作物学报 ›› 2011, Vol. 37 ›› Issue (06): 935-942.doi: 10.3724/SP.J.1006.2011.00935
• 综述 • 下一篇
赵开军1,2,*,李岩强1,3,王春连1,2,高英1,2
ZHAO Kai-Jun1,2,*,LI Yan-Qiang1,3,WANG Chun-Lian1,2,GAO Ying1,2
摘要: 植物定植在充满各种病原菌的环境中却能健康生长,显示其拥有一套免疫系统以应对病原物的侵染。最近,人们发现植物免疫系统至少包括2个层次:第一层为病原相关分子模式(PAMP)激发的免疫性(PTI),即植物通过细胞表面模式识别受体(PRRs)对病原菌的PAMPs进行分子识别,从而启动植物的防卫反应;第二层为病原菌效应子激发的免疫性(ETI),即有些毒性强的病原菌通过产生效应子(effectors)来抑制PTI,从而突破植物的第一道防线,而植物又进化出新的分子受体(例如R基因编码的NBS-LRR蛋白质)以侦察病原菌效应子并启动第二道防卫反应。数亿年来,病原菌的侵染和植物的防卫交替进行,促进了病原菌和植物基因组的共进化。最新的研究还发现,黄单胞杆菌TAL effectors和寄主植物DNA 的相互识别中,利用了精准的分子密码。TAL effector类蛋白识别植物靶基因的启动子序列,识别模式是2个氨基酸识别一个核苷酸。通过这种识别,TAL effector操控植物靶基因的表达,引起寄主植物的感病或抗病反应。上述抗病分子机理研究的突破,将对植物抗病育种产生重要影响。
[1]Bill B. A Short History of Nearly Everything. New York: Broadway Books, 2003. pp 188-202 [2]Butterfield N J. “Probable proterozoic fungi”. Paleobiology, 2005, 31: 165-182 [3]Takken F L W, Tameling W I L. To nibble at plant resistance proteins. Science, 2009, 324: 744-745 [4]Boller T, He S Y. Innate immunity in plants: an arms race between pattern recognition receptors in plants and effectors in microbial pathogens. Science, 2009, 324: 742-744 [5]Boch J, Scholze H, Schornack S, Landgraf A, Hahn S, Kay S, Lahaye T, Nickstadt A, Bonas U. Breaking the code of DNA binding specificity of TAL-type III effectors. Science, 2009, 326: 1509-1512 [6]Moscou M J, Bogdanove A J. A simple cipher governs DNA recognition by TAL effectors. Science, 2009, 326: 1501 [7]Jones J D G, Dangl J L. The plant immune system. Nature, 2006, 444: 323-329 [8]Dangl J L, Jones J D G. Plant pathogens and integrated defense responses to infection. Nature, 2001, 411: 826-833 [9]Ausubel F M. Are innate immune signaling pathways in plants and animals conserved? Nat Immunol, 2005, 6: 973-979 [10]Chisholm S T, Coaker G, Day B, Staskawicz B J. Host-microbe interactions: shaping the evolution of the plant immune response. Cell, 2006, 124: 803-814 [11]Boller T, Felix G. A renaissance of elicitors: perception of microbe-associated molecular patterns and danger signals by pattern-recognition receptors. Annu Rev Plant Biol, 2009, 60: 379-406 [12]Navarro L, Jay F, Nomura K, He S Y, Voinnet O. Suppression of the MicroRNA pathway by bacterial effector proteins. Science, 2008, 321: 964-967 [13]Göhre V, Spallek T, Häweker H, Mersmann S, Mentzel T, Boller T, Torres M, Mansfield J W, Robatzek S. Plant pattern-recognition receptor FLS2 is directed for degradation by the bacterial ubiquitin ligase AvrPtoB. Curr Biol, 2008, 23: 1824-1832 [14]Zipfel C, Robatzek S, Navarro L, Oakeley E J, Jones J D, Felix G, Boller T. Bacterial disease resistance in Arabidopsis through flagellin perception. Nature, 2004, 428: 764-767 [15]Gómez-Gómez L, Boller T. FLS2: an LRR receptor-like kinase involved in the perception of the bacterial elicitor flagellin in Arabidopsis. Mol Cell, 2000, 5: 1003-1011 [16]Sun W, Dunning F M, Pfund C, Weingarten R, Bent A F. Within-species flagellin polymorphism in Xanthomonas campestris pv. campestris and its impact on elicitation of Arabidopsis FLAGELLIN SENSING2-dependent defenses. Plant Cell, 2006, 18: 764-779 [17]Robatzek S, Bittel P, Chinchilla D, Köchner P, Felix G, Shiu S H, Boller T. Molecular identification and characterization of the tomato flagellin receptor LeFLS2, an orthologue of Arabidopsis FLS2 exhibiting characteristically different perception specificities. Plant Mol Biol, 2007, 64: 539-547 [18]Takai R, Isogai A, Seiji S, Che F S. Analysis of flagellin perception mediated by flg22 receptor OsFLS2 in rice. Mol