Functions of rice NAC transcriptional factors, ONAC122 and ONAC131, in defense responses against Magnaporthe grisea
详细信息 查看全文
- 作者：Lijun Sun (1)
Huijuan Zhang (1)
Dayong Li (1)
Lei Huang (1)
Yongbo Hong (1)
Xin Shun Ding (2)
Richard S. Nelson (2)
Xueping Zhou (1)
Fengming Song (1) - 关键词：Rice (Oryza sativa L.) ; NAC transcription factor ; ONAC122 and ONAC131 ; Defense response ; Magnaporthe grisea ; Virus ; induced gene silencing
- 刊名：Plant Molecular Biology
- 出版年：2013
- 出版时间：2 - January 2013
- 年：2013
- 卷：81
- 期：1
- 页码：41-56
- 全文大小：866KB
- 参考文献：1. Aaron S, Mark E (2009) Recent advances and emerging trends in plant hormone signaling. Nature 459:1071鈥?078 CrossRef
2. Abbruscato P, Nepusz T, Mizzi L, Del Corvo M, Morandini P, Fumasoni I, Michel C, Paccanaro A, Guiderdoni E, Schaffrath U, Morel JB, Piffanelli P, Faivre-Rampant O (2012) OsWRKY22, a monocot WRKY gene, plays a role in the resistance response to blast. Mol Plant Pathol 13:828鈥?41
3. Agrawal GK, Jwa NS, Rakwal R (2000) A novel rice ( / Oryza sativa L.) acidic / PR1 gene highly responsive to cut, phytohormones, and protein phosphatase inhibitors. Biochem Biophys Res Commun 274:157鈥?65 CrossRef
4. Ahn IP, Kim S, Kang S, Suh SC, Lee YH (2005) Rice defense mechanisms against / Cochliobolus miyabeanus and / Magnaporthe grisea are distinct. Phytopathology 95:1248鈥?255 CrossRef
5. Aida M, Ishida T, Fukaki H, Fujisawa H, Tasaka M (1997) Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant. Plant Cell 9:841鈥?57 CrossRef
6. Bent AF, Mackey D (2007) Elicitors, effectors, and / R genes: the new paradigm and a lifetime supply of questions. Annu Rev Phytopathol 45:399鈥?36 CrossRef
7. Biruma M, Martin T, Fridborg I, Okori P, Dixelius C (2012) Two loci in sorghum with NB-LRR encoding genes confer resistance to / Colletotrichum sublineolum. Theor Appl Genet 124:1005鈥?015 CrossRef
8. Boller T, Felix G (2009) A renaissance of elicitors: perception of microbe-associated molecular patterns and danger signals by pattern-recognition receptors. Annu Rev Plant Biol 60:379鈥?06 CrossRef
9. Boller T, He SY (2009) Innate immunity in plants: an arms race between pattern recognition receptors in plants and effectors in microbial pathogens. Science 324:742鈥?44 CrossRef
10. Bu Q, Jiang H, Li CB, Zhai Q, Zhang J, Wu X, Sun J, Xie Q, Li C (2008) Role of the / Arabidopsis thaliana NAC transcription factors ANAC019 and ANAC055 in regulating jasmonic acid-signaled defense responses. Cell Res 18:756鈥?67 CrossRef
11. Chakravarthy S, Vela鈥瞫quez AC, Ekengren SK, Collmer A, Martin GB (2010) Identification of / Nicotiana benthamiana genes involved in pathogen-associated molecular pattern-triggered immunity. Mol Plant鈥揗icrobe Interact 23: 715鈥?26
12. Chern MS, Fitzgerald HA, Canlas PE, Navarre DA, Ronald PC (2005) Over-expression of rice NPR1 homologue leads to constitutive activation of defense response and hypersensitivity to light. Mol Plant-Microbe Interact 18:511鈥?20 CrossRef
13. Delessert C, Kazan K, Wilsom LW, Straetend VD, Manners J, Dennis ES, Dolferus R (2005) The transcription factor ATAF2 represses the expression of pathogenesis-related genes in Arabidopsis. Plant J 43:745鈥?57 CrossRef
