基因)。在成株期和幼苗期接种禾谷镰刀菌,两近等基因系的抗性差异均显著。用2个近等基因系的幼根接种禾谷镰刀菌,进行转录组分析研究。结果表明,与NIL-S相比,NIL-R在接种禾谷镰刀菌后,乙烯(ethylene,ET)合成、信号途径基因,病程相关蛋白、脱氧雪腐镰刀菌烯醇毒素(deoxynivalenol,DON)解毒基因等呈现特异上调表达。与NIL-S相比,有1170个基因在NIL-R对照组中表达量较高,其中水杨酸(salicylic acid,SA)、茉莉酸(jasmonic acid,JA)和乙烯合成和信号介导途径以及苯丙烷合成途径中的基因显著富集;接种禾谷镰刀菌6 h或18 h后,病程相关蛋白、激素JA和ET合成基因、DON解毒基因在NIL-R中表达量较高。
[1] Yang Q, Yin G M, Guo Y L, Zhang D F, Chen S J, Xu M L. A major QTL for resistance to Gibberella stalk rot in maize. Theor Appl Genet, 2010, 121: 673–687
[2] Ali M L, Taylor J H, Jie L, Sun G L, William M, Kasha K J, Reid L M, Pauls K P. Molecular mapping of QTLs for resistance to Gibberella ear rot, in corn, caused by Fusarium graminearum. Genome, 2005, 48: 521–533 [3] Schweiger W, Steiner B, Ametz C, Siegwart G, Wiesenberger G, Berthiller F, Lemmens M, Jia H Y, Adam G, Muehlbauer G J. Transcriptomic characterization of two major Fusarium resistance quantitative trait loci (QTLs), Fhb1 and Qfhs. Ifa-5A, identifies novel candidate genes. Mol Plant Pathol, 2013, 14: 772–785 [4] Boddu J, Cho S, Kruger W M, Muehlbauer G J. Transcriptome analysis of the barley-Fusarium graminearum interaction. Mol Plant-Microbe Interact, 2006, 19: 407–417 [5] Goswami R S, Kistler H C. Pathogenicity and in planta mycotoxin accumulation among members of the Fusarium graminearum species complex on wheat and rice. Phytopathology, 2005, 95: 1397–1404 [6] Urban M, Daniels S, Mott E, Hammond-Kosack K. Arabidopsis is susceptible to the cereal ear blight fungal pathogens Fusarium graminearum and Fusarium culmorum. Plant J, 2002, 32: 961–973 [7] McMullen M, Jones R, Gallenberg D. Scab of wheat and barley: a re-emerging disease of devastating impact. Plant Dis, 1997, 81: 1340–1348 [8] Rocha O, Ansari K, Doohan F M. Effects of trichothecene mycotoxins on eukaryotic cells: a review. Food Addit Contam, 2005, 22: 369–378 [9] Pestka J J, Zhou H R, Moon Y, Chung Y J. Cellular and molecular mechanisms for immune modulation by deoxynivalenol and other trichothecenes: unraveling a paradox. Toxicol Lett, 2004, 153: 61–73 [10] Pestka J J. Deoxynivalenol-induced proinflammatory gene expression: Mechanisms and pathological sequelae. Toxins, 2010, 2: 1300–1317 [11] Miller J D, Ewen M A. Toxic effects of deoxynivalenol on ribosomes and tissues of the spring wheat cultivars Frontana and Casavant. Nat Toxins, 1997, 5: 234–237 [12] Desjardins A E, Proctor R H, Bai G H, McCormick S P, Shaner G, Buechley G, Hohn T M. Reduced virulence of trichothecene-nonproducing mutants of Gibberella zeae in wheat field tests. Mol Plant-Microbe Interact, 1996, 9: 775–781 [13] Langevin F, Eudes F, Comeau A. Effect of trichothecenes produced by Fusarium graminearum during Fusarium head blight development in six cereal species. Eur J Plant Pathol, 2004, 110: 735–746 [14] Harris L, Desjardins A E, Plattner R, Nicholson P, Butler G, Young J, Weston G, Proctor R, Hohn T. Possible role of trichothecene mycotoxins in virulence of Fusarium graminearum on maize. Plant Dis, 1999, 83: 954–960 [15] Desmond O J, Manners J M, Stephens A E, Maclean D J, Schenk P M, Gardiner D M, Munn A M, Kazan K. The Fusarium mycotoxin deoxynivalenol elicits hydrogen peroxide production, programmed cell death and defence responses in wheat. Mol Plant Pathol, 2008, 9: 435–445 [16] Jia H Y, Cho S, Muehlbauer G J. Transcriptome analysis of a wheat near-isogenic line pair carrying Fusarium head blight-resistant and-susceptible alleles. Mol Plant-Microbe Interact, 2009, 22: 1366–1378 [17] Poppenberger B, Berthiller F, Lucyshyn D, Sieberer T, Schuhmacher R, Krska R, Kuchler K, Glossl J, Luschnig C, Adam G. Detoxification of the Fusarium mycotoxin deoxynivalenol by a UDP-glucosyltransferase from Arabidopsis thaliana. J Biol Chem, 2003, 278: 47905–47914 [18] Muhitch M J, McCormick S P, Alexander N J, Hohn T M. Transgenic expression of the TRI101 or PDR5 gene increases resistance of tobacco to the phytotoxic effects of the trichothecene 4,15-diacetoxyscirpenol. Plant Sci, 2000, 157: 201–207 [19] Boddu J, Cho S, Muehlbauer G J. Transcriptome