Skip to main content
Log in

Dependence of Root Cell Growth and Division on Root Diameter

  • Developmental Biology of Plants
  • Published:
Russian Journal of Developmental Biology Aims and scope Submit manuscript

Abstract

Primary roots of 98 species from different families of monocotyledonous and dicotyledonous plants and adventitious roots obtained from bulbs and rhizomes of 24 monocot species were studied. Root growth rate, root diameter, length of the meristem and elongation zones, number of meristematic cells in a file of cortical cells, and length of fully elongated cells were evaluated in each species after the onset of steady growth. The mitotic cycle duration and relative cell elongation rate were calculated. In all species, the meristem length was approximately equal to two root diameters. When comparing different species, the rate of root growth increased with a larger root diameter. This was due to an increase in the number of meristematic cells in a row and, to a lesser degree, to a greater length of fully elongated cells. The duration of the mitotic cycle and the relative cell elongation rate did not correlate with the root diameter. It is suggested that the meristem size depends on the level of nutrient inflow from upper tissues, and is thereby controlled during further 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.

Institutional subscriptions

Similar content being viewed by others

References

  • Dello Ioio, R., Linhares, F.S., Scacchi, E., et al., Cytokinins determine Arabidopsis root-meristem size by controlling cell differentiation, Curr. Biol., 2007, vol. 17, pp. 678–682.

    Article  Google Scholar 

  • Erickson, R.O. and Sax, K.B., Elemental growth rate of the primary root of Zea mays, Proc. Am. Philos. Soc., 1956, vol. 100, pp. 499–514.

    Google Scholar 

  • Galinha, C., Hofhuis, H., Luijten, M., et al., PLETHORA proteins as dose-dependent master regulators of Arabidopsis root development, Nature, 2007, vol. 449, pp. 1053–1057.

    Article  CAS  PubMed  Google Scholar 

  • Gazques, A. and Beemster, G.T.S., What determines organ size differences between species? A meta-analysis of the cellular basis, New Phytol., 2017. doi 10.1111/nph.14573

    Google Scholar 

  • Goodvin, R.H. and Avers, C.J., Studies on roots. III. An analysis of root growth in Phleum pretense using photomicrographic records, Am. J. Bot., 1956, vol. 43, pp. 479–487.

    Article  Google Scholar 

  • Grif, V.G., Ivanov, V.B., and Machs, E.M., Cell cycle and its parameters in flowering plants, Cytologia, 2002, vol. 44, pp. 936–980.

    CAS  Google Scholar 

  • Hacham, Y., Holland, N., Butterfield, C., et al., Brassinosteroid perception in the epidermis controls root meristem size, Stem Cells Dev., 2011, vol. 138, pp. 839–848.

    CAS  Google Scholar 

  • Ivanov, V.B., Kletochnye osnovy rosta rastenii (Cellular Basis of Plant Growth), Moscow: Nauka, 1977.

    Google Scholar 

  • Ivanov, V.B. and Dubrovsky, J.G., Estimation of the cellcycle duration in the root apical meristem: a model of linkage between cell-cycle duration, rate of cell production, and rate of root growth, Int. J. Plant Sci., 1997, vol. 158, pp. 757–763.

    Google Scholar 

  • Ivanov, V.B., Kletochnye mekhanizmy rosta rastenii (Cellular Mechanisms of Plant Growth), Moscow: Nauka, 2011.

    Google Scholar 

  • Ivanov, V.B. and Dubrovsky, J.G., Longitudinal zonation pattern in plant roots: conflicts and solutions, Trends Plant Sci., 2013, vol. 18, pp. 237–243.

    Article  CAS  PubMed  Google Scholar 

  • Kudo, T., Kiba, T., and Sakakibara, H., Metabolism and long-distance translocation of cytokinins, J. Integ. Plant Biol., 2010, vol. 52, no. 1, pp. 53–60.

    Article  CAS  Google Scholar 

  • Kutschera, L., Lichtenegger, E., and Sobotik, M., Wurzelatlas mitteleuropaischer Grunlandpflanzen, Bd. 1: Monocotyledoneae, Stuttgart, Jena, New York: Gustav Fisher, 1982.

    Google Scholar 

  • Kutschera, L., Sobotik, M., and Lichtenegger, E., Wurzelatlas mitteleuropaischer Grunlandpflanzen, Bd. 2: Pteridophyta und Dicotyledoneae (Magnoliopsida), Teil 1: Morphologie, Anatomie, Okologie, Verbereitung, Soziologie, Wirtschaft, Stuttgart, Jena, New York: Gustav Fisher, 1992.

    Google Scholar 

  • Kutschera-Mitter, L., Erklarungen des geotropen Wachstums aus Standort und Bau der Pflanzen, in Land- und forstwirtschaftliche Forschung in Osterreic, 1972, vol. 5, pp. 40–89.

    Google Scholar 

  • Malamy, J.E. and Benfey, P.N., Organization and cell differentiation in lateral roots of Arabidopsis thaliana, Development, 1997, vol. 124, pp. 33–44.

    CAS  PubMed  Google Scholar 

  • Muller, B., Stosser, M., and Tardieu, F., Spatial distributions of tissue expansion and cell division rates are related to irradiance and to sugar content in the growing zone of maize roots, Plant Cell Environ., 1998, vol. 21, pp. 149–158.

    Article  CAS  Google Scholar 

  • Shafiq, S., Chen, C., Yang, J., et al., DNA topoisomerase 1 prevents R-loop accumulation to modulate auxin-regulated root development in rice, Mol. Plant, 2017. doi 10.1016/j.molp.2017.04.001

    Google Scholar 

  • Shmanaeva, T.N. and Leman, V.M., Effect of temporary darkness on the morphogenesis of tomatoes and the nucleic acid content in the apical meristem, Izv. TSKhA, 1970, vol. 2, pp. 25–32.

    Google Scholar 

  • Su, Y.-H., Liu, Y.-B., and Zhang, X.-S., Auxin-cytokinin interaction regulates meristem development, Mol. Plant, 2011, vol. 4, pp. 616–625.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ubeda-Tomas, S., Federici, F., Casimiro, I., et al., Gibberellin signaling in the endodermis control Arabidopsis root meristem size, Curr. Biol., 2009, vol. 19, pp. 1194–1199.

    Article  CAS  PubMed  Google Scholar 

  • Verbelen, J.P., De Cnodder, T., Le, J., et al., The root apex of Arabidopsis thaliana consists of four distinct zones of growth activities: meristematic zone, transition zone, fast elongation zone and growth terminating zone, Plant Signal. Behav., 2006, vol. 1, pp. 296–304.

    PubMed  Google Scholar 

  • Werner, T., Holst, K., Pors, Y., et al., Cytokinin deficiency causes distinct changes of sink and source parameters in tobacco shoots and roots, J. Exp. Bot., 2008, vol. 59, pp. 2659–2672.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Zhukovskaya, N.V., Bystrova, E.I., and Ivanov, V.B., Length of meristematic and fully elongated root cells related to haploid DNA content, Russ. J. Dev. Biol., 2016, vol. 47, pp. 326–334.

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to N. V. Zhukovskaya.

Additional information

Original Russian Text © E.I. Bystrova, N.V. Zhukovskaya, V.B. Ivanov, 2018, published in Ontogenez, 2018, Vol. 49, No. 2.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bystrova, E.I., Zhukovskaya, N.V. & Ivanov, V.B. Dependence of Root Cell Growth and Division on Root Diameter. Russ J Dev Biol 49, 79–86 (2018). https://doi.org/10.1134/S1062360418020029

Download citation

  • Received:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1062360418020029

Keywords

Navigation