Response of cytokinin concentration in the xylem exudate of bean (Phaseolus vulgaris L.) plants to decapitation and auxin treatment, and relationship to apical dominance

Bangerth, F.

doi:10.1007/bf00197546

Cited by 220Plant Molecular Biology ResearchPlant Parasitism and ResistancePlant Physiology and Cultivation Studies

Response of cytokinin concentration in the xylem exudate of bean (Phaseolus vulgaris L.) plants to decapitation and auxin treatment, and relationship to apical dominance

Bangerth, F.·1994·Planta

DOI 10.1007/bf00197546

Open this paper in CoChat — free account

Integrity signals

Registry

Crossref · 10.1007/bf00197546

Cites

20 of 20 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Decrease of auxin in the stem after decapitation leads to increased cytokinin biosynthesis.
“In contrast, the decrease of auxin in the stem after removal of the main auxin biosynthesis site by decapitation will lead to increased cytokinin biosynthesis (Bangerth, 1994; Figure 2B).”
From Shaping plant architecture (2015) · cites this paper as Bangerth, 1994
Apical auxin influences the export of cytokinins from roots.
“The export of cytokinins from roots has been shown to be in¯uenced by apical auxin, and this has led to the hypothesis that inhibition by apical auxin is mediated wholly or partly by its in¯uence on cytokinin export from the roots (Bangerth, 1994).”
From The hormonal regulation of axillary bud growth in Arabidopsis (2000) · cites this paper as Bangerth, 1994

A MODIFIED NINHYDRIN REAGENT FOR THE PHOTOMETRIC DETERMINATION OF AMINO ACIDS AND RELATED COMPOUNDS
Moore, S., & Stein, W. H. (1954) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)71178-2 · Cited by 3,028 · see citing works
The role of auxins and cytokinins in the release of buds from dominance
Sachs, T., & Thimann, K. V. (1967) · American Journal of Botany · doi:10.1002/j.1537-2197.1967.tb06901.x · Cited by 429 · see citing works
Dominance among fruits/sinks and the search for a correlative signal
Bangerth, F. K. (1989) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1989.tb05487.x · Cited by 264 · see citing works
Self-citation
The role of hormones in apical dominance. New approaches to an old problem in plant development
Cline, M. G. (1994) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1994.tb02216.x · Cited by 241 · see citing works
The synthesis, transport and metabolism of endogenous cytokinins
STADEN, J. V., & DAVEY, J. E. (1979) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1979.tb00780.x · Cited by 238 · see citing works
Localization of Cytokinin Biosynthetic Sites in Pea Plants and Carrot Roots
Chen, C.-M., Ertl, J. R., Leisner, S. M., & Chang, C.-C. (1985) · Plant Physiology · doi:10.1104/pp.78.3.510 · Cited by 160 · see citing works
Effects of fruit set sequence and defoliation on cell number, cell size and hormone levels of tomato fruits (Lycopersicon esculentum Mill.) within a truss
Bohner, J., & Bangerth, F. K. (1988) · Plant Growth Regulation · doi:10.1007/bf00028237 · Cited by 139 · see citing works
Self-citation
Radioimmunoassays for trans-zeatin and related cytokinins
Weiler, E. W. (1980) · Planta · doi:10.1007/bf00380877 · Cited by 134 · see citing works
The effect of auxin concentration on cytokinin stability and metabolism
Palni, L. M. S., Burch, L. R., & Horgan, R. (1988) · Planta · doi:10.1007/bf00394775 · Cited by 127 · see citing works
THE INTERACTION BETWEEN GROWTH PROMOTERS IN APICAL DOMINANCE
Woolley, D. J., & Wareing, P. F. (1972) · New Phytologist · doi:10.1111/j.1469-8137.1972.tb01957.x · Cited by 74 · see citing works
Apical Dominance inPhaseolus vulgarisL.
KNOX, J. P., & Wareing, P. F. (1984) · Journal of Experimental Botany · doi:10.1093/jxb/35.2.239 · Cited by 58 · see citing works
The role of auxin efflux carriers in the reversible loss of polar auxin transport in the pea (Pisum sativum L.) stem
Morris, D., & Johnson, C. (1990) · Planta · doi:10.1007/bf00202333 · Cited by 55 · see citing works
Identification of Cytokinins from Xylem Exudate of Phaseolus vulgaris L
Palmer, M. V., & Wong, O. (1985) · PLANT PHYSIOLOGY · doi:10.1104/pp.79.1.296 · Cited by 37 · see citing works
Loading and translocation of various cytokinins in phloem and xylem of the seedlings of Ricinus communis L.
Komor, E., Liegl, I., & Schobert, C. (1993) · Planta · doi:10.1007/bf00199757 · Cited by 35 · see citing works
The possible role of cytokinins, ethylene and indoleacetic acid in apical dominance
Li, C. J., & Bangerth, F. (1992) · Current Plant Science and Biotechnology in Agriculture · doi:10.1007/978-94-011-2458-4_50 · Cited by 34 · see citing works
Self-citation
Reversal of the Direction of Photosynthate Allocation in Urtica dioica L. Plants by Increasing Cytokinin Import into the Shoot
Fetene, M., & Beck, E. (1993) · Botanica Acta · doi:10.1111/j.1438-8677.1993.tb00746.x · Cited by 32 · see citing works
The effects of decapitation on the distribution of cytokinins and growth of Phaseolus vulgaris plants
Staden, J. V., & Carmi, A. (1982) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1982.tb00282.x · Cited by 28 · see citing works
Mass-spectrometric quantitation of cytokinins in tobacco crown-gall tumours induced by mutated octopine Ti plasmids of Agrobacterium tumefaciens
McGaw, B. A., Horgan, R., Heald, J. K., Wullems, G. J., & Schilperoort, R. A. (1988) · Planta · doi:10.1007/bf00392449 · Cited by 26 · see citing works
Apical Dominance in Phaseolus vulgaris L.: The Possible Roles of Abscisic and Indole-3-Acetic Acid
Knox, J., & Wareing, P. F. (1984) · Journal of Experimental Botany · Cited by 24 · see citing works
Root cytokinins of Phaseolus vulgaris L.
Scott, I. M., & Horgan, R. (1984) · Plant Science Letters · doi:10.1016/0304-4211(84)90129-9 · Cited by 19 · see citing works

