The choice of auxin analogue for in vitro root induction influences post-induction root development in Eucalyptus grandis

Previous studies on in vitro rooting for improved micropropagation of eucalypts indicated that root graviperception and post-acclimatisation architecture are determined by the relative exogenous auxin analogue and its stability, supplied during the pre-rooting culture stages. The specific roles of indole-3-acetic acid (IAA) and indole-3-butyric acid (IBA) in the rooting medium on the in vitro root morphological processes were explored using a good-rooting clone. In vitro rooting percentage was significantly reduced when either of the auxin inhibitors 2,3,5-triiodobenzoic acid (TIBA) and ρ-chlorophenoxyisobutyric acid (PCIB) or the auxin antagonist kinetin was supplied at rooting, with or without exogenous auxin. For all treatments, at the time of root induction, shoots did not possess a vascular cambium, only procambial tissue, from where adventitious roots formed. However, when the inhibitors or the antagonist were supplied to the roots 3 days after root induction, they affected root growth and graviperception. Kinetin and PCIB significantly reduced the mean root diameter from 552.8 µm (control) to 129.2 µm and 278.6 µm, respectively, over 3 weeks. While the PCIB treatment resulted in a significant increase in delta root length over this period, the TIBA treatment significantly decreased delta root length and increased mean root diameter to 833.4 µm. Restricting IAA transport with TIBA further altered root vascular patterning and, as with PCIB, resulted in the collapse of the columella region. Nevertheless, only a disruption in IAA transport and subsequent auxin distribution by TIBA treatment resulted in altered root graviperception. The results suggest the necessary inclusion of IAA in eucalypt micropropagation protocols to ensure good quality roots.

The choice of auxin analogue for in vitro root induction influences post-induction root development in Eucalyptus grandis

Previous studies on in vitro rooting for improved micropropagation of eucalypts indicated that root graviperception and post-acclimatisation architecture are determined by the relative exogenous auxin analogue and its stability, supplied during the pre-rooting culture stages. The specific roles of indole-3-acetic acid (IAA) and indole-3-butyric acid (IBA) in the rooting medium on the in vitro root morphological processes were explored using a good-rooting clone. In vitro rooting percentage was significantly reduced when either of the auxin inhibitors 2,3,5-triiodobenzoic acid (TIBA) and ρ-chlorophenoxyisobutyric acid (PCIB) or the auxin antagonist kinetin was supplied at rooting, with or without exogenous auxin. For all treatments, at the time of root induction, shoots did not possess a vascular cambium, only procambial tissue, from where adventitious roots formed. However, when the inhibitors or the antagonist were supplied to the roots 3 days after root induction, they affected root growth and graviperception. Kinetin and PCIB significantly reduced the mean root diameter from 552.8 µm (control) to 129.2 µm and 278.6 µm, respectively, over 3 weeks. While the PCIB treatment resulted in a significant increase in delta root length over this period, the TIBA treatment significantly decreased delta root length and increased mean root diameter to 833.4 µm. Restricting IAA transport with TIBA further altered root vascular patterning and, as with PCIB, resulted in the collapse of the columella region. Nevertheless, only a disruption in IAA transport and subsequent auxin distribution by TIBA treatment resulted in altered root graviperception. The results suggest the necessary inclusion of IAA in eucalypt micropropagation protocols to ensure good quality roots.

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  • Aloni R, Langhans M, Aloni E, Ullrich CI (2004). Role of cytokinin in the regulation of root gravitropism. Planta 220: 177–182.
  • Baltierra XC, Montenegro G, De García E (2004). Ontogeny of in vitro rooting processes in Eucalyptus globulus. In Vitro Cell Dev Biol Plant 40: 499–503.
  • Bell DT, van der Moezel PG, Bennett IJ, McComb JA, Wilkins CF, Marshall SCB, Morgan AL (1993). Comparisons of growth of Eucalyptus camaldulensis from seeds and tissue culture: root, shoot and leaf morphology of 9-month-old plants grown in deep sand and sand over clay. For Ecol Manag 57: 125–139.
  • Bennett MJ, Marchant A, Green HG, May ST, Ward SP, Millner PA, Walker AR, Schulz B, Feldman KA (1996). Arabidopsis AUX1 gene: a permease-like regulator of root gravitropism. Science 273: 948–950.
  • Berleth T, Mattsson J, Hardtke CS (2000). Vascular continuity and auxin signals. Trends Plant Sci 5: 387–393.
  • Blilou I, Xu J, Wildwater M, Willemson V, Papnov 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.
  • Brault M, Maldiney R (1999). Mechanisms of cytokinin action. Plant Physiol Biochem 37: 403–412.
  • Campilho A, Lindgren O, Helariutta Y (2009). Vascular morphogenesis during root development. In: Beeckman T, editor. Annual Plant Reviews Volume 37: Root Development. Oxford, UK: Wiley-Blackwell, pp. 39–63.
