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Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis
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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“Novel roles for SL in plant architecture, other than shoot branching, have been recently suggested for dwarfism (Lin et al., 2009) and root architecture (Koltai et al., 2009;Kapulnik et al., 2011;Ruyter-Spira et al., 2011).”
From The Pea TCP Transcription Factor PsBRC1 Acts Downstream of Strigolactones to Control Shoot Branching (2012) · cites this paper as Kapulnik et al., 2011
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InfluentialPossible Roles of Strigolactones during Leaf Senescence
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BackgroundThe Role of Strigolactones in Nutrient-Stress Responses in Plants
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BackgroundBiological Functions of Strigolactones and Their Crosstalk With Other Phytohormones
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BackgroundStrigolactone: An Emerging Growth Regulator for Developing Resilience in Plants
Alvi, A. F., Sehar, Z., Fatma, M., Masood, A., & Khan, N. A. (2022) · Plants · doi:10.3390/plants11192604 · Cited by 91
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“…elongation and leaf senescence in Arabidopsis, and there is evidence for somewhat different interactions and independent effects of each hormone (Kapulnik et al., 2011; Ueda and Kusaba, 2015), reflecting the common observation that plant-hormone interactions are often specific to a given…”
BackgroundKoren, D., Resnick, N., Gati, E. M., Belausov, E., Weininger, S., Kapulnik, Y., & Koltai, H. (2013) · New Phytologist · doi:10.1111/nph.12189 · Cited by 77
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“In contrast, SLs exert inhibitory effects on lateral root formation under normal Pi-sufficient conditions (Ruyter-Spira et al. 2011; Kapulnik et al. 2011b).”
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“A racemic mix of GR24 (GR24rac) that was shown to regulate root growth (Kapulnik et al., 2011; Ruyter-Spira et al., 2011; Rasmussen et al., 2012) and that can also be perceived by KAI2 (Scaffidi et al.”
BackgroundVillaécija‐Aguilar, J. A., Körösy, C., Maisch, L., Hamon‐Josse, M., Petrich, A., Magosch, S., Chapman, P., Bennett, T., & Gutjahr, C. (2021) · Current Biology · doi:10.1016/j.cub.2021.10.044 · Cited by 76
Quain, M. D., Makgopa, M. E., Márquez‐García, B., Comadira, G., Fernández‐García, N., Olmos, E., Schnaubelt, D., Kunert, K. J., & Foyer, C. H. (2014) · Plant Biotechnology Journal · doi:10.1111/pbi.12193 · Cited by 76
The role of strigolactones in root development
Sun, H., Tao, J., Gu, P., Xu, G., & Zhang, Y. (2015) · Plant Signaling & Behavior · doi:10.1080/15592324.2015.1110662 · Cited by 77
“In terms of seminal root and AR elongation and LR formation, based on an analysis of SL and auxin signaling mutants, it was found that auxin signaling acts downstream of SLs.(4,7,9,22) SLs may affect root growth via changes in auxin polar transport from shoot to root and/or auxin efflux in roots.”
BackgroundStrigolactones interact with other phytohormones to modulate plant root growth and development
Sun, H., Li, W., Burritt, D. J., Tian, H., Zhang, H., Liang, X., Miao, Y., Mostofa, M. G., & Tran, L. P. (2022) · The Crop Journal · doi:10.1016/j.cj.2022.07.014 · Cited by 77
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“Subsequent analyses revealed additional functions of strigolactones in plant growth, which included the regulation of the root system development [6,7], the elongation of the mesocotyl and stem [8,9], secondary growth [10], and shoot gravitropism [11].”
BackgroundA new role for glutathione in the regulation of root architecture linked to strigolactones
Márquez‐García, B., Njo, M. F., Beeckman, T., Goormachtig, S., & Foyer, C. H. (2013) · Plant Cell & Environment · doi:10.1111/pce.12172 · Cited by 71
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InfluentialSelf-citationPandya‐Kumar, N., Shema, R., Kumar, M., Mayzlish‐Gati, E., Levy, D., Zemach, H., Belausov, E., Wininger, S., Abu‐Abied, M., Kapulnik, Y., et al. (2014) · New Phytologist · doi:10.1111/nph.12744 · Cited by 70
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“, 2009); strigolactones can increase root hair length by interfering with the regulation of cell expansion by auxin, indicating that strigolactones play a role in the late stages of root hair formation (Kapulnik et al., 2011).”
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“Although SLs control root morphology such as root hair elongation and lateral root development in Arabidopsis [15,16], these differences between wild-type and SL-deficient mutants in rice were not observed under our growth conditions.”
