A. Bleecker and H. Kende, Ethylene: A Gaseous Signal Molecule in Plants, Annual Review of Cell and Developmental Biology, vol.16, issue.1, pp.1-18, 2000.
DOI : 10.1146/annurev.cellbio.16.1.1

P. Johnson and J. Ecker, THE ETHYLENE GAS SIGNAL TRANSDUCTION PATHWAY: A Molecular Perspective, Annual Review of Genetics, vol.32, issue.1, pp.227-254, 1998.
DOI : 10.1146/annurev.genet.32.1.227

J. Pirrello, F. Jaimes-miranda, M. Sanchez-ballesta, B. Tournier, Q. Khalil-ahmad et al., Sl-ERF2, a Tomato Ethylene Response Factor Involved in Ethylene Response and Seed Germination, Plant and Cell Physiology, vol.47, issue.9, pp.1195-1205, 2006.
DOI : 10.1093/pcp/pcj084

L. Benavente and J. Alonso, Molecular mechanisms of ethylene signaling in Arabidopsis, Molecular BioSystems, vol.102, issue.3-4, pp.165-173, 2006.
DOI : 10.1039/b513874d

M. Ohme-takagi and H. Shinshi, Ethylene-Inducible DNA Binding Proteins That Interact with an Ethylene-Responsive Element, THE PLANT CELL ONLINE, vol.7, issue.2, pp.173-182, 1995.
DOI : 10.1105/tpc.7.2.173

R. Solano, A. Stepanova, Q. Chao, and J. Ecker, Nuclear events in ethylene signaling: a transcriptional cascade mediated by ETHYLENE-INSENSITIVE3 and ETHYLENE-RESPONSE-FACTOR1, Genes & Development, vol.12, issue.23, pp.3703-3714, 1998.
DOI : 10.1101/gad.12.23.3703

J. Riechmann, J. Heard, G. Martin, L. Reuber, C. Jiang et al., Arabidopsis Transcription Factors: Genome-Wide Comparative Analysis Among Eukaryotes, Science, vol.290, issue.5499, pp.2105-2110, 2000.
DOI : 10.1126/science.290.5499.2105

K. Jofuku, B. Boer, M. Van-montagu, and J. Okamuro, Control of Arabidopsis Flower and Seed Development by the Homeotic Gene APETALA2, THE PLANT CELL ONLINE, vol.6, issue.9, pp.1211-1225, 1994.
DOI : 10.1105/tpc.6.9.1211

Y. Kagaya, K. Ohmiya, and T. Hattori, RAV1, a novel DNA-binding protein, binds to bipartite recognition sequence through two distinct DNA-binding domains uniquely found in higher plants, Nucleic Acids Research, vol.27, issue.2, pp.470-478, 1999.
DOI : 10.1093/nar/27.2.470

Y. Sakuma, Q. Liu, J. Dubouzet, H. Abe, K. Shinozaki et al., DNA-Binding Specificity of the ERF/AP2 Domain of Arabidopsis DREBs, Transcription Factors Involved in Dehydration- and Cold-Inducible Gene Expression, Biochemical and Biophysical Research Communications, vol.290, issue.3, pp.998-1009, 2002.
DOI : 10.1006/bbrc.2001.6299

M. Allen, K. Yamasaki, M. Ohme-takagi, M. Tateno, and M. Suzuki, A novel mode of DNA recognition by a ??-sheet revealed by the solution structure of the GCC-box binding domain in complex with DNA, The EMBO Journal, vol.17, issue.18, pp.5484-5496, 1998.
DOI : 10.1093/emboj/17.18.5484

S. Nole-wilson and B. Krizek, DNA binding properties of the Arabidopsis floral development protein AINTEGUMENTA, Nucleic Acids Research, vol.28, issue.21, pp.4076-4082, 2000.
DOI : 10.1093/nar/28.21.4076

T. Nakano, K. Suzuki, T. Fujimura, and H. Shinshi, Genome-Wide Analysis of the ERF Gene Family in Arabidopsis and Rice, PLANT PHYSIOLOGY, vol.140, issue.2, pp.411-432, 2006.
DOI : 10.1104/pp.105.073783

J. Zhuang, B. Cai, R. Peng, B. Zhu, J. X. Xue et al., Genome-wide analysis of the AP2/ERF gene family in Populus trichocarpa, Biochemical and Biophysical Research Communications, vol.371, issue.3, pp.468-474, 2008.
DOI : 10.1016/j.bbrc.2008.04.087

