J. A. Aguilar-martínez, C. Poza-carrión, and P. Cubas, Arabidopsis BRANCHED1 acts as an integrator of branching signals within axillary buds, Plant Cell, vol.19, pp.458-472, 2007.

A. W. Alberts, Discovery, biochemistry and biology of lovastatin, Am J Cardiol, vol.62, pp.10-15, 1988.

I. Antoniadi, L. Pla-cková, B. Simonovik, K. Dole-zal, C. Turnbull et al., Cell-type-specific cytokinin distribution within the Arabidopsis primary root apex, Plant Cell, vol.27, pp.1955-1967, 2015.

J. Balla, P. Kalousek, V. Reinöhl, J. Friml, and S. Procházka, Competitive canalization of PIN-dependent auxin flow from axillary buds controls pea bud outgrowth, Plant J, vol.65, pp.571-577, 2011.

F. Bangerth, Response of cytokinin concentration in the xylem exudate of bean (Phaseolus vulgaris L.) plants to decapitation and auxin treatment, and relationship to apical dominance, Planta, vol.194, pp.439-442, 1994.

F. Barbier, T. Péron, M. Lecerf, M. D. Perez-garcia, Q. Barrière et al., Sucrose is an early modulator of the key hormonal mechanisms controlling bud outgrowth in Rosa hybrida, J Exp Bot, vol.66, pp.2569-2582, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01378956

F. F. Barbier, J. E. Lunn, and C. A. Beveridge, Ready, steady, go! A sugar hit starts the race to shoot branching, Curr Opin Plant Biol, vol.25, pp.39-45, 2015.

T. Bennett, T. Sieberer, B. Willett, J. Booker, C. Luschnig et al., The Arabidopsis MAX pathway controls shoot branching by regulating auxin transport, Curr Biol, vol.16, pp.553-563, 2006.

V. Bergougnoux, D. Zalabák, M. Jandová, O. Novák, A. Wiese-klinkenberg et al., Effect of blue light on endogenous isopentenyladenine and endoreduplication during photomorphogenesis and de-etiolation of tomato (Solanum lycopersicum L.) seedlings, PLoS ONE, vol.7, p.45255, 2012.

S. Bihmidine, C. T. Hunter, . Iii, C. E. Johns, K. E. Koch et al., Regulation of assimilate import into sink organs: update on molecular drivers of sink strength, Front Plant Sci, vol.4, p.177, 2013.

N. Braun, A. De-saint-germain, J. P. Pillot, S. Boutet-mercey, M. Dalmais et al., The pea TCP transcription factor PsBRC1 acts downstream of strigolactones to control shoot branching, Plant Physiol, vol.158, pp.225-238, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01019430

W. G. Brenner, G. A. Romanov, I. Köllmer, L. Bürkle, and T. Schmülling, Immediate-early and delayed cytokinin response genes of Arabidopsis thaliana identified by genome-wide expression profiling reveal novel cytokinin-sensitive processes and suggest cytokinin action through transcriptional cascades, Plant J, vol.44, pp.314-333, 2005.

P. B. Brewer, E. A. Dun, B. J. Ferguson, C. Rameau, and C. A. Beveridge, Strigolactone acts downstream of auxin to regulate bud outgrowth in pea and Arabidopsis, Plant Physiol, vol.150, pp.482-493, 2009.

M. Carabelli, M. Possenti, G. Sessa, A. Ciolfi, M. Sassi et al., Canopy shade causes a rapid and transient arrest in leaf development through auxin-induced cytokinin oxidase activity, Genes Dev, vol.21, pp.1863-1868, 2007.

L. Q. Chen, X. Q. Qu, B. H. Hou, D. Sosso, S. Osorio et al., Sucrose efflux mediated by SWEET proteins as a key step for phloem transport, Science, vol.335, pp.207-211, 2012.

X. Chen, X. Zhou, L. Xi, J. Li, R. Zhao et al., Roles of DgBRC1 in regulation of lateral branching in chrysanthemum (Dendranthema 3 grandiflora cv. Jinba), PLoS ONE, vol.8, p.61717, 2013.