Lahari, Z., Ullah, C., Kyndt, T., Gershenzon, J., & Gheysen, G. (2019) · New Phytologist · doi:10.1111/nph.15953 · Cited by 73
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“…in plant Numerous studies described the prominence of newly recognized SLs nd their derivatives in hormonal crosstalk while the development of oot in many plant varieties ( Kapulnik et al., 2011a ; Ruyter-Spira et al., 011 ; Mayzlish-Gati et al., 2012 ; Sun et al., 2014 ; De Cuyper et al., 014 ).”
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Strigolactones fine-tune the root system
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“In addition, strigolactones regulate several aspects of shoot and root development and thus influence overall plant architecture [8–12].”
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“Moreover, SLs regulate the elongation of root hairs in Arabidopsis (Arabidopsis thaliana) (Koltai et al., 2010; Kapulnik et al., 2011), which is also a singlecell model similar to cotton fiber cell.”
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“In flowering plants, SLs have also been implicated in development [19] as new hormonal players in the suppression of the outgrowth of preformed axillary buds [20,21], in root system architecture, adventitious rooting, secondary growth and reproductive development [22-25].”
BackgroundStes, E., Depuydt, S., Keyser, A. D., Matthys, C., Audenaert, K., Yoneyama, K., Werbrouck, S., Goormachtig, S., & Vereecke, D. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv309 · Cited by 66
“For instance, they control light-dependent photomorphogenesis during seed germination, influence root architecture, impact senescence, and affect flower development (Snowden et al., 2005; Shen et al., 2007; Agusti et al., 2011; Domagalska and Leyser, 2011; Kapulnik et al., 2011; Ruyter-Spira et al., 2011; Rasmussen et…”
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Rehman, N. U., Ali, M., Ahmad, M. Z., Liang, G., & Zhao, J. H. (2017) · Microbial Pathogenesis · doi:10.1016/j.micpath.2017.11.049 · Cited by 67
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“In addition to their role in controlling shoot branching, SLs are relevant molecules that modulate the coordinated development of roots (e.g., primary and lateral root development, root hair elongation) and shoots (Akiyama et al. 2005; Gomez-Roldan et al. 2008; Kapulnik et al. 2011; Koltai 2011).”
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“More recently, a study reported that SL is required for shoot elongation by its mediation of gibberellin metabolism and signaling in rice [116].”
BackgroundYi, F., Song, A., Cheng, K., Liu, J., Wang, C., Shao, L., Wu, S., Wang, P., Zhu, J., Liang, Z., et al. (2023) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiad053 · Cited by 65
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“This was particularly interesting because LP conditions promote SL biosynthesis in the Arabidopsis wild-type (Kohlen et al., 2011; Mayzlish-Gati et al., 2012).”
BackgroundRice DWARF14 acts as an unconventional hormone receptor for strigolactone
Yao, R., Wang, L., Li, Y., Chen, L., Li, S., Du, X., Wang, B., Yan, J., Li, J., & Xie, D. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/ery014 · Cited by 60
“Moreover, SLs also regulate hypocotyl elongation, root growth, leaf development and senescence (Snowden et al., 2005; Kapulnik et al., 2011; Ruyter-Spira et al., 2011; Waters et al., 2012b; Waters and Smith, 2013; Yamada et al., 2014; Soundappan et al., 2015; Ueda and Kusaba, 2015; Wang et al.,…”
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“SLs exert positive and negative regulation as they promote branching of the symbiotic arbuscular mycorrhizal (AM) fungi [14], regulate development of root meristems [15] and inhibit shoot branching by controlling axillary meristem cells growth [16–18].”
Self-citationMarzec, M., & Melzer, M. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19071887 · Cited by 60
“High concentrations of racGR24 (10 μM) decreased the number of LR in max2 signalling mutant in an MAX2-independet manner [35,36].”
BackgroundStrigolactones: New Physiological Roles for an Ancient Signal
Foo, E., & Reid, J. B. (2012) · Journal of Plant Growth Regulation · doi:10.1007/s00344-012-9304-6 · Cited by 60
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“In vascular plants, SLs stimulate stem thickening, leaf senescence, root hair elongation, and primary root growth and suppress adventitious root formation (Agusti et al., 2011; Kapulnik et al., 2011; Rasmussen et al., 2012; Ruyter-Spira et al., 2011; Ueda & Kusaba, 2015; Yamada et al., 2014).”