14. Ding XS, Schneider WL, Chaluvadi SR, Mian MA, Nelson RS (2006) Characterization of a Brome mosaic virus strain and its use as a vector for gene silencing in monocotyledonous hosts. Mol Plant-Microbe Interact 19:1229鈥?239 CrossRef
15. Ding XS, Chaluvadi SR, Nelson RS (2007) Analysis of gene function in rice through virus-induced gene silencing. Methods Mol Biol 354:145鈥?60
16. Ding XS, Ballard K, Nelson RS (2010) Improving virus induced gene silencing (VIGS) in rice through / Agrobacterium infiltration. In: Biology of molecular plant-microbe interactions vol. 7. In: Antoun H, Avis T, Brisson L, Pr茅vost D, and Trepanier M, (eds), International society for molecular plant-microbe interactions, St. Paul, MN, Paper 59
17. Dodds PN, Rathjen JP (2010) Plant immunity: towards an integrated view of plant鈥損athogen interactions. Nature Rev Genet 11:539鈥?48 CrossRef
18. Eulgem T, Somssich IE (2007) Networks of WRKY transcription factors in defense signaling. Curr Opin Plant Biol 10:366鈥?71 CrossRef
19. Fang Y, You J, Xie K, Xie W, Xiong L (2008) Systematic sequence analysis and identification of tissue-specific or stress-responsive genes of NAC transcription factor family in rice. Mol Genet Genomics 280:547鈥?63 CrossRef
20. Feussner I, Wasternack C (2002) The lipoxygenase pathway. Annu Rev Plant Biol 53:275鈥?97 CrossRef
21. Gutterson N, Reuber TL (2004) Regulation of disease resistance pathways by AP2/ERF transcription factors. Curr Opin Plant Biol 7:465鈥?71 CrossRef
22. Hearne PQ, Knorr DA, Hillman BI, Morris TJ (1990) The complete structure and synthesis of infectious RNA from clones of tomato bushy stunt virus. Virology 177:141鈥?51 CrossRef
23. Hein I, Barciszewska-Pacak M, Hrubikova K, Williamson S, Dinesen M, Soenderby IE, Sundar S, Jarmolowski A, Shirasu K, Lacomme C (2005) Virus-induced gene silencing-based functional characterization of genes associated with powdery mildew resistance in barley. Plant Physiol 138:2155鈥?164 CrossRef
24. Hiratsu K, Matsui K, Koyama T, Ohme-Takagi M (2003) Dominant repression of target genes by chimeric repressors that include the EAR motif, a repression domain, in Arabidopsis. Plant J 34:733鈥?39 CrossRef
25. Hu HH, Dai MQ, Yao JL, Xiao BZ, Li XH, Zhang QF, Xiong LZ (2006) Overexpressing a NAM, ATAF, and CUC (NAC) transcription factor enhances drought resistance and salt tolerance in rice. Proc Natl Acad Sci USA 103:12987鈥?2992 CrossRef
26. Jensen MK, Rung JH, Gregersen PL, Gjetting T, Fuglsang AT, Hansen M, Joehnk N, Lyngkjaer MF, Collinge DB (2007) The HvNAC6 transcription factor: a positive regulator of penetration resistance in barley and Arabidopsis. Plant Mol Biol 65:137鈥?50 CrossRef
27. Jensen MK, Hagedorn PH, de Torres-Zabala M, Grant MR, Rung JH, Collinge DB, Lyngkjaer MF (2008) Transcriptional regulation by an NAC (NAM鈥揂TAF1, 2鈥揅UC2) transcription factor attenuates ABA signaling for efficient basal defense towards / Blumeria graminis f. sp. / hordei in Arabidopsis. Plant J 56:867鈥?80 CrossRef
28. Jia Y, Valent B, Lee F (2003) Determination of host responses to / Magnaporthe grisea on detached rice leaves using a spot inoculation method. Plant Dis 87:129鈥?33 CrossRef
29. Jones JD, Dangl JL (2006) The plant immune system. Nature 444:323鈥?29 CrossRef
