D. B. Egli, SOYPOD: A Model of Fruit Set in Soybean, Agronomy Journal, vol.102, issue.1, pp.39-47, 2010.
DOI : 10.2134/agronj2009.0222

A. M. Wubs, Quantifying abortion rates of reproductive organs and effects of contributing factors using time-to-event analysis, Functional Plant Biology, vol.38, issue.5, pp.431-440, 2011.
DOI : 10.1071/FP10249

L. M. Jablonski, Plant reproduction under elevated CO2 conditions: a meta-analysis of reports on 79 crop and wild species, New Phytologist, vol.89, issue.1, pp.9-26, 2002.
DOI : 10.1071/PP00043

D. W. Lawlor, Carbon and nitrogen assimilation in relation to yield: mechanisms are the key to understanding production systems, Journal of Experimental Botany, vol.53, issue.370, pp.773-787, 2002.
DOI : 10.1093/jexbot/53.370.773

Q. Tan, Increased Phloem Transport of S-Methylmethionine Positively Affects Sulfur and Nitrogen Metabolism and Seed Development in Pea Plants, PLANT PHYSIOLOGY, vol.154, issue.4, pp.1886-1896, 2010.
DOI : 10.1104/pp.110.166389

M. J. Foulkes, Raising yield potential of wheat. III. Optimizing partitioning to grain while maintaining lodging resistance, Journal of Experimental Botany, vol.62, issue.2, pp.469-486, 2011.
DOI : 10.1093/jxb/erq300

L. Urban, Interpreting the decrease in leaf photosynthesis during flowering in mango, Tree Physiology, vol.28, issue.7, pp.1025-1036, 2008.
DOI : 10.1093/treephys/28.7.1025

URL : https://hal.archives-ouvertes.fr/hal-00964538

K. Wingenter, Increased Activity of the Vacuolar Monosaccharide Transporter TMT1 Alters Cellular Sugar Partitioning, Sugar Signaling, and Seed Yield in Arabidopsis, PLANT PHYSIOLOGY, vol.154, issue.2, pp.665-677, 2010.
DOI : 10.1104/pp.110.162040

E. D. Smidansky, Expression of a modified ADP-glucose pyrophosphorylase large subunit in wheat seeds stimulates photosynthesis and carbon metabolism, Planta, vol.119, issue.4, pp.965-976, 2007.
DOI : 10.1007/s00425-006-0400-3

K. H. Jensen, Universality of phloem transport in seed plants, Plant, Cell & Environment, vol.22, issue.3, pp.1065-1076, 2012.
DOI : 10.1111/j.1365-3040.2011.02472.x

D. R. Froelich, Phloem Ultrastructure and Pressure Flow: Sieve-Element-Occlusion-Related Agglomerations Do Not Affect Translocation, The Plant Cell, vol.23, issue.12, pp.4428-4445, 2011.
DOI : 10.1105/tpc.111.093179

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3269875

C. Zhang, 13C-photosynthate accumulation in Japanese pear fruit during the period of rapid fruit growth is limited by the sink strength of fruit rather than by the transport capacity of the pedicel, Journal of Experimental Botany, vol.56, issue.420, pp.2713-2719, 2005.
DOI : 10.1093/jxb/eri264

N. Gould, Direct measurements of sieve element hydrostatic pressure reveal strong regulation after pathway blockage, Functional Plant Biology, vol.31, issue.10, pp.987-993, 2004.
DOI : 10.1071/FP04058

R. Hiyane, Sucrose feeding reverses shade-induced kernel losses in maize, Annals of Botany, vol.106, issue.3, pp.395-403, 2010.
DOI : 10.1093/aob/mcq132

K. Esau, R. Holt, W. Werner, and D. , Vascular Differentiation in Plants A dual switch in phloem unloading during ovule development in Arabidopsis, Protoplasma, vol.248, pp.225-235, 1965.