Receptors, repressors, PINs: a playground for strigolactone signaling
Koltai, H. (2014) · Trends in Plant Science · doi:10.1016/j.tplants.2014.06.008 · Cited by 58
Self-citationLiu, G., Pfeifer, J., Francisco, R. D. B., Emonet, A., Stirnemann, M., Gübeli, C., Hutter, O., Sasse, J., Mattheyer, C., Stelzer, E. H. K., et al. (2017) · New Phytologist · doi:10.1111/nph.14847 · Cited by 57
“As a further step, plant-specific members of cytochrome P450 mono-oxygenases, MORE AXILLARY BRANCHES1 (MAX1) and MAX1 homologs produce canonical SLs such as orobanchol and ent-2 0 -epi-5- deoxystrigol (Zhang et al. , 2014a), respectively most abundant in Petunia hybrida and Oryza sativa (Kretzschmar et al. , 2012; Xie…”
InfluentialHaq, B. U., Ahmad, M. Z., Rehman, N. U., Wang, J., Li, P., Li, D., & Zhao, J. H. (2017) · BMC Plant Biology · doi:10.1186/s12870-017-1182-4 · Cited by 59
“As for the root growth, the knockout mutation in max3 resulted in shorter primary root and root hair lengths, but longer lateral root length [28, 30].”
Gao, J., Zhang, T., Xu, B., Jia, L., Xiao, B., Liu, H., Liu, L., Yan, H., & Xia, Q. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19041062 · Cited by 57
Ahmad, M. Z., Rehman, N. U., Yu, S., Zhou, Y., Haq, B. U., Wang, J., Li, P., Zeng, Z., & Zhao, J. H. (2019) · The Plant Journal · doi:10.1111/tpj.14545 · Cited by 57
Konstantinova, N., Korbei, B., & Luschnig, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052749 · Cited by 56
A Fluorescent Alternative to the Synthetic Strigolactone GR24
Rasmussen, A., Heugebaert, T. S. A., Matthys, C., Deun, R. V., Boyer, F., Goormachtig, S., Stevens, C. V., & Geelen, D. (2012) · Molecular Plant · doi:10.1093/mp/sss110 · Cited by 61
Phytohormone regulation of root growth triggered by P deficiency or Al toxicity
Sun, L., Tian, J., Zhang, H., & Liao, H. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw188 · Cited by 56
Exogenous strigolactones impact metabolic profiles and phosphate starvation signalling in roots
Gamir, J., Torres‐Vera, R., Rial, C., Berrio, E., Campos, P. M., Varela, R. M., Macías, F. A., Pozo, M. J., Flors, V., & Lopez-Raez, J. A. (2020) · Plant Cell & Environment · doi:10.1111/pce.13760 · Cited by 54
Koltai, H. (2012) · Annals of Botany · doi:10.1093/aob/mcs216 · Cited by 54
“…mutants have been found to be insensitive to SLs. Mutations in MAX2 confer an over-shooting phenotype (Stirnberg et al., 2002); this phenotype was not repressed by application of GR24 (a bioactive, synthetic SL; Johnson et al., 1981; Umehara et al., 2008) and was not associated with reduced…”
BackgroundSelf-citationStrigolactone, a key regulator of nutrient allocation in plants
Umehara, M. (2011) · Plant Biotechnology · doi:10.5511/plantbiotechnology.11.1109a · Cited by 53
“SLs affect not only lateral root development but also root hair elongation in Arabidopsis (Kapulnik et al. 2011).”
BackgroundKumar, M., Pandya‐Kumar, N., Dam, A., Haor, H., Mayzlish‐Gati, E., Belausov, E., Wininger, S., Abu‐Abied, M., McErlean, C. S. P., Bromhead, L. J., et al. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/eru513 · Cited by 51
“In roots, SLs regulate lateral-root formation and induce root-hair elongation (Kapulnik et al., 2011).”
BackgroundSelf-citationQuantitative analysis of plant hormones based on LC-MS/MS
Chu, J., Fang, S., Xin, P., Guo, Z., & Chen, Y. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-811562-6.00014-1 · Cited by 55
Combined toxic effects of anatoxin-a and microcystin-LR on submerged macrophytes and biofilms
Li, Q., Gu, P., Zhang, C., Luo, X., Zhang, H., Zhang, J., & Zheng, Z. (2020) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2020.122053 · Cited by 51
Mishra, S., Levengood, H., Fan, J., & Zhang, C. (2024) · Plants · doi:10.3390/plants13223144 · Cited by 60
Fernández‐Aparicio, M., Westwood, J. H., & Rubiales, D. (2011) · Botany · doi:10.1139/b11-075 · Cited by 53
Kaniganti, S., Bhattacharya, J., Petla, B. P., & Reddy, P. S. (2022) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2022.105072 · Cited by 50
Santoro, V., Schiavon, M., Gresta, F., Ertani, A., Cardinale, F., Sturrock, C. J., Celi, L., & Schubert, A. (2020) · Plants · doi:10.3390/plants9050612 · Cited by 49
“thaliana, primary root elongation was accompanied with a decrease of lateral root density and delayed development [14,30,38].”
