Cited by 197Insect-Plant Interactions and ControlPlant-Microbe Interactions and ImmunityPlant biochemistry and biosynthesis

The DOI matches its Crossref record; 137 of the 137 references it cites were found in a registry or an index.

Defence on demand: mechanisms behind optimal defence patterns

Open access

Meldau, Stefan, Erb, Matthias, Baldwin, Ian T.·2012·Annals of Botany

DOI 10.1093/aob/mcs212PMC PMC3503495

Open this paper in CoChat — free account Open PDF

Abstract

BACKGROUND: The optimal defence hypothesis (ODH) predicts that tissues that contribute most to a plant's fitness and have the highest probability of being attacked will be the parts best defended against biotic threats, including herbivores. In general, young sink tissues and reproductive structures show stronger induced defence responses after attack from pathogens and herbivores and contain higher basal levels of specialized defensive metabolites than other plant parts. However, the underlying physiological mechanisms responsible for these developmentally regulated defence patterns remain unknown. SCOPE: This review summarizes current knowledge about optimal defence patterns in above- and below-ground plant tissues, including information on basal and induced defence metabolite accumulation, defensive structures and their regulation by jasmonic acid (JA). Physiological regulations underlying developmental differences of tissues with contrasting defence patterns are highlighted, with a special focus on the role of classical plant growth hormones, including auxins, cytokinins, gibberellins and brassinosteroids, and their interactions with the JA pathway. By synthesizing recent findings about the dual roles of these growth hormones in plant development and defence responses, this review aims to provide a framework for new discoveries on the molecular basis of patterns predicted by the ODH. CONCLUSIONS: Almost four decades after its formulation, we are just beginning to understand the underlying molecular mechanisms responsible for the patterns of defence allocation predicted by the ODH. A requirement for future advances will be to understand how developmental and defence processes are integrated.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1093/aob/mcs212

Cites

0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

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?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