D. B. Fisher and C. E. Cash-clark, Sieve Tube Unloading and Post-Phloem Transport of Fluorescent Tracers and Proteins Injected into Sieve Tubes via Severed Aphid Stylets, Plant Physiology, vol.123, issue.1, pp.125-137, 2000.
DOI : 10.1104/pp.123.1.125

W. H. Zhang, : Nutrient loading of developing seeds, Functional Plant Biology, vol.34, issue.4, pp.314-331, 2007.
DOI : 10.1071/FP06271

R. Schmidt, The amino acid permease AAP8 is important for early seed development in Arabidopsis thaliana, Planta, vol.40, issue.4, p.805, 2007.
DOI : 10.1007/s00425-007-0527-x

A. Sanders, AAP1 regulates import of amino acids into developing Arabidopsis embryos, The Plant Journal, vol.12, issue.4, pp.540-552, 2009.
DOI : 10.1111/j.1365-313X.2009.03890.x

F. Li, Characterization of Sucrose transporter alleles and their association with seed yield-related traits in Brassica napus L, BMC Plant Biology, vol.11, issue.1, p.168, 2011.
DOI : 10.1006/meth.2001.1262

T. M. Burch-smith and P. C. Zambryski, Plasmodesmata Paradigm Shift: Regulation from Without Versus Within, Annual Review of Plant Biology, vol.63, issue.1, pp.239-260, 2012.
DOI : 10.1146/annurev-arplant-042811-105453

G. Cai, Distribution of Callose Synthase, Cellulose Synthase, and Sucrose Synthase in Tobacco Pollen Tube Is Controlled in Dissimilar Ways by Actin Filaments and Microtubules, PLANT PHYSIOLOGY, vol.155, issue.3, pp.1169-1190, 2011.
DOI : 10.1104/pp.110.171371

A. Castro and C. Clément, Sucrose and starch catabolism in the anther of Lilium during its development: a comparative study among the anther wall, locular fluid and microspore/pollen fractions, Planta, vol.118, issue.6, pp.1573-1582, 2007.
DOI : 10.1007/s00425-006-0443-5

M. Goetz, Induction of male sterility in plants by metabolic engineering of the carbohydrate supply, Proceedings of the National Academy of Sciences, vol.98, issue.11, pp.6522-6527, 2001.
DOI : 10.1073/pnas.091097998

P. K. Koonjul, Selective transcriptional down-regulation of anther invertases precedes the failure of pollen development in waterstressed wheat, J. Exp. Bot, vol.56, pp.179-190, 2005.

S. N. Oliver, ABA Regulates Apoplastic Sugar Transport and is a Potential Signal for Cold-Induced Pollen Sterility in Rice, Plant and Cell Physiology, vol.48, issue.9, pp.1319-1330, 2007.
DOI : 10.1093/pcp/pcm100

E. Pressman, The Effect of Heat Stress on Tomato Pollen Characteristics is Associated with Changes in Carbohydrate Concentration in the Developing Anthers, Annals of Botany, vol.90, issue.5, pp.631-636, 2002.
DOI : 10.1093/aob/mcf240

X. Ji, Importance of pre-anthesis anther sink strength for maintenance of grain number during reproductive stage water stress in wheat, Plant, Cell & Environment, vol.107, issue.Special Issue, pp.926-942, 2010.
DOI : 10.1111/j.1365-3040.2010.02130.x

J. E. Mclaughlin and J. S. Boyer, Glucose Localization in Maize Ovaries When Kernel Number Decreases at Low Water Potential and Sucrose is Fed to the Stems, Annals of Botany, vol.94, issue.1, pp.75-86, 2004.
DOI : 10.1093/aob/mch123

J. E. Mclaughlin and J. S. Boyer, Sugar-responsive Gene Expression, Invertase Activity, and Senescence in Aborting Maize Ovaries at Low Water Potentials, Annals of Botany, vol.94, issue.5, pp.675-689, 2004.
DOI : 10.1093/aob/mch193

