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Strigolactones and the Regulation of Pea Symbioses in Response to Nitrate and Phosphate Deficiency
Open accessAbstract
New roles for the recently identified group of plant hormones, the strigolactones, are currently under active investigation. One of their key roles is to regulate plant symbioses. These compounds act as a rhizosphere signal in arbuscular mycorrhizal symbioses and as a positive regulator of nodulation in legumes. The phosphorous and nitrogen status of the soil has emerged as a powerful regulator of strigolactone production. However, until now, the potential role of strigolactones in regulating mycorrhizal development and nodulation in response to nutrient deficiency has not been proven. In this paper, the role of strigolactone synthesis and response in regulating these symbioses is examined in pea (Pisum sativum L.). Pea is well suited to this study, since there is a range of well-characterized strigolactone biosynthesis and response mutants that is unique amongst legumes. Evidence is provided for a novel endogenous role for strigolactone response within the root during mycorrhizal development, in addition to the action of strigolactones on the fungal partner. The strigolactone response pathway that regulates mycorrhizal development also appears to differ somewhat from the response pathway that regulates nodulation. Finally, studies with strigolactone-deficient pea mutants indicate that, despite strong regulation of strigolactone production by both nitrogen and phosphate, strigolactones are not required to regulate these symbioses in response to nutrient deficiency.
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Nitrogen deficiency increased SL levels in roots and root exudates of sorghum and pea.
“Quantification of SLs in roots and root exudates of sorghum and pea plants grown under low nitrogen conditions showed that nitrogen deficiency increased SL levels in these plants (Yoneyama et al., 2007; Foo et al., 2013)”
From Shaping plant architecture (2015) · cites this paper as Foo et al., 2013
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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
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
Self-citationSorefan, 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
Self-citationMutational Analysis of Branching in Pea. Evidence That Rms1 and Rms5 Regulate the Same Novel Signal
Morris, S. E., Turnbull, C. G. N., Murfet, I. C., & Beveridge, C. A. (2001) · Plant Physiology · doi:10.1104/pp.126.3.1205 · Cited by 208
Pea has its tendrils in branching discoveries spanning a century from auxin to strigolactones
Beveridge, C. A., Dun, E. A., & Rameau, C. (2009) · Plant Physiology · doi:10.1104/pp.109.143909 · Cited by 79
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Research works printed but not linked: 46
- Balzergue, 2010, The regulation of arbuscular mycorrhizal symbiosis by phosphate involves early and systemic signaling events, J. Exp. Bot, 62, 1049, 10.1093/jxb/erq335 · DOI
- Besserer, 2008, GR24, a synthetic analog of strigolactones, stimulates the mitosis and growth of the arbuscular mycorrhizal fungus Gigaspora rosea by boosting its energy metabolism, Plant Physiol, 148, 402, 10.1104/pp.108.121400 · DOI
- Besserer, 2006, Strigolactones stimulate arbuscular mycorrhizal fungi by activating mitochondria, PLOS Biology, 4, e226, 10.1371/journal.pbio.0040226 · DOI
- Beveridge, 1994, Branching mutant rms-2 in Pisum sativum: grafting studies and endogenous indole-3-acetic acid levels, Plant Physiol, 104, 953, 10.1104/pp.104.3.953 · DOI · Paper page
- Beveridge, 1996, Branching in pea: action of genes Rms3 and Rms4, Plant Physiol, 110, 859, 10.1104/pp.110.3.859 · DOI
- Beveridge, 1997, 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), Plant Physiol, 115, 1251, 10.1104/pp.115.3.1251 · DOI
- Breuillin, 2010, Phosphate systemically inhibits development of arbuscular mycorrhiza in Petunia hybrid and represses genes involved in mycorrhizal functioning, Plant J, 64, 1002, 10.1111/j.1365-313X.2010.04385.x · DOI
