Cited by 502Plant Parasitism and ResistancePlant biochemistry and biosynthesisPlant Molecular Biology Research

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Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis

Kapulnik, Yoram, Delaux, Pierre-Marc, Resnick, Natalie, Mayzlish-Gati, Einav, Wininger, Smadar, Bhattacharya, Chaitali, Séjalon-Delmas, Nathalie, Combier, Jean-Philippe, Bécard, Guillaume, Belausov, Eduard, Beeckman, Tom, Dor, Evgenia, Hershenhorn, Joseph, Koltai, Hinanit·2011·Planta

DOI 10.1007/s00425-010-1310-y

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Abstract

Strigolactones (SLs) have been proposed as a new group of plant hormones, inhibiting shoot branching, and as signaling molecules for plant interactions. Here, we present evidence for effects of SLs on root development. The analysis of mutants flawed in SLs synthesis or signaling suggested that the absence of SLs enhances lateral root formation. In accordance, roots grown in the presence of GR24, a synthetic bioactive SL, showed reduced number of lateral roots in WT and in max3-11 and max4-1 mutants, deficient in SL synthesis. The GR24-induced reduction in lateral roots was not apparent in the SL signaling mutant max2-1. Moreover, GR24 led to increased root-hair length in WT and in max3-11 and max4-1 mutants, but not in max2-1. SLs effect on lateral root formation and root-hair elongation may suggest a role for SLs in the regulation of root development; perhaps, as a response to growth conditions.

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GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants.
Jefferson, R., Kavanagh, T. A., & Bevan, M. W. (1987) · The EMBO Journal · doi:10.1002/j.1460-2075.1987.tb02730.x · Cited by 9,854
Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi
Akiyama, K., Matsuzaki, K.-I., & Hayashi, H. (2005) · Nature · doi:10.1038/nature03608 · Cited by 2,429
Strigolactone inhibition of shoot branching
Gomez-Roldan, V., Fermas, S., Brewer, P. B., Puech-Pagès, V., Dun, E. A., Pillot, J.-P., Letisse, F., Matusova, R., Danoun, S., Portais, J.-C., et al. (2008) · Nature · doi:10.1038/nature07271 · Cited by 2,281
Self-citation
Inhibition of shoot branching by new terpenoid plant hormones
Umehara, M., Hanada, A., Yoshida, S., Akiyama, K., Arite, T., Takeda-Kamiya, N., Magome, H., Kamiya, Y., Shirasu, K., Yoneyama, K., et al. (2008) · Nature · doi:10.1038/nature07272 · Cited by 2,105
Aux/IAA Proteins Repress Expression of Reporter Genes Containing Natural and Highly Active Synthetic Auxin Response Elements
Ulmasov, T., Murfett, J., Hagen, G., & Guilfoyle, T. J. (1997) · The Plant Cell · doi:10.1105/tpc.9.11.1963 · Cited by 2,086
The role of nutrient availability in regulating root architecture
López‐Bucio, J., Cruz‐Ramírez, A., & Herrera‐Estrella, L. (2003) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(03)00035-9 · Cited by 1,528
An Auxin-Dependent Distal Organizer of Pattern and Polarity in the Arabidopsis Root
Sabatini, S., Beis, D., Wolkenfelt, H., Murfett, J., Guilfoyle, T. J., Malamy, J. E., Benfey, P. N., Leyser, O., Bechtold, N., Weisbeek, P. J., et al. (1999) · Cell · doi:10.1016/s0092-8674(00)81535-4 · Cited by 1,367
Organization and cell differentiation in lateral roots of Arabidopsis thaliana
Malamy, J. E., & Benfey, P. N. (1997) · Development · doi:10.1242/dev.124.1.33 · Cited by 1,259
Auxin Transport Promotes Arabidopsis Lateral Root Initiation
Casimiro, I., Marchant, A., Bhalerao, R. P., Beeckman, T., Dhooge, S., Swarup, R., Graham, N. S., Inzé, D., Sandberg, G., Casero, P. J., et al. (2001) · The Plant Cell · doi:10.1105/tpc.13.4.843 · Cited by 1,066
Self-citation
Strigolactones Stimulate Arbuscular Mycorrhizal Fungi by Activating Mitochondria
Besserer, A., Puech‐Pagès, V., Kiefer, P., Roldán, M. V. G., Jauneau, A., Roy, S., Portais, J., Roux, C. P., Bécard, G., & Séjalon‐Delmas, N. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040226 · Cited by 920
Self-citation

