Abstract
Parasitic weeds of the genera Striga and Orobanche are considered the most damaging agricultural agents in the developing world. An essential step in parasitic seed germination is sensing a group of structurally related compounds called strigolactones that are released by host plants. Although this makes strigolactone synthesis and action a major target of biotechnology, little fundamental information is known about this hormone. Chemical genetic screening using Arabidopsis thaliana as a platform identified a collection of related small molecules, cotylimides, which perturb strigolactone accumulation. Suppressor screens against select cotylimides identified light-signaling genes as positive regulators of strigolactone levels. Molecular analysis showed strigolactones regulate the nuclear localization of the COP1 ubiquitin ligase, which in part determines the levels of light regulators such as HY5. This information not only uncovers new functions for strigolactones but was also used to identify rice cultivars with reduced capacity to germinate parasitic seed.
This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
Strigolactones: diversity, perception, and hydrolysis
Phytochemistry Reviews Open Access 23 January 2023
-
Probing strigolactone perception mechanisms with rationally designed small-molecule agonists stimulating germination of root parasitic weeds
Nature Communications Open Access 09 July 2022
Access options
Subscribe to this journal
Receive 12 print issues and online access
$259.00 per year
only $21.58 per issue
Rent or buy this article
Get just this article for as long as you need it
$39.95
Prices may be subject to local taxes which are calculated during checkout








References
Santner, A. & Estelle, M. Recent advances and emerging trends in plant hormone signalling. Nature 459, 1071–1078 (2009).
Sakamoto, T. Phytohormones and rice crop yield: strategies and opportunities for genetic improvement. Transgenic Res. 15, 399–404 (2006).
Park, S.Y. et al. Abscisic acid inhibits type 2C protein phosphatases via the PYR/PYL family of START proteins. Science 324, 1068–1071 (2009).
Wang, Z.Y. et al. Nuclear-localized BZR1 mediates brassinosteroid-induced growth and feedback suppression of brassinosteroid biosynthesis. Dev. Cell 2, 505–513 (2002).
Savaldi-Goldstein, S. et al. New auxin analogs with growth-promoting effects in intact plants reveal a chemical strategy to improve hormone delivery. Proc. Natl. Acad. Sci. USA 105, 15190–15195 (2008).
Stirnberg, P., van De Sande, K. & Leyser, H.M. MAX1 and MAX2 control shoot lateral branching in Arabidopsis. Development 129, 1131–1141 (2002).
Booker, J. et al. MAX3/CCD7 is a carotenoid cleavage dioxygenase required for the synthesis of a novel plant signaling molecule. Curr. Biol. 14, 1232–1238 (2004).
Gomez-Roldan, V. et al. Strigolactone inhibition of shoot branching. Nature 455, 189–194 (2008).
Umehara, M. et al. Inhibition of shoot branching by new terpenoid plant hormones. Nature 455, 195–200 (2008).
Akiyama, K., Matsuzaki, K. & Hayashi, H. Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi. Nature 435, 824–827 (2005).
Govindarajulu, M. et al. Nitrogen transfer in the arbuscular mycorrhizal symbiosis. Nature 435, 819–823 (2005).
Joel, D.M. et al. Biology and management of weedy root parasites. Hortic. Rev. (Am. Soc. Hortic. Sci.) 33, 267–349 (2007).
López-Ráez, J.A. et al. Strigolactones: ecological significance and use as a target for parasitic plant control. Pest Manag. Sci. 65, 471–477 (2009).
Scholes, J.D. & Press, M.C. Striga infestation of cereal crops - an unsolved problem in resource limited agriculture. Curr. Opin. Plant Biol. 11, 180–186 (2008).
Humphrey, A.J., Galster, A.M. & Beale, M.H. Strigolactones in chemical ecology: waste products or vital allelochemicals? Nat. Prod. Rep. 23, 592–614 (2006).
Finkelstein, R. et al. Molecular aspects of seed dormancy. Annu. Rev. Plant Biol. 59, 387–415 (2008).
Seo, M. et al. Interaction of light and hormone signals in germinating seeds. Plant Mol. Biol. 69, 463–472 (2009).
Gazzarrini, S. et al. The transcription factor FUSCA3 controls developmental timing in Arabidopsis through the hormones gibberellin and abscisic acid. Dev. Cell 7, 373–385 (2004).
Huq, E. et al. Phytochrome-interacting factor 1 is a critical bHLH regulator of chlorophyll biosynthesis. Science 305, 1937–1941 (2004).
Franklin, K.A. et al. The signal transducing photoreceptors of plants. Int. J. Dev. Biol. 49, 653–664 (2005).
Nott, A. et al. Plastid-to-nucleus retrograde signaling. Annu. Rev. Plant Biol. 57, 739–759 (2006).