Flagged first, then by citations

Sorted by citations

Signal integration in the control of shoot branching
Domagalska, M. A., & Leyser, O. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3088 · Cited by 835 · see citing works
Molecular Basis of Plant Architecture
Wang, Y., & Li, J. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092902 · Cited by 643 · see citing works
MAX4 and RMS1 are orthologous dioxygenase-like genes that regulate shoot branching in Arabidopsis and pea
Sorefan, K., Booker, J., Haurogné, K., Goussot, M., Bainbridge, K., Foo, E., Chatfield, S., Ward, S., Beveridge, C., Rameau, C., et al. (2003) · Genes & Development · doi:10.1101/gad.256603 · Cited by 604 · see citing works
MAX1 Encodes a Cytochrome P450 Family Member that Acts Downstream of MAX3/4 to Produce a Carotenoid-Derived Branch-Inhibiting Hormone
Booker, J., Sieberer, T., Wright, W. J., Williamson, L. C., Willett, B., Stirnberg, P., Turnbull, C. G. N., Srinivasan, M., Goddard, P., & Leyser, O. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.01.009 · Cited by 556 · see citing works
Auxin, cytokinin and the control of shoot branching
Müller, D., & Leyser, O. (2011) · Annals of Botany · doi:10.1093/aob/mcr069 · Cited by 545 · see citing works
Auxin controls local cytokinin biosynthesis in the nodal stem in apical dominance
Tanaka, M., Takei, K., Kojima, M., Sakakibara, H., & Mori, H. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02656.x · Cited by 512 · see citing works
The Pea TCP Transcription Factor PsBRC1 Acts Downstream of Strigolactones to Control Shoot Branching
Braun, N., de Saint Germain, A., Pillot, J.-P., Boutet-Mercey, S., Dalmais, M., Antoniadi, I., Li, X., Maia-Grondard, A., Le Signor, C., Bouteiller, N., et al. (2012) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.182725 · Cited by 486 · see citing works
Hormonal changes in relation to biomass partitioning and shoot growth impairment in salinized tomato (Solanum lycopersicum L.) plants
Albacete, A. A., Ghanem, M. E., Martínez‐Andújar, C., Acosta, M., Sánchez‐Bravo, J., Martı́nez, V., Lutts, S., Dodd, I. C., & Pérez‐Alfocea, F. (2008) · Journal of Experimental Botany · doi:10.1093/jxb/ern251 · Cited by 484 · see citing works
Antagonistic action of strigolactone and cytokinin in bud outgrowth control
Dun, E. A., de Saint Germain, A., Rameau, C., & Beveridge, C. A. (2012) · Plant Physiology · doi:10.1104/pp.111.186783 · Cited by 466 · see citing works
Strigolactone can promote or inhibit shoot branching by triggering rapid depletion of the auxin efflux protein PIN1 from the plasma membrane
Shinohara, N., Taylor, C., & Leyser, O. (2013) · PLoS Biology · doi:10.1371/journal.pbio.1001474 · Cited by 438 · see citing works
Interactions between Auxin and Strigolactone in Shoot Branching Control
Hayward, A. C., Stirnberg, P., Beveridge, C. A., & Leyser, O. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.137646 · Cited by 430 · see citing works
Rapid effects of nitrogen form on leaf morphogenesis in tobacco
Walch‐Liu, P., Neumann, G., Bangerth, F. K., & Engels, C. (2000) · Journal of Experimental Botany · doi:10.1093/jexbot/51.343.227 · Cited by 391 · see citing works
Self-citation
Auxin-cytokinin interactions in the control of shoot branching
Shimizu-Sato, S., Tanaka, M., & Mori, H. (2009) · Plant Molecular Biology · doi:10.1007/s11103-008-9416-3 · Cited by 387 · see citing works
Strigolactones enhance competition between shoot branches by dampening auxin transport
Crawford, S., Shinohara, N., Sieberer, T., Williamson, L., George, G., Hepworth, J., Müller, D., Domagalska, M. A., & Leyser, O. (2010) · Development · doi:10.1242/dev.051987 · Cited by 384 · see citing works
Hormonal control of shoot branching
Ongaro, V., & Leyser, O. (2007) · Journal of Experimental Botany · doi:10.1093/jxb/erm134 · Cited by 373 · see citing works
Micrografting techniques for testing long‐distance signalling in Arabidopsis
Turnbull, C. G. N., Booker, J. P., & Leyser, H. M. O. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01419.x · Cited by 365 · see citing works
Control of Outgrowth and Dormancy in Axillary Buds
Shimizu‐Sato, S., & Mori, H. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.010841 · Cited by 364 · see citing works
Multiple pathways regulate shoot branching
Rameau, C., Bertheloot, J., Leduc, N., Andrieu, B., Foucher, F., & Sakr, S. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00741 · Cited by 357 · see citing works
SHOOT BRANCHING
McSteen, P., & Leyser, O. (2005) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.56.032604.144122 · Cited by 356 · see citing works
Roles for Auxin, Cytokinin, and Strigolactone in Regulating Shoot Branching
Ferguson, B. J., & Beveridge, C. A. (2009) · Plant Physiology · doi:10.1104/pp.109.135475 · Cited by 355 · see citing works
Hormonal signaling in rootstock–scion interactions