Plant-Microbe Interact, 2008, 12: 1635-1642 [19]Kunze G, Zipfel C, Robatzek S, Niehaus K, Boller T, Felix G. The N terminus of bacterial elongation factor Tu elicits innate immunity in Arabidopsis plants. Plant Cell, 2004, 16: 3496-3507 [20]Zipfel C, Kunze G, Chinchilla D, Caniard A, Jones J D G. Perception of the bacterial PAMP EF-Tu by the receptor EFR restricts Agrobacterium- mediated transformation. Cell, 2006, 125: 749-760 [21]Lee S W, Han S W, Sririyanum M, Park C J, Seo Y S, Ronald P C. A type I-secreted, sulfated peptide triggers XA21-mediated innate immunity. Science, 2009, 326: 850-853 [22]Kaku H, Nishizawa Y, Ishii-Minami N, Akimoto-Tomiyama C, Dohmae N. Plant cells recognize chitin fragments for defense signaling through a plasma membrane receptor. Proc Natl Acad Sci USA, 2006, 103: 11086-11091 [23]Shimizu T, Nakano T, Akamizawa D, Desaki Y, Ishii-Minami N, Nishizawa Y, Minami E, Okada K, Yamane H, Kaku H, Shibuya N. Two LysM receptor molecules, EBiP and OsCERK1, cooperatively regulate chitin elicitor signaling in rice. Plant J, 2010, 64: 204-214 [24]Miya A, Albert P, Shinya T, Desaki Y, Ichimura K. CERK1, a LysM receptor kinase, is essential for chitin elicitor signaling in Arabidopsis. Proc Natl Acad Sci USA, 2007, 104: 19613-19618 [25]Chen L, Hamada S, Fujiwara M, Zhu T, Thao N P, Wong H L, Krishna P, Ueda T, Kaku H, Shibuya N, Kawasaki T, Shimamoto K. The Hop/Sti1-Hsp90 chaperone complex facilitates the maturation and transport of a PAMP receptor in rice innate immunity. Cell Host & Microbe, 2010, 7: 185-196 [26]Felix G, Boller T. Molecular sensing of bacteria in plants-the highly conserved RNA-binding motif RNP-1 of bacterial cold shock proteins is recognized as an elicitor signal in tobacco. J Biol Chem, 2003, 278: 6201-6218 [27]Watt S A, Tellstrom V, Patschkowski T, Niehaus K. Identification of the bacterial superoxide dismutase (SodM) as plant-inducible elicitor of an oxidative burst reaction in tobacco cell suspension cultures. J Biotechnol, 2006, 126: 78-86 [28]Kim J G, Jeon E, Oh J, Moon J S, Hwang I. Mutational analysis of Xanthomonas harpin HpaG identifies a key functional region that elicits the hypersensitive response in nonhost plants. J Bacteriol, 2004, 186: 6239-6247 [29]Brunner F, Rosahl S, Lee J, Rudd J J, Geiler C, Kauppinen S. Pep-13, a plant defense-inducing pathogenassociated pattern from Phytophthora transglutaminases. EMBO J, 2002, 21: 6681-6688 [30]Boller T. Chemoperception of microbial signals in plant cells. Annu Rev Plant Physiol Plant Mol Biol, 1995, 46: 189-214 [31]Granado J, Felix G, Boller T. Perception of fungal sterols in plants (subnanomolar concentrations of ergosterol elicit extracellular alkalinization in tomato cells. Plant Physiol, 1995, 107: 485-490 [32]Erbs G, Silipo A, Aslam S, De Castro C, Liparoti V, Flagiello A, Pucci P, Lanzetta R, Parrilli M, Molinaro A, Newman M A, Cooper R M. Peptidoglycan and muropeptides from pathogens Agrobacterium and Xanthomonas elicit plant innate immunity: structure and activity. Chem & Biol, 2008, 15: 438-448 [33]Silipo A, Sturiale L, Garozzo D, Erbs G, Jensen T T, Lanzetta R, Dow J M, Parrilli M, Newman M A, Molinaro A. The acylation and phosphorylation pattern of lipid from Xanthomonas campestris strongly influence its ability to trigger the innate immune response in Arabidopsis. Chem Biol Chem, 2008, 9: 896-904 [34]Dulla G, Lindow S E. Quorum size of Pseudomonas syringae is small and dictated by water availability on the leaf surface. Proc Natl Acad Sci USA, 2008, 