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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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“Total chlorophyll was measured as previously described (Kong et al., 2006) with the following minor modifications: Chlorophyll was extracted from fresh samples in 95%ethanol, and the absorbance was measured at 665, 645, and 652 nm.”
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“GR24 treatment also led to an increase in root-hair length in wild-type and SL-deficient mutants, but not in SL-insensitive mutants [127].”
Science and application of strigolactones
Aliche, E. B., Screpanti, C., Mesmaeker, A. D., Munnik, T., & Bouwmeester, H. J. (2020) · New Phytologist · doi:10.1111/nph.16489 · Cited by 123
“…it has been reported that SLs regulate auxin-efflux carriers like PIN1 that influence auxin levels in root cells and thus affect root hair growth, thereby introducing another layer of hormonal control of root hair development centred around SLs (Koltai et al. , 2010; Kapulnik et al. , 2011).”
Norman, J. V., Zhang, J., Cazzonelli, C. I., Pogson, B. J., Harrison, P. J., Bugg, T. D. H., Chan, K. X., Thompson, A. J., & Benfey, P. N. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1403016111 · Cited by 123
“We were able to exclude primary roles for the known apocarotenoid signaling molecules, ABA and strigolactone, in LR prepatterning; however, these results do not preclude ABA and strigolactone from acting later at LR emergence and meristem activation as previously described (56, 70).”
Contribution of strigolactone in plant physiology, hormonal interaction and abiotic stresses
Bhoi, A., Yadu, B., Chandra, J., & Keshavkant, S. (2021) · Planta · doi:10.1007/s00425-021-03678-1 · Cited by 127
Passaia, G., Queval, G., Bai, J., Margis-Pinheiro, M. M. A. N., & Foyer, C. H. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/ert486 · Cited by 123
“SLs inhibit lateral root initiation (Kapulnik et al., 2011) by blocking auxin transport (Bennett et al.”
BackgroundA Pivotal Role of Hormones in Regulating Cotton Fiber Development
Xiao, G., Zhao, P., & Zhang, Y. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00087 · Cited by 125
Quantitative Analysis of Lateral Root Development: Pitfalls and How to Avoid Them
DUBROVSKY, J. G., & Forde, B. (2012) · The Plant Cell · doi:10.1105/tpc.111.089698 · Cited by 120
Smoke and Hormone Mirrors: Action and Evolution of Karrikin and Strigolactone Signaling
Morffy, N., Faure, L., & Nelson, D. C. (2016) · Trends in Genetics · doi:10.1016/j.tig.2016.01.002 · Cited by 120
Chesterfield, R. J., Vickers, C. E., & Beveridge, C. A. (2020) · Trends in Plant Science · doi:10.1016/j.tplants.2020.06.005 · Cited by 117
Waters, M. T., & Smith, S. M. (2012) · Molecular Plant · doi:10.1093/mp/sss127 · Cited by 119
“, 2012), roothair elongation (Kapulnik et al., 2011), and secondary thickening of the cambium (Agusti et al.”
BackgroundKarrikin and Cyanohydrin Smoke Signals Provide Clues to New Endogenous Plant Signaling Compounds
Flematti, G. R., Waters, M. T., Scaffidi, A., Merritt, D. J., Ghisalberti, E. L., Dixon, K. W., & Smith, S. M. (2012) · Molecular Plant · doi:10.1093/mp/sss132 · Cited by 115
Auxin, the organizer of the hormonal/environmental signals for root hair growth
Lee, R. D.-W., & Cho, H. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00448 · Cited by 113
Cuyper, C. D., Fromentin, J., Yocgo, R. E. E., Keyser, A. D., Guillotin, B., Kunert, K. J., Boyer, F., & Goormachtig, S. (2014) · Journal of Experimental Botany · doi:10.1093/jxb/eru404 · Cited by 114
“In Arabidopsis, the lateral root density of wild-type plants and strigolactone-deficient mutants decreases after GR24 treatment (Kapulnik et al., 2011a).”
BackgroundResultInfluentialAndreo‐Jiménez, B., Ruyter-Spira, C. P., Bouwmeester, H. J., & Lopez-Raez, J. A. (2015) · Plant and Soil · doi:10.1007/s11104-015-2544-z · Cited by 115
“2015 ; Kapulnik et al .”
Strigolactones and their crosstalk with other phytohormones
Omoarelojie, L. O., Kulkarni, M. G., Finnie, J. F., & Staden, J. V. (2019) · Annals of Botany · doi:10.1093/aob/mcz100 · Cited by 115
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 114
How drought and salinity affect arbuscular mycorrhizal symbiosis and strigolactone biosynthesis?
Lopez-Raez, J. A. (2015) · Planta · doi:10.1007/s00425-015-2435-9 · Cited by 113
“…secondary growth, reproductive development, leaf senescence and defence responses (Gomez-Roldan et al. 2008; Umehara et al. 2008; Agusti et al. 2011; Kapulnik et al. 2011; Ruyter-Spira et al. 2011; Kohlen et al. 2012; Rasmussen et al. 2012; Koltai 2013; Torres-Vera et al. 2014; Yamada et al. 2014).”