M. I. Zanor, RNA Interference of LIN5 in Tomato Confirms Its Role in Controlling Brix Content, Uncovers the Influence of Sugars on the Levels of Fruit Hormones, and Demonstrates the Importance of Sucrose Cleavage for Normal Fruit Development and Fertility, PLANT PHYSIOLOGY, vol.150, issue.3, pp.1204-1218, 2009.
DOI : 10.1104/pp.109.136598

Y. Jin, Posttranslational Elevation of Cell Wall Invertase Activity by Silencing Its Inhibitor in Tomato Delays Leaf Senescence and Increases Seed Weight and Fruit Hexose Level, THE PLANT CELL ONLINE, vol.21, issue.7, pp.2072-2089, 2009.
DOI : 10.1105/tpc.108.063719

X. Sun, Transcriptional and hormonal signaling control of Arabidopsis seed development, Current Opinion in Plant Biology, vol.13, issue.5, pp.611-620, 2010.
DOI : 10.1016/j.pbi.2010.08.009

H. Tanaka, Spatiotemporal asymmetric auxin distribution: a means to coordinate plant development, Cellular and Molecular Life Sciences, vol.63, issue.23, pp.2738-2754, 2006.
DOI : 10.1007/s00018-006-6116-5

M. Riefler, Arabidopsis Cytokinin Receptor Mutants Reveal Functions in Shoot Growth, Leaf Senescence, Seed Size, Germination, Root Development, and Cytokinin Metabolism, THE PLANT CELL ONLINE, vol.18, issue.1, pp.40-54, 2006.
DOI : 10.1105/tpc.105.037796

I. Roxrud, GASA4, One of the 14-Member Arabidopsis GASA Family of Small Polypeptides, Regulates Flowering and Seed Development, Plant and Cell Physiology, vol.48, issue.3, pp.471-483, 2007.
DOI : 10.1093/pcp/pcm016

N. Takahashi, shk1-D, a dwarf Arabidopsis mutant caused by activation of the CYP72C1 gene, has altered brassinosteroid levels, The Plant Journal, vol.7, issue.Suppl., pp.13-22, 2005.
DOI : 10.1111/j.1365-313X.2005.02357.x

S. Tanabe, A Novel Cytochrome P450 Is Implicated in Brassinosteroid Biosynthesis via the Characterization of a Rice Dwarf Mutant, dwarf11, with Reduced Seed Length, THE PLANT CELL ONLINE, vol.17, issue.3, pp.776-790, 2005.
DOI : 10.1105/tpc.104.024950

I. Olimpieri, Tomato fruit set driven by pollination or by the parthenocarpic fruit allele are mediated by transcriptionally regulated gibberellin biosynthesis, Planta, vol.17, issue.Suppl, pp.877-888, 2007.
DOI : 10.1007/s00425-007-0533-z

T. Pandolfini, Molecular dissection of the role of auxin in fruit initiation, Trends in Plant Science, vol.12, issue.8, pp.327-329, 2007.
DOI : 10.1016/j.tplants.2007.06.011

J. C. Serrani, Inhibition of Auxin Transport from the Ovary or from the Apical Shoot Induces Parthenocarpic Fruit-Set in Tomato Mediated by Gibberellins, PLANT PHYSIOLOGY, vol.153, issue.2, pp.851-862, 2010.
DOI : 10.1104/pp.110.155424

P. Hazra, Altered gibberellin and auxin levels in the ovaries in the manifestation of genetic parthenocarpy in tomato (Solanum lycopersicum), Curr. Sci, vol.99, pp.1439-1443, 2010.

