Abstract
Germination is the first crucial step in the life cycle of obligate root parasitic Orobanchaceae, which cannot survive on their own. Therefore, germination of the tiny seeds with minimal reserves should occur only near host roots. These parasites detect the presence of hosts by using root-derived signalling molecules belonging to several distinct classes of metabolites. Strigolactones, the most important germination stimulants, are derived from carotenoids through the action of carotenoid isomerase, carotenoid cleavage dioxygenases, and possibly a cytochrome P450 enzyme. Strigolactone production is increased under phosphate and nitrogen deficiencies. Strigolactones also attract arbuscular mycorrhizal fungi and act as plant hormones that decrease shoot and increase root branching. Various strigolactones have been identified, and the biological processes have differential sensitivity to different strigolactones. Germination stimulants may be a target for the control of parasitic weeds, but considering their other biological functions, such strategies need to be carefully analyzed for unwanted side effects.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Akiyama K, Matsuzaki K, Hayashi H (2005) Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi. Nature 435:824–827
Akiyama K, Ogasawara S, Ito S, Hayashi H (2010) Structural requirements of strigolactones for hyphal branching in AM fungi. Plant Cell Physiol 51:1104–1117
Alder A, Jamil M, Marzorati M, Bruno M, Vermathen M, Bigler P, Ghisla S, Bouwmeester HJ, Beyer P, Al-Babili S (2012) The path from β-carotene to carlactone, a strigolactone-like plant hormone. Science 335:1348–1351
Al-Ghazi Y, Muller B, Pinloche S, Tranbarger TJ, Nacry P, Rossignol M, Tardieu F, Doumas P (2003) Temporal responses of Arabidopsis root architecture to phosphate starvation: evidence for the involvement of auxin signalling. Plant Cell Environ 26:1053–1066
Arite T, Iwata H, Ohshima K, Maekawa M, Nakajima M, Kojima M, Sakakibara H, Kyozuka J (2007) DWARF10, an RMS1/MAX4/DAD1 ortholog, controls lateral bud outgrowth in rice. Plant J 51:1019–1029
Arite T, Umehara M, Ishikawa S, Hanada A, Maekawa M, Yamaguchi S, Kyozuka J (2009) D14, a strigolactone-insensitive mutant of rice, shows an accelerated outgrowth of tillers. Plant Cell Physiol 50:1416–1424
Auger B, Pouvreau J-B, Pouponneau K, Yoneyama K, Montiel G et al (2012) Germination stimulants of Phelipanche ramosa in the rhizosphere of Brassica napus are derived from the glucosinolate pathway. Mol Plant Microbe Interact 25:993–1004
Awad AA, Sato D, Kusumoto D, Kamioka H, Takeuchi Y, Yoneyama K (2006) Characterization of strigolactones, germination stimulants for the root parasitic plants Striga and Orobanche, produced by maize, millet and sorghum. Plant Growth Regul 48:221–227
Ayongwa GC, Stomph TJ, Emechebe AM, Kuyper TW (2006) Root nitrogen concentration of sorghum above 2% produces least Striga hermonthica seed stimulation. Ann Appl Biol 149:255–262
Babalola OO, Osir EO, Sanni AI (2002) Characterization of potential ethylene-producing rhizosphere bacteria of Striga-infested maize and sorghum. Afr J Biotechnol 1:67–69
Babiker AG, Ejeta G, Butler LG, Woodson WR (1993a) Ethylene biosynthesis and strigol-induced germination of Striga asiatica. Physiol Plant 88:359–365
Babiker AGT, Butler KG, Ejeta G, Woodson WR (1993b) Enhancement of ethylene biosynthesis and germination by cytokinins and 1-aminocyclopropane-1-carboxylic acid in Striga asiatica seeds. Physiol Plant 89:21–26
Baldwin IT, Staszak-Kozinski L, Davidson R (1994) Up in smoke: smoke-derived germination cues for postfire annual, Nicotiana attenuata Torr. ex. Watson. J Chem Ecol 20:2345–2371
Balzergue C, Puech-Pags V, Bécard G, Rochange SF (2011) The regulation of arbuscular mycorrhizal symbiosis by phosphate in pea involves early and systemic signalling events. J Exp Bot 62:1049–1060
Bar Nun N, Mayer AM (2005) Smoke chemicals and coumarin promote the germination of the parasitic weed Orobanche aegyptiaca. Isr J Plant Sci 53:97–101
