Skip to main content

Regulation of cell division in the shoot apex

  • Chapter
Molecular and Cell Biology of the Plant Cell Cycle

Abstract

The aim of this paper is to explore how changes in the plane, and in the rate, of cell division affect primordium initiation in the shoot apex. Leaf initiation is characterised by a change in the plane of cell division in incipient primordia or changes in the rate of cell division, or both. We refer to published work on the preprophase band (PPB) and the phragmosome to indicate how planes of cell division are predicted in plant cells and argue that the presence of F-actin in PPBs may be a potential substrate for key regulatory cell cycle protein kinases. However the key signalling molecules that may cause a repositioning of PPBs during leaf initiation are unknown. We also attempt to make a link between homeotic, or organ identity genes and the regulation of cell size during floral morphogenesis. Here, emphasis is placed on a model by EM Lord proposing that homeotic genes have heterochronic function. In keeping with a timer mechanism would be genes which regulate cell size at division. The timing mechanism could act first, through homeotic genes determining where and when flower primordia are initiated and second, through genes which cause cell size to alter in cells which are determined as a particular floral primordium.

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

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 39.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Bernier G, Kinet J-M and Bronchart R (1967) Cellular events at the meristem during floral evocation in Sinapis alba L. Physiol Veg 5: 311–324.

    Google Scholar 

  2. Coen ES (1991) The role of homeotic genes in flower development and evolution. Annu Rev Pl Physiol Pl Mol Biol 42: 241–279.

    Article  Google Scholar 

  3. Coen ES and Meyerowitz EM (1991) The war of the whorls: genetic interactions controlling flower development. Nature 353: 31–37.

    Article  PubMed  CAS  Google Scholar 

  4. Evans LT (1971) The nature of floral induction. In: The Induction of Flowering. LT Evans (ed) , pp. 457–480. Melbourne: Macmillan.

    Google Scholar 

  5. Flanders DJ, Rawlins DJ, Shaw PJ and Lloyd CW (1990) Nucleus-associated microtubules help determine the division plane of plant epidermal cells: Avoidance of four-way junctions and the role of cell geometry. J Cell Biol 110: 1111–1122.

    Article  PubMed  CAS  Google Scholar 

  6. Francis D (1991) The cell cycle in plant development. Tansley Rev No. 38 New Phytol 122: 1–20.

    Article  Google Scholar 

  7. Francis D and Lyndon RF (1979) Synchronisation of cell division in the shoot apex of Silene in relation to flower initiation. Planta 145: 151–157.

    Article  CAS  Google Scholar 

  8. Francis D, Rembur J and Nougarède A (1988) Changements dans la composition polypetidique du méristème de Silene coeli-rosa (L.) au cours de 1’induction florale. Comptes Rendues Acad Sci Paris Ser III 307: 763–770.

    CAS  Google Scholar 

  9. Goodbody KC, Venverloo J and Lloyd CW (1991) Laser microsurgery demonstrates that cytoplasmic strands anchoring the nucleus across the vacuole of premitotic cells are under tension. Implications for division plane alignment. Development 113: 931–939.

    Google Scholar 

  10. Grose S and Lyndon RF (1984) Inhibition of growth and synchronised cell division in the shoot apex in relation to flowering in Silene. Planta 161: 289–294.

    Article  Google Scholar 

  11. Gunning BES (1982) The cytokinetic apparatus: its developmental and spatial regulation. In: The Cytoskeleton in Plant Growth and Development. CW Lloyd (ed), pp. 229–292. New York: Academic Press Inc.

    Google Scholar 

  12. Herbert RJ (1992) Cellular and molecular studies on the shoot terminal meristem of Pharbitis nil Chois. cv. Violet during floral evocation Ph D Thesis, Univ Wales.

    Google Scholar 

  13. Herbert RJ, Francis D and Ormrod JC (1992) Cellular and morphological changes at the terminal shoot apex of the short day plant Pharbitis nil Chois. cv. Violet, during the transition to flowering. Physiol Pl 86: 85–92.

    Article  Google Scholar 

  14. Hill JP and Lord EM (1989) Floral development in Arabidopsis thaliana: a comparison of the wild type and the homeotic pistillata mutant. Can J Bot 67: 2922–2936.

    Article  Google Scholar 

  15. Jacqmard A, Raju MVS, Kinet J-M and Bernier G (1976) The early action of the floral stimulus on mitotic activity and DNA synthesis in the apical meristem of Xanthium strumarium. Am J Bot 63: 166–174.

    Article  CAS  Google Scholar 

  16. Lord EM (1991) The concepts of heterochrony and homeosis in the study of floral morphogenesis. In: G Bernier (ed.) Flowering Newslett 11: 4–13.