G. Zhang, M. Chen, X. Chen, Z. Xu, S. Guan et al., Phylogeny, gene structures, and expression patterns of the ERF gene family in soybean (Glycine max L.), Journal of Experimental Botany, vol.59, issue.15, pp.4095-4107, 2008.
DOI : 10.1093/jxb/ern248

S. Fujimoto, M. Ohta, A. Usui, H. Shinshi, and M. Ohme-takagi, Arabidopsis Ethylene-Responsive Element Binding Factors Act as Transcriptional Activators or Repressors of GCC Box-Mediated Gene Expression, THE PLANT CELL ONLINE, vol.12, issue.3, pp.393-404, 2000.
DOI : 10.1105/tpc.12.3.393

B. Tournier, M. Sanchez-ballesta, B. Jones, E. Pesquet, F. Regad et al., New members of the tomato ERF family show specific expression pattern and diverse DNA-binding capacity to the GCC box element, FEBS Letters, vol.5, issue.1-3, pp.149-154, 2003.
DOI : 10.1016/S0014-5793(03)00757-9

S. Chakravarthy, R. Tuori, D. Ascenzo, M. Fobert, P. Despres et al., The Tomato Transcription Factor Pti4 Regulates Defense-Related Gene Expression via GCC Box and Non-GCC Box cis Elements, THE PLANT CELL ONLINE, vol.15, issue.12, pp.3033-3050, 2003.
DOI : 10.1105/tpc.017574

K. Sasaki, I. Mitsuhara, S. Seo, H. Ito, H. Matsui et al., Two novel AP2/ERF domain proteins interact with cis-element VWRE for wound-induced expression of the Tobacco tpoxN1 gene, The Plant Journal, vol.6, issue.6, pp.1079-1092, 2007.
DOI : 10.1111/j.1365-313X.2007.03111.x

Y. Gu, C. Yang, V. Thara, J. Zhou, and G. Martin, Pti4 Is Induced by Ethylene and Salicylic Acid, and Its Product Is Phosphorylated by the Pto Kinase, THE PLANT CELL ONLINE, vol.12, issue.5, pp.771-786, 2000.
DOI : 10.1105/tpc.12.5.771

S. Yamamoto, K. Suzuki, and H. Shinshi, Elicitor-responsive, ethylene-independent activation of GCC box-mediated transcription that is regulated by both protein phosphorylation and dephosphorylation in cultured tobacco cells, The Plant Journal, vol.11, issue.5, pp.571-579, 1999.
DOI : 10.1093/emboj/16.11.3207

J. Dubouzet, Y. Sakuma, Y. Ito, M. Kasuga, E. Dubouzet et al., L., encode transcription activators that function in drought-, high-salt- and cold-responsive gene expression, The Plant Journal, vol.6, issue.4, pp.751-763, 2003.
DOI : 10.1046/j.1365-313X.2003.01661.x

Q. Liu, M. Kasuga, Y. Sakuma, H. Abe, S. Miura et al., Two Transcription Factors, DREB1 and DREB2, with an EREBP/AP2 DNA Binding Domain Separate Two Cellular Signal Transduction Pathways in Drought- and Low-Temperature-Responsive Gene Expression, Respectively, in Arabidopsis, THE PLANT CELL ONLINE, vol.10, issue.8, pp.1391-1406, 1998.
DOI : 10.1105/tpc.10.8.1391

E. Stockinger, S. Gilmour, and M. Thomashow, Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/DRE, a cis-acting DNA regulatory element that stimulates transcription in response to low temperature and water deficit, Proceedings of the National Academy of Sciences, vol.94, issue.3, pp.1035-1040, 1997.
DOI : 10.1073/pnas.94.3.1035

A. Aharoni, S. Dixit, R. Jetter, E. Thoenes, G. Van-arkel et al., The SHINE Clade of AP2 Domain Transcription Factors Activates Wax Biosynthesis, Alters Cuticle Properties, and Confers Drought Tolerance when Overexpressed in Arabidopsis, THE PLANT CELL ONLINE, vol.16, issue.9, pp.2463-2480, 2004.
DOI : 10.1105/tpc.104.022897

P. Broun, P. Poindexter, E. Osborne, C. Jiang, and J. Riechmann, WIN1, a transcriptional activator of epidermal wax accumulation in Arabidopsis, Proceedings of the National Academy of Sciences, vol.101, issue.13, pp.4706-4711, 2004.
DOI : 10.1073/pnas.0305574101

