Inhibition of shoot branching by new terpenoid plant hormones

Nature

Volumn 455, Issue 7210, 2008, Pages 195-200

  Umehara, Mikihisa ^a   Hanada, Atsushi ^a   Yoshida, Satoko ^a   Akiyama, Kohki ^b   Arite, Tomotsugu ^c   Takeda Kamiya, Noriko ^a   Magome, Hiroshi ^a   Kamiya, Yuji ^a   Shirasu, Ken ^a   Yoneyama, Koichi ^d   Kyozuka, Junko ^c   Yamaguchi, Shinjiro ^a  

^a RIKEN Center for Sustainable Resource Science   (Japan)

^b Osaka Prefecture University   (Japan)

^c UNIVERSITY OF TOKYO   (Japan)

^d UTSUNOMIYA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

LACTONE DERIVATIVE; PHYTOHORMONE; STRIGOLACTONE; TERPENOID; UNCLASSIFIED DRUG;

ARBUSCULAR MYCORRHIZA; BIOLOGICAL DEVELOPMENT; CAROTENOID; ENDOGENOUS GROWTH; EXUDATION; FUNGUS; HORMONE; MUTATION; PARASITE; SHOOT GROWTH; TERPENE; WEED;

ARTICLE; MYCORRHIZA; NONHUMAN; ORGANISMAL INTERACTION; PARASITIC PLANT; PLANT ROOT; PRIORITY JOURNAL; SYMBIOSIS;

ARABIDOPSIS; GENE EXPRESSION REGULATION, PLANT; LACTONES; MUTATION; ORYZA SATIVA; PLANT GROWTH REGULATORS; PLANT ROOTS; PLANT SHOOTS; SEEDLING; TERPENES;

ARBUSCULAR; FUNGI;

EID: 51649112342     PISSN: 00280836     EISSN: 14764679     Source Type: Journal    
DOI: 10.1038/nature07272     Document Type: Article

References (44)