G. L. Rotino, Genetic engineering of parthenocarpic plants, Nature Biotechnology, vol.11, issue.13, pp.1398-1401, 1997.
DOI : 10.1016/0304-4238(79)90002-5

N. Carmi, Induction of parthenocarpy in tomato via specific expression of the rolB gene in the ovary, Planta, vol.217, issue.5, pp.726-735, 2003.
DOI : 10.1007/s00425-003-1052-1

J. Wu, Identification, isolation and expression analysis of auxin response factor (ARF) genes in Solanum lycopersicum, Plant Cell Reports, vol.53, issue.11, pp.2059-2073, 2011.
DOI : 10.1007/s00299-011-1113-z

C. Audran-delalande, Genome-Wide Identification, Functional Analysis and Expression Profiling of the Aux/IAA Gene Family in Tomato, Plant and Cell Physiology, vol.53, issue.4, pp.659-672, 2012.
DOI : 10.1093/pcp/pcs022

T. J. Guilfoyle and G. Hagen, Auxin response factors, Current Opinion in Plant Biology, vol.10, issue.5, pp.453-460, 2007.
DOI : 10.1016/j.pbi.2007.08.014

H. Wang, 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

S. Chaabouni, 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

W. Deng, The tomato SlIAA15 is involved in trichome formation and axillary shoot development, New Phytologist, vol.40, issue.2, pp.379-390, 2012.
DOI : 10.1111/j.1469-8137.2012.04053.x

M. Goetz, Expression of Aberrant Forms of AUXIN RESPONSE FACTOR8 Stimulates Parthenocarpy in Arabidopsis and Tomato, PLANT PHYSIOLOGY, vol.145, issue.2, pp.351-366, 2007.
DOI : 10.1104/pp.107.104174

N. Dharmasiri and M. Estelle, Auxin signaling and regulated protein degradation, Trends in Plant Science, vol.9, issue.6, pp.302-308, 2004.
DOI : 10.1016/j.tplants.2004.04.003

J. W. Wang, Control of Root Cap Formation by MicroRNA-Targeted Auxin Response Factors in Arabidopsis, THE PLANT CELL ONLINE, vol.17, issue.8, pp.2204-2216, 2005.
DOI : 10.1105/tpc.105.033076

P. Ru, Plant fertility defects induced by the enhanced expression of microRNA167, Cell Research, vol.52, issue.11, pp.457-465, 2006.
DOI : 10.1038/36856

J. Zhang, A single-base deletion mutation in SlIAA9 gene causes tomato (Solanum lycopersicum) entire mutant, Journal of Plant Research, vol.40, issue.6, pp.671-678, 2007.
DOI : 10.1007/s10265-007-0109-9

J. C. Serrani, Auxin-induced fruit-set in tomato is mediated in part by gibberellins, The Plant Journal, vol.18, issue.6, pp.922-934, 2008.
DOI : 10.1111/j.1365-313X.2008.03654.x

M. Jong, The role of auxin and gibberellin in tomato fruit set, Journal of Experimental Botany, vol.60, issue.5, pp.1523-1532, 2009.
DOI : 10.1093/jxb/erp094

W. H. Vriezen, Changes in tomato ovary transcriptome demonstrate complex hormonal regulation of fruit set, New Phytologist, vol.17, issue.0, pp.60-76, 2008.
DOI : 10.1104/pp.108.3.929

J. C. Serrani, Gibberellin Regulation of Fruit Set and Growth in Tomato, PLANT PHYSIOLOGY, vol.145, issue.1, pp.246-257, 2007.
DOI : 10.1104/pp.107.098335

L. Pascual, Transcriptomic analysis of tomato carpel development reveals alterations in ethylene and gibberellin synthesis during pat3/pat4 parthenocarpic fruit set, BMC Plant Biology, vol.9, issue.1, p.67, 2009.
DOI : 10.1186/1471-2229-9-67

H. Wang, 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

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700536

L. Nitsch, Abscisic acid levels in tomato ovaries are regulated by LeNCED1 and SlCYP707A1, Planta, vol.17, issue.6, pp.1335-1346, 2009.
DOI : 10.1007/s00425-009-0913-7