105: 3082-3087 [35]Johnson L. Iron and siderophores in fungal-host interactions. Mycol Res, 2008, 112: 170-183 [36]Abramovitch R B, Anderson J C, Martin G B. Bacterial elicitation and evasion of plant innate immunity. Nat Rev Mol Cell Biol, 2006, 7: 601-611 [37]Ellis J G, Dodds P N, Lawrence G J. Flax rust resistance gene specificity is based on direct resistance avirulence protein interactions. Annu Rev Phytopathol, 2007, 45: 289-306 [38]Kamoun S. Groovy times: filamentous pathogen effectors revealed. Curr Opin Plant Biol, 2007, 10: 358-365 [39]Xiang T, Zong N, Zou Y, Wu Y, Zhang J, Xing W, Li Y, Tang X, Zhu L, Chai J, Zhou J M. Pseudomonas syringae effector AvrPto blocks innate immunity by targeting receptor kinases. Curr Biol, 2008, 18: 74-80 [40]Shan L, He P, Li J, Heese A, Peck S C, Nürnberger T, Martin G B, Sheen J. Bacterial effectors target the common signaling partner BAK1 to disrupt multiple MAMP Receptor-Signaling complexes and impede plant immunity. Cell Host & Microbe, 2008, 4: 17-27 [41]Chinchilla D, Zipfel C, Robatzek S, Kemmerling B, Nurnberger T. A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence. Nature, 2007, 448: 497-500 [42]Heese A, Hann D R, Gimenez-Ibanez S, Jones A M E, He K, Li J, Schroeder J I, Peck S C, Rathjen J P. The receptor-like kinase SERK3/BAK1 is a central regulator of innate immunity in plants. Proc Natl Acad Sci USA, 2002, 104: 12217-12222 [43]Zhang J, Shao F, Li Y, Cui H, Chen L, Li H, Zou Y, Long C, Lan L, Chai J, Chen S, Tang X, Zhou J M. A Pseudomonas syringae effector inactivates MAPKs to suppress PAMP-induced immunity in plants. Cell Host & Microbe, 2007, 1: 175-185 [44]Block A, Li G Y, Fu Z Q, Alfano J R. Phytopathogen type III effector weaponry and their plant targets. Curr Opin Plant Biol, 2008, 11: 396-403 [45]Wang Y, Li J, Hou S, Wang X, Li Y, Ren D, Chen S, Tang X, Zhou J. A Pseudomonas syringae ADP-Ribosyltransferase inhibits Arabidopsis mitogen-activated protein kinase kinases. Plant Cell, 2010, 22: 2033-2044 [46]Melotto M, Underwood W, Koczan J, Nomura K, He S Y. Plant stomata function in innate immunity against bacterial invasion. Cell, 2006, 126: 969-980 [47]Groll M, Schellenberg B, Bachmann A S, Archer C R, Huber R, Powell T K, Lindow S, Kaiser M, Dudler R. A plant pathogen virulence factor inhibits the eukaryotic proteasome by a novel mechanism. Nature, 2008, 452: 755-758 [48]Aslam S N, Newman M A, Erbs G, Morrissey K L, Chinchilla D, Boller T, Jensen T T, De Castro C, Ierano T, Molinaro A, Jackson R W, Knight M R, Cooper R M. Bacterial polysaccharides suppress induced innate immunity by calcium chelation. Curr Biol, 2008, 18: 1078-1183 [49]Meyers B C, Kozik A, Griego A, Kuang H H, Michelmore R W. Genome-wide analysis of NBS-LRR-encoding genes in Arabidopsis. Plant Cell, 2003, 15: 809-834 [50]Caplan J, Padmanabhan M, Dinesh-Kumar S P. Plant NB-LRR immune receptors: from recognition to transcriptional reprogramming. Cell Host & Microbe, 2008, 3: 126-135 [51]Lotze M T, Zeh H J, Rubartelli A, Sparvero L J, Amoscato A A, Washburn N R, Devera M E, Liang X, Tör M, Billiar T. The grateful dead: damage associated molecular pattern molecules and reduction/oxidation regulate immunity. Immunologcal Rev, 2007, 220: 60-81 [52]Kay S, Bonas U. How Xanthomonas type III effectors manipulate the host plant. Curr Opin Microbiol, 2009, 12: 37-43 [53]White F F, Yang B. Host and pathogen factors controlling the Rice-Xanthomonas oryzae interaction. Plant Physiol, 2009, 150: 1677-1686 [54]Kay S, Hahn S, Marois