Show all 52 references

Research works printed but not linked: 1

Hewitt EJ (1966) Sand and water culture method used in the study of plant nutrition, The Eastern Press, 2nd edn. Commonwealth Agricultural Bureau, London

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“[26] Kapulnik Y, Delaux PM, Resnick N, Mayzlish-Gati E, Wininger S, Bhattacharya C, Séjalon-Delmas N, Combier JP, Bécard G, Belausov E, Beeckman T, Dor E, Hershenhorn J, Koltai H.”
Background
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Peña, E. M. B., Bucio, J. L., Macías‐Rodríguez, L., & Cortés, C. N. M. (2015) · Ciencia Nicolaita · doi:10.35830/cn.vi66.225
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“, Kapulnik, Y., and Koltai, H. (2013). Strigolactone signaling in the endodermis is sufficient to restore root responses and involves SHORT HYPOCOTYL 2 (SHY2) activity.”
Background
Molecular regulation of drought tolerance in rice
Haider, I. (2014) · doi:10.18174/287484
Karrikin-sensing protein KAI2 is a new player in regulating root growth patternsPreprint
Swarbreck, S. M., Guerringue, Y., Matthus, E., Jamieson, F. J. C., & Davies, J. M. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/195891
“…of the structural similarities between KAR and the SL analogue GR24rac (Zwanenburg et al., 2009), and the already established role of GR24rac in regulating root growth (Ruyter-Spira et al., 2011; Kapulnik et al., 2011; Rasmussen et al., 2012), we tested the effect of GR24rac on root skewing.”
Background
Use of strigolactone for stress relief and increased productivity in high-yielding environments
Harmon, A. W. (2017) · Illinois Digital Environment for Access to Learning and Scholarship (University of Illinois at Urbana-Champaign)
Exploring the resistance against root parasitic plants in Arabidopsis and tomato
Cheng, X. (2017) · doi:10.18174/423176
Strigolactone defective mutants of Arabidopsis exhibit delayed sepal senescencePreprint
Xu, X., Jibran, R., Wang, Y., Dong, L., Floková, K., Esfandiari, A., McLachlan, A., Heiser, A., Sutherland‐Smith, A. J., Bouwmeester, H. J., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.01.07.897272
Carotenoid biosynthesis and metabolism in potato tubers
Pasare, S. A. (2013) · OpenGrey (Institut de l'Information Scientifique et Technique)
A synthetic biology toolbox for examining and engineering strigolactone biosynthesis
Wood, R. (2020) · The University of Queensland · doi:10.14264/uql.2020.1007
Regulation of root architecture by Pseudomonas oryzihabitans is mediated by strigolactones and redox processes.Preprint
Cantabella, D., Karpińska, B., Teixidó, N., Dolcet-Sanjuan, R., & Foyer, C. H. (2020) · doi:10.22541/au.159819295.56193824
Cortical microtubule remodelling during strigolactone- and light-mediated growth inhibition of Arabidopsis hypocotylsPreprint
Krasylenko, Y. A., Komis, G., Hlynska, S., Vavrdová, T., Ovečka, M., Pospíšil, T., & Šamaj, J. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.12.07.414524
Impact of abiotic stress on the root growth and development
Kumari, S., Patra, D., Mishra, N., & Panigrahi, K. C. S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85193-0.00016-4
Cross-talk of NO and phytohormones in the regulation of plant development
Kaszler, N., Benkő, P., & Gémes, K. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-818797-5.00026-1
From bottom to top : tweaking auxin homeostasis to deal with salt stress
Koevoets, I. T. (2021) · doi:10.18174/542084
Strigolactones Affect Growth Parameters and Some Antioxidant Enzyme Activities in Wheat (Triticum aestivum L.) under Salt Stress
Önay, E., & Demirbaş, S. (2023) · International Journal of Innovative Approaches in Agricultural Research · doi:10.29329/ijiaar.2023.568.8
“This result is consistent with studies about GR24 pre-treatment in Arabidopsis by (Kapulnik et al., 2011), in wheat by Kausar & Shahbaz (2017), in rapeseed by Ma et al. (2017), and in rice by Ling et al. (2020).”
Karrikins – effect on plants, interaction with other growth regulators, and potential use in horticulture
Marciniak, P., Sochacki, D., & Nowakowska, K. (2023) · Acta Scientiarum Polonorum Hortorum Cultus · doi:10.24326/asphc.2023.4678
Photomodulation of strigolactones in mediating sunflower seedling growth