R. Alba, Transcriptome and Selected Metabolite Analyses Reveal Multiple Points of Ethylene Control during Tomato Fruit Development, THE PLANT CELL ONLINE, vol.17, issue.11, pp.2954-2965, 2005.
DOI : 10.1105/tpc.105.036053

F. Carrari, Integrated Analysis of Metabolite and Transcript Levels Reveals the Metabolic Shifts That Underlie Tomato Fruit Development and Highlight Regulatory Aspects of Metabolic Network Behavior, PLANT PHYSIOLOGY, vol.142, issue.4, pp.1380-1396, 2006.
DOI : 10.1104/pp.106.088534

F. Csukasi, Gibberellin biosynthesis and signalling during development of the strawberry receptacle, New Phytologist, vol.19, issue.2, pp.376-390, 2011.
DOI : 10.1111/j.1469-8137.2011.03700.x

J. Rohrmann, Combined transcription factor profiling, microarray analysis and metabolite profiling reveals the transcriptional control of metabolic shifts occurring during tomato fruit development, The Plant Journal, vol.95, issue.6, pp.999-1013, 2011.
DOI : 10.1111/j.1365-313X.2011.04750.x

R. Karlova, Transcriptome and Metabolite Profiling Show That APETALA2a Is a Major Regulator of Tomato Fruit Ripening, The Plant Cell, vol.23, issue.3, pp.923-941, 2011.
DOI : 10.1105/tpc.110.081273

A. Fait, Reconfiguration of the Achene and Receptacle Metabolic Networks during Strawberry Fruit Development, PLANT PHYSIOLOGY, vol.148, issue.2, pp.730-750, 2008.
DOI : 10.1104/pp.108.120691

V. A. Lombardo, Metabolic Profiling during Peach Fruit Development and Ripening Reveals the Metabolic Networks That Underpin Each Developmental Stage, PLANT PHYSIOLOGY, vol.157, issue.4, pp.1696-1710, 2011.
DOI : 10.1104/pp.111.186064

S. Osorio, ) Mutants Reveals Novel Regulatory Interactions, Plant Physiology, vol.157, issue.1, pp.405-425, 2011.
DOI : 10.1104/pp.111.175463

A. Zamboni, Identification of Putative Stage-Specific Grapevine Berry Biomarkers and Omics Data Integration into Networks, PLANT PHYSIOLOGY, vol.154, issue.3, pp.1439-1459, 2010.
DOI : 10.1104/pp.110.160275

Z. X. Ren, The auxin receptor homologue in Solanum lycopersicum stimulates tomato fruit set and leaf morphogenesis, Journal of Experimental Botany, vol.62, issue.8, pp.2815-2826, 2011.
DOI : 10.1093/jxb/erq455

M. Jong, The Solanum lycopersicum AUXIN RESPONSE FACTOR 7 (SlARF7) mediates cross-talk between auxin and gibberellin signalling during tomato fruit set and development, Journal of Experimental Botany, vol.62, issue.2, pp.617-626, 2011.
DOI : 10.1093/jxb/erq293

M. Egea-cortines, Polyamine levels in pollinated and auxin-induced fruit of tomato (Lycopersicon esculentum) during development, Physiologia Plantarum, vol.83, issue.1, pp.14-20, 1993.
DOI : 10.1007/BF00117588

K. L. Bologa, A Bypass of Sucrose Synthase Leads to Low Internal Oxygen and Impaired Metabolic Performance in Growing Potato Tubers, PLANT PHYSIOLOGY, vol.132, issue.4, pp.2058-2072, 2003.
DOI : 10.1104/pp.103.022236

A. Hackel, Sucrose transporter LeSUT1 and LeSUT2 inhibition affects tomato fruit development in different ways, The Plant Journal, vol.12, issue.2, pp.180-192, 2006.
DOI : 10.1111/j.1365-313X.2005.02572.x

L. Q. Chen, Sucrose Efflux Mediated by SWEET Proteins as a Key Step for Phloem Transport, Science, vol.335, issue.6065, pp.207-211, 2012.
DOI : 10.1126/science.1213351

