Skip to main content
Log in

Strigolactones’ Effect on Root Growth and Root-Hair Elongation May Be Mediated by Auxin-Efflux Carriers

  • Published:
Journal of Plant Growth Regulation Aims and scope Submit manuscript

Abstract

Strigolactones are a new group of plant hormones that play a pivotal role in the regulation of aboveground plant architecture. However, the mechanisms governing their regulation of plant growth and development are unknown. We characterized the effect of a synthetic strigolactone (GR24) on tomato (Solanum lycopersicon) roots and present evidence for its relationship with the plant hormone auxin. We demonstrate that strigolactones interfere with the inhibitory effect of exogenously applied auxin on root elongation. This GR24-induced root elongation is conveyed via an increase in root cell length accompanied by a reduction in cell diameter, and it occurs despite strigolactone’s reduction of cell division (detected as reduction of CYCB1;1 transcript). In addition, high concentrations of strigolactone lead to asymmetric root growth and inhibition of root-hair elongation. Exogenous application of NAA or IAA was unable to restore symmetric root growth and root-hair elongation in the presence of strigolactone. However, application of NPA, an auxin-efflux inhibitor, did restore root-hair elongation in the presence of strigolactone. Similarly, exogenous application of 2,4-D, a synthetic auxin that is not secreted by efflux carriers, restored root-hair elongation and symmetric growth in the presence of strigolactone. Nevertheless, 2,4-D was unable to prevent root elongation by strigolactones. Therefore, strigolactones’ effect on root growth and root-hair elongation appears to be mediated via an effect on auxin-efflux carriers. Nevertheless, more than one mechanism may govern strigolactones’ effect on root growth.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

References

  • Akiyama K, Matsuzaki K, Hayashi H (2005) Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi. Nature 435:824–827

    Article  CAS  PubMed  Google Scholar 

  • Bennett T, Sieberer T, Willett B, Booker J, Luschnig C, Leyser O (2006) The Arabidopsis MAX pathway controls shoot branching by regulating auxin transport. Curr Biol 16:553–563

    Article  CAS  PubMed  Google Scholar 

  • Besserer A, Bécard G, Jauneau A, Roux C, Séjalon-Delmas N (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 148:402–413

    Article  CAS  PubMed  Google Scholar 

  • Blilou I, Xu J, Wildwater M, Willemsen V, Paponov I, Friml J, Heidstra R, Aida M, Palme K, Scheres B (2005) The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots. Nature 433:39–44

    Article  CAS  PubMed  Google Scholar 

  • 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

    Article  CAS  PubMed  Google Scholar 

  • 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

    Article  CAS  PubMed  Google Scholar 

  • Brewer PB, Dun EA, Ferguson BJ, Rameau C, Beveridge CA (2009) Strigolactone acts downstream of auxin to regulate bud outgrowth in pea and Arabidopsis. Plant Physiol 150:482–493

    Article  CAS  PubMed  Google Scholar 

  • Cande WZ, Ray PM (1976) Nature of cell-to-cell transfer of auxin in polar transport. Planta 129:43–52

    Article  CAS  Google Scholar 

  • 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

    Article  CAS  PubMed  Google Scholar 

  • Delbarre A, Muller P, Imhoff V, Guern J (1996) Comparison of mechanisms controlling uptake and accumulation of 2, 4-dichlorophenoxy acetic acid, naphthalene-1-acetic acid, and indole-3-acetic acid in suspension-cultured tobacco cells. Planta 198:532–541

    Article  CAS  Google Scholar 

  • Dewitte W, Murray JA (2003) The plant cell cycle. Annu Rev Plant Biol 54:235–264

    Article  CAS  PubMed  Google Scholar 

  • Eshed Y, Abu-Abied M, Saranga Y, Zamir D (1992) Lycopersicon esculentum lines containing small overlapping introgressions from L. pennellii. Theor Appl Genet 83:1027–1034

    Article  CAS  Google Scholar 

  • Ferguson BJ, Beveridge CA (2009) Roles for auxin, cytokinin and strigolactone in regulating shoot branching. Plant Physiol 149:1929–1944

    Article  CAS  PubMed  Google Scholar 

  • Foo E, Turnbull CG, Beveridge CA (2001) Long-distance signaling and the control of branching in the rms1 mutant of pea. Plant Physiol 126:203–209