BackgroundAt MYB 93 is a novel negative regulator of lateral root development in Arabidopsis
Gibbs, D. J., Voß, U., Harding, S. A., Fannon, J. M., Moody, L. A., Yamada, E., Swarup, K., Nibau, C., Bassel, G. W., Choudhary, A., et al. (2014) · New Phytologist · doi:10.1111/nph.12879 · Cited by 106
“…School of Biosciences, University of Nottingham, Nottingham LE12 5RD, UK; 3School of Biosciences, University of Nottingham, Nottingham, LE12 5RD, UK Author for correspondence: Juliet Coates Tel: +44 121 414 5478 Email: j.c.coates@bham.ac.uk Received: 28 March 2014 Accepted: 7 May 2014 New…”
BackgroundAvenaol, a germination stimulant for root parasitic plants from Avena strigosa
Kim, H. I., Kisugi, T., Khetkam, P., Xie, X., Yoneyama, K., Uchida, K., Yokota, T., Nomura, T., McErlean, C. S. P., & Yoneyama, K. (2014) · Phytochemistry · doi:10.1016/j.phytochem.2014.03.030 · Cited by 109
Rozpądek, P., Domka, A., Nosek, M., Ważny, R., Jędrzejczyk, R. J., Wiciarz, M., & Turnau, K. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.00441 · Cited by 107
“Recently, the plant hormone strigolactone (SL) has been recognized due to its role in root and shoot architecture determination and plant interactions in the rhizosphere (Rochange, 2010; Foo and Reid, 2013; Koltai and Kapulnik, 2013; Pandya-Kumar et al., 2014; Chen et al., 2015; van Zeijl et al., 2015).”
BackgroundStrigolactones positively regulate defense against root-knot nematodes in tomato
Xu, X., Fang, P., Zhang, H., Chi, C., Song, L., Xia, X., Shi, K., Zhou, Y., Zhou, J., & Yu, J. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/ery439 · Cited by 103
Recent Advances in Strigolactone Research: Chemical and Biological Aspects
Seto, Y., Kameoka, H., Yamaguchi, S., & Kyozuka, J. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs142 · Cited by 98
“In contrast, SLs exert inhibitory effects on lateral root formation under normal Pi-sufficient conditions (Kapulnik et al. 2011a, Ruyter-Spira et al. 2011).”
BackgroundZhang, S., Huang, L., Yan, A., Liu, Y., Liu, B., Yu, C., Zhang, A., Schiefelbein, J., & Gan, Y. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw400 · Cited by 97
“Strigolactone, another recently reported hormone, also promotes root hair elongation (Kapulnik et al. , 2011).”
Strigolactone signalling: standing on the shoulders of DWARFs
Bennett, T., & Leyser, O. (2014) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2014.08.001 · Cited by 95
Jamil, M., Charnikhova, T. V., Houshyani, B., van Ast, A., & Bouwmeester, H. J. (2011) · Planta · doi:10.1007/s00425-011-1520-y · Cited by 98
“Differences in resistance in the germination phase as well as in post-attachment resistance were recently also reported for the New Rice for Africa NERICA’s (Cissoko et al. 2011; Jamil et al. 2011b).”
BackgroundMethodInfluentialAuxin-Regulated Lateral Root OrganogenesisPreprint
Cavallari, N., Artner, C., & Benková, E. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a039941 · Cited by 97
Palková, Z., & Váchová, L. (. (2012) · Springer eBooks · doi:10.1007/978-94-007-4264-2 · Cited by 93
Strigolactones spatially influence lateral root development through the cytokinin signaling network
Jiang, L., Matthys, C., Márquez‐García, B., Cuyper, C. D., Smet, L. D., Keyser, A. D., Boyer, F., Beeckman, T., Depuydt, S., & Goormachtig, S. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv478 · Cited by 96
Self-citationPlant hormones as signals in arbuscular mycorrhizal symbiosis
Miransari, M., Abrishamchi, A., Khoshbakht, K., & Niknam, V. (2012) · Critical Reviews in Biotechnology · doi:10.3109/07388551.2012.731684 · Cited by 92
New Strigolactone Analogs as Plant Hormones with Low Activities in the Rhizosphere
Boyer, F., Germain, A. D. S., Pouvreau, J., Clavé, G., Pillot, J.-P., Roux, A., Rasmussen, A., Depuydt, S., Lauressergues, D., Frey, N. F. D., et al. (2013) · Molecular Plant · doi:10.1093/mp/sst163 · Cited by 98
Role of strigolactones: Signalling and crosstalk with other phytohormones
Faizan, M., Faraz, A., Sami, F., Siddiqui, H., Yusuf, M., Gruszka, D., & Hayat, S. (2020) · Open Life Sciences · doi:10.1515/biol-2020-0022 · Cited by 98
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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