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Role of Ascorbate in the Regulation of the Arabidopsis thaliana Root Growth by Phosphate Availability

DOI: 10.1155/2012/580342

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Abstract:

Arabidopsis root system responds to phosphorus (P) deficiency by decreasing primary root elongation and developing abundant lateral roots. Feeding plants with ascorbic acid (ASC) stimulated primary root elongation in seedlings grown under limiting P concentration. However, at high P, ASC inhibited root growth. Seedlings of ascorbate-deficient mutant (vtc1) formed short roots irrespective of P availability. P-starved plants accumulated less ascorbate in primary root tips than those grown under high P. ASC-treatment stimulated cell divisions in root tips of seedlings grown at low P. At high P concentrations ASC decreased the number of mitotic cells in the root tips. The lateral root density in seedlings grown under P deficiency was decreased by ASC treatments. At high P, this parameter was not affected by ASC-supplementation. vtc1 mutant exhibited increased lateral root formation on either, P-deficient or P-sufficient medium. Irrespective of P availability, high ASC concentrations reduced density and growth of root hairs. These results suggest that ascorbate may participate in the regulation of primary root elongation at different phosphate availability via its effect on mitotic activity in the root tips. 1. Introduction It has been reported that phosphorus (P) availability affects root architecture in Arabidopsis. Seedlings of this plant, exposed to low P concentration (1?μM), formed a highly branched root system with abundant lateral roots and a short primary root. Under these growth conditions primary, and secondary roots had an abundance of long root hairs. Under high P concentrations (1?mM), the root system was composed of a long primary root with few lateral roots and short root hairs [1–3]. P deficiency responses of the root system are dependent on changes in cell proliferation. Under low P conditions, the reduction in primary root growth is due to inhibition of cell division and cell differentiation within the primary root meristem. The mitotic activity is relocated to the sites of lateral root formation, resulting in increased lateral root density. However, similar to the primary root tip, cell differentiation in older lateral roots occurs within the apical root meristem, which results in the arrest of lateral root elongation [4]. Besides the reduction in cell division rate, low P treatment inhibits cell elongation and reduces the number of cells in root elongation zone [4, 5]. Little is known about the mechanisms underlying the alteration in growth and development of Arabidopsis roots after plants are exposed to limiting P supply. It has been