analysis of trichothecene-induced gene expression in barley. Mol Plant-Microbe Interact, 2007, 20: 1364–1375 [20] Gardiner S A, Boddu J, Berthiller F, Hametner C, Stupar R M, Adam G, Muehlbauer G J. Transcriptome analysis of the barley-deoxynivalenol interaction: evidence for a role of glutathione in deoxynivalenol detoxification. Mol Plant-Microbe Interact, 2010, 23: 962–976 [21] Schweiger W, Boddu J, Shin S, Poppenberger B, Berthiller F, Lemmens M, Muehlbauer G J, Adam G. Validation of a candidate deoxynivalenol-inactivating UDP-glucosyltransferase from barley by heterologous expression in yeast. Mol Plant-Microbe Interact, 2010, 23: 977–986 [22] Kruger W M, Pritsch C, Chao S, Muehlbauer G J. Functional and comparative bioinformatic analysis of expressed genes from wheat spikes infected with Fusarium graminearum. Mol Plant-Microbe Interact, 2002, 15: 445–455 [23] Zhu Q H, Stephen S, Kazan K, Jin G, Fan L, Taylor J, Dennis E S, Helliwell C A, Wang M B. Characterization of the defense transcriptome responsive to Fusarium oxysporum-infection in Arabidopsis using RNA-seq. Gene, 2013, 512: 259–266 [24] Lanubile A, Ferrarini A, Maschietto V, Delledonne M, Marocco A, Bellin D. Functional genomic analysis of constitutive and inducible defense responses to Fusarium verticillioides infection in maize genotypes with contrasting ear rot resistance. BMC Genomics, 2014, 15: 710 [25] Buerstmayr H, Steiner B, Lemmens M, Ruckenbauer P. Resistance to Fusarium head blight in winter wheat: heritability and trait associations. Crop Sci, 2000, 40: 1012–1018 [26] Trapnell C, Roberts A, Goff L, Pertea G, Kim D, Kelley D R, Pimentel H, Salzberg S L, Rinn J L, Pachter L. Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks. Nat Protocols, 2012, 7: 562–578 [27] Anders S, Huber W. Differential expression analysis for sequence count data. Genome Biol, 2010, 11: R106 [28] Conesa A, Götz S, García-Gómez JM, Terol J, Talón M, Robles M. Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics, 2005, 21: 3674–3676 [29] Ashburner M, Ball C A, Blake J A, Botstein D, Butler H, Cherry J M, Davis A P, Dolinski K, Dwight S S, Eppig J T. Gene Ontology: tool for the unification of biology. Nat Genet, 2000, 25: 25–29 [30] Gimenez-Ibanez S, Solano R. Nuclear jasmonate and salicylate signaling and crosstalk in defense against pathogens. Front Plant Sci, 2013, 4: 7 [31] Xiao J, Jin X H, Jia X P, Wang H Y, Cao A Z, Zhao W P, Pei H Y, Xue Z K, He L Q, Chen Q G, Wang X. Transcriptome-based discovery of pathways and genes related to resistance against Fusarium head blight in wheat landrace Wangshuibai. BMC Genomics, 2013, 14: 197 [32] Li G L, Yen Y. Jasmonate and ethylene signaling pathway may mediate Fusarium head blight resistance in wheat. Crop Sci, 2008, 48: 1888–1896 [33] Ding L N, Xu H B, Yi H Y, Yang L M, Kong Z X, Zhang L X, Xue S L, Jia H Y, Ma Z Q. Resistance to hemi-biotrophic F. graminearum infection is associated with coordinated and ordered expression of diverse defense signaling pathways. PloS One, 2011, 6: e19008 [34] Steiner B, Kurz H, Lemmens M, Buerstmayr H. Differential gene expression of related wheat lines with contrasting levels of head blight resistance after Fusarium graminearum inoculation. Theor Appl Genet, 2009, 118: 753–764 [35] Ye J R, Guo Y L, Zhang D F, Zhang N, Wang C, Xu M L. Cytological and molecular characterization of quantitative trait locus qRfg1, which confers resistance to Gibberella stalk rot in maize. Mol Plant-Microbe Interact, 2013, 26: 1417–1428 [36] Hamzehzarghani H, Kushalappa A C, Dion Y, Rioux S, Comeau A, Yaylayan V, Marshall W D, Mather D E. Metabolic profiling and factor analysis to discriminate quantitative resistance in wheat cultivars against Fusarium head blight. Physiol Mol Plant Pathol, 2005, 66: 119–133 [37] Chinchilla D, Zipfel C, Robatzek S, Kemmerling B, Nürnberger T, Jones J D, Felix G, Boller T. A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence. Nature, 2007, 448: 497–500 |
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