30. Kachroo A, Kachroo P (2007) Salicylic acid-, jasmonic acid and ethylene-mediated regulation of plant defense signaling. Genet Eng (NY) 28:55鈥?3 CrossRef
31. Kaneda T, Taga Y, Takai R, wano M, Matsui H, Takayama S, Isoga A, Che FS (2009) The transcription factor OsNAC4 is a key positive regulator of plant hypersensitive cell death. EMBO J 28: 926鈥?36
32. Le DT, Nisjiyama R, Watanabe Y, Mochida K, Yamaquchi-Shinozaki K, Shinozaki K, Tran LS (2011) Genome-wide survey and expression analysis of the plant-specific NAC transcription factor family in soybean during development and dehydration stress. DNA Res 18:263鈥?76 CrossRef
33. Li W, Zhong S, Li G, Li Q, Mao B, Deng Y, Zhang H, Zeng L, Song F, He Z (2011) Rice RING protein OsBBI1 with E3 ligase activity confers broad-spectrum resistance against / Magnaporthe oryzae by modifying the cell wall defence. Cell Res 21:835鈥?48 CrossRef
34. Lin RM, Zhao WS, Meng XB, Wang M, Peng YL (2007) Rice gene OsNAC19 encodes a novel NAC-domain transcription factor and responds to infection by / Magnaporthe grisea. Plant Sci 172:120鈥?30 CrossRef
35. Liu Y, Schiff M, Dinesh-Kumar SP (2002) Virus-induced gene silencing in tomato. Plant J 31:777鈥?86 CrossRef
36. Liu JL, Wang XJ, Mitchell T, Hu YJ, Liu XL, Dai LY, Wang GL (2010) Recent progress and understanding of the molecular mechanisms of the rice-Magnaporthe oryzae interaction. Mol Plant Pathol 11:419鈥?27 CrossRef
37. Livak KJ, Schmittgen TD (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta DeltaC (T)) method. Methods 25:402鈥?08 CrossRef
38. Mitsuda N, Hiratsu K, Todaka D, Nakashima K, Yamaguchi-Shinozaki K, Ohme-Takagi M (2006) Efficient production of male and female sterile plants by expression of a chimeric repressor in Arabidopsis and rice. Plant Biotechnol J 4:325鈥?32 CrossRef
39. Mitsuda N, Umemura Y, Ikeda M, Shikata M, Koyama T, Matsui K, Narumi T, Aida R, Sasaki K, Hiyama T, Higuchi Y, Ono M, Isuzugawa K, Saitoh K, Endo R, Ikeda K, Nakatsuka T, Nishihara M, Yamamura S, Yamamura T, Terakawa T, Ohtsubo N, Ohme-Takagi M (2008) FioreDB: a database of phenotypic information induced by the chimeric repressor silencing technology (CRES-T) in Arabidopsis and floricultural plants. Plant Biotechnol 25:37鈥?3 CrossRef
40. Mitsuhara I, Iwai T, Seo S, Yanagawa Y, Kawahigasi H, Hirose S, Ohkawa Y, Ohashi Y (2008) Characteristic expression of twelve rice PR1 family genes in response to pathogen infection, wounding, and defense-related signal compounds. Mol Genet Genomics 279:415鈥?27 CrossRef
41. Motoyasu Y, Takumi S, Muneo Y, Takahiko H, Akio M, Hirohiko H, Toshihiro O (2009) Disruption of a novel gene for a NAC-domain protein in rice confers resistance to Rice dwarf virus. Plant J 57:615鈥?25 CrossRef
42. Nakashima K, Tran LP, Nguyen DV, Fujita M, Maruyama K, Todaka D, Ito Y, Hayashi N, Shinozaki K, Yamaguchi-Shinozaki K (2007) Functional analysis of a NAC-type transcription factor OsNAC6 involved in abiotic and biotic stress-responsive gene expression in rice. Plant J 51:617鈥?30 CrossRef
43. Nakashima K, Takasaki H, Mizoi J, Shinozaki K, Yamaguchi-Shinozaki K (2012) NAC transcription factors in plant abiotic stress responses. Biochim Biophys Acta 1819:97鈥?03 CrossRef