E, Hause G, Bonas U. A bacterial effector acts as a plant transcription factor and induces a cell size regulator. Science, 2007, 318: 648-651 [55]Römer P, Hahn S, Jordan T, Strauss T, Bonas U, Lahaye T. Plant pathogen recognition mediated by promoter activation of the pepper Bs3 resistance gene. Science, 2007, 318: 645-648 [56]Sugio A, Yang B, Zhu T, White F F. Two type III effector genes of Xanthomonas oryzae pv. oryzae control the induction of the host genes OsTFIIAγ1 and OsTFX1 during bacterial blight of rice. Proc Natl Acad Sci USA, 2007, 104: 10720-10725 [57]Yang B, Sugio A, White F F. Os8N3 is a host disease-susceptibility gene for bacterial blight of rice. Proc Nat Acad Sci USA, 2006, 103: 10503-10508 [58]Gu K, Yang B, Tian D, Wu L, Wang D, Sreekala C, Yang F, Chu Z, Wang G L, White F F, Yin Z. R gene expression induced by a type-III effector triggers disease resistance in rice. Nature, 2005, 435: 1122-1125 [59]Schornack S, Meyer A, Römer P, Jordan T, Lahaye T. Gene-for-gene-mediated recognition of nuclear-targeted AvrBs3-like bacterial effector proteins. J Plant Physiol, 2006, 163: 256-272 [60]Van den Ackerveken G, Marois E, Bonas U. Recognition of the bacterial avirulence protein AvrBs3 occurs inside the host plant cell. Cell, 1996, 87: 1307-1316 [61]Conrads-Strauch J H K, Bonas U. Race-specificity of plant resistance to bacterial spot disease determined by repetitive motifs in a bacterial avirulence protein. Nature, 1992, 356: 172-174 [62]Yang B, Sugio A, White F F. Avoidance of host recognition by alterations in the repetitive and C-terminal regions of AvrXa7, a type III effector of Xanthomonas oryzae pv. oryzae. Mol Plant-Microbe Interact, 2005, 18: 142-149 [63]Bonas U, Stall R E, Staskawicz B. Genetic and Structural characterization of the avirulence gene avrBs3 from Xanthomonas campestris pv. vesicatoria. Mol Gen Genet, 1989, 218: 127-136 [64]Li T, Huang S, Jiang W Z, Wright D, Spalding M H, Weeks D P, Yang B. TAL nucleases (TALNs): hybrid proteins composed of TAL effectors and FokI DNA-cleavage domain. Nucl Acids Res, 2011, 39: 359-372 [65]Christian M, Cermak T, Doyle E L, Schmidt C, Zhang F, Hummel A, Bogdanove A J, Voytas D F. TAL effector nucleases create targeted DNA double-strand breaks. Genetics, 2010, 186: 757-761 [66]Lacombe S, Rougon-Cardoso A, Sherwood E, Peeters N, Dahlbeck D, van Esse H P, Smoker M, Rallapalli G, Thomma B, Staskawicz B, Jones J, Zipfel C. Interfamily transfer of a plant pattern-recognition receptor confers broad-spectrum bacterial resistance. Nat Biotechnol, 2010, 28: 365-369 [67]Römer P, Recht S, Lahaye T. A single plant resistance gene promoter engineered to recognize multiple TAL effectors from disparate pathogens. Proc Natl Acad Sci USA, 2009, 106: 20526-20531 [68]Zou L-F(邹丽芳), Chen G-Y(陈功友), Wu X-M(武晓敏), Wang J-S(王金生). Cloning and analysis of diverse members of avrBs3/PthA Family of Xanthomonas oryzae pv. oryzicola. Sci Agric Sin (中国农业科学), 2005, 38(5): 929-935 (in Chinese with English abstract) [69]Zhao B, Zhao B, Lin X, Poland J, Trick H, Leach J, Hulbert S. A maize resistance gene functions against bacterial streak disease in rice. Proc Natl Acad Sci USA, 2005, 102: 15383-15388 [70]Tian D, Yin Z. Constitutive heterologous expression of avrXa27 in rice containing the R gene Xa27 confers enhanced resistance to compatible Xanthomonas oryzae strains. Mol Plant Pathol, 2009, 10: 29-39 |
[1] | 赵海涵, 练旺民, 占小登, 徐海明, 张迎信, 程式华, 楼向阳, 曹立勇, 洪永波. 水稻协优9308重组自交系群体白叶枯病抗性的全基因组关联分析[J]. 作物学报, 2022, 48(1): 121-137. |
|