Skip to main content
Log in

Cytokinesis and nodal anatomy in the charophycean green alga Chara zeylanica

  • Original Papers
  • Published:
Protoplasma Aims and scope Submit manuscript

Summary

Cell plate formation in Chara zeylanica was compared with recent models of cytokinesis in higher plants in order to gain insight into the evolutionary origin of plant cytokinetic processes. Transmission electron microscopy (TEM) reveals that while cytokinesis in C. zeylanica bears many features in common with that in higher plants, there are significant differences. Unlike that in higher plants, cytokinesis in C. zeylanica begins with a congregation of smooth membrane tubules that are closely associated with endoplasmic reticulum (ER) and Golgi membranes. Mitochondria and other organelles excluded by the phragmoplast in higher plants are present as well. Unlike in higher plants, phragmoplast microtubules persist throughout cytokinesis in C. zeylanica, and the cell plate generally forms across the whole cell at once, though development is patchy, due to small regions developing at different rates; the ends of the plate form last. By identifying aspects of cytokinesis that are different in C. zeylanica and plants, our study indicates which cytokinetic features are more likely to be derived, and which are more likely to be ancestral. In addition, we demonstrated that all nodal cells of C. zeylanica are interconnected via plasmodesmata, lending support to the idea that, while Chara spp. are generally considered to be filamentous organisms, nodal regions may be thought of as meristemlike tissues.

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.

Similar content being viewed by others

Abbreviations

HPF:

high-pressure freezing

KFe:

potassium ferricyanide

SCF:

stepwise chemical fixation

TEM:

transmission electron microscopy

References

  • Bold HC, Wynne MJ (1985) Introduction to the algae, 2nd edn. Prentice-Hall, Englewood Cliffs, NJ

    Google Scholar 

  • Brown RC, Lemmon BE, Graham LE (1994) Morphogenetic plastid migration and microtubule arrays in mitosis and cytokinesis in the green alga Coleochaete orbicularis. Am J Bot 81: 127–133

    Article  Google Scholar 

  • Cook ME, Graham LE, Botha CEJ, Lavin CA (1997) Comparative ultrastructure of plasmodesmata of Chara and selected bryophytes: toward an elucidation of the evolutionary origin of plant plasmodesmata. Am J Bot 84: 1169–1178

    Article  CAS  Google Scholar 

  • Cronshaw J, Esau K (1968) Cell division in leaves of Nicotiana. Protoplasma 65: 1–24

    Article  CAS  Google Scholar 

  • Cutter EG, Hung CY (1972) Symmetric and asymmetric mitosis and cytokinesis in the root tip of Hydrocharis morsus-ranae L. J Cell Sci 11: 723–737

    CAS  PubMed  Google Scholar 

  • Ding B, Turgeon R, Parthasarathy MV (1992) Substructure of freeze-substituted plasmodesmata. Protoplasma 169: 28–41

    Article  Google Scholar 

  • Evert RF, Deshpande BP (1970) An ultrastructural study of cell division in the cambium. Am J Bot 57: 942–961

    Article  Google Scholar 

  • Frame P, Sawa T (1975) Comparative anatomy of Charophyta II: the axial nodal complex — an approach to the taxonomy of Lamprothamnion. J Phycol 11: 202–205

    Google Scholar 

  • Franceschi VR, Ding B, Lucas WJ (1994) Mechanism of plasmodesmata formation in characean algae in relation to evolution of intercellular communication in higher plants. Planta 192: 347–358

    Article  Google Scholar 

  • Fritsch FE (1935) The structure and reproduction of the algae, vol 1. Macmillan, New York

    Google Scholar 

  • Graham LE (1993) Origin of land plants. Wiley, New York

    Google Scholar 

  • — (1996) Green algae to land plants: an evolutionary transition. J Plant Res 109: 241–251

    Article  Google Scholar 

  • —, Kaneko Y (1991) Subcellular structures of relevance to the origin of land plants (embryophytes) from green algae. Crit Rev Plant Sci 10: 323–342