L. Van-der-fits and J. Memelink, ORCA3, a Jasmonate-Responsive Transcriptional Regulator of Plant Primary and Secondary Metabolism, Science, vol.289, issue.5477, pp.295-297, 2000.
DOI : 10.1126/science.289.5477.295

J. Zhang, C. Broeckling, E. Blancaflor, M. Sledge, L. Sumner et al., Overexpression of WXP1, a putative Medicago truncatula AP2 domain-containing transcription factor gene, increases cuticular wax accumulation and enhances drought tolerance in transgenic alfalfa (Medicago sativa), The Plant Journal, vol.6, issue.5, pp.689-707, 2005.
DOI : 10.1111/j.1365-313X.2005.02405.x

H. Banno, Y. Ikeda, Q. Niu, and N. Chua, Overexpression of Arabidopsis ESR1 Induces Initiation of Shoot Regeneration, THE PLANT CELL ONLINE, vol.13, issue.12, pp.2609-2618, 2001.
DOI : 10.1105/tpc.13.12.2609

G. Chuck, M. Muszynski, E. Kellogg, S. Hake, and R. Schmidt, The Control of Spikelet Meristem Identity by the branched silkless1 Gene in Maize, Science, vol.298, issue.5596, pp.1238-1241, 2002.
DOI : 10.1126/science.1076920

E. Van-der-graaff, A. Dulk-ras, P. Hooykaas, and B. Keller, Activation tagging of the LEAFY PETIOLE gene affects leaf petiole development in Arabidopsis thaliana, Development, vol.127, pp.4971-4980, 2000.

W. Chen, N. Provart, J. Glazebrook, F. Katagiri, H. Chang et al., Expression Profile Matrix of Arabidopsis Transcription Factor Genes Suggests Their Putative Functions in Response to Environmental Stresses, THE PLANT CELL ONLINE, vol.14, issue.3, pp.559-574, 2002.
DOI : 10.1105/tpc.010410

J. Park, C. Park, S. Lee, B. Ham, R. Shin et al., Overexpression of the Tobacco Tsi1 Gene Encoding an EREBP/AP2-Type Transcription Factor Enhances Resistance against Pathogen Attack and Osmotic Stress in Tobacco, THE PLANT CELL ONLINE, vol.13, issue.5, pp.1035-1046, 2001.
DOI : 10.1105/tpc.13.5.1035

R. Brown, K. Kazan, K. Mcgrath, D. Maclean, and J. Manners, A Role for the GCC-Box in Jasmonate-Mediated Activation of the PDF1.2 Gene of Arabidopsis, PLANT PHYSIOLOGY, vol.132, issue.2, pp.1020-1032, 2003.
DOI : 10.1104/pp.102.017814

O. Lorenzo, R. Piqueras, J. Sánchez-serrano, and R. Solano, ETHYLENE RESPONSE FACTOR1 Integrates Signals from Ethylene and Jasmonate Pathways in Plant Defense, THE PLANT CELL ONLINE, vol.15, issue.1, pp.165-178, 2003.
DOI : 10.1105/tpc.007468

N. Wehner, L. Hartmann, A. Ehlert, S. Böttner, L. Oñate-sánchez et al., High-throughput protoplast transactivation (PTA) system for the analysis of Arabidopsis transcription factor function, The Plant Journal, vol.39, issue.3, pp.560-569, 2011.
DOI : 10.1111/j.1365-313X.2011.04704.x

S. Altschul, W. Gish, W. Miller, E. Myers, and D. Lipman, Basic local alignment search tool, Journal of Molecular Biology, vol.215, issue.3, pp.403-410, 1990.
DOI : 10.1016/S0022-2836(05)80360-2

S. Sato and . Consortium, The tomato genome sequence provides insights into fleshy fruit evolution, Nature, vol.63, issue.7400, pp.635-641, 2012.
DOI : 10.1038/nature11119

M. Sharma, R. Kumar, A. Solanke, R. Sharma, A. Tyagi et al., Identification, phylogeny, and transcript profiling of ERF family genes during development and abiotic stress treatments in tomato, Molecular Genetics and Genomics, vol.391, issue.6, pp.455-475, 2010.
DOI : 10.1007/s00438-010-0580-1