Bharti, N. (2023) · THE SCIENTIFIC TEMPER · doi:10.58414/scientifictemper.2023.14.2.49
“Photomodulation of GR24-induced genes has also been demonstrated in the leaves of plants exposed to different light regimes (Guo et al. , 2008).”
BackgroundInfluential
Strigolactone receptor DAD2 promotes lateral root formation in Petunia hybridaPreprint
Khuvung, K., Courty, P., & Reinhardt, D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.28.609930
Strigalakton Uygulamalarının Bitkilerde Abiyotik Stres Şartlarına Toleransı Artırmadaki Etkileri
Yüce, M., & Yıldırım, E. (2024) · Erciyes Tarım ve Hayvan Bilimleri Dergisi · doi:10.55257/ethabd.1552107
Diverse Roles of Strigolactones in Plant Growth and Development
Hussain, A., Wani, K. I., & Faizan, S. (2025) · Wiley eBooks · doi:10.1002/9781394302826.ch4
Regulation of Phosphorus Nutrition in Tomato Plants
Santoro, V., Schiavon, M., Prandi, C., & Celi, L. (2025) · doi:10.1002/9781394302826.ch5
Strigolactones and Biological Activity
Yoneyama, K., Xie, X., Yoneyama, K., & Nomura, T. (2025) · Springer eBooks · doi:10.1007/978-3-642-36202-6_155-1
Strigolactone (GR24) mediated in vitro flowering, seed production, and regeneration of plants in Hedyotis biflora (L.) Lam
Manokari, M., Faisal, M., Alatar, A. A., Ahmad, Z., & Shekhawat, M. S. (2025) · The Journal of Horticultural Science and Biotechnology · doi:10.1080/14620316.2025.2513699
Additional file 1 of Strigolactones affect the yield of Tartary buckwheat by regulating endogenous hormone levels
Tang, Z., Huang, X., & Huang, K. (2024) · Figshare · doi:10.6084/m9.figshare.26710979
Comparative transcriptome analysis to identify the key genes and metabolic pathways involved in the Brassica napus semi-dwarf mutant zs-d
Zhang, M., Yang, Q., Xu, J., Zeng, Y., Wang, F., Chen, P., Zhang, C., Ge, X., & Liu, C. (2025) · Scientia Horticulturae · doi:10.1016/j.scienta.2025.114562
Effects of Abscisic Acid and Strigolactone on the Yield and Economic Benefit of Tartary Buckwheat
Dai, L., Cai, F., Lu, D., Tang, J., Huang, K., & HUANG, X. (2025) · Journal of soil science and plant nutrition · doi:10.1007/s42729-025-02928-5
Overexpression of DWARF14-LIKE2 in Arabidopsis thaliana alters multiple traits related to plant morphology and osmotic and salt stress tolerance
Nie, X., Li, L., Zhu, C., Yang, K., Li, Q., Fu, J., Xing, M., Wang, M., Nelson, D. C., Feng, X., et al. (2026) · Plant Cell Reports · doi:10.1007/s00299-026-03742-8
Synthèse et évaluations biologiques de strigolactones, nouvelle classe d'hormones végétales
Chen, V. X. (2011) · theses.fr (ABES) · doi:10.70675/f67ba35cz2dd7z4b27z98feza6ea8d9a669d
Rôle des alpha-tubulines fongiques dans la symbiose ectomycorhizienne et dans les interactions champignons plantes
Perrin, A. (2013) · theses.fr (ABES) · doi:10.70675/3376022dz4a3az45c3z8061zb6d0fa7bff1f
Vers la compréhension de la stimulation du développement racinaire par les signaux symbiotiques chez les légumineuses
Buhian, W. P. C. (2021) · theses.fr (ABES) · doi:10.70675/4d4d8f0bz1ab8z499bz865fz69350644d14c
Utilisation de miPEPs pour étudier et contrôler l'interaction Orobanche cumana - Tournesol
Tourneur, S. (2021) · doi:10.70675/69c5c763zc53cz44e7z9cfcz6eb9ce818980
Temporal Dynamics of Auxins and Strigolactones in the Root Emergence Zone of Chestnut Cuttings During Adventitious Root Formation
Kunc, P., Medič, A., Veberič, R., Grohar, M. C., & Osterc, G. (2026) · Horticulturae · doi:10.3390/horticulturae12050575
The regulatory roles of 24-epibrassinolide and GR24 in the growth and morpho-anatomical adaptations of spinach seedlings grown under salt stress
Sağlam, S., Şahin, A. A., SEVEN, S., & Pınar, N. M. (2026) · Plant Biosystems - An International Journal Dealing with all Aspects of Plant Biology · doi:10.1007/s44473-026-00201-w
Foliar GR24 and γ-aminobutyric acid modulate redox signaling, root-system architecture, and mineral homeostasis in tellurite-stressed wheat ( Triticum aestivum L.)
Haider, I., Rehman, S. U., Iqbal, Z., Mahmood, A., Zaheer, A., Nadeem, M. Y., Mubushar, M., & Tahir, M. U. (2026) · Plant Signaling & Behavior · doi:10.1080/15592324.2026.2728143
“25,26 The synthetic analog GR24 reproduces many of these responses and is the standard experimental tool in the field.”
Influential