    Google Scholar 

  17. Lyndon RF (1970) Planes of cell division and growth in the shoot apex of Pisum Ann Bot 34: 19–28.

    Google Scholar 

  18. Lyndon RF (1983) The mechanism of leaf initiation. In: The Growth and Functioning of Leaves. JE Dale and FL Milthorpe (eds), pp. 3–24. Cambridge: Cambridge Univ Press.

    Google Scholar 

  19. Lyndon RF (1990) Plant Development. The Cellular Basis. London, New York: Unwin Hyman Inc.

    Google Scholar 

  20. Lyndon RF and Francis D (1984) The response of the shoot apex to light-generated signals from the leaves. In: Light and the Flowering Process. D Vince-Prue B Thomas and KE Cockshull (eds), pp. 171–192. London: Acad Press.

    Google Scholar 

  21. Lyndon RF and Cunninghame ME (1986) Control of shoot apical development via cell division. In: Plasticity in Plants, 40th Sym Soc Exp Biol. AJ Trewavas and DH Jennings (eds), pp. 233–255. Cambridge: Company of Biologists.

    Google Scholar 

  22. Lyndon RF and Francis D (1992) Plant and organ development. Plant Mol Biol 19: 51–68.

    Article  PubMed  CAS  Google Scholar 

  23. Miller MB and Lyndon RF (1976) Rates of cell division in the shoot apex of Silene during the transition to flowering. J Exp Bot 27: 1142–1153.

    Article  Google Scholar 

  24. Mineyuki Y, Yamashita M and Nagahama Y (1991) p34cdc2 kinase homologue in the preprophase band. Protoplasma 162: 182–186.

    Article  CAS  Google Scholar 

  25. Palevitz BA (1987) Actin in the preprophase band of Allium cepa J Cell Biol 104: 1515–1519.

    Article  PubMed  CAS  Google Scholar 

  26. Pickett-Heaps JD and Northcote DH (1966) Organisation of microtubules and endoplasmic reticulum during mitosis and cytokinesis in wheat meristems. J Cell Sci 1: 109–120.

    PubMed  CAS  Google Scholar 

  27. Selker JML and Green PB (1984) Organogenesis in Graptopetalatum paraguayense E Walther: shifts in orientation of cortical microtubule arrays are associated with periclinal divisions. Planta 160: 289–297.

    Article  Google Scholar 

  28. Sinnott E and Bloch R (1940) Cytoplasmic behaviour during division in vacuolate plant cells. Proc Natl Acad Sci USA 26: 223–227.

    Article  PubMed  CAS  Google Scholar 

  29. Sommer H, Beltran J, Huijser, Pape H, Loning W, Saedler H and Schwarz-Sommer Z (1990) Deficiens ,a homeotic gene involved in the control of flower morphogenesis in Antirrhinum majus: the protein shows homology to transcription factors. EMBO J 9: 605–613.

    PubMed  CAS  Google Scholar 

  30. Staiger CJ and Lloyd CW (1991) The plant cytoskeleton. Curr Opinion Cell Biol 3: 33–42.

    Article  PubMed  CAS  Google Scholar 

  31. Taylor M, Francis D, Rembur J and Nougarède A (1990) Changes to proteins in the shoot meristem of Silene coeli-rosa during the transition to flowering. Plant Cell Physiol 31: 1169–1176.

    CAS  Google Scholar 

  32. Traas JA, Doonan JH, Rawlins DJ, Shaw PJ, Watts J and Lloyd CW (1987) An actin network is present in the cytoplasm throughout the cell cycle of carrot cells and associates with the dividing nucleus. J Cell Biol 105: 387–395.

    Article  PubMed  CAS  Google Scholar 

  33. Verde F, Labbé JC, Dorée M and Karseti E (1990) Regulation of microtubule dynamics by cdcl protein kinase in cell-free extracts of Xenopus eggs. Nature 343: 233–238.

    Article  PubMed  CAS  Google Scholar 

  34. Wick SM and Duniec J (1983) Immunofluorescence microscopy of tubulin and microtubule arrays in plant cells. I. Preprophase band development and concomitant appearance of nuclear envelope-associated tubulin. J Cell Biol 97: 235–243.

    Article  PubMed  CAS  Google Scholar 

  35. Yamashita M, Yoshikuni M, Hirai T, Fukada S and Nagahama Y (1991) A monoclonal antibody against the PSTAIR sequence of p34cdc2, catalytic subunit of maturation-promotion factor and key regulator of the cell cycle. Develop Growth & Differ 33: 617–624.

    Article  CAS  Google Scholar 

Download references

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1993 Springer Science+Business Media Dordrecht

About this chapter

Cite this chapter

Francis, D., Herbert, R.J. (1993). Regulation of cell division in the shoot apex. In: Ormrod, J.C., Francis, D. (eds) Molecular and Cell Biology of the Plant Cell Cycle. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-1789-0_15

Download citation

  • DOI: https://doi.org/10.1007/978-94-011-1789-0_15

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-4787-6

  • Online ISBN: 978-94-011-1789-0

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics