Three ERF transcription factors from Chinese wild grapevine Vitis pseudoreticulata participate in different biotic and abiotic stress-responsive pathways

Journal of Plant Physiology

Volumn 170, Issue 10, 2013, Pages 923-933

  Zhu, Ziguo ^a,b   Shi, Jiangli ^a,b   Xu, Weirong ^a,b   Li, Huie ^a,b   He, Mingyang ^a,b   Xu, Yan ^a,b   Xu, Tengfei ^a,b   Yang, Yazhou ^a,b   Cao, Jiangling ^a,b   Wang, Yuejin ^a,b  

^a NORTHWEST A F UNIVERSITY   (China)

^b AGRO ENVIRONMENTAL PROTECTION INSTITUTE   (China)

Author keywords

Abiotic and biotic stresses; Chinese wild Vitis pseudoreticulata; Disease resistance to powdery mildew; Ethylene response factor; Grapevine

Indexed keywords

PHYTOHORMONE; PLANT DNA; TRANSCRIPTION FACTOR; VEGETABLE PROTEIN;

AMINO ACID SEQUENCE; ARTICLE; ASCOMYCETES; CELL FRACTIONATION; CHEMISTRY; CHINA; DISEASE RESISTANCE; DROUGHT; DRUG EFFECT; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; MICROBIOLOGY; MOLECULAR GENETICS; PHYLOGENY; PHYSIOLOGICAL STRESS; PHYSIOLOGY; PLANT DISEASE; PLANT GENE; PLANT LEAF; PROTEIN BINDING; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS; TEMPERATURE; TOBACCO; TRANSCRIPTION INITIATION; TRANSGENIC PLANT; VITIS;

AMINO ACID SEQUENCE; ASCOMYCOTA; CHINA; DISEASE RESISTANCE; DNA, PLANT; DROUGHTS; GENE EXPRESSION REGULATION, PLANT; GENES, PLANT; MOLECULAR SEQUENCE DATA; PHYLOGENY; PLANT DISEASES; PLANT GROWTH REGULATORS; PLANT LEAVES; PLANT PROTEINS; PLANTS, GENETICALLY MODIFIED; PROTEIN BINDING; SEQUENCE ALIGNMENT; SEQUENCE ANALYSIS, PROTEIN; STRESS, PHYSIOLOGICAL; SUBCELLULAR FRACTIONS; TEMPERATURE; TOBACCO; TRANSCRIPTION FACTORS; TRANSCRIPTIONAL ACTIVATION; VITIS;

ARABIDOPSIS; BACTERIA (MICROORGANISMS); ERYSIPHALES; NICOTIANA OBTUSIFOLIA; NICOTIANA TABACUM; RALSTONIA SOLANACEARUM; TEREBRANTIA; VITIS; VITIS PSEUDORETICULATA;

EID: 84878110156     PISSN: 01761617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jplph.2013.01.017     Document Type: Article

References (62)

1. Balague C., Bouchez O., Huard C., Lorrain S., Roby D. Ethylene is one of the key elements for cell death and defense response control in the Arabidopsis lesion mimic mutant vad1. Plant Physiol 2007, 145:465-477.
2. Barker C.L., Donald T., Pauquet J., Ratnaparkhe M.B., Bouquet A., Adam-Blondon A.F., et al. Dry I, genetic and physical mapping of the grapevine powdery mildew resistance gene, Run1, using a bacterial artificial chromosome library. Theor Appl Genet 2005, 111:370-377.
3. Bellin D., Peressotti E., Merdinoglu D., Wiedemann-Merdinoglu S., Adam-Blondon A.F., Cipriani G., et al. Resistance to Plasmopara viticola in grapevine 'Bianca' is controlled by a major dominant gene causing localised necrosis at the infection site. Theor Appl Genet 2009, 120:163-176.
4. Brederode F.T., Linthorst H.J., Bol J.F. Differential induction of acquired resistance and PR gene expression in tobacco by virus infection, ethephon treatment, UV light and wounding. Plant Mol Biol 1991, 17:1117-1125.
5. Chen L., Zhang Z., Liang H., Liu H., Du L., Xu H., et al. Overexpression of TiERF1 enhances resistance to sharp eyespot in transgenic wheat. J Exp Bot 2008, 59:4195-4204.
6. Coleman C., Copetti D., Cipriani G., Hoffman S., Kozman P., Kovacs L., et al. The powdery mildew resistance gene REN1 co-segregates with an NBS-LRR gene cluster in two Central Asian grapevines. BMC Genet 2009, 10:89.
7. Dong N., Liu X., Lu Y., Du L., Xu H., Liu H., et al. Overexpression of TaPIEP1, a pathogen-induced ERF gene of wheat, confers host-enhanced resistance to fungal pathogen Bipolaris sorokiniana. Funct Integr Genomic 2010, 10:215-226.
8. Fischer U., Droge-Laser W. Overexpression of NtERF5, a new member of the tobacco ethylene response transcription factor family enhances resistance to Tobacco mosaic virus. Mol Plant Microbe Interact 2004, 17:1162-1171.
9. Fujimoto S.Y., Ohta M., Usui A., Shinshi H., Ohme-Takagi M. Arabidopsis ethylene-responsive element binding factors act as transcriptional activators or repressors of GCC box-mediated gene expressio. Plant Cell 2000, 12:393-404.
10. Fujita M., Fujita Y., Noutoshi Y., Takahashi F., Narusaka Y., Yamaguchi-Shinozaki K., et al. Crosstalk between abiotic and biotic stress responses: a current view from the points of convergence in the stress signaling networks. Curr Opin Plant Biol 2006, 9:436-442.
11. Gu Y.Q., Wildermuth M.C., Chakravarthy S., Loh Y.T., Yang C., He X., et al. Tomato transcription factors pti4, pti5, and pti6 activate defense responses when expressed in Arabidopsis. Plant Cell 2002, 14:817-831.
12. Guo Z.J., Chen X.J., Wu X.L., Ling J.Q., Xu P. Overexpression of the AP2/EREBP transcription factor OPBP1 enhances disease resistance and salt tolerance in tobacco. Plant Mol Biol 2004, 55:607-618.
13. Gutterson N., Reuber T.L. Regulation of disease resistance pathways by AP2/ERF transcription factors. Curr Opin Plant Biol 2004, 7:465-471.
14. Hattori Y., Nagai K., Furukawa S., Song X.J., Kawano R., Sakakibara H., et al. The ethylene response factors SNORKEL1 and SNORKEL2 allow rice to adapt to deep water. Nature 2009, 460:1026-1030.
15. He P., Warren R.F., Zhao T., Shan L., Zhu L., Tang X., Zhou J.M. Overexpression of Pti5 in tomato potentiates pathogen-induced defense gene expression and enhances disease resistance to Pseudomonas syringae pv. tomato. Mol Plant Microbe Interact 2001, 14:1453-1457.
16. Horsch R.B., Fry J.E., Eichlotz D., Rogers S.G., Frakey R.T. A simple and general method for transferring genes into plants. Science 1985, 1229-1231.
17. Jaillon O., Aury J.M., Noel B., Policriti A., Clepet C., Casagrande A., et al. The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla. Nature 2007, 449:463-468.
18. Jung C., Lyou S., Yeu S., Kim M., Rhee S., et al. Microarray-based screening of jasmonate-responsive genes in Arabidopsis thaliana. Plant Cell Rep 2007, 26:1053-1063.
19. Jung J., Won S.Y., Suh S.C., Kim H.R., Wing R., Jeong Y., et al. The barley ERF-type transcription factor HvRAF confers enhanced pathogen resistance and salt tolerance in Arabidopsis. Planta 2007, 225:575-588.
20. Li H., Xu Y., Xiao Y., Zhu Z., Xie X., Zhao H., et al. Expression and functional analysis of two genes encoding transcription factors, VpWRKY1 and VpWRKY2, isolated from Chinese wild Vitis pseudoreticulata. Planta 2010, 232:1325-1337.