    Article  Google Scholar 

  • —, Delwiche CF, Mishler B (1991) Phylogenetic connections between the “green algae” and the “bryophytes”. Adv Bryol 4: 213–244

    Google Scholar 

  • Gunning BES (1982) The cytokinetic apparatus: its development and spatial regulation. In: Lloyd CW (ed) The cytoskeleton in plant growth and development. Academic Press, London, pp 229–292

    Google Scholar 

  • Hawes CR, Juniper BE, Horne JC (1981) Low and high voltage electron microscopy of mitosis and cytokinesis in maize roots. Planta 152: 397–407

    Article  CAS  Google Scholar 

  • Hepler PK (1981) The structure of the endoplasmic reticulum revealed by osmium tetroxide potassium ferricyanide staining. Eur J Cell Biol 26: 102–110

    CAS  PubMed  Google Scholar 

  • — (1982) Endoplasmic reticulum in the formation of the cell plate and plasmodesmata. Protoplasma 111: 121–133

    Article  Google Scholar 

  • —, Newcomb EH (1967) Fine structure of cell plate formation in the apical meristem of Phaseolus roots. J Ultrastruct Res 19: 498–513

    Article  CAS  Google Scholar 

  • Kaplan DR, Hagemann W (1991) The relationship of cell and organism in vascular plants. BioScience 41.: 693–703

    Article  Google Scholar 

  • Manhardt JR (1994) Phylogenetic analysis of green plant rbcL sequences. Mol Phylogenet Evol 3: 114–127

    Article  Google Scholar 

  • McCourt RM, Karol KG, Guerlesquin M, Feist M (1996) Phytogeny of extant genera in the family Characeae (Charales, Charophyceae) based on rbcL sequences and morphology. Am J Bot 83: 125–131

    Article  Google Scholar 

  • Mishler BD, Lewis LA, Buchheim MA, Renzaglia KS, Garbary DJ, Delwiche CF, Zechman FW, Kantz TS, Chapman RL (1994) Phylogenetic relationships of the “green algae” and “bryophytes”. Ann Missouri Bot Garden 81: 451–483

    Article  Google Scholar 

  • Pickett-Heaps JD (1967a) Ultrastructure and differentiation in Chara sp. I: vegetative cells. Aust J Biol Sci 20: 539–551

    Article  Google Scholar 

  • — (1967b) Ultrastructure and differentiation in Chara sp. II: mitosis. Aust J Biol Sci 20: 883–894

    Article  Google Scholar 

  • — (1975) Green algae. Sinauer Associates, Sunderland, Mass

    Google Scholar 

  • Porter KR, Machado RD (1997) Studies on the endoplasmic reticulum IV: its form and distribution during mitosis in cells of onion root tip. J Biophys Biochem Cytol 7: 167–180

    Article  Google Scholar 

  • Samuels AL, Giddings TH Jr, Staehelin LA (1995) Cytokinesis in tobacco BY-2 and root tip cells: a new model of cell plate formation in higher plants. J Cell Biol 130: 1345–1357

    Article  CAS  Google Scholar 

  • Staehelin LA, Hepler, PK (1996) Cytokinesis in higher plants. Cell 84: 821–824

    Article  CAS  Google Scholar 

  • Sundaralingam VS (1954) The developmental morphology of Chara zeylanica. J Ind Bot Soc 33: 272–297

    Google Scholar 

  • Taylor DP (1988) Direct measurement of the osmotic effects of buffers and fixatives in Nitella flexilis. J Microsc 150: 71–80

    Article  CAS  Google Scholar 

  • Whaley WG, Dauwalder M, Kephart JE (1966) The Golgi apparatus and an early stage of cell plate formation. J Ultrastruct Res 15: 169–180

    Article  CAS  Google Scholar 

  • Wood RD (1967) Charophytes of North America. Stella's Printing, West Kingston

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Cook, M.E., Graham, L.E. & Lavin, C.A. Cytokinesis and nodal anatomy in the charophycean green alga Chara zeylanica . Protoplasma 203, 65–74 (1998). https://doi.org/10.1007/BF01280588

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01280588

Keywords

Navigation