J. Zhou, X. Tang, and G. Martin, The Pto kinase conferring resistance to tomato bacterial speck disease interacts with proteins that bind a cis-element of pathogenesis-related genes, The EMBO Journal, vol.16, issue.11, pp.3207-3218, 1997.
DOI : 10.1093/emboj/16.11.3207

Z. Huang, Z. Zhang, X. Zhang, H. Zhang, D. Huang et al., Tomato TERF1 modulates ethylene response and enhances osmotic stress tolerance by activating expression of downstream genes, FEBS Letters, vol.12, issue.1-3, pp.110-116, 2004.
DOI : 10.1016/j.febslet.2004.07.064

H. Zhang, D. Zhang, J. Chen, Y. Yang, Z. Huang et al., Tomato stress-responsive factor TSRF1 interacts with ethylene responsive element GCC box and regulates pathogen resistance to Ralstonia solanacearum, Plant Molecular Biology, vol.16, issue.Suppl, pp.825-834, 2004.
DOI : 10.1007/s11103-005-2140-3

Y. Pan, G. Seymour, C. Lu, Z. Hu, X. Chen et al., An ethylene response factor (ERF5) promoting adaptation to drought and salt tolerance in tomato, Plant Cell Reports, vol.60, issue.2, pp.349-360, 2012.
DOI : 10.1007/s00299-011-1170-3

H. Wang, Z. Huang, Q. Chen, Z. Zhang, H. Zhang et al., Ectopic overexpression of tomato JERF3 in tobacco activates downstream gene expression and enhances salt tolerance, Plant Molecular Biology, vol.16, issue.2, pp.183-192, 2004.
DOI : 10.1007/s11103-004-0113-6

S. Kagale and K. Rozwadowski, EAR motif-mediated transcriptional repression in plants, Epigenetics, vol.59, issue.2, pp.141-146, 2011.
DOI : 10.1111/j.1365-313X.2010.04112.x

N. Gutterson and T. Reuber, Regulation of disease resistance pathways by AP2/ERF transcription factors, Current Opinion in Plant Biology, vol.7, issue.4, pp.465-471, 2004.
DOI : 10.1016/j.pbi.2004.04.007

F. Licausi, M. Kosmacz, D. Weits, B. Giuntoli, F. Giorgi et al., Oxygen sensing in plants is mediated by an N-end rule pathway for protein destabilization, Nature, vol.2, issue.7373, pp.419-422, 2011.
DOI : 10.1038/nature10536

A. Andriankaja, A. Boisson-dernier, L. Frances, L. Sauviac, A. Jauneau et al., AP2-ERF Transcription Factors Mediate Nod Factor Dependent Mt ENOD11 Activation in Root Hairs via a Novel cis-Regulatory Motif, THE PLANT CELL ONLINE, vol.19, issue.9, pp.2866-2885, 2007.
DOI : 10.1105/tpc.107.052944

L. Wu, X. Chen, H. Ren, Z. Zhang, H. Zhang et al., ERF protein JERF1 that transcriptionally modulates the expression of abscisic acid biosynthesis-related gene enhances the tolerance under salinity and cold in tobacco, Planta, vol.53, issue.Suppl, pp.815-825, 2007.
DOI : 10.1007/s00425-007-0528-9

Z. Xu, L. Xia, M. Chen, X. Cheng, R. Zhang et al., Isolation and molecular characterization of the Triticum aestivum L. ethylene-responsive factor 1 (TaERF1) that increases multiple stress tolerance, Plant Molecular Biology, vol.16, issue.6, pp.719-732, 2007.
DOI : 10.1007/s11103-007-9237-9

J. Jung, S. Won, S. Suh, H. Kim, R. Wing et al., The barley ERF-type transcription factor HvRAF confers enhanced pathogen resistance and salt tolerance in Arabidopsis, Planta, vol.102, issue.3, pp.575-588, 2007.
DOI : 10.1007/s00425-006-0373-2

G. Chen, Z. Hu, and D. Grierson, Differential regulation of tomato ethylene responsive factor LeERF3b, a putative repressor, and the activator Pti4 in ripening mutants and in response to environmental stresses, Journal of Plant Physiology, vol.165, issue.6, pp.662-670, 2008.
DOI : 10.1016/j.jplph.2007.03.006

A. Hirota, T. Kato, H. Fukaki, M. Aida, and M. Tasaka, The Auxin-Regulated AP2/EREBP Gene PUCHI Is Required for Morphogenesis in the Early Lateral Root Primordium of Arabidopsis, THE PLANT CELL ONLINE, vol.19, issue.7, pp.2156-2168, 2007.
DOI : 10.1105/tpc.107.050674

A. Lehman, R. Black, and J. Ecker, HOOKLESS1, an Ethylene Response Gene, Is Required for Differential Cell Elongation in the Arabidopsis Hypocotyl, Cell, vol.85, issue.2, pp.183-194, 1996.
DOI : 10.1016/S0092-8674(00)81095-8

V. Raz and J. Ecker, Regulation of differential growth in the apical hook of Arabidopsis, Development, vol.126, pp.3661-3668, 1999.