Berner DK, Schaad NW, Völksch B (1999) Use of ethylene-producing bacteria for stimulation of Striga spp. seed germination. Biol Control 15:274–282
Besserer A, Puech-Pagès V, Kiefer P, Gomez-Roldan V, Jauneau A, Roy S, Portais J-C, Roux C, Bécard G, Séjalon-Delmas N (2006) Strigolactones stimulate arbuscular mycorrhizal fungi by activating mitochondria. PLoS Biol 4:1239–1247
Bonser AM, Lynch J, Snapp S (1996) Effect of phosphorus deficiency on growth angle of basal roots in Phaseolus vulgaris. New Phytol 132:281–288
Booker J, Auldridge M, Wills S, McCarty D, Klee H, Leyser O (2004) MAX3/CCD7 is a carotenoid cleavage dioxygenase required for the synthesis of a novel plant signalling molecule. Curr Biol 14:1232–1238
Booker J, Sieberer T, Wright W, Williamson L, Willett B, Stirnberg P, Turnbull C, Srinivasan M, Goddard P, Leyser O (2005) 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
Bouwmeester HJ, Matusova R, Zhongkui S, Beale MH (2003) Secondary metabolite signalling in host-parasitic plant interactions. Curr Opin Plant Biol 6:358–364
Bouwmeester HJ, Roux C, Lopez-Raez JA, Bécard G (2007) Rhizosphere communication of plants, parasitic plants and AM fungi. Trends Plant Sci 12:224–230
Brown NAC, van Staden J (1997) Smoke as a germination cue: a review. Plant Growth Regul 22:115–124
Brown R, Johnson AW, Robinson E, Todd AR (1949) The stimulant involved in the germination of Striga hermonthica. Proc R Soc Lond B Biol Sci 136:395–404
Brown R, Greenwood AD, Johnson AW, Long AG (1951a) The stimulant involved in the germination of Orobanche minor Sm. 1. Assay technique and bulk preparation of the stimulant. Biochem J 48:559–564
Brown R, Greenwood AD, Johnson AW, Long AG, Tyler GL (1951b) The stimulant involved in the germination of Orobanche minor Sm. 2. Chromatographic purification of crude concentrates. Biochem J 48:564–568
Brown R, Greenwood AD, Johnson AW, Lansdown AR, Long AG, Suderland N (1952a) The Orobanche germination factor. III. Concentration of the factor by counter current distribution. Biochem J 52:571–574
Brown R, Johnson AW, Robinson E, Tyler GL (1952b) The Striga germination factor. II. Chromatographic purification of crude concentrates. Biochem J 50:596–600
Butler LG (1995) Chemical communication between the parasitic weed Striga and its crop host. A new dimension in allelochemistry. In: Inderjit KM, Dakshini M, Enhelling FA (eds) Allelopathy, organisms, processes and applications. American Chemical Society, Washington, DC, pp 158–166
Cardoso C, Ruyter-Spira C, Bouwmeester HJ (2011) Strigolactones and root infestation by plant-parasitic Striga, Orobanche and Phelipanche spp. Plant Sci 180:414–420
Chae HS, Yoneyama K, Takeuchi Y, Joel DM (2004) Fluridone and norflurazon, carotenoid-biosynthesis inhibitors, promote seed conditioning and germination of the holoparasite Orobanche minor. Physiol Plant 120:328–337
Chang M, Netzly DG, Butler LG, Lynn DG (1986) Chemical regulation of distance: characterization of the first natural host germination stimulant for Striga asiatica. J Am Chem Soc 108:7858–7860
Chen VX, Boyer FD, Rameau C, Retailleau P, Vors JP, Beau JM (2010) Stereochemistry, total synthesis, and biological evaluation of the new plant hormone solanacol. Chem Eur J 16:13941–13945
Chittapur BM, Hunshal CS, Shenoy H (2001) Allelopathy in parasitic weed management: role of catch and trap crops. Allelopathy J 8:147–160
Chiwocha SDS, Dixon KW, Flematti GR, Ghisalbert EL, Merritt DJ, Nelson DC, Riseborough J-AM, Smith SM, Stevens JC (2009) Karrikins: a new family of plant growth regulators in smoke. Plant Sci 177:252–256
Cline M (1997) Concepts and terminology of apical dominance. Am J Bot 84:1064
Cook CE, Whichard LP, Turner B, Wall ME, Egley GH (1966) Germination of witchweed (Striga lutea Lour.): isolation and properties of a potent stimulant. Science 154:1189–1190
Cook CE, Whichard LP, Wall ME, Egley GH, Coggon P, Luhan PA, McPhail AT (1972) Germination stimulants. II. The structure of strigol – a potent seed germination stimulant for witchweed (Striga lutea Lour.). J Am Chem Soc 94:6198–6199