Authors: Kapulnik, Y., Delaux, P.-M., Resnick, N., Mayzlish-Gati, E., Wininger, S., Bhattacharya, C., Séjalon-Delmas, N., Combier, J.-P., Bécard, G., Belausov, E., Beeckman, T., Dor, E., Hershenhorn, J., & Koltai, H.
Affiliations: Agricultural Research Organization (IL)
Université Toulouse III - Paul Sabatier (FR)
Ghent University (BE)
Corresponding author: Koltai, Hinanit
ORCID: Delaux, Pierre-Marc
Combier, Jean-Philippe
Bécard, Guillaume
Belausov, Eduard
Beeckman, Tom
Dor, Evgenia
Koltai, Hinanit
Venue: Planta
Publisher: Springer Science and Business Media LLC
Published: 2010-11-16
Volume: 233
Issue: 1
Pages: 209-216
ISSN: 0032-0935 (ISSN-L)
1432-2048
DOI: 10.1007/s00425-010-1310-y
OpenAlex: W2072398514
Cited by: 502
References: 52
Citations by year: 2026: 12 · 2025: 28 · 2024: 29 · 2023: 24 · 2022: 41 · 2021: 43 · 2020: 31 · 2019: 28 · 2018: 31 · 2017: 32 · 2016: 31 · 2015: 32 · 2014: 42 · 2013: 42 · 2012: 35
FWCI: 37.69
Type: journal article
Language: en
Open access: closed
Licence: www.springer.com/tdm (tdm)
Locations: Planta (publishedVersion)
PubMed (publishedVersion)
Ghent University Academic Bibliography (Ghent University) (submittedVersion)
Topics: Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Parasitism and Resistance
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Molecular Biology Research
Keywords: strigolactones, lateral root formation, root hair elongation, root development, GR24, MAX2, strigolactone biosynthesis, strigolactone signaling, Arabidopsis thaliana, plant hormones
MeSH terms: Analysis of Variance, Lactones, Mutation, Arabidopsis, Plant Roots, Organogenesis

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Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis

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