  • Chen R, Rosen E, Masson PH (1999). Gravitropism in higher plants. Plant Physiol 120: 343–350.
  • Christie AE, Leopold AC (1965). On the manner of triiodobenzoic acid inhibition of auxin transport. Plant Cell Physiol 6: 337– 3 de Assis TF, Fett-Neto AG, Alfenas AC (2004). Current techniques and prospects for the clonal propagation of hardwoods with emphasis on Eucalyptus. In: Walter C, Carson M, editors. Plantation Forest Biotechnology for the 21st Century. Trivandrum, India: Research Signpost, pp. 303–333.
  • De Klerk G-J, Van der Krieken W, De Jong J (1999). The formation of adventitious roots: new concepts, new possibilities. In Vitro Cell Dev Biol Plant 35: 189–199.
  • De Rybel B, Audenaert D, Beeckman T, Kepinski T (2009). The past, present and future of chemical biology in auxin research. ACS Chem Biol 4: 987–998.
  • 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.
  • Denison NP, Kietzka JE (1993a). The development and utilization of vegetative propagation in Mondi for commercial afforestation programmes. S Afr Forest J 165: 47–54.
  • Denison NP, Kietzka JE (1993b). The use and importance of hybrid intensive forestry in South Africa. S Afr Forest J 165: 55–60.
  • Eldridge K, Davidson J, Harwood C, van Wyk G (1994). Eucalypt Domestication and Breeding. London: Claredon Press.
  • Epstein E, Ludwig-Müller J (1993). Indole-3-butyric acid in plants: occurrence, biosynthesis, metabolism, and transport. Physiol Plant 88: 382–389.
  • Friml J (2003). Auxin transport – shaping the plant. Curr Opin Plant Biol 6: 7–12.
  • Gälweiler L, Guan C, Müller A, Wiseman E, Mendgen K, Yephremov A, Palme K (1998). Regulation of polar auxin transport by AtPIN1 in Arabidopsis vascular tissue. Science 282: 2226–2230.
  • Geldner N, Friml J, Stierhof Y-D, Jürgens G, Palme K (2001). Auxin transport inhibitors block PIN1 cycling and vesicle trafficking. Nature 413: 425–428.
  • George EF, Hall MA, De Klerk G-J (2008). Plant Propagation by Tissue Culture. 3rd ed. The Netherlands: Springer.
  • Hammer Ø, Harper DAT, Ryan PD (2001). PAST: Paleontological Statistics Software Package for education and data analysis. Palaeontologia Electron 4: 9.
  • Hartmann HT, Kester DE, Davies FT, Geneve RL (1997) Plant Propagation: Principles and Practices. 6th ed. London, UK: Prentice Hall International.
  • Jones NB, Van Staden J (1997). Micropropagation of Eucalyptus. In: Bajaj YPS, editor. Biotechnology in Agriculture and Forestry Volume 39: High-tech and Micropropagation. Berlin: SpringerVerlag, pp. 286–329.
  • Kerk NM, Feldman LJ (1995). A biochemical model for the initiation and maintenance of the quiescent centre: implications for the organization of root meristems. Development 121: 2825–2833.
  • Kerk NM, Jiang K, Feldman LJ (2000). Auxin metabolism in the root apical meristem. Plant Physiol 122: 925–932.
  • Kramer EM, Bennett MJ (2006). Auxin transport: a field in flux. Trends Plant Sci 11: 383–386.
  • Kuderová A, Hejátko J (2009). Spatiotemporal aspect of cytokininauxin interaction in hormonal regulation of the root meristem. Plant Signal Behav 4: 156–157.
  • Le Roux JJ, Van Staden J (1991). Micropropagation and tissue culture of Eucalyptus – a review. Tree Physiol 9: 435–477.
  • Ludwig-Müller J (2000). Indole-3-butyric acid in plant growth and development. Plant Growth Regul 32: 219–230.
  • Ludwig-Müller J, Vertocnik A, Town CD (2005). Analysis of indole3-butyric acid-induced adventitious root formation on Arabidopsis stem segments. J Exp Bot 56: 2095–2105.
  • Luijten M, Heidstra R (2009). Arabidopsis root development. In: Beeckman T, editor. Annual Plant Reviews Volume 37: Root Development. Oxford, UK: Wiley-Blackwell, pp. 1–38.
  • Mankessi F, Saya A, Baptiste C, Nourissier S, Monteuuis O (2009). In vitro rooting of genetically related Eucalyptus urophylla × Eucalyptus grandis clones in relation to the time spent in culture. Trees 23: 931–940.
  • Mattsson J, Renee Sung Z, Berleth T (1999). Responses of plant vascular systems to auxin transport inhibition. Development 126: 2979–2991.
  • Merkle SA, Nairn CJ (2005). Hardwood tree biotechnology. In Vitro Cell Dev Bio Plant 41: 602–619.