D. Choubane, A. Rabot, E. Mortreau, J. Legourrierec, T. Péron et al., Photocontrol of bud burst involves gibberellin biosynthesis in Rosa sp, J Plant Physiol, vol.169, pp.1271-1280, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00841832

D. N. Crowell and M. S. Salaz, Inhibition of growth of cultured tobacco cells at low concentrations of lovastatin is reversed by cytokinin, Plant Physiol, vol.100, pp.2090-2095, 1992.

I. B. D'agostino, J. Deruère, and J. J. Kieber, Characterization of the response of the Arabidopsis response regulator gene family to cytokinin, Plant Physiol, vol.124, pp.1706-1717, 2000.

, Plant Physiol, vol.172, 2016.

S. Dal-santo, M. Fasoli, E. Cavallini, G. B. Tornielli, M. Pezzotti et al., PhEXPA1, a Petunia hybrida expansin, is involved in cell wall metabolism and in plant architecture specification, Plant Signal Behav, vol.6, pp.2031-2034, 2011.

S. M. De-jager, S. Maughan, W. Dewitte, S. Scofield, and J. Murray, The developmental context of cell-cycle control in plants, Semin Cell Dev Biol, vol.16, pp.385-396, 2005.

S. Demotes-mainard, L. Huché-thélier, P. Morel, R. Boumaza, V. Guérin et al., Temporary water restriction or light intensity limitation promotes branching in rose bush, Sci Hortic (Amsterdam), vol.150, pp.432-440, 2013.

S. Demotes-mainard, T. Péron, A. Corot, J. Bertheloot, L. Gourrierec et al., Plant responses to red and far-red lights, applications in horticulture, Environ Exp Bot, vol.121, pp.4-21, 2016.

M. L. Devitt and J. P. Stafstrom, Cell cycle regulation during growthdormancy cycles in pea axillary buds, Plant Mol Biol, vol.29, pp.255-265, 1995.

S. Djennane, H. Oyant, L. Kawamura, K. Lalanne, D. Laffaire et al., Impacts of light and temperature on shoot branching gradient and expression of strigolactone synthesis and signalling genes in rose, Plant Cell Environ, vol.37, pp.742-757, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01153739

R. S. Drummond, B. J. Janssen, Z. Luo, C. Oplaat, S. E. Ledger et al., Environmental control of branching in petunia, Plant Physiol, vol.168, pp.735-751, 2015.

A. Dubois, S. Carrere, O. Raymond, B. Pouvreau, L. Cottret et al., Transcriptome database resource and gene expression atlas for the rose, BMC Genomics, vol.13, p.638, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00841830

E. A. Dun, A. De-saint-germain, C. Rameau, and C. A. Beveridge, Antagonistic action of strigolactone and cytokinin in bud outgrowth control, Plant Physiol, vol.158, pp.487-498, 2012.
URL : https://hal.archives-ouvertes.fr/hal-01004268

S. El-showk, R. Ruonala, and Y. Helariutta, Crossing paths: cytokinin signalling and crosstalk, Development, vol.140, pp.1373-1383, 2013.

B. J. Ferguson and C. A. Beveridge, Roles for auxin, cytokinin, and strigolactone in regulating shoot branching, Plant Physiol, vol.149, pp.1929-1944, 2009.

S. A. Finlayson, S. R. Krishnareddy, T. H. Kebrom, and J. J. Casal, Phytochrome regulation of branching in Arabidopsis, Plant Physiol, vol.152, pp.1914-1927, 2010.

A. J. Fleming, S. Mcqueen-mason, T. Mandel, and C. Kuhlemeier, Induction of leaf primordia by the cell wall protein expansin, Science, vol.276, pp.1415-1418, 1997.

K. Floková, D. Tarkowská, O. Miersch, M. Strnad, C. Wasternack et al., UHPLC-MS/MS based target profiling of stress-induced phytohormones, Phytochemistry, vol.105, pp.147-157, 2014.

E. Foo, S. E. Morris, K. Parmenter, N. Young, H. Wang et al., Feedback regulation of xylem cytokinin content is conserved in pea and Arabidopsis, Plant Physiol, vol.143, pp.1418-1428, 2007.

