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Organization of actin filaments in regenerating and outgrowing subprotoplasts from pollen tubes ofNicotiana tabacum L.

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Abstract

The dynamics of actin-filament organization in pollen-tube subprotoplasts ofNicotiana tabacum L. cv. Samsun during regeneration and outgrowth was examined using phalloidin probes and a non-fixation method. A succession of actin arrays was examined during subprotoplast regeneration that strongly resembled the actin dynamics described for developing microspores by Van Lammeren et al. (1989, Planta178, 531–539) and activated pollen by Tiwari and Polito (1988, Protoplasma147, 5–15). At the end of the succession the actin filaments often became extended between two opposite polar foci. The ordering of the cortical actin filaments reflected a polarity in the subprotoplasts which determined the plane of outgrowth. The site of outgrowth was often marked by a ring of actin filaments. As growth proceeded and tube-like structures were formed, the arrangement of cortical actin filaments was found to be transverse to the elongation axis. Since the patterns of actin distribution were identical in both caryoplasts and cytoplasts, it was concluded that the pollen-tube cytoplasm has the intrinsic capacity of reorganizing actin filaments and imposing polarity on the spherical subprotoplasts.

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References

  • Anderson, J.M., Soll, D.R. (1986) Differences in actin localization during bud and hypha formation in the yeastCandida albicans. J. Gen. Microbiol.132, 2035–2047

    CAS  PubMed  Google Scholar 

  • Bajer, A.S., Mole-Bajer, J. (1986) Reorganization of microtubules in endosperm cell and cell fragments of the higher plantHaemanthus in vivo. J. Cell Biol.102, 263–281

    Article  CAS  PubMed  Google Scholar 

  • Bershadsky, A.D., Vasiliev, J.M. (eds.) (1988) Cytoskeleton, Plenum Press, New York

    Google Scholar 

  • Cresti, M., Pacini, E., Ciampolini, F., Sarfatti, G. (1977) Germination and early tube development in vitro ofLycopersicum peruvianum pollen: ultrastructural features. Planta136, 239–247

    Article  Google Scholar 

  • Derksen, J., Traas, J.A. (1984) Growth of tobacco pollen tubes in vitro; effects of drug inteference with the cytoskeleton. In: Proc. 8th Int. Symp. Sexual Reproduction in seed plants, ferns and mosses, 20–24 August 1984, pp. 64–70, Willemse, M.T.M., Van Went, J.L., eds. Pudoc, Wageningen, The Netherlands

    Google Scholar 

  • Derksen, J., Traas, J.A., Oostendorp, T. (1986) Distribution of actin filaments in differentiating cells ofEquisetum hyemale root tips. Plant Sci.43, 77–81

    Article  CAS  Google Scholar 

  • Franke, W.W., Herth, W., VanDerWoude, W.J., Moore, D.J. (1972) Tubular and filamentous structures in pollen tubes: possible involvement as guide elements in protoplasmic streaming and vectorial migration of secretory vesicles. Planta105, 317–341

    Article  Google Scholar 

  • Galway, M.E., Hardham, A.R. (1988) Microtubule reorganization, cell wall synthesis and establishment of the axis of elongation in regenerating protoplasts of the algaMougeotia. Protoplasma135, 130–143

    Article  Google Scholar 

  • Gelfand, V.I., Glushankova, N.A., Ivanova, O.Y., Mittelman, L.A., Pletyushkina, O.Y., Vasiliev, J.M., Gelfand, I.M. (1985) Polarization of cytoplasmic fragments microsurgically detached from mouse fibroblasts. Cell Biol. Int. Rep.9, 883–892

    Article  CAS  PubMed  Google Scholar 

  • Hasezawa, S., Hogetsu, T., Syono, K. (1989) Changes of actin filaments and cellulose fibrils in elongating cells derived from tobacco protoplasts. J. Plant Physiol.134, 115–119

    Google Scholar 

  • Herth, W., Franke, W.W., VanDerWoude, W.J. (1972) Cytochalasin stops tip growth in plants. Naturwissenschaften59, 38–39

    Article  CAS  Google Scholar 

  • Heslop-Harrison, J., Heslop-Harrison, Y., Cresti, M., Tiezzi, A., Ciampolini, F. (1986) Actin during pollen germination. J. Cell Sci.86, 1–8

    CAS  Google Scholar 

  • Heslop-Harrison, J., Heslop-Harrison, Y., Cresti, M., Tiezzi, A., Moscatelli, A. (1988) Cytoskeletal elements, cell shaping and movement in the angiosperm pollen tube. J. Cell Sci.91, 49–60

    Google Scholar 

  • Hussey, P.J., Traas, J.A., Gull, K., Lloyd, C.W. (1987) Isolation of cytoskeletons from synchronized plant cells: the interphase microtubule array utilizes multiple tubuline isotypes. J. Cell Sci.88, 225–230

    CAS  Google Scholar 

  • Kilmartin, J.V., Adams, A.E.M. (1984) Structural rearrangements of tubulin and actin during the cell cycle of the yeastSaccharomyces. J. Cell Biol.98, 922–933