References

[1]  L. C. Williamson, S. P. C. P. Ribrioux, A. H. Fitter, and H. M. O. Leyser, “Phosphate availability regulates root system architecture in Arabidopsis,” Plant Physiology, vol. 126, no. 2, pp. 875–882, 2001.
[2]  J. López-Bucio, E. Hernández-Abreu, L. Sánchez-Calderón, M. F. Nieto-Jacobo, J. Simpson, and L. Herrera-Estrella, “Phosphate availability alters architecture and causes changes in hormone sensitivity in the Arabidopsis root system,” Plant Physiology, vol. 129, no. 1, pp. 244–256, 2002.
[3]  J. López-Bucio, E. Hernández-Abreu, L. Sánchez-Calderón et al., “An auxin transport independent pathway is involved in phosphate stress-induced root architectural alterations in Arabidopsis. Identification of BIG as a mediator of auxin in pericycle cell activation,” Plant Physiology, vol. 137, no. 2, pp. 681–691, 2005.
[4]  L. Sánchez-Calderón, J. López-Bucio, A. Chacón-López, A. Gutiérrez-Ortega, E. Hernández-Abreu, and L. Herrera-Estrella, “Characterization of low phosphorus insensitive mutants reveals a crosstalk between low phosphorus-induced determinate root development and the activation of genes involved in the adaptation of Arabidopsis to phosphorus deficiency,” Plant Physiology, vol. 140, no. 3, pp. 879–889, 2006.
[5]  L. Sánchez-Calderón, J. López-Bucio, A. Chacón-López et al., “Phosphate starvation induces a determinate developmental program in the roots of Arabidopsis thaliana,” Plant and Cell Physiology, vol. 46, no. 1, pp. 174–184, 2005.
[6]  S. Svistoonoff, A. Creff, M. Reymond et al., “Root tip contact with low-phosphate media reprograms plant root architecture,” Nature Genetics, vol. 39, no. 6, pp. 792–796, 2007.
[7]  C. A. Ticconi, R. D. Lucero, S. Sakhonwasee et al., “ER-resident proteins PDR2 and LPR1 mediate the developmental response of root meristems to phosphate availability,” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 33, pp. 14174–14179, 2009.
[8]  H. Rouached, A. B. Arpat, and Y. Poirier, “Regulation of phosphate starvation responses in plants: signaling players and cross-talks,” Molecular Plant, vol. 3, no. 2, pp. 288–299, 2010.
[9]  P. Nacry, G. Canivenc, B. Muller et al., “A role for auxin redistribution in the responses of the root system architecture to phosphate starvation in Arabidopsis,” Plant Physiology, vol. 138, no. 4, pp. 2061–2074, 2005.
[10]  R. Shin and D. P. Schachtman, “Hydrogen peroxide mediates plant root cell response to nutrient deprivation,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 23, pp. 8827–8832, 2004.
[11]  R. Shin, R. H. Berg, and D. P. Schachtman, “Reactive oxygen species and root hairs in Arabidopsis root response to nitrogen, phosphorus and potassium deficiency,” Plant and Cell Physiology, vol. 46, no. 8, pp. 1350–1357, 2005.
[12]  R. Liso, G. Calabrese, M. B. Bitonti, and O. Arrigoni, “Relationship between ascorbic acid and cell division,” Experimental Cell Research, vol. 150, no. 2, pp. 314–320, 1984.
[13]  N. M. Kerk and L. J. Feldman, “A biochemical model for the initiation and maintenance of the quiescent center: implications for organization of root meristems,” Development, vol. 121, no. 9, pp. 2825–2833, 1995.
[14]  G. Potters, N. Horemans, R. J. Caubergs, and H. Asard, “Ascorbate and dehydroascorbate influence cell cycle progression in a tobacco cell suspension,” Plant Physiology, vol. 124, no. 1, pp. 17–20, 2000.
[15]  R. Liso, A. M. Innocenti, M. B. Bitonti, and O. Arrigoni, “Ascorbic acid induced progression of quiescent centre cells from G1 to S phase,” New Phytologist, vol. 110, no. 4, pp. 469–471, 1988.
[16]  L. S. Lin and J. E. Varner, “Expression of ascorbic acid oxidase in zucchini squash (Cucurbita pepo L.),” Plant Physiology, vol. 96, no. 1, pp. 159–165, 1991.
[17]  M. A. Green and S. C. Fry, “Apoplastic degradation of ascorbate: novel enzymes and metabolites permeating the plant cell wall,” Plant Biosystems, vol. 139, no. 1, pp. 2–7, 2005.
[18]  P. L. Conklin, S. A. Saracco, S. R. Norris, and R. L. Last, “Identification of ascorbic acid-deficient Arabidopsis thaliana mutants,” Genetics, vol. 154, no. 2, pp. 847–856, 2000.
[19]  T. Murashige and F. Skoog, “A revised medium for rapid growth and bioassays with tobacco tissue culture,” Physiologia Plantarum, vol. 15, no. 3, pp. 437–497, 1962.
[20]  K. Kampfenkel, M. Van Montagu, and D. Inzé, “Extraction and determination of ascorbate and dehydroascorbate from plant tissue,” Analytical Biochemistry, vol. 225, no. 1, pp. 165–167, 1995.
[21]  P. Schopfer, C. Plachy, and G. Frahry, “Release of reactive oxygen intermediates (superoxide radicals, hydrogen peroxide, and hydroxyl radicals) and peroxidase in germinating radish seeds controlled by light, gibberellin, and abscisic acid,” Plant Physiology, vol. 125, no. 4, pp. 1591–1602, 2001.
[22]  X. Zhang, L. Zhang, F. Dong, J. Gao, D. W. Galbraith, and C. P. Song, “Hydrogen peroxide is involved in abscisic acid-induced stomatal closure in Vicia faba,” Plant Physiology, vol. 126, no. 4, pp. 1438–1448, 2001.
[23]  J. Foreman, V. Demidchik, J. H. F. Bothwell et al., “Reactive oxygen species produced by NADPH oxidase regulate plant cell growth,” Nature, vol. 422, no. 6930, pp. 442–446, 2003.
[24]  E. Olmos, G. Kiddle, T. K. Pellny, S. Kumar, and C. H. Foyer, “Modulation of plant morphology, root architecture, and cell structure by low vitamin C in Arabidopsis thaliana,” Journal of Experimental Botany, vol. 57, no. 8, pp. 1645–1655, 2006.
[25]  J. Tyburski, K. Dunajska, and A. Tretyn, “Reactive oxygen species localization in roots of Arabidopsis thaliana seedlings grown under phosphate deficiency,” Plant Growth Regulation, vol. 59, no. 1, pp. 27–36, 2009.
[26]  F. Lai, J. Thacker, Y. Li, and P. Doerner, “Cell division activity determines the magnitude of phosphate starvation responses in Arabidopsis,” Plant Journal, vol. 50, no. 3, pp. 545–556, 2007.
[27]  G. Potters, L. De Gara, H. Asard, and N. Horemans, “Ascorbate and glutathione: guardians of the cell cycle, partners in crime?” Plant Physiology and Biochemistry, vol. 40, no. 6-8, pp. 537–548, 2002.
[28]  K. Jiang, Y. L. Meng, and L. J. Feldman, “Quiescent center formation in maize roots is associated with an auxin-regulated oxidizing environment,” Development, vol. 130, no. 7, pp. 1429–1438, 2003.
[29]  J. T. Ward, B. Lahner, E. Yakubova, D. E. Salt, and K. G. Raghothama, “The effect of iron on the primary root elongation of Arabidopsis during phosphate deficiency,” Plant Physiology, vol. 147, no. 3, pp. 1181–1191, 2008.
[30]  L. Zheng, F. Huang, R. Narsai et al., “Physiological and transcriptome analysis of iron and phosphorus interaction in rice seedlings,” Plant Physiology, vol. 151, no. 1, pp. 262–274, 2009.
[31]  S. Abel, “Phosphate sensing in root development,” Current Opinion in Plant Biology, vol. 14, no. 3, pp. 303–309, 2011.
[32]  J. Jeong and M. L. Guerinot, “Homing in on iron homeostasis in plants,” Trends in Plant Science, vol. 14, no. 5, pp. 280–285, 2009.
[33]  J. Tyburski, K. Dunajska, and A. Tretyn, “A role for redox factors in shaping root architecture under phosphorus deficiency,” Plant Signaling and Behavior, vol. 5, no. 1, pp. 64–66, 2010.
[34]  T. R. Bates and J. P. Lynch, “Stimulation of root hair elongation in Arabidopsis thaliana by low phosphorus availability,” Plant, Cell and Environment, vol. 19, no. 5, pp. 529–538, 1996.

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