21. Liang H.X., Lu Y., Liu H.X., Wang F.D., Xin Z.Y., Zhang Z.Y. A novel activator-type ERF of Thinopyrum intermedium, TiERF1, positively regulates defence responses. J Exp Bot 2008, 59:3111-3120.
22. Licausi F., Giorgi F.M., Zenoni S., Osti F., Pezzotti M., Perata P. Genomic and transcriptomic analysis of the AP2/ERF superfamily in Vitis vinifera. BMC Genomics 2010, 11:719.
23. Liu W.Y., Chiou S.J., Ko C.Y., Lin T.Y. Functional characterization of three ethylene response factor genes from Bupleurum kaoi indicates that BkERFs mediate resistance to Botrytis cinerea. J Plant Physiol 2011, 168:375-381.
24. Livak K.J., Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(T)(-Delta Delta C) method. Methods 2001, 25:402-408.
25. Mare C., Mazzucotelli E., Crosatti C., Francia E., Stanca A.M., Cattivelli L. Hv-WRKY38: a new transcription factor involved in cold- and drought-response in barley. Plant Mol Biol 2004, 55:399-416.
26. McGrath K.C., Dombrecht B., Manners J.M., Schenk P.M., Edgar C.I., Maclean D.J., et al. Repressor- and activator-type ethylene response factors functioning in jasmonate signaling and disease resistance identified via a genome-wide screen of Arabidopsis transcription factor gene expression. Plant Physiol 2005, 139:949-959.
27. Meng X., Li F., Liu C., Zhang C., Wu Z., Chen Y. Isolation and characterization of an ERF transcription factor gene from cotton (Gossypium barbadense L.). Plant Mol Biol Rep 2010, 28:176-183.
28. Nakano T., Suzuki K., Fujimura T., Shinshi H. Genome-wide analysis of the ERF gene family in Arabidopsis and rice. Plant Physiol 2006, 140:411-432.
29. Nishiuchi T., Suzuki K., Kitajima S., Sato F., Shinshi H. Wounding activates immediate early transcription of genes for ERFs in tobacco plants. Plant Mol Biol 2002, 49:473-482.
30. Ohta M., Ohme-Takagi M., Shinshi H. Three ethylene-responsive transcription factors in tobacco with distinct transactivation functions. Plant J 2000, 22:29-38.
31. Onate-Sanchez L., Anderson J.P., Young J., Singh K.B. AtERF14, a member of the ERF family of transcription factors, plays a nonredundant role in plant defense. Plant Physiol January 2007, 143:400-409.
32. Pauquet J., Bouquet A., This P., Adam-Blondon A.F. Establishment of a local map of AFLP markers around the powdery mildew resistance gene Run1 in grapevine and assessment of their usefulness for marker assisted selection. Theor Appl Genet 2001, 103:1201-1210.
33. Peng S., Zhu Z., Zhao K., Shi J., Yang Y., He M., Wang Y. A novel heat shock transcription factor, VpHsf1, from Chinese Wild Vitis pseudoreticulata is involved in biotic and abiotic stresses. Plant Mol Biol Rep 2013, 31:240-247.
34. Quan R., Hu S., Zhang Z., Zhang H., Zhang Z., Huang R. Overexpression of an ERF transcriptionfactor TSRF1 improves rice drought tolerance. Plant Biotechnol J 2010, 8:476-488.
35. Rabbani M.A., Maruyma K., Abe H., Khan M.A., Katsura K., Ito Y., et al. Monitoring expression profiles of rice genes under cold, drought, and high-salinity stresses and abscisic acid application using cDNA microarray and RNA gel-blot analyses. Plant Physiol 2003, 133:1755-1767.
36. Sakuma Y., Liu Q., Dubouzet J.G., Abe H., Shinozaki K., Yamaguchi-Shinozaki K. DNA-binding specificity of the ERF/AP2 domain of Arabidopsis DREBs, transcription factors involved in dehydration- and cold-inducible gene expression. Biochemi Bioph Res Co 2002, 290:998-1009.
37. Santos-Rosa M., Poutaraud A., Merdinoglu D., Mestre P. Development of a transient expression system in grapevine via agro-infiltration. Plant Cell Rep 2008, 27:1053-1063.
38. Shan W., Marshall J.S., Hardham A.R. Gene expression in germinated cysts of Phytophthora nicotianae. Mol Plant Pathol 2004, 5:317-330.
39. Sherif S., El-Sharkawy I., Paliyath G., Jayasankar S. Differential expression of peach ERF transcriptional activators in response to signaling molecules and inoculation with Xanthomonas campestris pv. pruni. J Plant Physiol 2012, 169:731-739.
40. Song Y., Lin Y., Tong S., Hou H. Molecular cloning, promoter analysis, and expression profile of VvERF3b gene in Vitis vinifera. Biol Plantarum 2012, 56:31-36.
41. Sun Q.H., Gao F., Zhao L., Li K.P., Zhang J.R. Identification of a new 130 bp cis-acting element in the TsVP1 promoter involved in the salt stress response from Thellungiella halophila. BMC Plant Biol 2010, 10:90.