1. Beveridge, C. A., Ross, J. J. & Murfet, I. C. Branching mutant rms-2 in Pisum sativum. Grafting studies and endogenous indole-3-acetic acid levels. Plant Physiol. 104, 953-959 (1994).
2. Beveridge, C. A., Ross, J. J. & Murfet, I. C. Branching in pea (Action of Genes Rms3 and Rms4). Plant Physiol. 110, 859-865 (1996).
3. Beveridge, C. A., Symons, G. M. & Turnbull, C. G. Auxin inhibition of decapitation-induced branching is dependent on graft-transmissible signals regulated by genes Rms1 and Rms2. Plant Physiol. 123, 689-697 (2000).
4. Johnson, X. et al. Branching genes are conserved across species. Genes controlling a novel signal in pea are coregulated by other long-distance signals. Plant Physiol. 142, 1014-1026 (2006).
5. Stirnberg, P., van De Sande, K. & Leyser, O. MAX1 and MAX2 control shoot lateral branching in Arabidopsis. Development 129, 1131-1141 (2002).
6. Sorefan, K. et al. MAX4 and RMS1 are orthologous dioxygenase-like genes that regulate shoot branching in Arabidopsis and pea. Genes Dev. 17, 1469-1474 (2003).
7. 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).
8. Booker, J. et al. MAX1 encodes a cytochrome P450 family member that acts downstream of MAX3/4 to produce a carotenoid-derived branch-inhibiting hormone. Dev. Cell 8, 443-449 (2005).
9. Turnbull, C. G., Booker, J. P. & Leyser, O. Micrografting techniques for testing long-distance signalling in Arabidopsis. Plant J. 32, 255-262 (2002).
10. Snowden, K. C. et al. The Decreased apical dominance1/Petunia hybrida CAROTENOID CLEAVAGE DIOXYGENASE8 gene affects branch production and plays a role in leaf senescence, root growth, and flower development. Plant Cell 17, 746-759 (2005).
11. Simons, J. L., Napoli, C. A., Janssen, B. J., Plummer, K. M. & Snowden, K. C. Analysis of the DECREASED APICAL DOMINANCE genes of petunia in the control of axillary branching. Plant Physiol. 143, 697-706 (2007).
12. Ishikawa, S. et al. Suppression of tiller bud activity in tillering dwarf mutants of rice. Plant Cell Physiol. 46, 79-86 (2005).
13. Zou, J. et al. The rice HIGH-TILLERING DWARF1 encoding an ortholog of Arabidopsis MAX3 is required for negative regulation of the outgrowth of axillary buds. Plant J. 48, 687-698 (2006).
14. Arite, T. et al. DWARF10, an RMS1/MAX4/DAD1 ortholog, controls lateral bud outgrowth in rice. Plant J. 51, 1019-1029 (2007).
15. Ongaro, V. & Leyser, O. Hormonal control of shoot branching. J. Exp. Bot. 59, 67-74 (2008).
16. Schwartz, S. H., Qin, X. & Loewen, M. C. The biochemical characterization of two carotenoid cleavage enzymes from Arabidopsis indicates that a carotenoid-derived compound inhibits lateral branching. J. Biol. Chem. 279, 46940-46945 (2004).
17. Auldridge, M. E. et al. Characterization of three members of the Arabidopsis carotenoid cleavage dioxygenase family demonstrates the divergent roles of this multifunctional enzyme family. Plant J. 45, 982-993 (2006).
18. Lechner, E., Achard, P., Vansiri, A., Potuschak, T. & Genschik, P. F-box proteins everywhere. Curr. Opin. Plant Biol. 9, 631-638 (2006).
19. Cook, C. E. et al. Germination stimulants II. The structure of strigol-a potent seed germination stimulant for witchweed (Striga lutea Lour.). J. Am. Chem. Soc. 94, 6198-6199 (1972).
20. Humphrey, A. J. & Beale, M. H. Strigol: Biogenesis and physiological activity. Phytochemistry 67, 636-640 (2006).
21. Bouwmeester, H. J., Matusova, R., Zhongkui, S. & Beale, M. H. Secondary metabolite signalling in host-parasitic plant interactions. Curr. Opin. Plant Biol. 6, 358-364 (2003).
22. Akiyama, K., Matsuzaki, K. & Hayashi, H. Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi. Nature 435, 824-827 (2005).
23. Bradow, J. M., Connick, W. J. Jr, Pepperman, A. B. & Wartelle, L. H. Germination stimulation in wild oats (Avena fatua L.) by synthetic strigol analogues and gibberellic acid. J. Plant Growth Regul. 9, 35-41 (1990).
24. Bradow, J. M., Connick, W. J. & Pepperman, A. B. Comparison of the seed germination effects of synthetic analogs of strigol, gibberellic acid, cytokinins and other plant growth regulators. J. Plant Growth Regul. 7, 227-239 (1988).
25. Goldwasser, Y., Yoneyama, K., Xie, X. & Yoneyama, K. Production of strigolactones by Arabidopsis thaliana responsible for Orobanche aegyptiaca seed germination. Plant Growth Regul. 55, 21-28 (2008).
26. Yoneyama, K. et al. Strigolactones, host recognition signals for root parasitic plants and arbuscular mycorrhizal fungi, from Fabaceae plants. New Phytol. 179, 484-494 (2008).
27. Matusova, R. et al. The strigolactone germination stimulants of the plant-parasitic Striga and Orobanche spp. are derived from the carotenoid pathway. Plant Physiol. 139, 920-934 (2005).
28. López-Ráez, J. A. et al. Tomato strigolactones are derived from carotenoids and their biosynthesis is promoted by phosphate starvation. New Phytol. 178, 863-874 (2008).
29. Bouwmeester, H. J., Roux, C., Lopez-Raez, J. A. & Bécard, G. Rhizosphere communication of plants, parasitic plants and AM fungi. Trends Plant Sci. 12, 224-230 (2007).
30. Yoneyama, K. et al. 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, 125-132 (2007).
31. Yoneyama, K., Yoneyama, K., Takeuchi, Y. & Sekimoto, H. Phosphorus deficiency in red clover promotes exudation of orobanchol, the signal for mycorrhizal symbionts and germination stimulant for root parasites. Planta 225, 1031-1038 (2007).
32. Sugimoto, Y. & Ueyama, T. Production of (+)-5-deoxystrigol by Lotus japonicus root culture. Phytochemistry 69, 212-217 (2008).
33. Zou, J. et al. Characterizations and fine mapping of a mutant gene for high tillering and dwarf in rice (Oryza sativa L.). Planta 222, 604-612 (2005).
34. Gressel, J. et al. Major heretofore intractable biotic constraints to Africa food security that may be amenable to novel biotechnological solutions. Crop Prot. 23, 661-689 (2004).
35. Joel, D. M. The long-term approach to parasitic weeds control: manipulation of specific developmental mechanisms of the parasite. Crop Prot. 19, 753-758 (2000).
36. Xie, X. et al. 2′-Epi-orobanchol and solanacol, two unique strigolactones, germination stimulants for root parasitic weeds, produced by tobacco. J. Agric. Food Chem. 55, 8067-8072 (2007).
37. Cline, M. G. Apical dominance. Bot. Rev. 57, 318-358 (1991).
38. Magome, H., Yamaguchi, S., Hanada, A., Kamiya, Y. & Oda, K. dwarf and delayed-flowering 1, a novel Arabidopsis mutant deficient in gibberellin biosynthesis because of overexpression of a putative AP2 transcription factor. Plant J. 37, 720-729 (2004).
39. Kamachi, K., Yamaya, T., Mae, T. & Ojima, K. A role for glutamine synthetase in the recombination of leaf nitrogen during natural senescence in rice leaves. Plant Physiol. 96, 411-417 (1991).
40. Murashige, T. & Skoog, F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15, 473-497 (1962).
41. Norén, H., Svensson, P. & Andersson, B. A convenient and versatile hydroponic cultivation system for Arabidopsis thaliana. Physiol. Plant. 121, 343-348 (2004).
42. Varbanova, M. et al. Methylation of gibberellins by Arabidopsis GAMT1 and GAMT2. Plant Cell 19, 32-45 (2007).
43. Mangnus, E. M., Jan Dommerholt, F., de Jong, R. L. P. & Zwaneburg, B. Improved synthesis of strigol analogue GR24 and evaluation of the biological activity of its diastereomers. J. Agric. Food Chem. 40, 1230-1235 (1992).
44. Gurney, A. L., Slate, J., Press, C. & Scholes, J. D. A novel form of resistance in rice to the angiosperm parasite Striga hermonthica. New Phytol. 169, 199-208 (2006).