- Caba, 2000, Inoculation and nitrate alter phytohormone levels in soybean roots: differences between a supernodulating mutant and the wild type, Planta, 211, 98, 10.1007/s004250000265 · DOI
- Eskew, 1989, Nitrate inhibition of nodulation and nitrogen fixation by supernodulating nitrate-tolerant symbiosis mutants of soybean, Crop Sci, 29, 1491, 10.2135/cropsci1989.0011183X002900060035x · DOI
- Ferguson, 2010, Molecular analysis of legume nodule development and autoregulation, J. Integr. Plant Biol, 52, 61, 10.1111/j.1744-7909.2010.00899.x · DOI
- Foo, 2011, Strigolactones promote nodulation in pea, Planta, 234, 1073, 10.1007/s00425-011-1516-7 · DOI
- Foo, 2012, Strigolactones: new physiological roles for an ancient signal, J. Plant Growth Regul
- Forde, 2001, The nutritional control of root development, Plant Soil, 232, 51, 10.1023/A:1010329902165 · DOI
- Gu, 2011, How does phosphate status influence the development of the arbuscular mycorrhizal symbiosis?, Plant Signal. Behav, 6, 1300, 10.4161/psb.6.9.16365 · DOI
- Jamil, 2011, Quantification of the relationship between strigolactones and Strige hermonthica infection in rice under varying levels of nitrogen and phosphorus, Weed Res, 51, 373, 10.1111/j.1365-3180.2011.00847.x · DOI
- Johnson, 2006, Branching genes are conserved across species: genes controlling a novel signal in pea are coregulated by other long-distance signals, Plant Physiol, 142, 1014, 10.1104/pp.106.087676 · DOI · Paper page
- Kohlen, 2011, Strigolactones are transported through the xylem and play a key role in shoot architectural response to phosphate deficiency in nonarbuscular mycorrhizal host Arabidopsis, Plant Physiol, 155, 974, 10.1104/pp.110.164640 · DOI · Paper page
- Koltai, 2011, Strigolactones as mediators of plant growth responses to environmental conditions, Plant Signal. Behav, 6, 37, 10.4161/psb.6.1.13245 · DOI
- Kretzschmar, 2012, A petunia ABC protein controls strigolactone-dependent symbiotic signalling and branching, Nature, 483, 341, 10.1038/nature10873 · DOI
- López-Bucio, 2003, The role of nutrient availability in regulating root architecture, Curr. Op. Plant Biol, 6, 280, 10.1016/S1369-5266(03)00035-9 · DOI
- Markmann, 2009, Evolution of root endosymbiosis with bacteria: how novel are nodules?, Trends Plant Sci, 14, 77, 10.1016/j.tplants.2008.11.009 · DOI
- Mathesius, 2008, Auxin: at the root of nodule development?, Funct. Plant Biol, 35, 651, 10.1071/FP08177 · DOI
- McGonigle, 1990, A new method which gives an objective measure of colonization of roots by vesicular–arbuscular mycorrhizal fungi, New Phytol, 115, 495, 10.1111/j.1469-8137.1990.tb00476.x · DOI
- Mortier, 2012, Nodule numbers are governed by interactions between CLE peptides and cytokinin signalling, Plant J, 70, 367, 10.1111/j.1365-313X.2011.04881.x · DOI
- Mortier, 2012, Never too many? How legumes control nodule number, Plant Cell Environ, 35, 245, 10.1111/j.1365-3040.2011.02406.x · DOI
- Moscatiello, 2010, Flavonoid-induced calcium signalling in Rhizobium leguminosarum bv. Viciae, New Phytol, 188, 814, 10.1111/j.1469-8137.2010.03411.x · DOI
- Murfet, 2003, Branching in pea: double mutants of rms7 with rms1 through rms5, Pisum Genetics, 35, 15
- Nelson, 2011, F-box protein MAX2 has dual roles in karrikin and strigolactone signaling in Arabidopsis thaliana, Proc. Natl Acad. Sci. U S A, 108, 8897, 10.1073/pnas.1100987108 · DOI
- Proust, 2011, Strigolactones regulate protonema branching and act as a quorum sensing-like signal in the moss Physcomitrella patens, Development, 138, 1531, 10.1242/dev.058495 · DOI
- Rasmussen, 2012, Strigolactones suppress adventitious rooting in Arabidopsis and pea, Plant Physiol, 158, 1976, 10.1104/pp.111.187104 · DOI
- Reid, 2011, Molecular mechanisms controlling legume autoregulation of nodulation, Ann. Bot, 108, 789, 10.1093/aob/mcr205 · DOI
- Remy, 1994, Four hundred-million-year-old vesicular arbuscular mycorrhizae, Proc. Natl Acad. Sci. U S A, 91, 11841, 10.1073/pnas.91.25.11841 · DOI
- Ruyter-Spira, 2011, Physiological effects of the synthetic strigolactone analog GR24 on root system architecture in Arabidopsis: Another belowground role for strigolactones?, Plant Physiol, 155, 721, 10.1104/pp.110.166645 · DOI