44. Nuruzzaman M, Manimekalai R, Sharoni AM, Satoh K, Kondoh H, Ooka H, Kikuchi S (2010) Genome-wide analysis of NAC transcription factor family in rice. Gene 465:30鈥?4 CrossRef
45. Oh SK, Lee S, Yu SH, Choi D (2005) Expression of a novel NAC domain-containing transcription factor (CaNAC1) is preferentially associated with incompatible interactions between chili pepper and pathogens. Planta 222:876鈥?87 CrossRef
46. Olsen AN, Ernst HA, Leggio LL, Skriver K (2005) NAC transcription factors: structurally distinct, functionally diverse. Trends Plant Sci 10:79鈥?7 CrossRef
47. Ooka H, Satoh K, Doi K, Nagata T, Otomo Y, Murakami K, Matsubara K, Osato N, Kawai J, Carninci P, Hayashizaki Y, Suzuki K, Kojima K, Takahara Y, Yamamoto K, Kikuchi S (2003) Comprehensive analysis of NAC family genes in / Oryza sativa and / Arabidopsis thaliana. DNA Res 10:239鈥?47 CrossRef
48. Pacak A, Strozycki PM, Barciszewska-Pacak M, Alejska M, Lacomme C, Jarmo艂owski A, Szweykowska-Kuli艅ska Z, Figlerowicz M (2010) The brome mosaic virus-based recombination vector triggers a limited gene silencing response depending on the orientation of the inserted sequence. Arch Virol 155:169鈥?79 CrossRef
49. Purkayastha A, Dasgupta I (2009) Virus-induced gene silencing: a versatile tool for discovery of gene functions in plants. Plant Physiol Biochem 47:967鈥?76 CrossRef
50. Purkayastha A, Mathur S, Verma V, Sharma S, Dasgupta I (2010) Virus-induced gene silencing in rice using a vector derived from a DNA virus. Planta 232:1531鈥?540 CrossRef
51. Qi M, Yang Y (2002) Quantification of / Magnaporthe grisea during infection of rice plants using real-time polymerase chain reaction and Northern blot/phosphoimaging analyses. Phytopathology 92:870鈥?76 CrossRef
52. Qiu D, Xiao J, Ding X, Xiong M, Cai M, Cao Y, Li X, Xu C, Wang S (2007) OsWRKY13 mediates rice disease resistance by regulating defense-related genes in salicylate- and jasmonate-dependent signaling. Mol Plant-Microbe Interact. 20:492鈥?99 CrossRef
53. Robert-Sellaniantz A, Grant M, Jones JD (2011) Hormone crosstalk in plant disease and defense: more than just jasmonate-salicylate antagonism. Annu Rev Phytopathol 49:317鈥?43 CrossRef
54. Rushton PJ, Bokowiec MT, Han SC, Zhang HB, Brannock JF, Chen XF, Laudeman TW, Timko MP (2008) Tobacco transcription factors: novel insights into transcriptional regulation in the Solanaceae. Plant Physiol 147:280鈥?95 CrossRef
55. Scholthof HB (1999) Rapid delivery of foreign genes into plants by direct rub-inoculation with intact plasmid DNA of a Tomato bushy stunt virus gene vector. J Virol 73:7823鈥?829
56. Scofield SR, Nelson RS (2009) Resources for virus-induced gene silencing in the grasses. Plant Physiol 149:152鈥?57 CrossRef
57. Scofield SR, Huang L, Brandt AS, Gill BS (2005) Development of a virus-induced gene-silencing system for hexaploid wheat and its use in functional analysis of the / Lr21-mediated leaf rust resistance pathway. Plant Physiol 138:2165鈥?173 CrossRef
58. Shi B-J, Ding S-W, Symons RH (1997) Plasmid vector for cloning infectious cDNAs from plant RNA viruses: high infectivity of cDNA clones of tomato aspermy cucumovirus. J Gen Virol 78:1181鈥?185