I. Frébort, M. Kowalska, T. Hluska, J. Frébortová, and P. Galuszka, Evolution of cytokinin biosynthesis and degradation, J Exp Bot, vol.62, pp.2431-2452, 2011.

P. M. Furet, J. Lothier, S. Demotes-mainard, S. Travier, C. Henry et al., Light and nitrogen nutrition regulate apical control in Rosa hybrida L, J Plant Physiol, vol.171, pp.7-13, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01169241

B. Gillissen, L. Bürkle, B. André, C. Kühn, D. Rentsch et al., A new family of high-affinity transporters for adenine, cytosine, and purine derivatives in Arabidopsis, Plant Cell, vol.12, pp.291-300, 2000.

T. Girault, F. Abidi, M. Sigogne, S. Pelleschi-travier, R. Boumaza et al., Sugars are under light control during bud burst in Rosa sp, Plant Cell Environ, vol.33, pp.1339-1350, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00729623

T. Girault, V. Bergougnoux, D. Combes, J. D. Viemont, and N. Leduc, Light controls shoot meristem organogenic activity and leaf primordia growth during bud burst in Rosa sp, Plant Cell Environ, vol.31, pp.1534-1544, 2008.

E. González-grandío, C. Poza-carrión, C. Sorzano, and P. Cubas, BRANCHED1 promotes axillary bud dormancy in response to shade in Arabidopsis, Plant Cell, vol.25, pp.834-850, 2013.

. Guivarc'h-a, J. Rembur, M. Goetz, T. Roitsch, M. Noin et al., Local expression of the ipt gene in transgenic tobacco (Nicotiana tabacum L. cv. SR1) axillary buds establishes a role for cytokinins in tuberization and sink formation, J Exp Bot, vol.53, pp.621-629, 2002.

I. M. Guseinova, S. Y. Suleimanov, and J. A. Aliyev, The effect of norflurazon on protein composition and chlorophyll organization in pigmentprotein complex of photosystem II, Photosynth Res, vol.84, pp.71-76, 2005.

K. Hartig and E. Beck, Assessment of lovastatin application as tool in probing cytokinin-mediated cell cycle regulation, Physiol Plant, vol.125, pp.260-267, 2005.

A. Hartmann, M. Senning, P. Hedden, U. Sonnewald, and S. Sonnewald, Reactivation of meristem activity and sprout growth in potato tubers require both cytokinin and gibberellin, Plant Physiol, vol.155, pp.776-796, 2011.

C. Henry, A. Rabot, M. Laloi, E. Mortreau, M. Sigogne et al., Regulation of RhSUC2, a sucrose transporter, is correlated with the light control of bud burst in Rosa sp, Plant Cell Environ, vol.34, pp.1776-1789, 2011.
URL : https://hal.archives-ouvertes.fr/hal-01168877

L. Huché-thélier, L. Crespel, L. Gourrierec, J. Morel, P. Sakr et al., Light signaling and plant responses to blue and UV radiations: perspectives for applications in horticulture, Environ Exp Bot, vol.121, pp.22-38, 2016.

I. Hwang, J. Sheen, and B. Müller, Cytokinin signaling networks, Annu Rev Plant Biol, vol.63, pp.353-380, 2012.

T. Kakimoto, Identification of plant cytokinin biosynthetic enzymes as dimethylallyl diphosphate:ATP/ADP isopentenyltransferases, Plant Cell Physiol, vol.42, pp.677-685, 2001.

P. Kalousek, D. Buchtova, J. Balla, V. Reinoehl, and S. Prochazka, Cytokinins and polar transport of auxin in axillary pea buds, Acta Univ Agric Silvic Mendel Brun, vol.58, pp.79-87, 2010.

T. H. Kebrom, T. P. Brutnell, and S. A. Finlayson, Suppression of sorghum axillary bud outgrowth by shade, phyB and defoliation signalling pathways, Plant Cell Environ, vol.33, pp.48-58, 2010.

T. H. Kebrom, B. L. Burson, and S. A. Finlayson, Phytochrome B represses Teosinte Branched1 expression and induces sorghum axillary bud outgrowth in response to light signals, Plant Physiol, vol.140, pp.1109-1117, 2006.