J. Masucci and J. Schiefelbein, The rhd6 Mutation of Arabidopsis thaliana Alters Root-Hair Initiation through an Auxin- and Ethylene-Associated Process, Plant Physiology, vol.106, issue.4, pp.1335-1346, 1994.
DOI : 10.1104/pp.106.4.1335

R. Pitts, A. Cernac, and M. Estelle, Auxin and ethylene promote root hair elongation inArabidopsis, The Plant Journal, vol.222, issue.5, pp.553-560, 1998.
DOI : 10.1126/science.277.5329.1113

A. Rahman, T. Amakawa, N. Goto, and S. Tsurumi, Auxin is a Positive Regulator for Ethylene-Mediated Response in the Growth of Arabidopsis Roots, Plant and Cell Physiology, vol.42, issue.3, pp.301-307, 2001.
DOI : 10.1093/pcp/pce035

R. Harper, E. Stowe-evans, D. Luesse, H. Muto, K. Tatematsu et al., The NPH4 Locus Encodes the Auxin Response Factor ARF7, a Conditional Regulator of Differential Growth in Aerial Arabidopsis Tissue, THE PLANT CELL ONLINE, vol.12, issue.5, pp.757-770, 2000.
DOI : 10.1105/tpc.12.5.757

S. Chaabouni, B. Jones, C. Delalande, H. Wang, Z. Li et al., Sl-IAA3, a tomato Aux/IAA at the crossroads of auxin and ethylene signalling involved in differential growth, Journal of Experimental Botany, vol.60, issue.4, pp.1349-1362, 2009.
DOI : 10.1093/jxb/erp009

C. Chaabouni, A. Latché, J. Pech, and M. Bouzayen, Tomato Aux/IAA3 and HOOKLESS are important actors of the interplay between auxin and ethylene during apical hook formation, Plant Signal Behav, vol.4, pp.559-560, 2009.

H. Wang, N. Schauer, B. Usadel, P. Frasse, M. Zouine et al., Regulatory Features Underlying Pollination-Dependent and -Independent Tomato Fruit Set Revealed by Transcript and Primary Metabolite Profiling, THE PLANT CELL ONLINE, vol.21, issue.5, pp.1428-1452, 2009.
DOI : 10.1105/tpc.108.060830

H. Wang, B. Jones, Z. Li, P. Frasse, C. Delalande et al., The Tomato Aux/IAA Transcription Factor IAA9 Is Involved in Fruit Development and Leaf Morphogenesis, THE PLANT CELL ONLINE, vol.17, issue.10, pp.2676-2692, 2005.
DOI : 10.1105/tpc.105.033415

N. Saitou and M. Nei, The neighbor-joining method: a new method for reconstructing phylogenetic trees, Mol Biol Evol, vol.4, pp.406-425, 1987.

N. Takezaki, F. Figueroa, Z. Zaleska-rutczynska, N. Takahata, and J. Klein, The Phylogenetic Relationship of Tetrapod, Coelacanth, and Lungfish Revealed by the Sequences of Forty-Four Nuclear Genes, Molecular Biology and Evolution, vol.21, issue.8, pp.1512-1524, 2004.
DOI : 10.1093/molbev/msh150

E. Zuckerkandl and L. Pauling, In Evolving Genes and Proteins: Evolutionary divergence and convergence in proteins, H.J, vol.1965, pp.97-166

K. Tamura, J. Dudley, M. Nei, and S. Kumar, MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0, Molecular Biology and Evolution, vol.24, issue.8, pp.1596-1599, 2007.
DOI : 10.1093/molbev/msm092

T. Bailey and C. Elkan, Fitting a mixture model by expectation maximization to discover motifs in biopolymers, Proc Int Conf Intell Syst Mol Biol, vol.2, pp.28-36, 1994.