42. Swamy P.M., Smith B.N. Role of abscisic acid in plant stress tolerance. Curr Sci 1999, 76:1220-1227.
43. Thilmony R.L., Chen Z.T., Bressan R.A., Martin G.B. Expression of the tomato Pto gene in tobacco enhances resistance to Pseudomonas-Syringae Pv Tabaci expressing avrPto. Plant Cell 1995, 7:1529-1536.
44. Tian Y., Zhang H.W., Pan X.W., Chen X.L., Zhang Z.J., Lu X.Y., et al. Overexpression of ethylene response factor TERF2 confers cold tolerance in rice seedlings. Transgenic Res 2011, 20:857-866.
45. Velasco R., Zharkikh A., Troggio M., Cartwright D.A., Cestaro A., Pruss D., et al. A high quality draft consensus sequence of the genome of a heterozygous grapevine variety. PLoS ONE 2007, 2:e1326.
46. Vomastek T., Iwanicki M.P., Schaeffer H., Tarcsafalvi A., Parsons J.T., Weber M.J. RACK1 targets the extracellular signal-regulated kinase/mitogen-activated protein kinase pathway to link integrin engagement with focal adhesion disassembly and cell motility. Mol Cell Biol 2007, 27:8296-8305.
47. Wan Y., Schwaninger H., He P., Wang Y. Comparison of resistance to powdery mildew and downy mildew in Chinese wild grapes. Vitis 2007, 46:132-136.
48. Wang Y., Liu Y., He P., Chen J., Lamikanra O., Lu J. Evaluation of foliar resistance to uncinula necator in Chinese wild vitis species. Vitis 1995, 34:159-164.
49. Xu W., Yu Y., Ding J., Hua Z., Wang Y. Characterization of a novel stilbene synthase promoter involved in pathogen- and stress-inducible expression from Chinese wild Vitis pseudoreticulata. Planta 2010, 231:475-487.
50. Xu Y., Chang P.F.L., Liu D., Narasimhan M.L., Raghothama K.G., Hasegawa P.M., et al. Plant defense genes are synergistically induced by ethylene and methyl jasmonate. Plant Cell 1994, 6:1077-1085.
51. Xu Z.S., Xia L.Q., Chen M., Cheng X.G., Zhang R.Y., Li L.C., et al. Isolation and molecular characterization of the Triticum aestivum L. ethylene-responsive factor 1 (TaERF1) that increases multiple stress tolerance. Plant Mol Biol 2007, 65:719-732.
52. Yu Y., Xu W., Wang S., Xu Y., Li H., Wang Y., et al. VpRFP1, a novel C4C4-type RING finger protein gene from Chinese wild Vitis pseudoreticulata, functions as a transcriptional activator in defence response of grapevine. J Exp Bot 2011, 62:5671-5682.
53. Yu Y., Xu W., Wang J., Wang L., Yao W., Xu Y., et al. A core functional region of the RFP1 promoter from Chinese wild grapevine is activated by powdery mildew pathogen and heat stress. Planta Planta 2013, 237:293-303.
54. Zhang G., Chen M., Li L., Xu Z., Chen X., Guo J., et al. Overexpression of the soybean GmERF3 gene, an AP2/ERF type transcription factor for increased tolerances to salt, drought, and diseases in transgenic tobacco. J Exp Bot 2009, 60:3781-3796.
55. Zhang H., Liu W., Wan L., Li F., Dai L., Li D., et al. Functional analyses of ethylene response factor JERF3 with the aim of improving tolerance to drought and osmotic stress in transgenic rice. Transgenic Res 2010, 19:809-818.
56. Zhang J., Wang Y.J., Wang X.P. An improved method for rapidly extracting total RNA from Vitis. J Fruit Sci 2003, 178-181. (in Chinese).
57. Zhang Z., Li F., Li D., Zhang H., Huang R. Expression of ethylene response factor JERF1 in rice improves tolerance to drought. Planta 2010, 232:765-774.
58. Zhang Z., Wang J., Zhang R., Huang R. The ethylene response factor AtERF98 enhances tolerance to salt through the transcriptional activation of ascorbic acid synthesis in Arabidopsis. Plant J 2012, 71:273-287.
59. Zhang Z., Yao W., Dong N., Liang H., Liu H., Huang R. A novel ERF transcription activator in wheat and its induction kinetics after pathogen and hormone treatments. J Exp Bot 2007, 58:2993-3003.
60. Zhu Q., Zhang J., Gao X., Tong J., Xiao L., Li W., et al. The Arabidopsis AP2/ERF transcription factor RAP2.6 participates in ABA, salt and osmotic stress responses. Gene 2010, 457:1-12.
61. Zhu Z., Shi J., Cao J., He M., Cao J., Wang Y. VpWRKY3, a biotic and abiotic stress-related transcription factor from the Chinese wild Vitis pseudoreticulata. Plant Cell Rep 2012, 31:2109-2120.
62. Zhu Z., Shi J., He M., Cao J., Wang Y. Isolation and functional characterization of a transcription factor VpNAC1 from Chinese wild Vitis pseudoreticulata. Biotechnol Lett 2012, 34:1335-1342.