    Article  CAS  PubMed  Google Scholar 

  • Kobayashi, H., Fukuda, H., Shibaoka, H. (1988) Interrelation between the spatial disposition of actin filaments and microtubules during the differentiation of tracheary elements in culturedZinnia cells. Protoplasma143, 29–37

    Article  Google Scholar 

  • Kroh, M., Knuiman, B. (1988) Development of subprotoplasts from in vitro-grown tobacco pollen tubes. Sex. Plant Reprod.1, 103–113

    Article  Google Scholar 

  • Lancelle, S.A., Cresti, M., Hepler, P.K. (1987) Ultrastructure of the cytoskeleton in freeze-substituted pollen tubes ofNicotiana alata. Protoplasma140, 141–150

    Article  Google Scholar 

  • Lloyd, C.W. (1984) Toward a dynamic helical model for the influence of microtubules on wall patterns in plants. Int. Rev. Cytol.86, 1–51

    Article  Google Scholar 

  • McNiven, M.A., Wang, M., Porter, K.R. (1984) Microtubule polarity and the direction of pigment transport reverse simultaneously in surgically severed melanophore arms. Cell37, 753–765

    Article  CAS  PubMed  Google Scholar 

  • Niggli, V., Burger, M.M. (1987) Interaction of the cytoskeleton with the plasma membrane. J. Membr. Biol.100, 97–121

    Article  CAS  PubMed  Google Scholar 

  • Pargney, J.-C. (1982) Etude des ultrastructures cellulaires au cours de la plasmolyse et de l'isolement des protoplastes issue de tube pollinique d'Iris pseudacorus et deClivia nobilis. Z. Pflanzenphysiol.107, 237–249

    Google Scholar 

  • Perdue, T.D., Parthasarathy, M.V. (1985) In situ localization of F-actin in pollen tubes. Eur. J. Cell Biol.39, 13–20

    Google Scholar 

  • Picton, J.M., Steer, M.W. (1981) Determination of secretory vesicle production rates by dictyosomes in pollen tubes ofTradescantia using cytochalasin D. J. Cell Sci.49 261–272

    CAS  PubMed  Google Scholar 

  • Pierson, E.S., Derksen, J., Traas, J.A. (1986) Organization of microfilaments and microtubules in pollen tubes grown in vitro or in vivo in various angiosperms. Eur. J. Cell Biol.41, 14–18

    Google Scholar 

  • Power, J.B. (1973) Isolation of mature pollen protoplasts. In: Plant tissue and cell culture, pp. 118–119, Street, H.E., ed., Blackwell, Oxford

    Google Scholar 

  • Schnepf, E. (1986) Cellular polarity. Annu. Rev. Plant Physiol.37, 23–37

    Article  CAS  Google Scholar 

  • Sheldon, J.M., Hawes, C. (1988) The actin cytoskeleton during male meiosis inLilium. Cell Biol. Int. Rep.12, 471–476

    Article  Google Scholar 

  • Siderov, V.A., Menczel, L., Nagy, F., Maliga, P. (1981) Chloroplast transfer inNicotiana based on metabolic complementation between irradiated and iodoacetate treated protoplasts. Planta152, 341–345

    Article  Google Scholar 

  • Staiger, C.J., Schliwa, M. (1987) Actin localization and function in higher plants. Protoplasma141, 1–12

    Article  CAS  Google Scholar 

  • Steer, M.W., Steer, J.M. (1989) Pollen tube tip growth. New Phytol.111, 323–358

    Article  Google Scholar 

  • Tang, X., Hepler, P.K., Scordilis, S.P. (1989) Immunochemical and immunocytochemical identification of a myosin heavy chain polypeptide inNicotiana pollen tubes. J. Cell Sci.92, 569–574

    CAS  PubMed  Google Scholar 

  • Tiwari, S.C., Polito, V.S. (1988) Spatial and temporal organization of actin during hydration, activation, and germination of pollen inPyrus communis L.: a population study. Protoplasma147, 5–15

    Article  Google Scholar 

  • Traas, J.A., Doonan, J.H., Rawlins, D.J., Shaw, P.J., Watts, J., Lloyd, C.W. (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  CAS  PubMed  Google Scholar 

  • Van Lammeren, A.A.M., Bednara, J., Willemse, M.T.M. (1989) Organization of the actin cytoskeleton during pollen development inGasteria verrucosa (Mill.) H. Duval visualized with rhodamine-phalloidin. Planta178, 531–539

    Article  Google Scholar 

  • Wang, Y., Yan, L. (1988) The membrane proteins of leaf cells ofVicia faba. Sci. Bull.33, 231–235

    CAS  Google Scholar 

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Rutten, T.L.M., Derksen, J. Organization of actin filaments in regenerating and outgrowing subprotoplasts from pollen tubes ofNicotiana tabacum L.. Planta 180, 471–479 (1990). https://doi.org/10.1007/BF02411443

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