Skip to main content
Log in

Regulation of developmental pathways in cultured microspores of tobacco and snapdragon by medium pH

  • Original Article
  • Published:
Planta Aims and scope Submit manuscript

Abstract

The regulation of developmental pathways in cultured microspores of tobacco (Nicotiana tabacum L) and snapdragon (Antirrhinum majus L) by medium pH is described for the first time. Unicellular tobacco and snapdragon microspores developed into normal, fertile pollen when cultured in media T1 and AT3 at pH 7.0 and 25°C for 6 and 8 days, respectively. First, pollen mitosis was asymmetric and mature pollen grains were filled with starch granules and germinated upon transfer to a germination medium. However, when tobacco and snapdragon microspores were cultured in media T1 and AT3, respectively, at pH 8.0–8.5 for 4–6 days at 25 °C, the frequency of symmetric division increased significantly with the formation two nuclei of equal size, and the gametophytic pathway was blocked, as seen by the lack of starch accumulation and the inhibition of pollen germination. The transfer of these microspores to embryogenesis medium AT3 at pH 6.5 resulted in the formation of multicellular structures in both species and, in tobacco, in the formation of embryos and plants. In order to understand the possible mechanisms of the action of high pH, sucrose metabolism was analysed in isolated microspores of tobacco cultured at various pH values. Invertase (EC 3.2.1.26) activity in microspores was maximal at pH 5.0 and strongly decreased at higher pH, leading to a slow-down of sucrose cleavage. At the same time the incorporation of 14C-labelled sucrose from the medium into microspores was drastically reduced at high pH. These data suggest that isolated microspores are not able to metabolise carbohydrates at high pH and thus undergo starvation stress, which was shown earlier to block the gametophytic pathway and trigger sporophytic development.

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.

Fig. 1a–e
Fig. 2a,b
Fig. 3
Fig. 4a–d
Fig. 5

Similar content being viewed by others

References

  • Barinova I, Zhexembekova M, Barsova E, Lukyanov S, Heberle-Bors E, Touraev A (2002) Antirrhinum majus microspore maturation and transient transformation in vitro. J Exp Bot 53:1119–29

    Article  CAS  PubMed  Google Scholar 

  • Benito Moreno RM, Macke F, Hauser M-T, Alwen A, Heberle-Bors E (1988) Sporophytes and male gametophytes from in vitro cultured, immature tobacco pollen. In: Cresti M, Jori P, Pacini E (eds) Sexual reproduction in higher plants. Springer, Berlin Heidelberg New York, pp 137–142

  • Custers JBM, Gordewener JHG, Nöllen Y, Dons JJM, Van Lookeren-Campagne MM (1994) Temperature controls both gametophytic and sporophytic development in microspore cultures of Brassica napus. Plant Cell Rep 13:267–271

    CAS  Google Scholar 

  • Indrianto A, Heberle-Bors E, Touraev A (1999) Assessment of various stresses and carbohydrates for their effect on the induction of embryogenesis in isolated wheat microspores. Plant Sci 143:71–79

    Article  CAS  Google Scholar 

  • Indrianto A, Barinova J, Touraev A, Heberle-Bors E (2001) Tracking individual wheat microspores in vitro: identification of embryogenic microspores and body axis formation in the embryo. Planta 212:163–174

    Article  CAS  PubMed  Google Scholar 

  • Kyo M, Harada H (1986) Control of the developmental pathway of tobacco pollen in vitro. Planta 168:427–432

    CAS  Google Scholar 

  • Kumlehn J, Lörz H (1999) Monitoring sporophytic development of individual microspores of barley (Hordeum vulgare L.). In: Clément C, Pacini E, Audran (eds) Anther and pollen: from biology to biotechnology. Springer, Berlin Heidelberg New York, pp 183–190

  • Lowry OH, Rosebrough NJ, Lewis Farr A, Randall RJ (1951) Protein measurement with the folin phenol reagent. J Biochem 193:265–275

    CAS  Google Scholar 

  • Maddison AL, Hedley PE, Meyer, RC, Aziz N, Davidson D, Machray GC (1999) Expression of tandem invertase genes associated with sexual and vegetative growth cycles in potato. Plant Mol Biol 41:741–751

    Article  CAS  Google Scholar 

  • Maliga P, Breznovitis A, Morton L (1973) Streptomycin-resistant plants from callus culture from haploid tobacco. Nature 244:29–30

    CAS  Google Scholar 

  • Miller WB, Ranwala AP (1994) Characterization of three soluble invertase forms from Lilium longiflorum flower buds. Physiol Plant 92:247–253

    Article  CAS  Google Scholar 

  • Pasternak TP, Prinsen E, Ayaydin F, Miskolczi P, Potters G, Asard H, Van Onckelen HA, Dudits D, Feher A (2002) The role of auxin, pH, and stress in the activation of embryogenic cell division in leaf protoplast-derived cells of alfalfa. Plant Physiol 129:1807–1819

    Article  CAS  PubMed  Google Scholar 

  • Sangwan RS, Sangwan-Norreel BS (1987) Ultrastructural cytology of plastids in pollen grains of certain androgenic and nonandrogenic plants. Protoplasma 138:11–22

    Google Scholar 

  • Scott P, Lyne RL, ap Rees T (1995) Metabolism of maltose and sucrose by microspores isolated from barley (Hordeum vulgare L.). Planta 197:435–441

    CAS  Google Scholar 

  • Smith DL, Krikorian AD (1990a) Somatic embryogenesis of carrot in hormone-free medium: external pH control over morphogenesis. Am J Bot 77:1634–1647

    CAS  PubMed  Google Scholar 

  • Smith DL, Krikorian AD (1990b) Somatic proembryo production from excised, wounded zygotic carrot embryos on hormone-free medium: evaluation of the effects of pH, ethylene and activated charcoal. Plant Cell Rep 9:34–37

    CAS  PubMed  Google Scholar 

  • Somogyi M (1952) Notes on sugar determination. J Biol Chem 195:19–23

    CAS  Google Scholar 

  • Touraev A, Heberle-Bors E (1999) Microspore embryogenesis and in vitro pollen maturation in tobacco. In: Hall R (eds) Plant cell culture protocols, vol 111. Humana Press, Totowa, NJ, pp 281–291

  • Touraev A, Pfosser M, Heberle-Bors E (2001) The microspore: a haploid multipurpose cell. Adv Bot Res 35:53–109

    Google Scholar 

  • Tupy J, Rihova L, Zarsky V (1991) Production of fertile tobacco pollen from microspores in suspension culture and its storage for in situ pollination. Sex Plant Reprod 4:284–287

    Google Scholar 

  • Twell D (1994) The diversity and regulation of gene expression in the pathway of male gametophyte development. In: Scott RG (ed) Molecular and cellular aspects of plant reproduction, vol 55. Cambridge University Press, Cambridge, pp 83–135

  • Zaki M, Dickinson H (1991) Microspore-derived embryos in Brassica: the significance of division symmetry in pollen mitosis I to embryogenic development. Sex Plant Reprod 4:48–55

    Google Scholar 

Download references

Acknowledgements

The authors specially thank Dr. V. Zarsky (Institute of Experimental Botany, Prague, Czech Republic) for critical reading the manuscript and very useful advice and Dr. Z. Schwarz-Sommer (MPI, Cologne, Germany) for providing A. majus seeds. I. Barinova and Ch. Clément contributed equally to this work.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Alisher Touraev.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Barinova, I., Clément, C., Martiny, L. et al. Regulation of developmental pathways in cultured microspores of tobacco and snapdragon by medium pH. Planta 219, 141–146 (2004). https://doi.org/10.1007/s00425-003-1202-5

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00425-003-1202-5

Keywords

Navigation