    Article  CAS  PubMed  Google Scholar 

  • Gal TZ, Aussenberg ER, Bordman S, Kapulnik Y, Koltai H (2006) Expression of a plant expansin is necessary for completion of the root knot nematode life cycle. Planta 4:1–8

    Google Scholar 

  • Goldwasser Y, Yoneyama K, Xie X, Yoneyama K (2008) Production of strigolactones by Arabidopsis thaliana responsible for Orobanche aegyptiaca seed germination. Plant Growth Regul 55:21–28

    Article  CAS  Google Scholar 

  • Gomez-Roldan V, Fermas S, Brewer PB, Puech-Pagès V, Dun EA, Pillot JP, Letisse F, Matusova R, Danoun S, Portais JC, Bouwmeester H, Bécard G, Beveridge CA, Rameau C, Rochange SF (2008) Strigolactone inhibition of shoot branching. Nature 455:189–194

    Article  CAS  PubMed  Google Scholar 

  • Hobbie L, Estelle M (1995) The axr4 auxin-resistant mutants of Arabidopsis thaliana define a gene important for root gravitropism and lateral root initiation. Plant J 7:211–220

    Article  CAS  PubMed  Google Scholar 

  • Johnson AW, Gowda G, Hassanali A, Knox J, Monaco S, Razavi Z, Rosebery G (1981) The preparation of synthetic analogues of strigol. J Chem Soc Perkin Trans 1:1734–1743

    Article  Google Scholar 

  • Klee H (2008) Plant biology: hormones branch out. Nature 455:176–177

    Article  CAS  PubMed  Google Scholar 

  • 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

    Article  CAS  PubMed  Google Scholar 

  • Lucas M, Godin C, Jay-Allemand C, Laplaze L (2008) Auxin fluxes in the root apex co-regulate gravitropism and lateral root initiation. J Exp Bot 59:55–66

    Article  CAS  PubMed  Google Scholar 

  • Marchant A, Kargul J, May ST, Muller P, Delbarre A, Perrot-Rechenmann C, Bennett MJ (1999) AUX1 regulates root gravitropism in Arabidopsis by facilitating auxin uptake within root apical tissues. EMBO J 18:2066–2073

    Article  CAS  PubMed  Google Scholar 

  • Matusova R, Rani K, Verstappen FW, Franssen MC, 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

    Article  CAS  PubMed  Google Scholar 

  • Ongaro V, Leyser O (2008) Hormonal control of shoot branching. J Exp Bot 59:67–74

    Article  CAS  PubMed  Google Scholar 

  • Pitts RJ, Cernac A, Estelle M (1998) Auxin and ethylene promote root hair elongation in Arabidopsis. Plant J 16:553–560

    Article  CAS  PubMed  Google Scholar 

  • Sato D, Awad AA, Takeuchi Y, Yoneyama K (2005) Confirmation and quantification of strigolactones, germination stimulants for root parasitic plants Striga and Orobanche, produced by cotton. Biosci Biotechnol Biochem 69:98–102

    Article  CAS  PubMed  Google Scholar 

  • Teale WD, Ditengou FA, Dovzhenko AD, Li X, Molendijk AM, Rupertia B, Paponov I, Palmel K (2008) Auxin as a model for the integration of hormonal signal processing and transduction. Mol Plant 1:229–237

    Article  CAS  PubMed  Google Scholar 

  • 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

    Article  CAS  PubMed  Google Scholar 

  • Vieten A, Sauer M, Brewer PB, Friml J (2007) Molecular and cellular aspects of auxin-transport-mediated development. Trends Plant Sci 12:160–168

    Article  CAS  PubMed  Google Scholar 

  • 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

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We thank Yogev Rosianski, Doron Meir, Hadas Veroslavsky, and Bruria Ben-Dor for their technical help. We are grateful to Drs. Kaori and Koichi Yoneyama for supplying us with GR24. The research was funded by the Chief Scientist Foundation, Israeli Ministry of Agriculture.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hinanit Koltai.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Koltai, H., Dor, E., Hershenhorn, J. et al. Strigolactones’ Effect on Root Growth and Root-Hair Elongation May Be Mediated by Auxin-Efflux Carriers. J Plant Growth Regul 29, 129–136 (2010). https://doi.org/10.1007/s00344-009-9122-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00344-009-9122-7

Keywords

Navigation