Daws MI, Pritchard HW, Van Staden J (2008) Butenolide from plant-derived smoke functions as a strigolactone analogue: evidence from parasitic weed seed germination. S Afr J Bot 74:116–120
Dayan FE, Howell JL, Weidenhamer JD (2009) Dynamic root exudation of sorgoleone and its in planta mechanism of action. J Exp Bot 60:2107–2117
Delaux P-M, Xie X, Timme RE, Puech-Pages V, Dunand C et al (2012) Origin of strigolactones in the green lineage. New Phytol 195:857–871
Dixon KW, Roche S, Pate JS (1995) The promotive effect of smoke derived from burnt native vegetation on seed germination of Western Australian plants. Oecologia 101:185–192
Dor E, Alperin B, Wininger S, Ben-Dor B, Somvanshi VS, Koltai H, Kapulnik Y, Hershenhorn J (2010) Characterization of a novel tomato mutant resistant to the weedy parasites Orobanche and Phelipanche spp. Euphytica 171:371–380
Ejeta G (2007) Breeding for Striga resistance in sorghum: exploitation of an intricate host-parasite biology. Crop Sci 47:S216–S227
El-Halmouch Y, Benharrat H, Thalouarn P (2006) Effect of root exudates from different tomato genotypes on broomrape (O. aegyptiaca) seed germination and tubercle development. Crop Prot 25:501–507
Evidente A, Andolfi A, Fiore M, Boari A, Vurro M (2006) Stimulation of Orobanche ramosa seed germination by fusicoccin derivatives: a structure–activity relationship study. Phytochemistry 67:19–26
Evidente A, Fernández-Aparicio M, Cimmino A, Rubiales D, Andolfi A, Motta A (2009) Peagol and peagoldione, two new strigolactone-like metabolites isolated from pea root exudates. Tetrahedron Lett 50:6955–6958
Evidente A, Cimmino A, Fernández-Aparicio M, Andolfi A, Rubiales D, Motta A (2010) Polyphenols, including the new peapolyphenols A-C, from pea root exudates stimulate Orobanche foetida seed germination. J Agric Food Chem 58:2902–2907
Evidente A, Cimmino A, Fernández-Aparicio M, Rubiales D, Andolfi A, Melck D (2011) Soyasapogenol B and trans-22-dehydrocampesterol from common vetch (Vicia sativa L.) root exudates stimulate broomrape seed germination. Pest Manag Sci 67:1015–1022
Fernández-Aparicio M, GarcÃa-Garrido JM, Ocampo JA, Rubiales D (2010) Colonisation of field pea roots by arbuscular mycorrhizal fungi reduces Orobanche and Phelipanche species seed germination. Weed Res 50:262–268
Fernández-Aparicio M, Yoneyama K, Rubiales D (2011) The role of strigolactones in host specificity of Orobanche and Phelipanche seed germination. Seed Sci Res 21:55–61
Flematti GR, Ghisalberti EL, Dixon KW, Trengrove RD (2004) A compound from smoke that promotes seed germination. Science 305:977
Foo E, Turnbull CGN, Beveridge CA (2001) Long-distance signalling and the control of branching in the rms1 mutant of pea. Plant Physiol 126:203–209
Fukui K, Ito S, Ueno K, Yamaguchi S, Kyozuka J, Asami T (2011) Inhibition of rice branching and promotion of Striga germination by debranone derivatives mimicking strigolactone function. Bioorg Med Chem Lett 21:4905–4908
Goldwasser Y, Yoder JI (2001) Differential induction of Orobanche seed germination by Arabidopsis thaliana. Plant Sci 160:951–959
Gomez-Roldan V, Fermas S, Brewer PB, Puech-Pagès V, Dun EA, Pillot J-P, Letisse F, Matusova R, Danoun S, Portais J-C, Bouwmeester H, Bécard G, Beveridge CA, Rameau C, Rochange SF (2008) Strigolactone inhibition of shoot branching. Nature 455:189–194
Hamiaux C, Drummond RSM, Janssen BJ, Ledger SE, Cooney JM, Newcomb RD, Snowden KC (2012) DAD2 is an α/β hydrolase likely to be involved in the perception of the plant branching hormone, strigolactone. Curr Biol 22:2032–2036
Harrison MJ (2005) Signalling in the arbuscular mycorrhizal symbiosis. Annu Rev Microbiol 59:19–42
Hauck C, Müller S, Schildknecht H (1992) A germination stimulant for parasitic flowering plants from Sorghum bicolor, a genuine host plant. J Plant Physiol 139:474–478
Hess DE, Ejeta G, Butler LG (1992) Selecting sorghum genotypes expressing a quantitative biosynthetic trait that confers resistance to Striga. Phytochemistry 31:493–497
Höniges A, Ardelean A, Xie X, Yoneyama K, Yoneyama K, Wegmann K (2012) Towards understanding Orobanche host-specificity. Rom Agric Res 29:313–322