URL : http://hdl.handle.net/11858/00-001M-0000-0014-2021-3

E. Fridman, Zooming In on a Quantitative Trait for Tomato Yield Using Interspecific Introgressions, Science, vol.305, issue.5691, pp.1786-1789, 2004.
DOI : 10.1126/science.1101666

N. Schauer, Comprehensive metabolic profiling and phenotyping of interspecific introgression lines for tomato improvement, Nature Biotechnology, vol.2, issue.4, pp.447-454, 2006.
DOI : 10.1038/nbt1192

T. D. Phuc, The influence of fruit load on the tomato pericarp metabolome in a Solanum chmielewskii introgression line population, Plant Physiol, vol.154, pp.1128-1142, 2010.

G. Gillaspy, Fruits: A Developmental Perspective, THE PLANT CELL ONLINE, vol.5, issue.10, pp.1439-1451, 1993.
DOI : 10.1105/tpc.5.10.1439

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC160374

B. Piechulla, Changes in Photosynthetic Capacity and Photosynthetic Protein Pattern during Tomato Fruit Ripening, PLANT PHYSIOLOGY, vol.84, issue.3, pp.911-917, 1987.
DOI : 10.1104/pp.84.3.911

H. Obiadalla-ali, Inhibition of chloroplastic fructose 1,6-bisphosphatase in tomato fruits leads to decreased fruit size, but only small changes in carbohydrate metabolism, Planta, vol.219, issue.3, pp.533-540, 2004.
DOI : 10.1007/s00425-004-1257-y

I. Kolotilin, Transcriptional Profiling of high pigment-2dg Tomato Mutant Links Early Fruit Plastid Biogenesis with Its Overproduction of Phytonutrients, PLANT PHYSIOLOGY, vol.145, issue.2, pp.389-401, 2007.
DOI : 10.1104/pp.107.102962

A. Lytovchenko, Tomato Fruit Photosynthesis Is Seemingly Unimportant in Primary Metabolism and Ripening But Plays a Considerable Role in Seed Development, PLANT PHYSIOLOGY, vol.157, issue.4, pp.1650-1663, 2011.
DOI : 10.1104/pp.111.186874

A. J. Matas, Tissue- and Cell-Type Specific Transcriptome Profiling of Expanding Tomato Fruit Provides Insights into Metabolic and Regulatory Specialization and Cuticle Formation, The Plant Cell, vol.23, issue.11, pp.3893-3910, 2011.
DOI : 10.1105/tpc.111.091173

L. Yin and H. Xue, The MADS29 Transcription Factor Regulates the Degradation of the Nucellus and the Nucellar Projection during Rice Seed Development, The Plant Cell, vol.24, issue.3, pp.1049-1065, 2012.
DOI : 10.1105/tpc.111.094854

H. J. Klee and J. J. Giovannoni, Genetics and Control of Tomato Fruit Ripening and Quality Attributes, Annual Review of Genetics, vol.45, issue.1, pp.41-59, 2011.
DOI : 10.1146/annurev-genet-110410-132507

D. Orzaez, A Visual Reporter System for Virus-Induced Gene Silencing in Tomato Fruit Based on Anthocyanin Accumulation, PLANT PHYSIOLOGY, vol.150, issue.3, pp.1122-1134, 2009.
DOI : 10.1104/pp.109.139006

L. Quadrana, Coupling Virus-Induced Gene Silencing to Exogenous Green Fluorescence Protein Expression Provides a Highly Efficient System for Functional Genomics in Arabidopsis and across All Stages of Tomato Fruit Development, PLANT PHYSIOLOGY, vol.156, issue.3, pp.1278-1291, 2011.
DOI : 10.1104/pp.111.177345