59. Shi Y, Qin Y, Cao Y, Sun H, Zhou T, Hong Y, Fan Z (2011) Influence of an m-type thioredoxin in maize on potyviral infection. Eur J Plant Pathol 131:317鈥?26 CrossRef
60. Shimono M, Sugano S, Nakayama A, Jiang CJ, Ono K, Toki S, Takatsuji H (2007) Rice WRKY45 plays a crucial role in benzothiadiazole-inducible blast resistance. Plant Cell 19:2064鈥?076 CrossRef
61. Shimono M, Koga H, Akagi A, Hayashi N, Goto S, Sawada M, Kurihara T, Matsushita A, Sugano S, Jiang CJ, Kaku H, Inoue H, Takatsuji H (2012) Rice WRKY45 plays important roles in fungal and bacterial disease resistance. Mol Plant Pathol 13:83鈥?4 CrossRef
62. Sindhu A, Chintamanani S, Brandt AS, Zanis M, Scofield SR, Johal GS (2008) A guardian of grasses: specific origin and conservation of a unique disease-resistance gene in the grass lineage. Proc Natl Acad Sci USA 105:1762鈥?767 CrossRef
63. Skamnioti P, Gurr SJ (2009) Against the grain: safeguarding rice from rice blast disease. Trends Biotechnol 27:141鈥?50 CrossRef
64. Takasaki H, Maruyama K, Kidokoro S, Ito Y, Fujita Y, Shinozaki K, Yamaguchi S-K, Nakashima K (2010) The abiotic stress-responsive NAC-type transcription factor OsNAC5 regulates stress-inducible genes and stress tolerance in rice. Mol Genet Genomics 284:173鈥?83 CrossRef
65. Tao Y, Xie Z, Chen W, Glazebrook J, Chang HS, Han B, Zhu T, Zou G, Katagiri F (2003) Quantitative nature of Arabidopsis responses during compatible and incompatible interactions with the bacterial pathogen / Pseudomonas syringae. Plant Cell 15:317鈥?30 CrossRef
66. Tao Z, Liu H, Qiu D, Zhou Y, Li X, Xu C, Wang S (2009) A pair of allelic WRKY genes play opposite roles in rice-bacteria interactions. Plant Physiol 151:936鈥?48 CrossRef
67. Tsuda K, Sato M, Stoddard T, Glazebrook J, Katagiri F (2009) Network properties of robust immunity in plants. PLoS Genet 5(12):e1000772 CrossRef
68. Valent B, Khang CH (2010) Recent advances in rice blast effector research. Curr Opin Plant Biol 13:434鈥?41 CrossRef
69. van der Linde K, Kastner C, Kumlehn J, Kahmann R, Doehlemann G (2011) Systemic virus-induced gene silencing allows functional characterization of maize genes during biotrophic interaction with / Ustilago maydis. New Phytol 189:471鈥?83 CrossRef
70. van Loon LC, Rep M, Pieterse CM (2006) Significance of inducible defense-related proteins in infected pants. Annu Rev Phytopathol 44:135鈥?62 CrossRef
71. Wang H, Hao J, Chen X, Hao Z, Wang X, Lou Y, Peng Y, Guo Z (2007) Overexpression of rice WRKY89 enhances ultraviolet B tolerance and disease resistance in rice plants. Plant Mol Biol 65:799鈥?15 CrossRef
72. Wang X, Basnayake BM, Zhang H, Li G, Li W, Virk N, Menqiste T, Song F (2009) The Arabidopsis ATAF1, a NAC transcription factor, is a negative regulator of defense responses against necrotrophic fungal and bacterial pathogens. Mol Plant-Microbe Interact 22:1227鈥?238 CrossRef
73. Wen N, Chu Z, Wang S (2003) Three types of defense-responsive genes are involved in resistance to bacterial blight and fungal blast diseases in rice. Mol Gen Genomics 269:331鈥?39 CrossRef
74. Wu Y, Deng Z, Lai J, Zhang Y, Yang C, Yin B, Zhao Q, Zhang L, Li Y, Yang C, Xie Q (2009) Dual function of Arabidopsis ATAF1 in abiotic and biotic stress responses. Cell Res 19:1279鈥?290 CrossRef
75. Xie GL, Mew TW (1998) A leaf inoculation method for detection of / Xanthomonas oryzae pv. / oryzicola from rice seed. Plant Dis 82:1007鈥?011 CrossRef
76. Yuan Y, Zhong S, Li Q, Zhu Z, Lou Y, Wang L, Wang J, Wang M, Li Q, Yang D, He Z (2007) Functional analysis of rice NPR1-like genes reveals that OsNPR1/NH1 is the rice orthologue conferring disease resistance with enhanced herbivore susceptibility. Plant Biotechnol J 5:313鈥?24 CrossRef
77. Zhang J, Zhou JM (2010) Plant immunity triggered by microbial molecular signatures. Mol Plant 3:783鈥?93 CrossRef
78. Zhang J, Peng Y, Guo Z (2008) Constitutive expression of pathogen-inducible OsWRKY31 enhances disease resistance and affects root growth and auxin response in transgenic rice plants. Cell Res 18:508鈥?21 CrossRef
79. Zhong R, Lee C, Ye ZH (2010) Evolutionary conservation of the transcriptional network regulating secondary cell wall biosynthesis. Trends Plant Sci 15:625鈥?32 CrossRef
80. Zhou H, Li S, Deng Z, Wang X, Chen T, Zhang J, Chen S, Ling H, Zhang A, Wang D, Zhang X (2007) Molecular analysis of three new receptor-like kinase genes from hexaploid wheat and evidence for their participation in the wheat hypersensitive response to stripe rust fungus infection. Plant J 52:420鈥?34 CrossRef - 作者单位：Lijun Sun (1)
Huijuan Zhang (1)
Dayong Li (1)
Lei Huang (1)
Yongbo Hong (1)
Xin Shun Ding (2)
Richard S. Nelson (2)
Xueping Zhou (1)
Fengming Song (1)
1. National Key Laboratory for Rice Biology, Institute of Biotechnology, Zhejiang University, Hangzhou, 310058, Zhejiang, China
2. Samuel Roberts Noble Foundation, Inc., 2510 Sam Noble Parkway, Ardmore, OK, 73401, USA - ISSN：1573-5028
文摘
NAC (NAM/ATAF/CUC) transcription factors have important functions in regulating plant growth, development, and abiotic and biotic stress responses. Here, we characterized two rice pathogen-responsive NAC transcription factors, ONAC122 and ONAC131. We determined that these proteins localized to the nucleus when expressed ectopically and had transcriptional activation activities. ONAC122 and ONAC131 expression was induced after infection by Magnaporthe grisea, the causal agent of rice blast disease, and the M. grisea-induced expression of both genes was faster and higher in the incompatible interaction compared with the compatible interaction during early stages of infection. ONAC122 and ONAC131 were also induced by treatment with salicylic acid, methyl jasmonate or 1-aminocyclopropane-1-carboxylic acid (a precursor of ethylene). Silencing ONAC122 or ONAC131 expression using a newly modified Brome mosaic virus (BMV)-based silencing vector resulted in an enhanced susceptibility to M. grisea. Furthermore, expression levels of several other defense- and signaling-related genes (i.e. OsLOX, OsPR1a, OsWRKY45 and OsNH1) were down-regulated in plants silenced for ONAC122 or ONAC131 expression via the BMV-based silencing system. Our results suggest that both ONAC122 and ONAC131 have important roles in rice disease resistance responses through the regulated expression of other defense- and signaling-related genes.