Muramoto, T. et al. The Arabidopsis photomorphogenic mutant hy1 is deficient in phytochrome chromophore biosynthesis as a result of a mutation in plastid heme oxygenase. Plant Cell 11, 335–348 (1999).
Davis, S.J. et al. The Arabidopsis thaliana HY1 locus, required for phytochrome-chromophore biosynthesis, encodes a protein related to heme oxygenases. Proc. Natl. Acad. Sci. USA 96, 6541–6546 (1999).
Kohchi, T. et al. The Arabidopsis HY2 gene encodes phytochromobilin synthase, a ferredoxin-dependent biliverdin reductase. Plant Cell 13, 425–436 (2001).
Izawa, T. et al. Phytochromes confer the photoperiodic control of flowering in rice (a short-day plant). Plant J. 22, 391–399 (2000).
Shen, H. et al. The F-box protein MAX2 functions as a positive regulator of photomorphogenesis in Arabidopsis. Plant Physiol. 145, 1471–1483 (2007).
Ang, L.H. et al. Molecular interaction between COP1 and HY5 defines a regulatory switch for light control of Arabidopsis development. Mol. Cell 1, 213–222 (1998).
Osterlund, M.T. et al. Targeted destabilization of HY5 during light-regulated development of Arabidopsis. Nature 405, 462–466 (2000).
von Arnim, A.G. & Deng, X.-W. Light inactivation of Arabidopsis photomorphogenic repressor COP1 involves a cell-specific regulation of its nucleocytoplasmic partitioning. Cell 79, 1035–1045 (1994).
Yi, C. & Deng, X.W. COP1 - from plant photomorphogenesis to mammalian tumorigenesis. Trends Cell Biol. 15, 618–625 (2005).
Goldwasser, Y. et al. Production of strigolactones by Arabidopsis thaliana responsible for Orobanche aegyptiaca seed germination. Plant Growth Regul. 55, 21–28 (2008).
Murashige, T. & Skoog, F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15, 473–497 (1962).
Clough, S.J. & Bent, A.F. Floral dip: a simplified method for Agrobacterium-mediated transformation in Arabidopsis thaliana. Plant J. 16, 735–743 (1998).
Stirnberg, P. et al. MAX2 participates in an SCF complex which acts locally at the node to suppress shoot branching. Plant J. 50, 80–94 (2007).
Acknowledgements
We thank D. Desveaux and S. Lumba for helpful discussion. We also thank the following researchers and the Ohio State Stock Center for providing materials: S.R. Cutler (Univ. California, Riverside), ABRC (T-DNA insertion lies); O. Leyser (Univ. York) (max1-1, max2-1, max3-9); T. Kohchi (Kyoto Univ.) (hy2-105); T. Sakai (RIKEN) (cry1 cry2); Y. Yamauchi, T. Izawa (Japanese National Institute of Agrobiological Sciences) and M. Nakazono (Univ. of Tokyo) (rice strains); M. Umehara (RIKEN) (rice instructions); A.G.T. Babiker (Sudan University of Science and Technology) (Striga hermonthica); M. Goldwasser (Hebrew Univ.) (Orobanche aegyptiaca); K. Yoneyama (Utsunomiya Univ.) (GR24); K. Shirasu and S. Yoshida (RIKEN) (Striga instructions); X.W. Deng (Yale Univ.) (HY5 antibody). We thank K. Akiyama (Osaka Prefecture Univ.) for the internal standard of 2′-epi-5DS.
Author information
Authors and Affiliations
Contributions
Y.T. performed the majority of the wet lab experiments with guidance from P.M. and E.N. D.V. and S.T. performed western blot analysis. A.H. contributed to strigolactone measurements in rice with guidance from S.Y. and Y.K. The project was conceived by Y.T. and P.M. and the manuscript written by P.M.
Corresponding author
Ethics declarations
Competing interests
The authors declare no competing financial interests.
Supplementary information
Supplementary Text and Figures
Supplementary Figs. 1–15 and Supplementary Methods (PDF 5323 kb)
Rights and permissions
About this article
Cite this article
Tsuchiya, Y., Vidaurre, D., Toh, S. et al. A small-molecule screen identifies new functions for the plant hormone strigolactone. Nat Chem Biol 6, 741–749 (2010). https://doi.org/10.1038/nchembio.435
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1038/nchembio.435
This article is cited by
-
Physiological and Molecular Role of Strigolactones as Plant Growth Regulators: A Review
Molecular Biotechnology (2023)
-
Strigolactones: diversity, perception, and hydrolysis
Phytochemistry Reviews (2023)
-
Probing strigolactone perception mechanisms with rationally designed small-molecule agonists stimulating germination of root parasitic weeds
Nature Communications (2022)
-
Strigolactones Stimulate High Light Stress Adaptation by Modulating Photosynthesis Rate in Arabidopsis
Journal of Plant Growth Regulation (2022)
-
Catabolism of strigolactones by a carboxylesterase
Nature Plants (2021)