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Transcriptome of Erysiphe necator-infected Vitispseudoreticulata leaves provides insight into grapevineresistance to powdery mildew 被引量:3

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摘要 Powdery mildew(PM),which is caused by the pathogen Erysiphe necator(Schw.)Burr.,is the single most damaging disease of cultivated grapes(Vitis vinifera)worldwide.However,little is known about the transcriptional response of grapes to infection with PM.RNA-seq analysis was used for deep sequencing of the leaf transcriptome to study PM resistance in Chinese wild grapes(V.pseudoreticulata Baihe 35-1)to better understand the interaction between host and pathogen.Greater than 100 million(M)90-nt cDNA reads were sequenced from a cDNA library derived from PM-infected leaves.Among the sequences obtained,6541 genes were differentially expressed(DEG)and were annotated with Gene Ontology terms and by pathway enrichment.The significant categories that were identified included the following:defense,salicylic acid(SA)and jasmonic acid(JA)responses;systemic acquired resistance(SAR);hypersensitive response;plant–pathogen interaction;flavonoid biosynthesis;and plant hormone signal transduction.Various putative secretory proteins were identified,indicating potential defense responses to PMinfection.In all,318 putative R-genes and 183 putative secreted proteins were identified,including the defense-related R-genes BAK1,MRH1 and MLO3 and the defense-related secreted proteins GLP and PR5.The expression patterns of 16 genes were further illuminated by RT-qPCR.The present study identified several candidate genes and pathways that may contribute to PM resistance in grapes and illustrated that RNA-seq is a powerful tool for studying gene expression.The RT-qPCR results reveal that effective resistance responses of grapes to PM include enhancement of JA and SAR responses and accumulation of phytoalexins.
出处 《Horticulture Research》 SCIE 2014年第1期86-97,共12页 园艺研究(英文)
基金 This research was supported by the‘948’Program,Ministry of Agriculture,China(Grant No.2011-G21),by the Program for Young Talents in Northwest A&F University(NCET-10-0692,QN2011052) by a grant from the Program for Innovative Research Team of Grape Germplasm Resource and Breeding(2013KCT-25)to Yan Xu。
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  • 1孙马,王跃进.中国野生葡萄染色体倍性研究[J].西北农业学报,2006,15(6):148-152. 被引量:21
  • 2王跃进,贺普超.中国葡萄属野生种叶片抗白粉病遗传研究[J].中国农业科学,1997,30(1):19-25. 被引量:41
  • 3Bradford M.M.,1976,A dye binding assay for protein,Anal.Biochem,72:248-254.
  • 4Cheung M.Y.,Zeng N.Y.,Suk-Wah T,Li W.Y.,Zhang Q.,Samuel S.M.,and Lam H.M.,2007,Expression of a RING-HC protein from rice improves resistance to Pseudomonas syringae pv.tomato DC3000 in transgenic Arabidopsis thaliana,Journal of Experimental Botany,58:4147-4159.
  • 5Claudio A.P.,and Weissman A.M.,2000,RING finger proteins:Mediators of ubiquitin ligase activity,Cell,102(1):549-552.
  • 6Wang Y.S.,Pi L.Y.,Chen X.H.,Chakrabarty P.K.,Jiang J.D.,De L.,Liu G.Z.,Li L.,Bennya U.,Oard J.,Ronald P.C.,and Song W.Y.,2006,Rice XA21 binding protein 3 is an ubiquitin ligase required for full Xa21-mediated disease resistance,The Plant Cell,18:3635-3646.
  • 7Deng X.W.,Caspar T.,and Quail P.H.,1991,Copl:A regulatory locus involved in light-controlled development and gene expression in Arabidopsis,Genes Development,5:1172-1182.
  • 8Deng X.W.,Matsui M.,Wei N.,Wagner D.,Chu A.M.,Feldmann K.A.,and Quail P.H.,1992,C0P1,an Arabidopsis regulatory gene,encodes a protein with both a zinc-binding motif and a G beta homologous domain,Cell,71:791-801.
  • 9Ellis C.,Turner J.G.,Devoto A.,2002,Protein complexes mediate signaling in plant responses to hormones,light,sucrose and pathogens,Plant Molecular Biology,50:971-980.
  • 10Fan J.L.,Quan S.,Travis O.,Chie A.,Joanne C,and Hu J.P.,2005,The Arabidopsis PEX12 gene is required for peroxisome biogenesis and is essential for development,Plant Physiology,139:231-239.

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