BackgroundRasmussen, A., Hu, Y., Depaepe, T., Vandenbussche, F., Boyer, F., Straeten, D. V. D., & Geelen, D. (2017) · Journal of Plant Growth Regulation · doi:10.1007/s00344-017-9692-8 · Cited by 49
Strigolactones can be a potential tool to fight environmental stresses in arid lands
Tariq, A., Ullah, I., Sardans, J., Graciano, C., Mussarat, S., Ullah, A., Zeng, F., Wang, W., Al‐Bakre, D. A., Ahmed, Z., et al. (2023) · Environmental Research · doi:10.1016/j.envres.2023.115966 · Cited by 51
Cohen, M., Prandi, C., Occhiato, E. G., Tabasso, S., Wininger, S., Resnick, N., Steinberger, Y., Koltai, H., & Kapulnik, Y. (2012) · Molecular Plant · doi:10.1093/mp/sss134 · Cited by 47
“GR24, GR5, and GR7 were prepared as reported by Johnson et al. (1981) and”
InfluentialSelf-citationStrigolactones Inhibit Caulonema Elongation and Cell Division in the Moss Physcomitrella patens
Hoffmann, B., Proust, H., Belcram, K., Labrune, C., Boyer, F., Rameau, C., & Bonhomme, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0099206 · Cited by 48
“Because karrikins promote Arabidopsis seed germination [41], we tested whether KAR1 has an effect on the germination of moss spores.”
BackgroundInfluentialLiu, Q., Zhang, Y., Matúšová, R., Charnikhova, T. V., Amini, M., Jamil, M., Fernández‐Aparicio, M., Huang, K., Timko, M. P., Westwood, J. H., et al. (2014) · New Phytologist · doi:10.1111/nph.12692 · Cited by 47
“…16.9 and 8.1) compared with untransformed max2-1, but still had significantly higher numbers of branches than WT. ShMAX2 complements the Arabidopsis max2-1 root growth phenotype Strigolactones affect root phenotypes in a MAX2dependent way (Kapulnik et al., 2011a; Ruyter-Spira et al., 2011).”
BackgroundInfluentialDo Phosphate and Cytokinin Interact to Regulate Strigolactone Biosynthesis or Act Independently?
Yoneyama, K., Xie, X., Nomura, T., & Yoneyama, K. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.00438 · Cited by 45
“Subsequent studies with SL mutants and on the effects of application of SL revealed that SLs are involved in the regulation of root architecture (Kapulnik et al., 2011; Ruyter-Spira et al., 2011; Arite et al., 2012), secondary growth (Agusti et al.”
BackgroundBouain, N., Doumas, P., & Rouached, H. (2016) · Current Genomics · doi:10.2174/1389202917666160331201812 · Cited by 46
“The SLs' ability to regulate root development may be executed by induction of the ethylene pathway in conjunction with regulation of auxin transport [72, 73].”
BackgroundVégh, A., Incze, N., Fábián, A., Huo, H., Bradford, K. J., Balázs, E., & Soós, V. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.01641 · Cited by 50
On the outside looking in: roles of endogenous and exogenous strigolactones
Aquino, B., Bradley, J. M., & Lumba, S. (2020) · The Plant Journal · doi:10.1111/tpj.15087 · Cited by 46
Strigolactones and Cytokinin Interaction in Buds in the Control of Rice Tillering
Zha, M., Zhao, Y., Wang, Y., Chen, B., & Tan, Z. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.837136 · Cited by 46
Altamura, M. M., Piacentini, D., Rovere, F. D., Fattorini, L., Falasca, G., & Betti, C. (2023) · Plants · doi:10.3390/plants12020413 · Cited by 46
Strigolactone and karrikin signal perception: receptors, enzymes, or both?
Janssen, B. J., & Snowden, K. C. (2012) · Frontiers in Plant Science · doi:10.3389/fpls.2012.00296 · Cited by 44
Kameoka, H., & Kyozuka, J. (2015) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2014.12.003 · Cited by 45
Lauressergues, D., André, O., Peng, J., Wen, J., Chen, R., Ratet, P., Tadege, M., Mysore, K. S., & Rochange, S. F. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru471 · Cited by 47
“In the last few years, more extensive characterization of the SL mutants in Arabidopsis, pea, and rice has established a role for SL in root architecture and root hair development (Kohlen et al., 2011; Kapulnik et al., 2011), mesocotyl elongation (Hu et al.”
Background
Metadata
- 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
- Venue
- Planta
- Published
- 2010-11-16
- Volume
- 233
- Issue
- 1
- Pages
- 209-216
- ISSN
- 0032-0935 (ISSN-L)
- 1432-2048
- 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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