E. Schijlen, Pathway engineering for healthy phytochemicals leading to the production of novel flavonoids in tomato fruit, Plant Biotechnology Journal, vol.100, issue.4, pp.433-444, 2006.
DOI : 10.1207/s15327914nc4801_14

T. Tohge and A. R. Fernie, Combining genetic diversity, informatics and metabolomics to facilitate annotation of plant gene function, Nature Protocols, vol.17, issue.6, pp.1210-1227, 2010.
DOI : 10.1080/0735-260291044232

Y. Iijima, Metabolite annotations based on the integration of mass spectral information, The Plant Journal, vol.12, issue.5, pp.949-962, 2008.
DOI : 10.1104/pp.105.060376

P. Giavalisco, C Isotope-Labeled Metabolomes Allowing for Improved Compound Annotation and Relative Quantification in Liquid Chromatography-Mass Spectrometry-based Metabolomic Research, Analytical Chemistry, vol.81, issue.15, pp.6546-6551, 2009.
DOI : 10.1021/ac900979e

M. Kojima, Highly Sensitive and High-Throughput Analysis of Plant Hormones Using MS-Probe Modification and Liquid Chromatography-Tandem Mass Spectrometry: An Application for Hormone Profiling in Oryza sativa, Plant and Cell Physiology, vol.50, issue.7, pp.1201-1214, 2009.
DOI : 10.1093/pcp/pcp057

O. Jaillon, The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla The genome of woodland strawberry (Fragaria vesca), Nature Nat. Genet, vol.449, issue.43, pp.463-465, 2007.

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

N. Schauer, Metabolic profiling of leaves and fruit of wild species tomato: a survey of the Solanum lycopersicum complex, Journal of Experimental Botany, vol.56, issue.410, pp.297-307, 2005.
DOI : 10.1093/jxb/eri057

A. R. Fernie and N. Schauer, Metabolomics-assisted breeding: a viable option for crop improvement? Trends Genet, pp.39-48, 2009.

G. Lebon, Sugars and flowering in the grapevine (Vitis vinifera L.), Journal of Experimental Botany, vol.59, issue.10, pp.2565-2578, 2008.
DOI : 10.1093/jxb/ern135

H. O. Ghiglione, Autophagy regulated by day length determines the number of fertile florets in wheat, The Plant Journal, vol.15, issue.6, pp.1010-1024, 2008.
DOI : 10.1111/j.1365-313X.2008.03570.x

M. F. Dreccer, Grain number and grain weight in wheat lines contrasting for stem water soluble carbohydrate concentration, Field Crops Research, vol.112, issue.1, pp.43-54, 2009.
DOI : 10.1016/j.fcr.2009.02.006

L. F. Marcelis, Flower and fruit abortion in sweet pepper in relation to source and sink strength, Journal of Experimental Botany, vol.55, issue.406, pp.2261-2268, 2004.
DOI : 10.1093/jxb/erh245

M. Lemaire-chamley, Changes in Transcriptional Profiles Are Associated with Early Fruit Tissue Specialization in Tomato, PLANT PHYSIOLOGY, vol.139, issue.2, pp.750-769, 2005.
DOI : 10.1104/pp.105.063719

J. Vrebalov, Fleshy Fruit Expansion and Ripening Are Regulated by the Tomato SHATTERPROOF Gene TAGL1, The Plant Cell, vol.21, issue.10, pp.3041-3062, 2009.
DOI : 10.1105/tpc.109.066936

C. Ampomah-dwamena, Down-Regulation of TM29, a Tomato SEPALLATA Homolog, Causes Parthenocarpic Fruit Development and Floral Reversion, PLANT PHYSIOLOGY, vol.130, issue.2, pp.605-617, 2002.
DOI : 10.1104/pp.005223

L. Pnueli, The TM5 MADS Box Gene Mediates Organ Differentiation in the Three Inner Whorls of Tomato Flowers, THE PLANT CELL ONLINE, vol.6, issue.2, pp.175-186, 1994.
DOI : 10.1105/tpc.6.2.175