- Schnabel, 2011, The ROOT DETERMINED NODULATION1 gene regulates nodule number in roots of Medicago truncatula and defines a highly conserved, uncharacterized plant gene family, Plant Physiol, 157, 328, 10.1104/pp.111.178756 · DOI
- Shen, 2012, MAX2 affects multiple hormones to promote photomorphogenesis, Mol. Plant, 5, 224, 10.1093/mp/sss029 · DOI
- Somers, 2009, Thinking outside the F-box: novel ligands for novel receptors, Cell, 14, 206
- Soto, 2010, First indications for the involvement of strigolactones on nodule formation in alfalfa (Medicago sativa), Soil Biol. Biochem, 42, 383, 10.1016/j.soilbio.2009.11.007 · DOI
- Tivendale, 2010, Reassessing the role of N-hydroxytryptamine in auxin biosynthesis, Plant Physiol, 154, 1957, 10.1104/pp.110.165803 · DOI
- Tsvetkova, 2007, Changes in phosphate fractions extracted from difference organs of phosphorus starved nitrogen fixing pea plants, J. Plant Nutr, 30, 2129, 10.1080/01904160701700616 · DOI
- Umehara, 2011, Strigolactone, a key regulator of nutrient allocation in plants, Plant Biotech, 28, 429, 10.5511/plantbiotechnology.11.1109a · DOI
- Umehara, 2010, Contribution of strigolactones to the inhibition of tiller bud outgrowth under phosphate deficiency in rice, Plant Cell Physiol, 51, 1118, 10.1093/pcp/pcq084 · DOI · Paper page
- Vance, 2003, Phosphorus acquisition and use: critical adaptations by plants for securing a non-renewable resource, New Phytol, 157, 423, 10.1046/j.1469-8137.2003.00695.x · DOI
- Vierheilig, 1998, Ink and vinegar, a simple staining technique for arbuscular-mycorrhizal fungi, Appl. Environ. Microbiol, 64, 5004, 10.1128/AEM.64.12.5004-5007.1998 · DOI
- Yoneyama, 2012, How do nitrogen and phosphorus deficiencies affect strigolactone production and exudation?, Planta, 235, 1197, 10.1007/s00425-011-1568-8 · DOI
- Yoneyama, 2007, Nitrogen deficiency as well as phosphorus deficiency in sorghum promotes the production and exudation of 5-deoxystrigol, the host recognition signal for arbuscular mycorrhizal fungi and root parasites, Planta, 227, 125, 10.1007/s00425-007-0600-5 · DOI · Paper page
- Yoneyama, 2007, Phosphorus deficiency in red clover promotes exudation of orobanchol, the signal for mycorrhizal symbionts and germination stimulant for root parasites, Planta, 225, 1031, 10.1007/s00425-006-0410-1 · DOI
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Teichmann, T., & Muhr, M. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00233 · Cited by 228
“…of SLs in roots and root exudates of sorghum and pea plants grown under low nitrogen conditions showed that nitrogen deficiency increased SL levels in these plants (Yoneyama et al., 2007; Foo et al., 2013), which points to SL-mediated suppression of bud outgrowth under nitrogen limitation.”
Background
Metadata
- Authors
- Foo, E., Yoneyama, K., Hugill, C. J., Quittenden, L. J., & Reid, J. B.
- Affiliations
- University of Tasmania (AU)
- Utsunomiya University (JP)
- Corresponding author
- Foo, Eloise
- Venue
- Molecular Plant
- Publisher
- Elsevier BV
- Published
- 2013-01
- Volume
- 6
- Issue
- 1
- Pages
- 76-87
- ISSN
- 1674-2052 (ISSN-L)
- OpenAlex
- W2023755292
- Cited by
- 242
- References
- 6
- Citations by year
- 2026: 13 · 2025: 13 · 2024: 7 · 2023: 21 · 2022: 23 · 2021: 15 · 2020: 16 · 2019: 15 · 2018: 21 · 2017: 25 · 2016: 12 · 2015: 16 · 2014: 25 · 2013: 17
- FWCI
- 22.30
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Molecular Plant (publishedVersion)
- PubMed (publishedVersion)
- eCite Digital Repository (University of Tasmania) (submittedVersion)
- Figshare (submittedVersion, cc-by)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Parasitism and Resistance
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Mycorrhizal Fungi and Plant Interactions
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Legume Nitrogen Fixing Symbiosis
- Keywords
- strigolactones, pea, Pisum sativum, arbuscular mycorrhizal symbiosis, root nodulation, legume symbiosis, nitrate deficiency, phosphate limitation, rhizosphere signaling, plant hormones
- MeSH terms
- Fertilizers, Lactones, Mutation, Nitrates, Phosphates, Symbiosis, Colony Count, Microbial, Signal Transduction, Pisum sativum, Mycorrhizae, Plant Root Nodulation
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