Humphrey AJ, Beale MH (2006) Strigol: biogenesis and physiological activity. Phytochemistry 67:636–640
Ito S, Kitahata N, Umehara M, Hanada A, Kato A, Ueno K, Mashiguchi K, Kyozuka J, Yoneyama K, Yamaguchi S, Asami T (2010) A new lead chemical for strigolactone biosynthesis inhibitors. Plant Cell Physiol 51:1143–1150
Jain R, Foy CL (1992) Nutrient effects on parasitism and germination of Egyptian broomrape (Orobanche aegyptiaca). Weed Technol 6:269–275
Jamil M, Charnikhova T, Verstappen F, Bouwmeester H (2010) Carotenoid inhibitors reduce strigolactone production and Striga hermonthica infection in rice. Arch Biochem Biophys 504:123–131
Jamil M, Charnikhova T, Cardoso C, Jamil T, Ueno K, Verstappen F, Asami T, Bouwmeester HJ (2011a) Quantification of the relationship between strigolactones and Striga hermonthica infection in rice under varying levels of nitrogen and phosphorus. Weed Res 51:373–385
Jamil M, Rodenburg J, Charnikhova T, Bouwmeester HJ (2011b) Pre-attachment Striga hermonthica resistance of NERICA cultivars based on low strigolactone production. New Phytol 192:964–975
Joel DM, Hershenhorn J, Eizenburg H, Aly R, Ejeta G, Rich PJ, Ransom JK, Sauerborn J, Rubiales D (2007) Biology and management of weedy root parasites. In: Janick J (ed) Horticultural reviews. Wiley, London, pp 267–349
Joel DM, Chaudhuri SK, Plakhine D, Ziadna H, Steffens JC (2011) Dehydrocostus lactone is exuded from sunflower roots and stimulates germination of the root parasite Orobanche cumana. Phytochemistry 72:624–634
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 (2011) Strigolactones affect lateral root formation and root-hair elongation in Arabidopsis. Planta 233:209–216
Keeley JE, Fotheringham CJ (1997) Trace gas emissions and smoke-induced seed germination. Science 276:1248–1250
Kim HI, Xie X, Kim HS, Chun JC, Yoneyama K, Nomura T, Takeuchi Y, Yoneyama K (2010) Structure-activity relationship of naturally occurring strigolactones in Orobanche minor seed germination stimulation. J Pestic Sci 35:344–347
Kisugi T, Xie X, Kim HI, Yoneyama K, Sado A, Akiyama K, Hayashi H, Uchida K, Yokota T, Nomura T, Yoneyama K (2013) Strigone, the first isolation and identification as a natural strigolactone from Houttuynia cordata. Phytochemistry 87:60–64
Kitahata N, Ito S, Kato A, Ueno K, Nakano T, Yoneyama K, Asami T (2011) Abamine as a basis for new designs of regulators of strigolactone production. J Pestic Sci 36:53–57
Kohlen W, Charnikhova T, Liu Q, Bours R, Domagalska MA, Beguerie S, Verstappen F, Leyser O, Bouwmeester H, Ruyter-Spira C (2011a) 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 155:974–987
Kohlen W, Ruyter-Spira C, Bouwmeester HJ (2011b) Strigolactones. A new musician in the orchestra of plant hormones. Botany 89:827–840
Kohlen W, Charnikhova T, Lammers M, Pollina T, Tóth P, Haider I, Pozo MJ, de Maagd RA, Ruyter-Spira C, Bouwmeester HJ, López-Ráez JA (2012) The tomato CAROTENOID CLEAVAGE DIOXYGENASE8 (SlCCD8) regulates rhizosphere signalling, plant architecture and affects reproductive development through strigolactone biosynthesis. New Phytol 196:535–547
Koltai H, Dor E, Hershenhorn J, Joel D, Weininger S, Lekalla S, Shealtiel H, Bahattacharya C, Eliahu E, Resnick N, Barg R, Kapulnik Y (2010a) Strigolactones’ effect on root growth and root-hair elongation may be mediated by auxin-efflux carriers. J Plant Growth Regul 29:129–136
Koltai H, LekKala SP, Bhattacharya C, Mayzlish-Gati E, Resnick N, Wininger S, Dor E, Yoneyama K, Yoneyama K, Hershenhorn J, Joel DM, Kapulnik Y (2010b) A tomato strigolactone-impaired mutant displays aberrant shoot morphology and plant interactions. J Exp Bot 61:1739–1749
Koltai H, Cohen M, Chesin O, Mayzlish-Gati E, Bécard G, Puech-Pagès V, Dor BB, Resnick N, Wininger S, Kapulnik Y (2011) Light is a positive regulator of strigolactone levels in tomato roots. J Plant Physiol 168:1993–1996
Kondo Y, Tadokoro E, Matsuura M, Iwasaki K, Sugimoto Y, Miyake H, Takikawa H, Sasaki M (2007) Synthesis and seed germination stimulating activity of some imino analogs of strigolactones. Biosci Biotechnol Biochem 71:2781–2786
Kusumoto D, Chae SH, Mukaida K, Yoneyama K, Joel DM, Takeuchi Y (2006) Effects of fluridone and norflurazon on conditioning and germination of Striga asiatica seeds. Plant Growth Regul 48:73–78
Ledger SE, Janssen BJ, Karunairetnam S, Wang T, Snowden KC (2010) Modified CAROTENOID CLEAVAGE DIOXYGENASE8 expression correlates with altered branching in kiwifruit (Actinidia chinensis). New Phytol 188:803–813
Lendzemo VW, Kuyper TW, Matusova R, Bouwmeester HJ, Van Ast A (2007) Colonization by arbuscular mycorrhizal fungi of sorghum leads to reduced germination and subsequent attachment and emergence of Striga hermonthica. Plant Signal Behav 2:58–62
Lin H, Wang R, Qian Q, Yan M, Meng X, Fu Z, Yan C, Jiang B, Su Z, Li J, Wang Y (2009) DWARF27, an iron-containing protein required for the biosynthesis of strigolactones, regulates rice tiller bud outgrowth. Plant Cell 21:1512–1525
Logan DC, Stewart GR (1991) Role of ethylene in the germination of the hemiparasite Striga hermonthica. Plant Physiol 97:1435–1438
López-Bucio J, Hernandez-Abreu E, Sanchez-Calderon L, Nieto-Jacobo MF, Simpson J, Herrera-Estrella L (2002) Phosphate availability alters architecture and causes changes in hormone sensitivity in the Arabidopsis root system. Plant Physiol 129:244–256
López-Ráez JA, Charnikhova T, Gómez-Roldán V, Matusova R, Kohlen W, De Vos R, Verstappen F, Puech-Pages V, Bécard G, Mulder P, Bouwmeester H (2008a) Tomato strigolactones are derived from carotenoids and their biosynthesis is promoted by phosphate starvation. New Phytol 178:863–874
López-Ráez JA, Charnikhova T, Mulder P, Kohlen W, Bino R, Levin I, Bouwmeester H (2008b) Susceptibility of the tomato mutant high pigment-2dg (hp-2 dg) to Orobanche spp. infection. J Agric Food Chem 56:6326–6332
López-Ráez JA, Matusova R, Cardoso C, Jamil M, Charnikhova T, Kohlen W, Ruyter-Spira C, Verstappen F, Bouwmeester H (2008c) Strigolactones: ecological significance and use as a target for parasitic plant control. Pest Manag Sci 64:471–477
López-Ráez JA, Kohlen W, Charnikhova T, Mulder P, Undas AK, Sergeant MJ, Verstappen F, Bugg TDH, Thompson AJ, Ruyter-Spira C, Bouwmeester H (2010) Does abscisic acid affect strigolactone biosynthesis? New Phytol 187:343–354
López-Ráez JA, Charnikhova T, Fernandez I, Bouwmeester HJ, Pozo MJ (2011) Arbuscular mycorrhizal symbiosis decreases strigolactone production in tomato. J Plant Physiol 168:294–297
Lynn DG, Chang M (1990) Phenolic signals in cohabitation: implications for plant development. Annu Rev Plant Physiol Plant Mol Biol 41:497–526
Ma Z, Baskin TI, Brown KM, Lynch JP (2003) Regulation of root elongation under phosphorus stress involves changes in ethylene responsiveness. Plant Physiol 131:1381–1390
MacÃas FA, GarcÃa-DÃaz MD, Pérez-de-Luque A, Rubiales D, Galindo JCG (2009) New chemical clues for broomrape-sunflower host–parasite interactions: synthesis of guaianestrigolactones. J Agric Food Chem 57:5853–5864
Matsuura H, Ohashi K, Sasako H, Tagawa N, Takano Y, Ioka Y, Nabeta K, Yoshihara T (2008) Germination stimulant from root exudates of Vigna unguiculata. Plant Growth Regul 54:31–36
Matusova R, Rani K, Verstappen FWA, Franssen MCR, Beale MH, Bouwmeester HJ (2005) The strigolactone germination stimulants of the plant-parasitic Striga and Orobanche spp. are derived from the carotenoid pathway. Plant Physiol 139:920–934
Mori K, Matsui J, Bando M, Kido M, Takeuchi Y (1998) Synthetic disproof against the structure proposed for alectrol, the germination stimulant from Vigna unguiculata. Tetrahedron Lett 39:6023–6026
Müller S, Hauck C, Schildknecht H (1992) Germination stimulants produced by Vigna unguiculata Walp cv Saunders Upright. J Plant Growth Regul 11:77–84
Mwakaboko AS, Zwanenburg B (2011) Strigolactone analogs derived from ketones using a working model for germination stimulants as a blueprint. Plant Cell Physiol 52:699–715
Nacry P, Canivenc G, Muller B, Azmi A, Van Onckelen H, Rossignol M, Doumas P (2005) A role for auxin redistribution in the responses of the root system architecture to phosphate starvation in Arabidopsis. Plant Physiol 138:2061–2074
Nefkens GHL, Thuring JWJF, Beenakkers MFM, Zwanenburg B (1997) Synthesis of a phthaloylglycine-derived strigol analogue and its germination stimulatory activity towards seeds of the parasitic weeds Striga hermonthica and Orobanche crenata. J Agric Food Chem 45:2273–2277
Nelson DC, Scaffidi A, Dun EA, Waters MT, Flematti GR, Dixon KW, Beveridge CA, Ghisalberti EL, Smith SM (2011) F-box protein MAX2 has dual roles in karrikin and strigolactone signalling in Arabidopsis thaliana. Proc Natl Acad Sci USA 108:8897–8902
Pérez de Luque AP, Galindo JCG, MacÃas FA, JorrÃn J (2000) Sunflower sesquiterpene lactone models induce Orobanche cumana seed germination. Phytochemistry 53:45–50
Pérez-Torres C-A, Lopez-Bucio J, Cruz-Ramirez A, Ibarra-Laclette E, Dharmasiri S, Estelle M, Herrera-Estrella L (2008) Phosphate availability alters lateral root development in Arabidopsis by modulating auxin sensitivity via a mechanism involving the TIR1 auxin receptor. Plant Cell 20:3258–3272
Pozo MJ, Azcón-Aguilar C (2007) Unraveling mycorrhiza-induced resistance. Curr Opin Plant Biol 10:393–398
Proust H, Hoffmann B, Xie X, Yoneyama K, Schaefer DG, Yoneyama K, Nogué F, Rameau C (2011) Strigolactones regulate protonema branching and act as a quorum sensing-like signal in the moss Physcomitrella patens. Development 138:1531–1539
Rani K, Zwanenburg B, Sugimoto Y, Yoneyama K, Bouwmeester HJ (2008) Biosynthetic considerations could assist the structure elucidation of host plant produced rhizosphere signalling compounds (strigolactones) for arbuscular mycorrhizal fungi and parasitic plants. Plant Physiol Biochem 46:617–626
Rubiales D, Verkleij J, Vurro M, Murdoch AJ, Joel DM (2009) Parasitic plant management in sustainable agriculture. Weed Res 49:1–5
Ruyter-Spira C, Kohlen W, Charnikhova T, van Zeijl A, van Bezouwen L et al (2011) Physiological effects of the synthetic strigolactone analog GR24 on root system architecture in Arabidopsis: another belowground role for strigolactones? Plant Physiol 155:721–734
Sánchez-Calderón L, Lopez-Bucio J, Chacon-Lopez A, Cruz-Ramirez A, Nieto-Jacobo F, Dubrovsky JG, Herrera-Estrella L (2005) Phosphate starvation induces a determinate developmental program in the roots of Arabidopsis thaliana. Plant Cell Physiol 46:174–184
Sergeant MJ, Li J-J, Fox C, Brookbank N, Rea D, Bugg TD, Thompson AJ (2009) Selective inhibition of carotenoid cleavage dioxygenases: phenotypic effects on shoot branching. J Biol Chem 284:5257–5264
Shen H, Luong P, Huq E (2007) The F-box protein MAX2 functions as a positive regulator of photomorphogenesis in Arabidopsis. Plant Physiol 145:1471–1483
Siame BP, Weerasuriya Y, Wood K, Ejeta G, Butler LG (1993) Isolation of strigol, a germination stimulant for Striga asiatica, from host plants. J Agric Food Chem 41:1486–1491
Sliwinska E, Bassel GW, Bewley JD (2009) Germination of Arabidopsis thaliana seeds is not completed as a result of elongation of the radicle but of the adjacent transition zone and lower hypocotyl. J Exp Bot 60:3587–3594
Snowden KC, Simkin AJ, Janssen BJ et al (2005) 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
Sorefan K, Booker J, Haurogné K et al (2003) MAX4 and RMS1 are orthologous dioxygenase-like genes that regulate shoot branching in Arabidopsis and pea. Genes Dev 17:1469–1474
Stirnberg P, van de Sande K, Leyser HMO (2002) MAX1 and MAX2 control shoot lateral branching in Arabidopsis. Development 129:1131–1141
Sugimoto Y, Ali AM, Yabuta S, Kinoshita H, Inanaga S, Itai A (2003) Germination strategy of Striga hermonthica involves regulation of ethylene biosynthesis. Physiol Plant 119:1–9
Sun Z, Matusova R, Bouwmeester HJ (2007) Germination of Striga and chemical signalling involved: a target for control methods. In: Gressel J, Ejeta G (eds) Integrating new technologies for Striga control: towards ending the witch-hunt. World Scientific, Singapore, pp 47–60
Sun Z, Has J, Walter MH et al (2008) Cloning and characterisation of a maize carotenoid cleavage dioxygenase (ZmCCD1) and its involvement in the biosynthesis of apocarotenoids with various roles in mutualistic and parasitic interactions. Planta 228:789–801
Taylor J, Harrier LA (2003) Expression studies of plant genes differentially expressed in leaf and root tissues of tomato colonised by the arbuscular mycorrhizal fungus Glomus mosseae. Plant Mol Biol 51:619–629
Toh S, Kamiya Y, Kawakami N, Nambara E, McCourt P, Tsuchiya Y (2012) Thermoinhibition uncovers a role for strigolactones in Arabidopsis seed germination. Plant Cell Physiol 53:107–117
Troughton A (1977) The effect of phosphorus nutrition upon the growth and morphology of young plants of Lolium perenne L. Ann Bot 41:85–92
Tsuchiya Y, McCourt P (2009) Strigolactones: a new hormone with a past. Curr Opin Plant Biol 12:556–561
Tsuchiya Y, Vidaurre D, Toh S, Hanada A, Nambara E, Kamiya Y, Yamaguchi S, McCourt P (2010) A small-molecule screen identifies new functions for the plant hormone strigolactone. Nat Chem Biol 6:741–749
Ueno K, Nomura S, Muranaka S, Mizutani M, Takikawa H, Sugimoto Y (2011) Ent-2′-epi-orobanchol and its acetate, as germination stimulants for Striga gesnerioides seeds isolated from cowpea and red clover. J Agric Food Chem 59:10485–10490
Umehara M, Hanada A, Yoshida S, Akiyama K, Arite T, Takeda-Kamiya N, Magome H, Kamiya Y, Shirasu K, Yoneyama K, Kyozuka J, Yamaguchi S (2008) Inhibition of shoot branching by new terpenoid plant hormones. Nature 455:195–200
Umehara M, Hanada A, Magome H, Takeda-Kamiya N, Yamaguchi S (2010) Contribution of strigolactones to the inhibition of tiller bud outgrowth under phosphate deficiency in rice. Plant Cell Physiol 51:1118–1126
Vaucher JP (1823) Mémoire sur la germination des orobanches. Mém Mus Hist nat Paris 10:261–273
Virtue JG, DeDear C, Potter MJ, Rieger M (2006) Potential use of isothiocyanates in branched broomrape eradication. In: Preston C, Watts JHW, Crossman ND (eds) 15th Australian weeds conference, Adelaide. pp 629–632
Vogel JT, Walter MH, Giavalisco P et al (2010) SlCCD7 controls strigolactone biosynthesis, shoot branching and mycorrhiza-induced apocarotenoid formation in tomato. Plant J 61:300–311
Waters MT, Nelson DC, Scaffidi A, Flematti GR, Sun YK, Dixon KW, Smith SM (2012) Specialisation within the DWARF14 protein family confers distinct responses to karrikins and strigolactones in Arabidopsis. Development 139:1285–1295
Weerasuriya Y, Siame BA, Hess D, Ejets G, Butler LG (1993) Influence of conditions and genotype on the amount of Striga germination stimulants exuded by root of several host crops. J Agric Food Chem 41:1492–1496
Westwood JH, Yoder JI, Timko MP, dePamphilis CW (2010) The evolution of parasitism in plants. Trends Plant Sci 15:227–235
Wigchert SCM, Kuiper E, Boelhouwer GJ, Nefkens GHL, Verkleij JAC, Zwanenburg B (1999) Dose–response of seeds of the parasitic weeds Striga and Orobanche toward the synthetic germination stimulants GR 24 and Nijmegen 1. J Agric Food Chem 47:1705–1710
Xie X, Kusumoto D, Takeuchi Y, Yoneyama K, Yamada Y, Yoneyama K (2007) 2′-Epi-orobanchol and solanacol, two unique strigolactones, germination stimulants for root parasitic weeds, produced by tobacco. J Agric Food Chem 55:8067–8072
Xie X, Yoneyama K, Kusumoto D, Yamada Y, Takeuchi Y, Sugimoto Y, Yoneyama K (2008a) Sorgomol, germination stimulant for root parasitic plants, produced by Sorghum bicolor. Tetrahedron Lett 49:2066–2068
Xie X, Yoneyama K, Kusumoto D, Yamada Y, Yokota T, Takeuchi Y, Yoneyama K (2008b) Isolation and identification of alectrol as (+)-orobanchyl acetate, a novel germination stimulant for root parasitic plants. Phytochemistry 69:427–431
Xie X, Yoneyama K, Harada Y, Fusegi N, Yamada Y, Ito S, Yokota T, Takeuchi Y, Yoneyama K (2009a) Fabacyl acetate, a germination stimulant for root parasitic plants from Pisum sativum. Phytochemistry 70:211–215
Xie X, Yoneyama K, Kurita J-Y, Harada Y, Yamada Y, Takeuchi Y, Yoneyama K (2009b) 7-Oxoorobanchyl acetate and 7-oxoorobanchol as germination stimulants for root parasitic plants from flax (Linum usitatissimum). Biosci Biotechnol Biochem 73:1367–1370
Xie X, Yoneyama K, Yoneyama K (2010) The strigolactone story. Annu Rev Phytopathol 48:93–117
Xie X, Yoneyama K, Kisugi T, Uchida K, Ito S, Akiyama K, Hayashi H, Yokota T, Nomura T, Yoneyama K (2012) Confirming stereochemical structures of strigolactones produced by rice and tobacco. Mol Plant 6:153–163
Yasuda N, Sugimoto Y, Kato M, Inanaga S, Yoneyama K (2003) (+)-Strigol, a witchweed seed germination stimulant, from Menispermum dauricum root culture. Phytochemistry 62:1115–1119
Yokota T, Sakai H, Okuno K, Yoneyama K, Takeuchi Y (1998) Alectrol and orobanchol, germination stimulants for Orobanche minor, from its host red clover. Phytochemistry 49:1967–1973
Yoneyama K, Ogasawara M, Takeuchi Y, Konnai M, Sugimoto Y, Seto H, Yoshida S (1998a) Effect of jasmonates and related compounds on seed germination of Orobanche minor Smith and Striga hermonthica (Del.) Benth. Biosci Biotechnol Biochem 62:1448–1450
Yoneyama K, Takeuchi Y, Ogasawara M, Konnai M, Sugimoto Y, Sassa T (1998b) Cotylenins and fusicoccins stimulate seed germination of Striga hermonthica (Del.) Benth and Orobanche minor Smith. J Agric Food Chem 46:1583–1586
Yoneyama K, Takeuchi Y, Yokota T (2001) Production of clover broomrape seed germination stimulants by red clover root requires nitrate but is inhibited by phosphate and ammonium. Physiol Plant 112:25–30
Yoneyama K, Xie X, Kusumoto D, Sekimoto H, Sugimoto Y, Takeuchi Y, Yoneyama K (2007a) 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
Yoneyama K, Yoneyama K, Takeuchi Y, Sekimoto H (2007b) Phosphorus deficiency in red clover promotes exudation of orobanchol, the signal for mycorrhizal symbionts and germination stimulant for root parasites. Planta 225:1031–1038
Yoneyama K, Xie X, Sekimoto H, Takeuchi Y, Ogasawara S, Akiyama K, Hayashi H, Yoneyama K (2008) Strigolactones, host recognition signals for root parasitic plants and arbuscular mycorrhizal fungi, from Fabaceae plants. New Phytol 179:484–494
Yoneyama K, Xie X, Yoneyama K, Takeuchi Y (2009) Strigolactones; structures and biological activities. Pest Manag Sci 65:467–470
Yoneyama K, Awad AA, Xie X, Yoneyama K, Takeuchi Y (2010) Strigolactones as germination stimulants for root parasitic plants. Plant Cell Physiol 51:1095–1103
Yoneyama K, Xie X, Kim HI, Kisugi T, Nomura T, Sekimoto H, Yokota T, Yoneyama K (2012) How do nitrogen and phosphorus deficiencies affect strigolactone production and exudation? Planta 235:1197–1207
Zehhar N, Ingouff M, Bouya D, Fer A (2002) Possible involvement of gibberellins and ethylene in Orobanche ramosa germination. Weed Res 42:464–469
Zhelev N (1987) The biological role of exogenic factors in broomrape germination. Rastenievudni Nauki 26:36–43 (in Bulgarian)
Zou J, Zhang S, Zhang W, Li G, Chen Z, Zhai W, Zhao X, Pan X, Xie Q, Zhu L (2006) 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
Zwanenburg B, Mwakaboko AS, Reizelman A, Anilkumar G, Sethumadhavan D (2009) Structure and function of natural and synthetic signalling molecules in parasitic weed germination. Pest Manag Sci 65:478–491
Acknowledgements
KY acknowledges grants from KAKENHI (18208010, 23338006) and Program for Promotion of Basic and Applied Researches for Innovations in Bio-oriented Industry. HB acknowledges funding by the Netherlands Organization for Scientific Research (NWO; VICI grant, 865.06.002 and Equipment grant, 834.08.001). He was co-financed by the Centre for BioSystems Genomics (CBSG) which is part of the Netherlands Genomics Initiative/Netherlands Organization for Scientific Research.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2013 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Yoneyama, K., Ruyter-Spira, C., Bouwmeester, H. (2013). Induction of Germination. In: Joel, D., Gressel, J., Musselman, L. (eds) Parasitic Orobanchaceae. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-38146-1_10
Download citation
DOI: https://doi.org/10.1007/978-3-642-38146-1_10
Published:
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-38145-4
Online ISBN: 978-3-642-38146-1
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)