JAZ repressor proteins are targets of the SCFCOI1 complex during jasmonate signalling
Thines, B. C., Katsir, L., Melotto, M., Niu, Y., Mandaokar, A. D., Liu, G., Nomura, K., He, S. Y., Howe, G. A., & Browse, J. (2007) · Nature · doi:10.1038/nature05960 · Cited by 2,512
Plant Immunity to Insect Herbivores
Howe, G. A., & Jander, G. (2007) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092825 · Cited by 2,493
The JAZ family of repressors is the missing link in jasmonate signalling
Chini, A., Fonseca, S., Santos-Fernandez, G., Adie, B. A. T., Chico, J. M., Lorenzo, Ó., García‐Casado, G., López‐Vidriero, I., Lozano, F. M., Ponce, M. R., et al. (2007) · Nature · doi:10.1038/nature06006 · Cited by 2,470
Gibberellin Metabolism and its Regulation
Yamaguchi, S. (2008) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.59.032607.092804 · Cited by 2,204
The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots
Blilou, I., Xu, J., Wildwater, M., Willemsen, V., Paponov, I. A., Friml, J., Heidstra, R., Aida, M., Palme, K. J., & Scheres, B. (2005) · Nature · doi:10.1038/nature03184 · Cited by 2,061
Hormone Crosstalk in Plant Disease and Defense: More Than Just JASMONATE-SALICYLATE Antagonism
Robert‐Seilaniantz, A., Grant, M., & Jones, J. D. G. (2011) · Annual Review of Phytopathology · doi:10.1146/annurev-phyto-073009-114447 · Cited by 1,996
Cytokinin-Deficient Transgenic Arabidopsis Plants Show Multiple Developmental Alterations Indicating Opposite Functions of Cytokinins in the Regulation of Shoot and Root Meristem Activity
Werner, T., Motyka, V., Laucou, V., Smets, R., Onckelen, H. A. V., & Schmülling, T. (2003) · The Plant Cell · doi:10.1105/tpc.014928 · Cited by 1,525
BAK1, an Arabidopsis LRR Receptor-like Protein Kinase, Interacts with BRI1 and Modulates Brassinosteroid Signaling
Li, J., Wen, J., Lease, K. A., Doke, J. T., Tax, F. E., & Walker, J. C. (2002) · Cell · doi:10.1016/s0092-8674(02)00812-7 · Cited by 1,450
A molecular framework for light and gibberellin control of cell elongation
de Lucas, M., Davière, J., Rodríguez-Falcón, M., Pontín, M., Iglesias‐Pedraz, J. M., Lorrain, S., Fankhauser, C., Blázquez, M. A., Titarenko, E., & Prat, S. (2008) · Nature · doi:10.1038/nature06520 · Cited by 1,320
GIBBERELLIN INSENSITIVE DWARF1 encodes a soluble receptor for gibberellin
Ueguchi‐Tanaka, M., Ashikari, M., Nakajima, M., Itoh, H., Katoh, E., Kobayashi, M., Chow, T., Hsing, Y.-I. C., Kitano, H., Yamaguchi, I., et al. (2005) · Nature · doi:10.1038/nature04028 · Cited by 1,302
BES1 Accumulates in the Nucleus in Response to Brassinosteroids to Regulate Gene Expression and Promote Stem Elongation
Yin, Y., Wang, Z., Mora‐García, S., Li, J., Yoshida, S., Asami, T., & Chory, J. (2002) · Cell · doi:10.1016/s0092-8674(02)00721-3 · Cited by 1,287
The evolutionary context for herbivore-induced plant volatiles: beyond the ‘cry for help’
Dicke, M., & Baldwin, I. T. (2010) · Trends in Plant Science · doi:10.1016/j.tplants.2009.12.002 · Cited by 1,258
Self-citation
BRI1/BAK1, a Receptor Kinase Pair Mediating Brassinosteroid Signaling
Nam, K. H., & Li, J. (2002) · Cell · doi:10.1016/s0092-8674(02)00814-0 · Cited by 1,217
Coordinated regulation of Arabidopsis thaliana development by light and gibberellins
Feng, S., Martínez, C., Gusmaroli, G., Wang, Y., Zhou, J., Wang, F., Chen, L., Yu, L., Iglesias‐Pedraz, J. M., Kircher, S., et al. (2008) · Nature · doi:10.1038/nature06448 · Cited by 1,118
NINJA connects the co-repressor TOPLESS to jasmonate signalling
Pauwels, L., Barbero, G. F., Geerinck, J., Tilleman, S., Grunewald, W., Pérez, A. C., Chico, J. M., Bossche, R. V., Sewell, J. A., Gil, E., et al. (2010) · Nature · doi:10.1038/nature08854 · Cited by 1,022
Direct control of shoot meristem activity by a cytokinin-activating enzyme
Kurakawa, T., Ueda, N., Maekawa, M., Kobayashi, K., Kojima, M., Nagato, Y., Sakakibara, H., & Kyozuka, J. (2007) · Nature · doi:10.1038/nature05504 · Cited by 989
A Genetic Framework for the Control of Cell Division and Differentiation in the Root Meristem
Ioio, R. D., Nakamura, K., Moubayidin, L., et al. (2008) · Science · doi:10.1126/science.1164147 · Cited by 944
Variation of glucosinolate accumulation among different organs and developmental stages of Arabidopsis thaliana
Brown, P. D., Tokuhisa, J. G., Reichelt, M., & Gershenzon, J. (2003) · Phytochemistry · doi:10.1016/s0031-9422(02)00549-6 · Cited by 942
Role of phytohormones in insect-specific plant reactions
Erb, M., Meldau, S., & Howe, G. A. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2012.01.003 · Cited by 939
Self-citation
The multifaceted role of ABA in disease resistance
Ton, J., Flors, V., & Mauch‐Mani, B. (2009) · Trends in Plant Science · doi:10.1016/j.tplants.2009.03.006 · Cited by 914
Auxin transport is sufficient to generate a maximum and gradient guiding root growth
Grieneisen, V. A., Xu, J., Marée, A. F. M., Hogeweg, P., & Scheres, B. (2007) · Nature · doi:10.1038/nature06215 · Cited by 892
Plant hormone jasmonate prioritizes defense over growth by interfering with gibberellin signaling cascade
Yang, D., Yao, J., Mei, C.-S., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1201616109 · Cited by 876
Genetic Characterization and Functional Analysis of the GID1 Gibberellin Receptors in Arabidopsis
Griffiths, J., Murase, K., Rieu, I., et al. (2006) · The Plant Cell · doi:10.1105/tpc.106.047415 · Cited by 853
COI1 is a critical component of a receptor for jasmonate and the bacterial virulence factor coronatine
Katsir, L., Schilmiller, A. L., Staswick, P., He, S. Y., & Howe, G. A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802332105 · Cited by 816
Auxin response factors ARF6 and ARF8 promote jasmonic acid production and flower maturation
Nagpal, P., Ellis, C., Weber, H. H., Ploense, S. E., Barkawi, L. S., Guilfoyle, T. J., Hagen, G., Alonso, J. M., Cohen, J. D., Farmer, E. E., et al. (2005) · Development · doi:10.1242/dev.01955 · Cited by 773
Adaptive Patterns in Alkaloid Physiology
McKey, D. (1974) · The American Naturalist · doi:10.1086/282909 · Cited by 750
KNOX Action in Arabidopsis Is Mediated by Coordinate Regulation of Cytokinin and Gibberellin Activities
Jasinski, S., Piazza, P., Craft, J., Hay, A., Woolley, L., Rieu, I., Phillips, A., Hedden, P., & Tsiantis, M. (2005) · Current Biology · doi:10.1016/j.cub.2005.07.023 · Cited by 749
DELLAs Control Plant Immune Responses by Modulating the Balance of Jasmonic Acid and Salicylic Acid Signaling
Navarro, L., Bari, R. P., Achard, P., Lisón, P., Nemri, A., Harberd, N. P., & Jones, J. D. G. (2008) · Current Biology · doi:10.1016/j.cub.2008.03.060 · Cited by 727
Arabidopsis MYC2 Interacts with DELLA Proteins in Regulating Sesquiterpene Synthase Gene Expression
Hong, G., Xue, X., Mao, Y., Wang, L.-J., & Chen, X. (2012) · The Plant Cell · doi:10.1105/tpc.112.098749 · Cited by 679
The control of developmental phase transitions in plants
Huijser, P., & Schmid, M. (2011) · Development · doi:10.1242/dev.063511 · Cited by 676
Sites and homeostatic control of auxin biosynthesis in Arabidopsis during vegetative growth
Ljung, K., Bhalerao, R. P., & Sandberg, G. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.01173.x · Cited by 653
Brassinosteroid Signal Transduction from Receptor Kinases to Transcription Factors
Kim, T., & Wang, Z. (2010) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.043008.092057 · Cited by 650
Localization of the auxin permease AUX1 suggests two functionally distinct hormone transport pathways operate in the Arabidopsis root apexPreprint
Swarup, R., Friml, J., Marchant, A., Ljung, K., Sandberg, G., Palme, K. J., & Bennett, M. J. (2001) · Genes & Development · doi:10.1101/gad.210501 · Cited by 645
Histidine Kinase Homologs That Act as Cytokinin Receptors Possess Overlapping Functions in the Regulation of Shoot and Root Growth in Arabidopsis
Nishimura, C., Ohashi, Y., Sato, S., Kato, T., Tabata, S., & Ueguchi, C. (2004) · The Plant Cell · doi:10.1105/tpc.021477 · Cited by 629
Auxin regulation of cytokinin biosynthesis in Arabidopsis thaliana : A factor of potential importance for auxin–cytokinin-regulated development
Nordström, A., Tarkowski, P., Tarkowska, D., Norbaek, R., Åstot, C., Dolezal, K., & Sandberg, G. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0402504101 · Cited by 574
Arabidopsis KNOXI Proteins Activate Cytokinin Biosynthesis
Yanai, O., Shani, E., Doležal, K., Tarkowski, P., Sablowski, R. W. M., Sandberg, G., Samach, A., & Ori, N. (2005) · Current Biology · doi:10.1016/j.cub.2005.07.060 · Cited by 567
The Arabidopsis BODENLOS gene encodes an auxin response protein inhibiting MONOPTEROS-mediated embryo patterningPreprint
Hamann, T., Benková, E., Bäurle, I., Kientz, M., & Jürgens, G. (2002) · Genes & Development · doi:10.1101/gad.229402 · Cited by 545
Convergent Evolution in Plant Specialized Metabolism
Pichersky, E., & Lewinsohn, E. (2011) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042110-103814 · Cited by 523
Brassinosteroids control meristem size by promoting cell cycle progression in Arabidopsis roots
González‐García, M. P., Vilarrasa‐Blasi, J., Zhiponova, M., Divol, F., Mora‐García, S., Russinova, E., & Caño‐Delgado, A. I. (2011) · Development · doi:10.1242/dev.057331 · Cited by 522
Transcriptional machineries in jasmonate-elicited plant secondary metabolism
Geyter, N. D., Gholami, A., Goormachtig, S., & Goossens, A. (2012) · Trends in Plant Science · doi:10.1016/j.tplants.2012.03.001 · Cited by 519
Molecular Interactions between the Specialist Herbivore Manduca sexta (Lepidoptera, Sphingidae) and Its Natural Host Nicotiana attenuata . III. Fatty Acid-Amino Acid Conjugates in Herbivore Oral Secretions Are Necessary and Sufficient for Herbivore-Specific Plant Responses
Halitschke, R., Schittko, U., Pohnert, G., Boland, W., & Baldwin, I. T. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.2.711 · Cited by 513
Self-citation
TOPLESS Regulates Apical Embryonic Fate in Arabidopsis
Long, J. A., Ohno, C. K., Smith, Z. R., & Meyerowitz, E. M. (2006) · Science · doi:10.1126/science.1123841 · Cited by 505
An Auxin Gradient and Maximum in the Arabidopsis Root Apex Shown by High-Resolution Cell-Specific Analysis of IAA Distribution and Synthesis
Petersson, S. V., Johansson, A. I., Kowalczyk, M., Makoveychuk, A., Wang, J. Y., Möritz, T., Grebe, M., Benfey, P. N., Sandberg, G., & Ljung, K. (2009) · The Plant Cell · doi:10.1105/tpc.109.066480 · Cited by 496
The Cytokinin-Activated Transcription Factor ARR2 Promotes Plant Immunity via TGA3/NPR1-Dependent Salicylic Acid Signaling in Arabidopsis
Choi, J., Huh, S. U., Kojima, M., Sakakibara, H., Paek, K.-H., & Hwang, I. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.07.011 · Cited by 470
An octadecanoid pathway mutant (JL5) of tomato is compromised in signaling for defense against insect attack.
Howe, G. A., Lightner, J. E., Browse, J., & Ryan, C. A. (1996) · The Plant Cell · doi:10.1105/tpc.8.11.2067 · Cited by 456
Molecular Interactions of a Soluble Gibberellin Receptor, GID1, with a Rice DELLA Protein, SLR1, and Gibberellin
Ueguchi‐Tanaka, M., Nakajima, M., Katoh, E., et al. (2007) · The Plant Cell · doi:10.1105/tpc.106.043729 · Cited by 449
Gibberellin Acts through Jasmonate to Control the Expression of MYB21, MYB24, and MYB57 to Promote Stamen Filament Growth in Arabidopsis
Cheng, H. S., Song, S., Xiao, L., et al. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000440 · Cited by 443
Interactions among PIN-FORMED and P-Glycoprotein Auxin Transporters in Arabidopsis
Blakeslee, J. J., Bandyopadhyay, A., Lee, O. R., Mravec, J., Titapiwatanakun, B., Sauer, M., Makam, S. N., Cheng, Y., Bouchard, R., Adamec, J., et al. (2007) · The Plant Cell · doi:10.1105/tpc.106.040782 · Cited by 434
A Molecular Framework for Plant Regeneration
Xu, J., Hofhuis, H. F., Heidstra, R., Sauer, M., Friml, J., & Scheres, B. (2006) · Science · doi:10.1126/science.1121790 · Cited by 398
The auxin-insensitive bodenlos mutation affects primary root formation and apical-basal patterning in the Arabidopsis embryo
Hamann, T., Mayer, U., & Jürgens, G. (1999) · Development · doi:10.1242/dev.126.7.1387 · Cited by 386
Gibberellin-GID1-DELLA: A Pivotal Regulatory Module for Plant Growth and Development
Sun, T. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.161554 · Cited by 386
Apical dominance
Cline, M. G. (1991) · The Botanical Review · doi:10.1007/bf02858771 · Cited by 380
Studies on the Growth Hormone of Plants: III. The Inhibiting Action of the Growth Substance on Bud Development
Thimann, K. V., & Skoog, F. (1933) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.19.7.714 · Cited by 380
Brassinosteroid perception in the epidermis controls root meristem size
Hacham, Y., Holland, N., Butterfield, C. N., Úbeda-Tomás, S., Bennett, M. J., Chory, J., & Savaldi‐Goldstein, S. (2011) · Development · doi:10.1242/dev.061804 · Cited by 375
SHOOT BRANCHING
McSteen, P., & Leyser, O. (2005) · Annual Review of Plant Biology · doi:10.1146/annurev.arplant.56.032604.144122 · Cited by 356
Antisense LOX expression increases herbivore performance by decreasing defense responses and inhibiting growth‐related transcriptional reorganization in Nicotiana attenuata
Halitschke, R., & Baldwin, I. T. (2003) · The Plant Journal · doi:10.1046/j.1365-313x.2003.01921.x · Cited by 342
Self-citation
Quantification, correlations and manipulations of wound-induced changes in jasmonic acid and nicotine in Nicotiana sylvestris
Baldwin, I. T., Zhang, Z., Diab, N., Ohnmeiss, T. E., McCLOUD, E. S., Lynds, G. Y., & Schmelz, E. A. (1997) · Planta · doi:10.1007/s004250050082 · Cited by 311
Self-citation
Gene expression and glucosinolate accumulation in Arabidopsis thaliana in response to generalist and specialist herbivores of different feeding guilds and the role of defense signaling pathways
Mewis, I., Tokuhisa, J. G., Schultz, J. C., Appel, H. M., Ulrichs, C., & Gershenzon, J. (2006) · Phytochemistry · doi:10.1016/j.phytochem.2006.09.004 · Cited by 305
Jasmonates: Structural Requirements for Lipid-Derived Signals Active in Plant Stress Responses and Development
Wasternack, C. H., & Kombrink, E. (2009) · ACS Chemical Biology · doi:10.1021/cb900269u · Cited by 278
Disruption of OPR7 and OPR8 Reveals the Versatile Functions of Jasmonic Acid in Maize Development and Defense
Yan, Y., Christensen, S. A., Isakeit, T., Engelberth, J., Meeley, R. B., Hayward, A., Emery, R. J. N., & Kolomiets, M. V. (2012) · The Plant Cell · doi:10.1105/tpc.111.094151 · Cited by 270
Ontogeny Constrains Systemic Protease Inhibitor Response in Nicotiana attenuata
van Dam, N. M., Horn, M., Mareš, M., & Baldwin, I. T. (2001) · Journal of Chemical Ecology · doi:10.1023/a:1010341022761 · Cited by 267
Self-citation
Gene networks controlling the initiation of flower development
Wellmer, F., & Riechmann, J. L. (2010) · Trends in Genetics · doi:10.1016/j.tig.2010.09.001 · Cited by 267
An Arabidopsis Mutant Defective in Jasmonate Response Is Allelic to the Auxin-Signaling Mutant axr1
Tiryaki, İ., & Staswick, P. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.005272 · Cited by 266
Induction and detoxification of maize 1,4‐benzoxazin‐3‐ones by insect herbivores
Glauser, G., Marti, G., Villard, N., Doyen, G. R., Wolfender, J., Turlings, T. C. J., & Erb, M. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04740.x · Cited by 256
Self-citation
R2R3-NaMYB8 Regulates the Accumulation of Phenylpropanoid-Polyamine Conjugates, Which Are Essential for Local and Systemic Defense against Insect Herbivores in Nicotiana attenuata
Kaur, H., Heinzel, N., Schöttner, M., Baldwin, I. T., & Gális, I. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.151738 · Cited by 254
Self-citation
Benzoic acid glucosinolate esters and other glucosinolates from Arabidopsis thaliana
Reichelt, M., Brown, P. D., Schneider, B., Oldham, N. J., Stauber, E. J., Tokuhisa, J. G., Kliebenstein, D. J., Mitchell‐Olds, T., & Gershenzon, J. (2002) · Phytochemistry · doi:10.1016/s0031-9422(02)00014-6 · Cited by 249
Can optimal defence theory be used to predict the distribution of plant chemical defences?
McCall, A. C., & Fordyce, J. A. (2010) · Journal of Ecology · doi:10.1111/j.1365-2745.2010.01693.x · Cited by 249
Manipulation of Endogenous Trypsin Proteinase Inhibitor Production inNicotiana attenuataDemonstrates Their Function as Antiherbivore Defenses
Zavala, J. A., Patankar, A. G., Gase, K., Hui, D., & Baldwin, I. T. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.103.035634 · Cited by 247
Self-citation
Co(i)‐ordinating defenses: NaCOI1 mediates herbivore‐ induced resistance in Nicotiana attenuata and reveals the role of herbivore movement in avoiding defenses
Paschold, A., Halitschke, R., & Baldwin, I. T. (2007) · The Plant Journal · doi:10.1111/j.1365-313x.2007.03119.x · Cited by 239
Self-citation
Methyl Jasmonate Application Induces Increased Densities of Glandular Trichomes on Tomato, Lycopersicon esculentum
Boughton, A. J., Hoover, K., & Felton, G. W. (2005) · Journal of Chemical Ecology · doi:10.1007/s10886-005-6228-7 · Cited by 238
Belowground Herbivory and Plant Defenses
van Dam, N. M. (2009) · Annual Review of Ecology Evolution and Systematics · doi:10.1146/annurev.ecolsys.110308.120314 · Cited by 224
Regulation of Root Greening by Light and Auxin/Cytokinin Signaling in Arabidopsis
Kobayashi, K., Baba, S., Obayashi, T., Sato, M., Toyooka, K., Keränen, M., Aro, E., Fukaki, H., Ohta, H., Sugimoto, K., et al. (2012) · The Plant Cell · doi:10.1105/tpc.111.092254 · Cited by 223
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
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 · Cited by 220
Cytokinins Mediate Resistance againstPseudomonas syringaein Tobacco through Increased Antimicrobial Phytoalexin Synthesis Independent of Salicylic Acid Signaling
Großkinsky, D. K., Naseem, M., Abdelmohsen, U. R., Plickert, N., Engelke, T., Griebel, T., Zeier, J., Novák, O., Strnad, M., Pfeifhofer, H. W., et al. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.182931 · Cited by 218
Jasmonic acid control of GLABRA3 links inducible defense and trichome patterning in Arabidopsis
Yoshida, Y., Sano, R., Wada, T., Takabayashi, J., & Okada, K. (2009) · Development · doi:10.1242/dev.030585 · Cited by 208
Hormone signaling in plant development
Durbak, A. R., Yao, H., & McSteen, P. (2012) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2011.12.004 · Cited by 204
OPTIMAL DEFENSE THEORY PREDICTS THE ONTOGENY OF AN INDUCED NICOTINE DEFENSE
Ohnmeiss, T. E., & Baldwin, I. T. (2000) · Ecology · doi:10.1890/0012-9658(2000)081[1765:odtpto]2.0.co;2 · Cited by 201
Self-citation
Expression of the Arabidopsis jasmonate signalling repressor JAZ1/TIFY10A is stimulated by auxin
Grunewald, W., Vanholme, B., Pauwels, L., Plovie, E. R., Inzé, D., Gheysen, G., & Goossens, A. (2009) · EMBO Reports · doi:10.1038/embor.2009.103 · Cited by 199
Jasmonate and ppHsystemin Regulate Key Malonylation Steps in the Biosynthesis of 17-Hydroxygeranyllinalool Diterpene Glycosides, an Abundant and Effective Direct Defense against Herbivores inNicotiana attenuata
Heiling, S., Schuman, M. C., Schöttner, M., Mukerjee, P., Berger, B., Schneider, B., Jassbi, A. R., & Baldwin, I. T. (2010) · The Plant Cell · doi:10.1105/tpc.109.071449 · Cited by 178
Self-citation
A specialist root herbivore exploits defensive metabolites to locate nutritious tissues
Robert, C. A. M., Veyrat, N., Glauser, G., Marti, G., Doyen, G. R., Villard, N., Gaillard, M. D. P., Köllner, T. G., Giron, D., Body, M. J. A., et al. (2011) · Ecology Letters · doi:10.1111/j.1461-0248.2011.01708.x · Cited by 176
Self-citation
MYB8 Controls Inducible Phenolamide Levels by Activating Three Novel Hydroxycinnamoyl-Coenzyme A:Polyamine Transferases in Nicotiana attenuata
Onkokesung, N., Gaquerel, E., Kotkar, H. M., Kaur, H., Baldwin, I. T., & Gális, I. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.187229 · Cited by 176
Self-citation
Variation of DIMBOA and related compounds content in relation to the age and plant organ in maize
Cambier, V., Hance, T., & de Hoffmann, E. (2000) · Phytochemistry · doi:10.1016/s0031-9422(99)00498-7 · Cited by 170
The Tomato odorless-2 Mutant Is Defective in Trichome-Based Production of Diverse Specialized Metabolites and Broad-Spectrum Resistance to Insect Herbivores
Kang, J.-H., Liu, G., Shi, F., Jones, A. D., Beaudry, R. M., & Howe, G. A. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.160192 · Cited by 169
Transport of exogenous auxin in two-branched dwarf pea seedlings (Pisum sativum L.): Some implications for polarity and apical dominance
Morris, D. A. (1977) · Planta · doi:10.1007/bf00387930 · Cited by 165
ARR1 Directly Activates Cytokinin Response Genes that Encode Proteins with Diverse Regulatory Functions
Taniguchi, M., Sasaki, N., Tsuge, T., Aoyama, T., & Oka, A. (2007) · Plant and Cell Physiology · doi:10.1093/pcp/pcl063 · Cited by 160
Brassinosteroids interact negatively with jasmonates in the formation of anti-herbivory traits in tomato
Campos, M. L., de Almeida, M., Rossi, M. L., Martinelli, A. P., Litholdo, C. G., Figueira, A., Rampelotti-Ferreira, F. T., Vendramim, J. D., Benedito, V. A., & Peres, L. E. P. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp270 · Cited by 157
Inducible Nicotine Production in Native Nicotiana as an Example of Adaptive Phenotypic Plasticity
Baldwin, I. T. (1999) · Journal of Chemical Ecology · doi:10.1023/a:1020880931488 · Cited by 154
Self-citation
Brassinosteroids Control the Proliferation of Leaf Cells of Arabidopsis thaliana
Nakaya, M., Tsukaya, H., Murakami, N., et al. (2002) · Plant and Cell Physiology · doi:10.1093/pcp/pcf024 · Cited by 150
Transcriptional Diversification and Functional Conservation between DELLA Proteins in Arabidopsis
Gallego‐Bartolomé, J., Minguet, E. G., Marin, J. A., Prat, S., Blázquez, M. A., & Alabadı́, D. (2010) · Molecular Biology and Evolution · doi:10.1093/molbev/msq012 · Cited by 148
Type‐A response regulators are required for proper root apical meristem function through post‐transcriptional regulation of PIN auxin efflux carriers
Zhang, W., To, J. P. C., Cheng, C., Schaller, G. E., & Kieber, J. J. (2011) · The Plant Journal · doi:10.1111/j.1365-313x.2011.04668.x · Cited by 130
Temporal and spatial variation in cyanogenic glycosides in Eucalyptus cladocalyx
Gleadow, R. M., & Woodrow, I. E. (2000) · Tree Physiology · doi:10.1093/treephys/20.9.591 · Cited by 128
Brassinosteroid Enhances Jasmonate‐Induced Anthocyanin Accumulation in Arabidopsis Seedlings
Peng, Z., Han, C., Yuan, L., Zhang, K., Huang, H., & Ren, C. (2011) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2011.01042.x · Cited by 126
AMP1 and MP antagonistically regulate embryo and meristem development in Arabidopsis
Vidaurre, D. P., Ploense, S. E., Krogan, N. T., & Berleth, T. (2007) · Development · doi:10.1242/dev.006759 · Cited by 123
Transformation of shoots into roots inArabidopsisembryos mutant at theTOPLESSlocus
Long, J. A., Woody, S., Poethig, R. S., Meyerowitz, E. M., & Barton, M. K. (2002) · Development · doi:10.1242/dev.129.12.2797 · Cited by 120
A Leaky Mutation in DWARF4 Reveals an Antagonistic Role of Brassinosteroid in the Inhibition of Root Growth by Jasmonate in Arabidopsis
Ren, C., Han, C., Peng, W., Huang, Y., Peng, Z., Xiong, X., Zhu, Q., Gao, B., & Xie, D. (2009) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.140202 · Cited by 115
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
Silencing Geranylgeranyl Diphosphate Synthase inNicotiana attenuataDramatically Impairs Resistance to Tobacco Hornworm
Jassbi, A. R., Gase, K., Hettenhausen, C., Schmidt, A., & Baldwin, I. T. (2007) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.108811 · Cited by 98
Self-citation
Early cytokinin response proteins and phosphoproteins of Arabidopsis thaliana identified by proteome and phosphoproteome profiling
Černý, M., Dyčka, F., Bobáľová, J., & Brzobohatý, B. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq322 · Cited by 74
Mechanisms of Optimal Defense Patterns in Nicotiana attenuata: Flowering Attenuates Herbivory-elicited Ethylene and Jasmonate SignalingF
Diezel, C., Allmann, S., & Baldwin, I. T. (2011) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2011.01086.x · Cited by 74
Self-citation
NaJAZh Regulates a Subset of Defense Responses against Herbivores and Spontaneous Leaf Necrosis inNicotiana attenuataPlants
Oh, Y., Baldwin, I. T., & Gális, I. (2012) · PLANT PHYSIOLOGY · doi:10.1104/pp.112.193771 · Cited by 74
Self-citation
Apical dominance and the levels of indole acetic acid in Phaseolus lateral buds
Hillman, J., Math, V. B., & Medlow, G. C. (1977) · Planta · doi:10.1007/bf00384970 · Cited by 56
Plasticity in allocation of nicotine to reproductive parts inNicotiana attenuata
Baldwin, I. T., & Karb, M. J. (1995) · Journal of Chemical Ecology · doi:10.1007/bf02033797 · Cited by 48
Self-citation
Ectopic expression of maize knotted1 results in the cytokinin-autotrophic growth of cultured tobacco tissues
Hewelt, A., Prinsen, E., Thomas, M., Onckelen, H. A. V., & Meins, F. (2000) · Planta · doi:10.1007/s004250050693 · Cited by 45
Hormonal input in plant meristems: A balancing act
Galinha, C., Bilsborough, G., & Tsiantis, M. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.09.007 · Cited by 44
A Model Without a Mimic: Aristolochic Acids from the California Pipevine Swallowtail, Battus philenor hirsuta, and Its Host Plant, Aristolochia californica
Fordyce, J. A. (2000) · Journal of Chemical Ecology · doi:10.1023/a:1005588829864 · Cited by 40
Ethylene-regulated transcription and crosstalk with jasmonic acid
Shinshi, H. (2008) · Plant Science · doi:10.1016/j.plantsci.2008.03.017 · Cited by 39
Influence of nitrogen availability on shoot development in young peach trees [ Prunus persica (L.) Batsch]
Médiène, S., Pagès, L., Jordan, M., Bot, J. L., & Adamowicz, S. (2002) · Trees · doi:10.1007/s00468-002-0204-4 · Cited by 26
Back to the past for pollination biology
Kessler, D., & Baldwin, I. T. (2011) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2011.03.023 · Cited by 22
Self-citation
Scopolamine in Brugmansia Suaveolens (Solanaceae): Defense, Allocation, Costs, and Induced Response
Alves, M. N., Sartoratto, A., & Trigo, J. R. (2007) · Journal of Chemical Ecology · doi:10.1007/s10886-006-9214-9
Environmental perception avenues: the interaction of cytokinin and environmental response pathways
ARGUESO, C. T., FERREIRA, F. J., & KIEBER, J. J. (2009) · Plant, Cell & Environment · doi:10.1111/j.1365-3040.2009.01940.x
Changes in resource concentration and defence during leaf development in a tough-leaved (Nothofagus moorei) and soft-leaved (Toona ciliata) species
Brunt, C., Read, J., & Sanson, G. D. (2006) · Oecologia · doi:10.1007/s00442-006-0369-4
Selection of plastid- and nuclear-encoded reference genes to study the effect of altered endogenous cytokinin content on photosynthesis genes in Nicotiana tabacum
Cortleven, A., Remans, T., Brenner, W. G., & Valcke, R. (2009) · Photosynthesis Research · doi:10.1007/s11120-009-9470-y
Extreme differences in pyrrolizidine alkaloid levels between leaves of Cynoglossum officinale
van Dam, N. M., Verpoorte, R., & van der Meijden, E. (1994) · Phytochemistry · doi:10.1016/s0031-9422(00)89519-9
Cytokinins Determine Arabidopsis Root-Meristem Size by Controlling Cell Differentiation
Ioio, R. D., Linhares, F. S., Scacchi, E., Casamitjana-Martinez, E., Heidstra, R., Costantino, P., & Sabatini, S. (2007) · Current Biology · doi:10.1016/j.cub.2007.02.047
Cytokinin Primes Plant Responses to Wounding and Reduces Insect Performance
Dervinis, C., Frost, C. J., Lawrence, S. D., Novak, N. G., & Davis, J. M. (2010) · Journal of Plant Growth Regulation · doi:10.1007/s00344-009-9135-2
Plants grow on brassinosteroids
Gudesblat, G. E., & Russinova, E. (2011) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2011.05.004
Distribution and concentration of total phenolics, condensed tannins, and nordihydroguaiaretic acid (NDGA) in creosotebush (Larrea tridentata)
Hyder, P. W., Fredrickson, E. L., Estell, R. E., Tellez, M., & Gibbens, R. P. (2002) · Biochemical Systematics and Ecology · doi:10.1016/s0305-1978(02)00050-9
Increased cytokinin levels in transgenic PSAG12–IPT tobacco plants have large direct and indirect effects on leaf senescence, photosynthesis and N partitioning
Jordi, W., Schapendonk, A., Davelaar, E., Stoopen, G. M., Pot, C. S., Visser, R. D., Rhijn, J. A. V., Gan, S., & Amasino, R. M. (2000) · Plant, Cell & Environment · doi:10.1046/j.1365-3040.2000.00544.x
Field Experiments with Transformed Plants Reveal the Sense of Floral Scents
Kessler, D., Gase, K., & Baldwin, I. T. (2008) · Science · doi:10.1126/science.1160072
Self-citation
Unpredictability of nectar nicotine promotes outcrossing by hummingbirds in Nicotiana attenuata
Kessler, D., Bhattacharya, S., Diezel, C., Rothe, E., Gase, K., Schöttner, M., & Baldwin, I. T. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.05008.x
Self-citation
Independently Silencing Two Photosynthetic Proteins in Nicotiana attenuata Has Different Effects on Herbivore Resistance
Mitra, S., & Baldwin, I. T. (2008) · Plant Physiology · doi:10.1104/pp.108.124354
Self-citation
Integrated Systems View on Networking by Hormones in Arabidopsis Immunity Reveals Multiple Crosstalk for Cytokinin
Naseem, M., Philippi, N., Hussain, A., Wangorsch, G., Ahmed, N., & Dandekar, T. (2012) · The Plant Cell · doi:10.1105/tpc.112.098335
Leaf Senescence Is Delayed in Tobacco Plants Expressing the Maize Homeobox Gene knotted1 under the Control of a Senescence-Activated Promoter
Ori, N., Juarez, M. T., Jackson, D., Yamaguchi, J., Banowetz, G. M., & Hake, S. (1999) · The Plant Cell · doi:10.2307/3870799
Altered cytokinin metabolism affects cytokinin, auxin, and abscisic acid contents in leaves and chloroplasts, and chloroplast ultrastructure in transgenic tobacco
Polanska, L., Vicankova, A., Novakova, M., Malbeck, J., Dobrev, P. I., Brzobohaty, B., Vankova, R., & Machackova, I. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl235
Testing the optimal defence hypothesis for two indirect defences: extrafloral nectar and volatile organic compounds
Radhika, V., Kost, C., Bartram, S., Heil, M., & Boland, W. (2008) · Planta · doi:10.1007/s00425-008-0749-6
Ontogenetic and spatio-temporal patterns of induced volatiles in Glycine max in the light of the optimal defence hypothesis
Rostás, M., & Eggert, K. (2008) · Chemoecology · doi:10.1007/s00049-007-0390-z
Nitrogen economics of root foraging: Transitive closure of the nitrate–cytokinin relay and distinct systemic signaling for N supply vs. demand
Ruffel, S., Krouk, G., Ristova, D., Shasha, D., Birnbaum, K. D., & Coruzzi, G. M. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1108684108
Regulation by Cytokinins of Endogenous Levels of Jasmonic and Salicylic Acids in Mechanically Wounded Tobacco Plants
Sano, H., Seo, S., Koizumi, N., Niki, T., Iwamura, H., & Ohashi, Y. (1996) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a029011
Cytokinin-mediated insect resistance in Nicotiana plants transformed with the ipt gene
Smigocki, A., Neal, J. W., McCanna, I., & Douglass, L. (1993) · Plant Molecular Biology · doi:10.1007/bf00029008
Bypassing Transcription: A Shortcut in Cytokinin-Auxin Interactions
Stepanova, A. N., & Alonso, J. M. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.09.016
Induced Resistance in Agricultural Crops: Effects of Jasmonic Acid on Herbivory and Yield in Tomato Plants
Thaler, J. S. (1999) · Environmental Entomology · doi:10.1093/ee/28.1.30
GLUCOSINOLATES AND TRICHOMES TRACK TISSUE VALUE IN TWO SYMPATRIC MUSTARDS
Traw, M. B., & Feeny, P. (2008) · Ecology · doi:10.1890/07-0729.1
Chapter 13 Adaptive Defense Responses to Pathogens and Insects
Walling, L. L. (2009) · Advances in Botanical Research · doi:10.1016/s0065-2296(09)51013-0
BAK1 regulates the accumulation of jasmonic acid and the levels of trypsin proteinase inhibitors in Nicotiana attenuata's responses to herbivory
Yang, D.-H., Hettenhausen, C., Baldwin, I. T., & Wu, J. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/erq298
Self-citation
Optimal defence, kin conflict and the distribution of furanocoumarins among offspring of wild parsnip
Zangerl, A. R., & Nitao, J. K. (1998) · Evolutionary Ecology · doi:10.1023/a:1006572805289
Cytokinin Stimulates Chloroplast Transcription in Detached Barley Leaves
Zubo, Y. O., Yamburenko, M. V., Selivankina, S. Y., Shakirova, F. M., Avalbaev, A. M., Kudryakova, N. V., Zubkova, N. K., Liere, K., Kulaeva, O. N., Kusnetsov, V. V., et al. (2008) · Plant Physiology · doi:10.1104/pp.108.122275

Research works printed but not linked: 20

Achard, 2009, Gibberellin signaling controls cell proliferation rate in Arabidopsis, Current Biology, 19, 1188, 10.1016/j.cub.2009.05.059 · DOI
Adio, 2011, Biosynthesis and defensive function of Ndelta-acetylornithine, a jasmonate-induced Arabidopsis metabolite, The Plant Cell, 23, 3303, 10.1105/tpc.111.088989 · DOI
An, 2011, Salicylic acid and its function in plant immunity, Journal of Integrative Plant Biology, 53, 412, 10.1111/j.1744-7909.2011.01043.x · DOI
Argueso, 2012, Two-component elements mediate interactions between cytokinin and salicylic acid in plant immunity, PloS Genetics, 8, e1002448, 10.1371/journal.pgen.1002448 · DOI
Baldwin, 1993, Alkaloidal responses to damage in Nicotiana native to North America, Journal of Chemical Ecology, 19, 1143, 10.1007/BF00987376 · DOI
Barrett, 2010, Understanding plant reproductive diversity, Philosophical Transactions of the Royal Society. B: Biological Sciences, 365, 99, 10.1098/rstb.2009.0199 · DOI
Barto, 2005, Testing the optimal defense theory and the growth-differentiation balance hypothesis in Arabidopsis thaliana, Oecologia, 146, 169, 10.1007/s00442-005-0207-0 · DOI
Bowers, 1992, Effcts of gnotype, habitat,and seasonal variation on iridoid glycoside content of Plantago lanceolata (Plantagiaceae) and the implications for insect herbivores, Oecologia, 91, 201, 10.1007/BF00317784 · DOI
Del Bianco, 2011, Context, specificity, and self-organization in auxin response, Cold Spring Harbor Perspectives in Biology, 3, a001578, 10.1101/cshperspect.a001578 · DOI
Haberlandt, 1913, The physiology of cellular division, Sitzungsberichte der Koniglich Preussischen Akademie der Wissenschaften, 318
He, 2002, The GSK3-like kinase BIN2 phosphorylates and destabilizes BZR1, a positive regulator of the brassinosteroid signaling pathway in Arabidopsis, Proceedings of the National Academy of Sciences of the USA, 99, 10185, 10.1073/pnas.152342599 · DOI
Higuchi, 2004, Arabidopsis lacking all the three cytokinin-receptors exists with a small body, Plant and Cell Physiology, 45, pS216
Köllner, 2004, The sesquiterpene hydrocarbons of maize (Zea mays) form five groups with distinct developmental and organ-specific distribution, Phytochemistry, 65, 1895, 10.1016/j.phytochem.2004.05.021 · DOI
Lara, 2004, Extracellular invertase is an essential component of cytokinin-mediated delay of senescence, The Plant Cell, 16, 1276, 10.1105/tpc.018929 · DOI
Li, 2002, Resistance of cultivated tomato to cell content-feeding herbivores is regulated by the octadecanoid-signaling pathway, Plant Physiology, 130, 494, 10.1104/pp.005314 · DOI
Miller, 1955, Kinetin, a cell division factor from deoxyribonucleic acid, Journal of the American Chemical Society, 77, 1392, 10.1021/ja01610a105 · DOI · Paper page
van Schie, 2007, Tomato linalool synthase is induced in trichomes by jasmonic acid, Plant Molecular Biology, 64, 251, 10.1007/s11103-007-9149-8 · DOI
Szemenyei, 2008, TOPLESS mediates auxin-dependent transcriptional repression during Arabidopsis embryogenesis, Science, 319, 1384, 10.1126/science.1151461 · DOI
Walling, 2009, Adaptive defense responses to pathogens and insects, Plant Innate Immunity, 51, 551
Xu, 2002, The SCFCOl1 ubiquitin-ligase complexes are required for jasmonate response in Arabidopsis, The Plant Cell, 14, 1919, 10.1105/tpc.003368 · DOI

Sorted by citations

Jasmonates: Biosynthesis, perception, signal transduction and action in plant stress response, growth and development. An update to the 2007 review in Annals of Botany
Wasternack, C., & Hause, B. (2013) · Annals of Botany · doi:10.1093/aob/mct067 · Cited by 2,629
Plant Secondary Metabolites as Defenses, Regulators, and Primary Metabolites: The Blurred Functional Trichotomy
Erb, M., & Kliebenstein, D. J. (2020) · Plant Physiology · doi:10.1104/pp.20.00433 · Cited by 1,333
Self-citation
Light Regulation of Plant Defense
Ballaré, C. L. (2014) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050213-040145 · Cited by 571
Explaining intraspecific diversity in plant secondary metabolites in an ecological context
Moore, B. D., Andrew, R. L., Külheim, C., & Foley, W. J. (2013) · New Phytologist · doi:10.1111/nph.12526 · Cited by 536
Integrating circadian dynamics with physiological processes in plants
Greenham, K. M., & Mcclung, C. (2015) · Nature reviews genetics · doi:10.1038/nrg3976 · Cited by 437

See all 197

Authors: Meldau, S., Erb, M., & Baldwin, I. T.
Affiliations: Max Planck Society (DE)
Corresponding author: Meldau, Stefan
ORCID: Erb, Matthias
Baldwin, Ian T.
Venue: Annals of Botany
Publisher: Oxford University Press (OUP)
Published: 2012-09-28
Volume: 110
Issue: 8
Pages: 1503-1514
ISSN: 0305-7364 (ISSN-L)
1095-8290
DOI: 10.1093/aob/mcs212
PMC: PMC3503495
OpenAlex: W2072280600
Cited by: 197
References: 0
Citations by year: 2026: 11 · 2025: 5 · 2024: 18 · 2023: 17 · 2022: 12 · 2021: 18 · 2020: 16 · 2019: 10 · 2018: 10 · 2017: 12 · 2016: 15 · 2015: 17 · 2014: 18 · 2013: 17
FWCI: 1.68
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: Annals of Botany (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
BORIS (University Library Bern) (submittedVersion, other-oa)
MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
Open Access CRIS of the University of Bern
Topics: Life Sciences › Agricultural and Biological Sciences › Insect Science › Insect-Plant Interactions and Control
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant-Microbe Interactions and Immunity
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
Keywords: induced defense, jasmonic acid, plant hormones, auxin, cytokinins, gibberellin, brassinosteroids, sink tissues, herbivory, plant development, plant-pathogen interaction, plant-herbivore interactions
MeSH terms: Plant Diseases, Plant Growth Regulators, Plants, Signal Transduction, Plant Components, Aerial, Plant Immunity, Herbivory, Plant Development

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

Defence on demand: mechanisms behind optimal defence patterns

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Metadata

Record

About these checks