T. H. Kebrom and J. E. Mullet, Photosynthetic leaf area modulates tiller bud outgrowth in sorghum, Plant Cell Environ, vol.38, pp.1471-1478, 2015.

T. H. Kebrom and J. E. Mullet, Transcriptome profiling of tiller buds provides new insights into PhyB regulation of tillering and indeterminate growth in sorghum, Plant Physiol, vol.170, pp.2232-2250, 2016.

J. J. Kieber and G. E. Schaller, Cytokinins. The Arabidopsis Book, vol.12, p.168, 2014.

T. Kudo, T. Kiba, and H. Sakakibara, Metabolism and long-distance translocation of cytokinins, J Integr Plant Biol, vol.52, pp.53-60, 2010.

T. Kurakawa, N. Ueda, M. Maekawa, K. Kobayashi, M. Kojima et al., Direct control of shoot meristem activity by a cytokinin-activating enzyme, Nature, vol.445, pp.652-655, 2007.

N. Leduc, H. Roman, F. Barbier, T. Péron, L. Huché-thélier et al., Light signaling in bud outgrowth and branching in plants, Plants (Basel), vol.3, pp.223-250, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01169243

L. Hir, R. Leduc, N. , J. E. Viemont, J. D. Pelleschi-travier et al., Variations in sucrose and ABA concentrations are concomitant with heteroblastic leaf shape changes in a rhythmically growing species (Quercus robur), Tree Physiol, vol.26, pp.229-238, 2006.

C. Li and F. Bangerth, Autoinhibition of indoleacetic acid transport in the shoots of two-branched pea (Pisum sativum) plants and its relationship to correlative dominance, Physiol Plant, vol.106, pp.415-420, 1999.

C. Li and F. Bangerth, Stimulatory effect of cytokinins and interaction with IAA on the release of lateral buds of pea plants from apical dominance, J Plant Physiol, vol.160, pp.1059-1063, 2003.

S. C. Liao, C. S. Lin, A. Y. Wang, and H. Y. Sung, Differential expression of genes encoding acid invertases in multiple shoots of bamboo in response to various phytohormones and environmental factors, J Agric Food Chem, vol.61, pp.4396-4405, 2013.

Y. Liu, J. Xu, Y. Ding, Q. Wang, G. Li et al., Auxin inhibits the outgrowth of tiller buds in rice (Oryza sativa L.) by downregulating OsIPT expression and cytokinin biosynthesis in nodes, Aust J Crop Sci, vol.5, pp.169-174, 2011.

E. López-juez, D. E. Magyar, Z. Khan, S. Hazeldine, S. De-jager et al., Distinct light-initiated gene expression and cell cycle programs in the shoot apex and cotyledons of Arabidopsis, Plant Cell, vol.20, pp.947-968, 2008.

M. Martín-trillo, E. G. Grandío, F. Serra, F. Marcel, M. L. Rodríguez-buey et al., Role of tomato BRANCHED1-like genes in the control of shoot branching, Plant J, vol.67, pp.701-714, 2011.

M. G. Mason, J. J. Ross, B. A. Babst, B. N. Wienclaw, and C. A. Beveridge, Sugar demand, not auxin, is the initial regulator of apical dominance, Proc Natl Acad Sci, vol.111, pp.6092-6097, 2014.

K. Miyawaki, M. Matsumoto-kitano, and T. Kakimoto, Expression of cytokinin biosynthetic isopentenyltransferase genes in Arabidopsis: tissue specificity and regulation by auxin, cytokinin, and nitrate, Plant J, vol.37, pp.128-138, 2004.

G. L. Moldovan, B. Pfander, and S. Jentsch, PCNA, the maestro of the replication fork, Cell, vol.129, pp.665-679, 2007.

D. Müller and O. Leyser, Auxin, cytokinin and the control of shoot branching, Ann Bot (Lond), vol.107, pp.1203-1212, 2011.

D. Müller, T. Waldie, K. Miyawaki, J. To, C. W. Melnyk et al., Cytokinin is required for escape but not release from auxin mediated apical dominance, Plant J, vol.82, pp.874-886, 2015.