  • Michniewicz M, Brewer PB, Friml J (1997). Polar auxin transport and asymmetric auxin distribution. The Arabidopsis Book 5: 1–
  • Mokotedi MEO, Watt MP, Pammenter NW, Blakeway FC (2000). In vitro rooting and subsequent survival of two clones of a coldtolerant Eucalyptus grandis × E. nitens hybrid. Hortscience 35: 1163–1165.
  • Mokotedi MEO, Watt MP, Pammenter NW (2010). Analysis of differences in field performance of vegetatively and seedpropagated Eucalyptus varieties II: vertical uprooting resistance. South For 72: 712–718.
  • Moore I (2002). Gravitropism: lateral thinking in auxin transport. Curr Biol 12: R452–R454.
  • Mravec J, Kubes M, Bielach A, Gaykova V, Petrášek J, Skůpa P, Chand S, Benková, Zažímalova E, Friml J (2008). Interaction of PIN and PGP transport mechanisms in auxin distributiondependent development. Development 135: 3345–3354.
  • Muday GK (2001). Auxins and tropisms. J Plant Growth Regul 20: 226–243.
  • Murashige T, Skoog F (1962). A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant 15: 473–497.
  • Nakhooda M, Watt MP, Mycock D (2011). Auxin stability and accumulation during in vitro shoot morphogenesis influences subsequent root induction and development in Eucalyptus grandis. Plant Growth Regul 65: 263–271.
  • Nakhooda M, Watt MP, Mycock D (2012). The properties and interaction of auxins and cytokinins influence rooting of shoot cultures of Eucalyptus. Afr J Biotech 11: 16568–16578.
  • Nordström A-C, Jacobs FA, Eliasson L (1991). Effect of exogenous indole-3-acetic acid and indole-3-butyric acid on internal levels of the respective auxins and their conjugation with aspartic acid during adventitious root formation in pea cuttings. Plant Physiol 96: 856–861.
  • Nourissier S, Monteuuis O (2008). In vitro rooting of two Eucalyptus urophylla × Eucalyptus grandis mature clones. In Vitro Cell Dev Biol Plant 44: 263–272.
  • Oono Y, Ooura C, Rahman A, Aspuria ET, Hayashi K-I, Tanaka A, Uchimiya H (2003). p-Chlorophenoxyisobutyric acid impairs auxin response in Arabidopsis root. Plant Physiol 133: 1135– 11
  • Parry G, Marchant A, May S, Swarup R, Swarup K, James N, Graham N, Allen T, Martucci T, Yemm A et al. (2001). Quick on the uptake: characterisation of a family of plant auxin influx carriers. J Plant Growth Dev 20: 217–225.
  • Pernisová M, Klíma P, Horák J, Válkova M, Malbeck J, Souček P, Reichman P, Hoyerová K, Dubová J, Friml J et al. (2009). Cytokinins modulate auxin-induced organogenesis in plants via regulation of the auxin efflux. Proc Natl Acad Sci USA 106: 3609–3614.
  • Rashotte AM, Brady SR, Reed RC, Ante SJ, Muday GK (2000). Basipetal auxin transport is required for gravitropism in roots of Arabidopsis. Plant Physiol 122: 481–490.
  • Spurr AR (1969). A low viscosity epoxy resin embedding medium for electron microscopy. J Ultrastruct Res 26: 31–43.
  • Su Y-H, Zhang X-S (2011). Auxin-cytokinin interaction regulates meristem development. Mol Plant 4: 616–625.
  • Swarup R, Bennett MJ (2009). Root gravitropism. In: Beeckman T, editor. Annual Plant Reviews Volume 37: Root Development. Oxford, UK: Wiley-Blackwell, pp. 157–174.
  • Terasaka K, Blakeslee JJ, Titapiwatanakun B, Peer WA, Bandyopadhyay A, Makam SN, Lee OR, Richards EL, Murphy AS, Sato F, et al. (2005). PGP4, an ATP binding cassette P-glycoprotein, catalyzes auxin transport in Arabidopsis thaliana roots. Plant Cell 17: 2922–2939.
  • Trindade H, Pais MS (1997). In vitro studies on Eucalyptus globulus rooting ability. In Vitro Cell Dev Biol Plant 33: 1–5.
  • Tromas A, Perrot-Rechenmann C (2010). Recent progress in auxin biology. Comtes Rendus Biol 333: 297–306.
  • Watt MP, Blakeway FC, Mokotedi MEO, Jain SM (2003). Micropropagation of Eucalyptus. In: Jain SM, Ishii K, editors. Micropropagation of Woody Trees and Fruits. Netherlands: Kluwer Academic Publishers, pp. 217–244.
  • Woodward AW, Bartel B (2005). Auxin: regulation, action and interaction. Ann Bot 95: 707–735.
  • Yasodha R, Sumathi R, Gurumuthi K (2004). Micropropagation for quality propagule production in plantation forestry. Indian J Biotechnol 3: 159–170.
  • Ye Z-H (2002). Vascular tissue differentiation and pattern formation in plants. Ann Rev Plant Biol 53: 183–202.
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