Aloni, B., Cohen, R., Karni, L., Aktaş, H., & Edelstein, M. (2010) · Scientia Horticulturae · doi:10.1016/j.scienta.2010.09.003 · Cited by 328 · see citing works
The Branching Gene RAMOSUS1 Mediates Interactions among Two Novel Signals and Auxin in Pea
Foo, E., Bullier, E., Goussot, M., Foucher, F., Rameau, C., & Beveridge, C. A. (2005) · The Plant Cell · doi:10.1105/tpc.104.026716 · Cited by 289 · see citing works
The hormonal regulation of axillary bud growth in Arabidopsis
Chatfield, S. P., Stirnberg, P., Forde, B. G., & Leyser, O. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00862.x · Cited by 284 · see citing works
Root-derived cytokinins as long-distance signals for NO3--induced stimulation of leaf growth
Rahayu, Y. S. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/eri107 · Cited by 277 · see citing works
Root-To-Shoot Signalling: Assessing The Roles of ‘Up’ In the Up and Down World of Long-Distance Signalling In Planta
Dodd, I. C. (2005) · Plant and Soil · doi:10.1007/s11104-004-0966-0 · Cited by 267 · see citing works
Auxin—cytokinin interactions in higher plants: old problems and new tools
Coenen, C., & Lomax, T. L. (1997) · Trends in Plant Science · doi:10.1016/s1360-1385(97)84623-7 · Cited by 266 · see citing works
Strigolactones: discovery of the elusive shoot branching hormone
Dun, E. A., Brewer, P. B., & Beveridge, C. A. (2009) · Trends in Plant Science · doi:10.1016/j.tplants.2009.04.003 · Cited by 256 · see citing works
The control of shoot branching: an example of plant information processing
Leyser, O. (2009) · Plant Cell & Environment · doi:10.1111/j.1365-3040.2009.01930.x · Cited by 253 · see citing works
Auxin cross-talk: integration of signalling pathways to control plant development
Swarup, R., Parry, G., Graham, N. S., Allen, T., & Bennett, M. J. (2002) · Springer eBooks · doi:10.1007/978-94-010-0377-3_12 · Cited by 248 · see citing works
grassy tillers1 promotes apical dominance in maize and responds to shade signals in the grasses
Whipple, C. J., Kebrom, T. H., Weber, A. L., Yang, F., Hall, D., Meeley, R., Schmidt, R., Doebley, J., Brutnell, T. P., & Jackson, D. P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1102819108 · Cited by 240 · see citing works
Regulation of shoot branching by auxin
Leyser, O. (2003) · Trends in Plant Science · doi:10.1016/j.tplants.2003.09.008 · Cited by 237 · see citing works
Shaping plant architecture
Teichmann, T., & Muhr, M. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00233 · Cited by 228 · see citing works
“In contrast, the decrease of auxin in the stem after removal of the main auxin biosynthesis site by decapitation will lead to increased cytokinin biosynthesis (Bangerth, 1994; Figure 2B).”
Background
Apical Dominance and Shoot Branching. Divergent Opinions or Divergent Mechanisms?
Dun, E. A., Ferguson, B. J., & Beveridge, C. A. (2006) · Plant Physiology · doi:10.1104/pp.106.086868 · Cited by 227 · see citing works
Root-to-shoot signalling: Assessing the roles of ‘up’ in the up and down world of long-distance signalling in planta
Dodd, I. C. (2005) · Plant ecophysiology · doi:10.1007/1-4020-4099-7_14 · Cited by 227 · see citing works
Auxin Acts in Xylem-Associated or Medullary Cells to Mediate Apical Dominance
Booker, J., Chatfield, S. P., & Leyser, O. (2003) · The Plant Cell · doi:10.1105/tpc.007542 · Cited by 221 · see citing works
The Plant Architecture of Rice (Oryza sativa)
Wang, Y., & Li, J. (2005) · Plant Molecular Biology · doi:10.1007/s11103-004-4038-x · Cited by 200 · see citing works
Cytokinin Targets Auxin Transport to Promote Shoot Branching
Waldie, T., & Leyser, O. (2018) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.01691 · Cited by 198 · see citing works
Defence on demand: mechanisms behind optimal defence patterns
Meldau, S., Erb, M., & Baldwin, I. T. (2012) · Annals of Botany · doi:10.1093/aob/mcs212 · Cited by 197 · see citing works
Control of axillary bud initiation and shoot architecture in Arabidopsis through the SUPERSHOOT gene
Tantikanjana, T., Yong, J. W. H., Letham, D. S., Griffith, M., Hussain, M., Ljung, K., Sandberg, G., & Sundaresan, V. (2001) · Genes & Development · doi:10.1101/gad.887301 · Cited by 194 · see citing works
Genes controlling plant architecture
Wang, Y., & Li, J. (2006) · Current Opinion in Biotechnology · doi:10.1016/j.copbio.2006.02.004 · Cited by 187 · see citing works
The interaction between nitrogen availability and auxin, cytokinin, and strigolactone in the control of shoot branching in rice (Oryza sativa L.)
Xu, J., Zha, M., Li, Y., Ding, Y., Chen, L., Ding, C., & Wang, S. (2015) · Plant Cell Reports · doi:10.1007/s00299-015-1815-8 · Cited by 185 · see citing works
BRANCHED1: A Key Hub of Shoot Branching