J. Nisler, M. Zatloukal, I. Popa, K. Dolezal, M. Strnad et al., Cytokinin receptor antagonists derived from 6-benzylaminopurine, Phytochemistry, vol.71, pp.823-830, 2010.

A. Nordström, P. Tarkowski, D. Tarkowska, R. Norbaek, C. Åstot et al., Auxin regulation of cytokinin biosynthesis in Arabidopsis thaliana: a factor of potential importance for auxincytokinin-regulated development, Proc Natl Acad Sci, vol.101, pp.8039-8044, 2004.

V. Ongaro and O. Leyser, Hormonal control of shoot branching, J Exp Bot, vol.59, pp.67-74, 2008.

M. W. Pfaffl, A new mathematical model for relative quantification in real-time RT-PCR, Nucleic Acids Res, vol.29, p.45, 2001.

R. K. Proels and T. Roitsch, Extracellular invertase LIN6 of tomato: a pivotal enzyme for integration of metabolic, hormonal, and stress signals is regulated by a diurnal rhythm, J Exp Bot, vol.60, pp.1555-1567, 2009.

A. Rabot, C. Henry, B. Baaziz, K. Mortreau, E. Azri et al., Insight into the role of sugars in bud burst under light in the rose, Plant Cell Physiol, vol.53, pp.1068-1082, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00841828

A. Rabot, V. Portemer, T. Péron, E. Mortreau, N. Leduc et al., Interplay of sugar, light and gibberellins in expression of Rosa hybrida vacuolar invertase 1 regulation, Plant Cell Physiol, vol.55, pp.1734-1748, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01379022

C. Rameau, J. Bertheloot, N. Leduc, B. Andrieu, F. Foucher et al., Multiple pathways regulate shoot branching, Front Plant Sci, vol.5, p.741, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01168759

S. K. Reddy and S. A. Finlayson, Phytochrome B promotes branching in Arabidopsis by suppressing auxin signaling, Plant Physiol, vol.164, pp.1542-1550, 2014.

S. K. Reddy, S. V. Holalu, J. J. Casal, and S. A. Finlayson, Abscisic acid regulates axillary bud outgrowth responses to the ratio of red to far-red light, Plant Physiol, vol.163, pp.1047-1058, 2013.

D. Reinhardt, F. Wittwer, T. Mandel, and C. Kuhlemeier, Localized upregulation of a new expansin gene predicts the site of leaf formation in the tomato meristem, Plant Cell, vol.10, pp.1427-1437, 1998.

D. Rittenberg and G. L. Foster, A new procedure for quantitative analysis by isotope dilution, with application to the determination of amino acids and fatty acids, J Biol Chem, vol.133, pp.737-744, 1940.

T. Roitsch and R. Ehneß, Regulation of source/sink relations by cytokinins, Plant Growth Regul, vol.32, pp.359-367, 2000.

G. A. Romanov, J. J. Kieber, and T. Schmülling, A rapid cytokinin response assay in Arabidopsis indicates a role for phospholipase D in cytokinin signalling, FEBS Lett, vol.515, pp.39-43, 2002.

T. Sachs and K. V. Thimann, Release of lateral buds from apical dominance, Nature, vol.201, pp.939-940, 1964.

T. Sachs and K. V. Thimann, The role of auxins and cytokinins in the release of buds from dominance, Am J Bot, vol.54, pp.136-144, 1967.

H. Sakakibara, Cytokinins: activity, biosynthesis, and translocation, Annu Rev Plant Biol, vol.57, pp.431-449, 2006.

T. Schlüter, J. Leide, and K. Conrad, Light promotes an increase of cytokinin oxidase/dehydrogenase activity during senescence of barley leaf segments, J Plant Physiol, vol.168, pp.694-698, 2011.

T. Schmülling, T. Werner, M. Riefler, E. Krupková, and I. Bartrina-y-manns, Structure and function of cytokinin oxidase/dehydrogenase genes of maize, rice, Arabidopsis and other species, J Plant Res, vol.116, pp.241-252, 2003.