Wang, M., Moigne, M.-A. L., Bertheloot, J., Crespel, L., Pérez-Garcia, M.-D., Ogé, L., Demotes‐Mainard, S., Hamama, L., Davière, J., & Sakr, S. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00076 · Cited by 184 · see citing works
Gibberellin Promotes Shoot Branching in the Perennial Woody PlantJatropha curcas
Ni, J., Gao, C., Chen, M.-S., Pan, B.-Z., Ye, K., & Xu, Z. (2015) · Plant and Cell Physiology · doi:10.1093/pcp/pcv089 · Cited by 179 · see citing works
The rms1 Mutant of Pea Has Elevated Indole-3-Acetic Acid Levels and Reduced Root-Sap Zeatin Riboside Content but Increased Branching Controlled by Graft-Transmissible Signal(s)
Beveridge, C. A., Symons, G. M., Murfet, I. C., Ross, J. J., & Rameau, C. (1997) · PLANT PHYSIOLOGY · doi:10.1104/pp.115.3.1251 · Cited by 178 · see citing works
Branching in Pea (Action of Genes Rms3 and Rms4)
Beveridge, C. A., Ross, J. J., & Murfet, I. C. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.3.859 · Cited by 174 · see citing works
Auxin cross-talk: integration of signalling pathways to control plant development
Swarup, R., Parry, G., Graham, N. S., Allen, T., & Bennett, M. J. (2002) · Plant Molecular Biology · doi:10.1023/a:1015250929138 · Cited by 169 · see citing works
Auxin Inhibition of Decapitation-Induced Branching Is Dependent on Graft-Transmissible Signals Regulated by GenesRms1andRms2
Beveridge, C. A., Symons, G. M., & Turnbull, C. G. N. (2000) · Plant Physiology · doi:10.1104/pp.123.2.689 · Cited by 162 · see citing works
Long-distance signalling and a mutational analysis of branching in pea
Beveridge, C. A. (2000) · Plant Growth Regulation · doi:10.1023/a:1010718020095 · Cited by 160 · see citing works
Long-Distance Signaling and the Control of Branching in therms1 Mutant of Pea
Foo, E., Turnbull, C. G. N., & Beveridge, C. A. (2001) · Plant Physiology · doi:10.1104/pp.126.1.203 · Cited by 160 · see citing works
Regulation of cytokinin content in plant cells
Kamínek, M., Motyka, V., & Vaňková, R. (1997) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1997.tb01053.x · Cited by 153 · see citing works
Exogenous Auxin Effects on Lateral Bud Outgrowth in Decapitated Shoots
CLINE, M. (1996) · Annals of Botany · doi:10.1006/anbo.1996.0119 · Cited by 144 · see citing works
Effect of apex excision and replacement by 1-naphthylacetic acid on cytokinin concentration and apical dominance in pea plants
Li, C.-J., Guevara, E., Herrera, J., & Bangerth, F. K. (1995) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1995.tb00955.x · Cited by 136 · see citing works
Self-citation
Auxin Dynamics after Decapitation Are Not Correlated with the Initial Growth of Axillary Buds
Morris, S. E., Cox, M. C. H., Ross, J. J., Krisantini, S., & Beveridge, C. A. (2005) · Plant Physiology · doi:10.1104/pp.104.058743 · Cited by 135 · see citing works
Changing concepts in plant hormone action
Gaspar, T., Kevers, C., Faivre‐Rampant, O., Crèvecoeur, M., Penel, C., Greppin, H., & Dommès, J. (2003) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1079/ivp2002393 · Cited by 133 · see citing works
Autoinhibition of indoleacetic acid transport in the shoots of two‐branched pea (Pisum sativum) plants and its relationship to correlative dominance
Li, C., & Bangerth, F. (1999) · Physiologia Plantarum · doi:10.1034/j.1399-3054.1999.106409.x · Cited by 130 · see citing works
Self-citation
5 Reevaluating Concepts of Apical Dominance and the Control of Axillary Bud Outgrowth
Napoli, C. A., Beveridge, C. A., & Snowden, K. C. (1998) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)60469-x · Cited by 130 · see citing works
Cytokinins Are Initial Targets of Light in the Control of Bud Outgrowth
Roman, H., Girault, T., Barbier, F. F., Péron, T., Brouard, N., Pěnčík, A., Novák, O., Vian, A., Sakr, S., Lothier, J., et al. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00530 · Cited by 125 · see citing works
Floral induction in mature, perennial angiosperm fruit trees: Similarities and discrepancies with annual/biennial plants and the involvement of plant hormones
Bangerth, K. F. (2009) · Scientia Horticulturae · doi:10.1016/j.scienta.2009.06.014 · Cited by 122 · see citing works
Mutual interaction of auxin and cytokinins in regulating correlative dominance
Bangerth, F. K., Li, C.-J., & Gruber, J. (2000) · Plant Growth Regulation · doi:10.1023/a:1010742721004 · Cited by 119 · see citing works
Self-citation
Factors involved in root formation in Medicago truncatula
Imin, N., Nizamidin, M., Wu, T., & Rolfe, B. G. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl224 · Cited by 118 · see citing works
Shoot branching
Ward, S. P., & Leyser, O. (2003) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2003.10.002 · Cited by 113 · see citing works
Auxin-Cytokinin Interactions in Wild-Type and Transgenic Tobacco
Eklöf, S., Åstot, C., Blackwell, J., Möritz, T., Olsson, O., & Sandberg, G. (1997) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a029157 · Cited by 113 · see citing works
Feedback regulation of xylem cytokinin content is conserved in pea and Arabidopsis
Foo, E., Morris, S. E., Parmenter, K., Young, N., Wang, H., Jones, A., Rameau, C., Turnbull, C. G. N., & Beveridge, C. A. (2007) · Plant Physiology · doi:10.1104/pp.106.093708 · Cited by 107 · see citing works
Dynamics of Strigolactone Function and Shoot Branching Responses in Pisum sativum
Dun, E. A., Germain, A. D. S., Rameau, C., & Beveridge, C. A. (2012) · Molecular Plant · doi:10.1093/mp/sss131 · Cited by 107 · see citing works
Mechanisms of cytokinin action
Brault, M., & Maldiney, R. (1999) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(99)80046-1 · Cited by 104 · see citing works
Light Regulation of Axillary Bud Outgrowth Along Plant Axes: An Overview of the Roles of Sugars and Hormones
Schneider, A., Godin, C., Boudon, F., Demotes‐Mainard, S., Sakr, S., & Bertheloot, J. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01296 · Cited by 102 · see citing works
In vitro propagation of the neotropical giant bamboo, Guadua angustifolia Kunth, through axillary shoot proliferation
Jiménez, V. M., Castillo, J. M. S., Tavares, E., Guevara, E., & Montiel, M. (2006) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-006-9120-4 · Cited by 96 · see citing works
Physiology of Spikelet Development on the Rice Panicle
Mohapatra, P. K., Panigrahi, R., & Turner, N. C. (2011) · Advances in agronomy · doi:10.1016/b978-0-12-385531-2.00005-0 · Cited by 96 · see citing works
Hormonal relationships in xylem sap of grafted and ungrafted Prunus rootstocks
Sorce, C., Massai, R., Picciarelli, P., & Lorenzi, R. (2002) · Scientia Horticulturae · doi:10.1016/s0304-4238(01)00338-7 · Cited by 95 · see citing works
Proper gibberellin localization in vascular tissue is required to control auxin‐dependent leaf development and bud outgrowth in hybrid aspen
Mauriat, M., Sandberg, L. G., & Möritz, T. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04635.x · Cited by 95 · see citing works
Effects of Nitrogen and 6‐Benzylaminopurine on Rice Tiller Bud Growth and Changes in Endogenous Hormones and Nitrogen
Liu, Y., Ding, Y., Wang, Q., Meng, D., & Wang, S. (2011) · Crop Science · doi:10.2135/cropsci2010.04.0217 · Cited by 93 · see citing works
MicroRNA393 is involved in nitrogen-promoted rice tillering through regulation of auxin signal transduction in axillary buds
Li, X., Xia, K., Liang, Z., Chen, K., Gao, C., & Zhang, M. (2016) · Scientific Reports · doi:10.1038/srep32158 · Cited by 80 · see citing works
Lessons from a century of apical dominance research
Beveridge, C. A., Rameau, C., & Yapa, A. W. (2023) · Journal of Experimental Botany · doi:10.1093/jxb/erad137 · Cited by 80 · see citing works
Auxin flow-mediated competition between axillary buds to restore apical dominance
Balla, J., Medveďová, Z., Kalousek, P., Matiješčuková, N., Friml, J., Reinöhl, V., & Procházka, S. (2016) · Scientific Reports · doi:10.1038/srep35955 · Cited by 80 · see citing works
Ethylene‐triggered abscisic acid: A principle in plant growth regulation?
Großmann, K., & Hansen, H. (2001) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2001.1130102.x · Cited by 77 · see citing works
Axillary bud outgrowth in herbaceous shoots: how do strigolactones fit into the picture?
Waldie, T., Hayward, A. C., & Beveridge, C. A. (2010) · Plant Molecular Biology · doi:10.1007/s11103-010-9599-2 · Cited by 73 · see citing works
Stress induced ethylene evolution and its possible relationship to auxin-transport, cytokinin levels, and flower bud induction in shoots of apple seedlings and bearing apple trees
Sanyal, D., & Bangerth, F. K. (1998) · Plant Growth Regulation · doi:10.1023/a:1005948918382 · Cited by 73 · see citing works
Self-citation
Involvement of endogenous plant hormones in the effect of mixed nitrogen source on growth and tillering of wheat
Chen, J., CHENG, S.-H., Cao, W., & Zhou, X. (1998) · Journal of Plant Nutrition · doi:10.1080/01904169809365385 · Cited by 72 · see citing works
Functional Analysis of the Tandem-Duplicated P450 Genes SPS/BUS/CYP79F1 and CYP79F2 in Glucosinolate Biosynthesis and Plant Development by Ds Transposition-Generated Double Mutants
Tantikanjana, T., Mikkelsen, M. D., Hussain, M., Halkier, B. A., & Sundaresan, V. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.040113 · Cited by 72 · see citing works
Bending Shoots Stimulates Flowering and Influences Hormone Levels in Lateral Buds of Japanese Pear
Ito, A., Yaegaki, H., Hayama, H., Kusaba, S., Yamaguchi, I., & Yoshioka, H. (1999) · HortScience · doi:10.21273/hortsci.34.7.1224 · Cited by 70 · see citing works
Signals Regulating Dormancy in Vegetative Buds
Chao, W. S., & Anderson, V. J. (2007) · Cited by 67 · see citing works
Signaling network regulating plant branching: Recent advances and new challenges
Kotov, A. A., Kotova, L. M., & Romanov, G. A. (2021) · Plant Science · doi:10.1016/j.plantsci.2021.110880 · Cited by 66 · see citing works
Identification and expression analysis of the IPT and CKX gene families during axillary bud outgrowth in apple ( Malus domestica Borkh.)
Tan, M., Li, G., Qi, S., Liu, X., Chen, X., Ma, J., Zhang, D., & Han, M. (2018) · Gene · doi:10.1016/j.gene.2018.01.101 · Cited by 66 · see citing works
Involvement of auxin and CKs in boron deficiency induced changes in apical dominance of pea plants (Pisum sativum L.)
Wang, G., Römheld, V., Li, C., & Bangerth, F. K. (2005) · Journal of Plant Physiology · doi:10.1016/j.jplph.2005.09.014 · Cited by 65 · see citing works
Self-citation
Interactions between Axillary Branches of Arabidopsis
Ongaro, V., Bainbridge, K., Williamson, L., & Leyser, O. (2008) · Molecular Plant · doi:10.1093/mp/ssn007 · Cited by 65 · see citing works
Auxin-Gibberellin Interactions in Pea: Integrating the Old with the New
Ross, J. J., O'Neill, D., & Rathbone, D. A. (2003) · Journal of Plant Growth Regulation · doi:10.1007/s00344-003-0021-z · Cited by 64 · see citing works
Sugars, hormones, and environment affect the dormancy status in underground adventitious buds of leafy spurge ( Euphorbia esula )
Chao, W. S., Serpe, M. D., Anderson, J. V., Gesch, R. W., & Horvath, D. P. (2006) · Weed Science · doi:10.1614/ws-05-088r.1 · Cited by 64 · see citing works
The interaction of cytokinin with other signals
Rashotte, A. M., Chae, H. S., Maxwell, B. B., & Kieber, J. J. (2005) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2005.00445.x · Cited by 63 · see citing works
The BUD2 mutation affects plant architecture through altering cytokinin and auxin responses in Arabidopsis
Cui, X., Ge, C., Wang, R., Wang, H., Chen, W., Fu, Z., Jiang, X., Li, J., & Wang, Y. (2010) · Cell Research · doi:10.1038/cr.2010.51 · Cited by 61 · see citing works
Effect of decapitation and nutrient applications on shoot branching, yield, and accumulation of secondary metabolites in leaves of Stevia rebaudiana Bertoni
Pal, P. K., Prasad, R., & Pathania, V. (2013) · Journal of Plant Physiology · doi:10.1016/j.jplph.2013.06.017 · Cited by 59 · see citing works
The pea branching RMS2 gene encodes the PsAFB4/5 auxin receptor and is involved in an auxin-strigolactone regulation loop
Ligerot, Y., Germain, A. D. S., Waldie, T., Troadec, C., Citerne, S., Kadakia, N., Pillot, J.-P., Prigge, M. J., Aubert, G., Bendahmane, A., et al. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1007089 · Cited by 58 · see citing works
Modulating tiller formation in cereal crops by the signalling function of fertilizer nitrogen forms
Bauer, B. L., & von Wirén, N. (2020) · Scientific Reports · doi:10.1038/s41598-020-77467-3 · Cited by 57 · see citing works
Cytokinin/Auxin Control of Apical Dominance in Ipomoea nil
Cline, M. G., Wesse, T., & Iwamura, H. (1997) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a029218 · Cited by 57 · see citing works
Sucrose/cytokinin interaction in Sinapis alba at floral induction: a shoot‐to‐root‐to‐shoot physiological loop
Havelange, A., Lejeune, P., & Bernier, G. (2000) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2000.100316.x · Cited by 55 · see citing works
Roles of DgBRC1 in Regulation of Lateral Branching in Chrysanthemum (Dendranthema ×grandiflora cv. Jinba)
Chen, X., Zhou, X., Xi, L., Li, J., Zhao, R., Ma, N., & Zhao, L. (2013) · PLoS ONE · doi:10.1371/journal.pone.0061717 · Cited by 54 · see citing works
Rhizobium-induced elevation in xylem cytokinin delivery in pigeonpea induces changes in shoot development and leaf physiology
Yong, J. W. H., Letham, D. S., Wong, S., & Farquhar, G. D. (2014) · Functional Plant Biology · doi:10.1071/fp14066 · Cited by 52 · see citing works
Transcriptome analysis revealed the interaction among strigolactones, auxin, and cytokinin in controlling the shoot branching of rice
Zha, M., Imran, M., Wang, Y., Xu, J., Ding, Y., & Wang, S. (2019) · Plant Cell Reports · doi:10.1007/s00299-018-2361-y · Cited by 49 · see citing works
Role of AUX1 in the control of organ identity during in vitro organogenesis and in mediating tissue specific auxin and cytokinin interaction in Arabidopsis
Kakani, A., Li, G., & Peng, Z. (2008) · Planta · doi:10.1007/s00425-008-0846-6 · Cited by 49 · see citing works
Cytokinins in Rosa hybrida in relation to bud break
Dieleman, J. A., Verstappen, F. W. A., Nicander, B., Kuiper, D., Tillberg, E., & Tromp, J. J. (1997) · Physiologia Plantarum · doi:10.1034/j.1399-3054.1997.990314.x · Cited by 45 · see citing works
Unlocking the Multifaceted Mechanisms of Bud Outgrowth: Advances in Understanding Shoot Branching
Yuan, Y., Khourchi, S., Li, S., Du, Y., & Delaplace, P. (2023) · Plants · doi:10.3390/plants12203628 · Cited by 44 · see citing works

Role of acropetal water transport in regulation of cytokinin levels in stems of pea seedlings
Kotov, A. A., & Kotova, L. M. (2015) · Russian Journal of Plant Physiology · doi:10.1134/s1021443715020090 · Cited by 12 · see citing works
Auxin and Cytokinins in the Control of Apical Dominance in Pea — A Differential Response Due to Bud Position
Blažková, J., Krekule, J., Macháčková, I., & Procházka, S. (1999) · Journal of Plant Physiology · doi:10.1016/s0176-1617(99)80246-6 · Cited by 15 · see citing works
Effect of apex excision and replacement by 1-naphthylacetic acid on cytokinin concentration and apical dominance in pea plants
Li, C.-J., Guevara, E., Herrera, J., & Bangerth, F. K. (1995) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1995.tb00955.x · Cited by 136 · see citing works
Self-citation
Auxin-cytokinin interactions in the control of shoot branching
Shimizu-Sato, S., Tanaka, M., & Mori, H. (2009) · Plant Molecular Biology · doi:10.1007/s11103-008-9416-3 · Cited by 387 · see citing works
The effects of decapitation on the distribution of cytokinins and growth of Phaseolus vulgaris plants
Staden, J. V., & Carmi, A. (1982) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1982.tb00282.x · Cited by 28 · see citing works

Authors: Bangerth, F.
Affiliations: University of Hohenheim (DE)
Corresponding author: Bangerth, F.
Venue: Planta
Publisher: Springer Science and Business Media LLC
Published: 1994-08
Volume: 194
Issue: 3
ISSN: 0032-0935 (ISSN-L)
1432-2048
DOI: 10.1007/bf00197546
OpenAlex: W1999306802
Cited by: 220
References: 20
Citations by year: 2026: 2 · 2025: 1 · 2024: 4 · 2023: 7 · 2022: 1 · 2021: 3 · 2020: 5 · 2019: 3 · 2018: 8 · 2017: 4 · 2016: 4 · 2015: 10 · 2014: 5 · 2013: 8 · 2012: 7
FWCI: 8.92
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Planta (publishedVersion)
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Parasitism and Resistance
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Physiology and Cultivation Studies
Keywords: cytokinins, xylem exudate, Phaseolus vulgaris, beans, decapitation, apical dominance, auxin, naphthaleneacetic acid, polar auxin transport, auxin-cytokinin interaction, shoot tip removal

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Response of cytokinin concentration in the xylem exudate of bean (Phaseolus vulgaris L.) plants to decapitation and auxin treatment, and relationship to apical dominance

Integrity signals

Claims the paper makes

Claims other papers make about this one

Cites

Cited by

Related

Record

About these checks