S. Shimizu and H. Mori, Analysis of cycles of dormancy and growth in pea axillary buds based on mRNA accumulation patterns of cell cyclerelated genes, Plant Cell Physiol, vol.39, pp.255-262, 1998.

L. Spíchal, T. Werner, I. Popa, M. Riefler, T. Schmülling et al., The purine derivative PI-55 blocks cytokinin action via receptor inhibition, FEBS J, vol.276, pp.244-253, 2009.

A. Sturm and G. Q. Tang, The sucrose-cleaving enzymes of plants are crucial for development, growth and carbon partitioning, Trends Plant Sci, vol.4, pp.401-407, 1999.

H. Su, S. D. Abernathy, R. H. White, and S. A. Finlayson, Photosynthetic photon flux density and phytochrome B interact to regulate branching in Arabidopsis, Plant Cell Environ, vol.34, pp.1986-1998, 2011.

K. Takei, H. Sakakibara, and T. Sugiyama, Identification of genes encoding adenylate isopentenyltransferase, a cytokinin biosynthesis enzyme, in Arabidopsis thaliana, J Biol Chem, vol.276, pp.26405-26410, 2001.

K. Takei, N. Ueda, K. Aoki, T. Kuromori, T. Hirayama et al., AtIPT3 is a key determinant of nitratedependent cytokinin biosynthesis in Arabidopsis, Plant Cell Physiol, vol.45, pp.1053-1062, 2004.

M. Tanaka, K. Takei, M. Kojima, H. Sakakibara, and H. Mori, Auxin controls local cytokinin biosynthesis in the nodal stem in apical dominance, Plant J, vol.45, pp.1028-1036, 2006.

M. Taniguchi, T. Kiba, H. Sakakibara, C. Ueguchi, T. Mizuno et al., Expression of Arabidopsis response regulator homologs is induced by cytokinins and nitrate, FEBS Lett, vol.429, pp.259-262, 1998.

T. H. Thomas, Hormonal control of assimilate movement and compartmentation, Growth Substances, pp.350-359, 1985.

C. G. Turnbull, M. A. Raymond, I. C. Dodd, and S. E. Morris, Rapid increases in cytokinin concentration in lateral buds of chickpea (Cicer arietinum L.) during release of apical dominance, Planta, vol.202, pp.271-276, 1997.

Y. Ueda, S. Nishihara, H. Tomita, and Y. Oda, Photosynthetic response of Japanese rose species Rosa bracteata and Rosa rugosa to temperature and light, Sci Hortic (Amsterdam), vol.84, pp.365-371, 2000.

T. Werner, K. Holst, Y. Pörs, A. Guivarc'h, A. Mustroph et al., Cytokinin deficiency causes distinct changes of sink and source parameters in tobacco shoots and roots, J Exp Bot, vol.59, pp.2659-2672, 2008.

C. D. Whitty and R. H. Hall, A cytokinin oxidase in Zea mays, Can J Biochem, vol.52, pp.789-799, 1974.

J. Xu, M. Zha, Y. Li, Y. Ding, L. Chen et al., The interaction between nitrogen availability and auxin, cytokinin, and strigolactone in the control of shoot branching in rice, Oryza sativa L.). Plant Cell Rep, vol.34, pp.1647-1662, 2015.

S. Yoshida, T. Mandel, and C. Kuhlemeier, Stem cell activation by light guides plant organogenesis, Genes Dev, vol.25, pp.1439-1450, 2011.

S. Zenoni, M. Fasoli, G. B. Tornielli, D. Santo, S. Sanson et al., Overexpression of PhEXPA1 increases cell size, modifies cell wall polymer composition and affects the timing of axillary meristem development in Petunia hybrida, New Phytol, vol.191, pp.662-677, 2011.

N. Zieslin and M. J. Tsujita, Response of miniature roses to supplementary illumination. 1. Light intensity, Sci Hortic (Amsterdam), vol.42, pp.113-121, 1990.

R. Zrenner, M. Salanoubat, L. Willmitzer, and U. Sonnewald, Evidence of the crucial role of sucrose synthase for sink strength using transgenic potato plants (Solanum tuberosum L.), Plant J, vol.7, pp.97-107, 1995.