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Cytoskeletal aspects of nuclear migration during tip-growth in the fernAdiantum protonemal cell

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Summary

In the tip-growing protonemal cell, the nucleus migrates with the tip as it grows, keeping a constant distance between them. Cytoskeletal control of this nuclear migration was analyzed inAdiantum capillus-veneris. Using rhodamine-phalloidin (Rh-Phal), tubulin antibodies and confocal laser scanning microscopy, we found the presence of microtubule (MT) and microfilament (MF) strands connecting the cell nucleus to the cortex of the growing apex. The strands come from the apical end of the spindle-shaped nucleus and run through the endoplasm, arriving at the apical cortex, where a circular arrangement of MTs and MFs is present. Strands of MFs and MTs were also found to emanate from the proximal end of the nucleus and extend towards the cortex of the basal part of the cell. Double staining of MTs and MFs revealed a co-localization of these cytoskeletal elements. When MF strands were disrupted by cytochalasin B (CB), tip-growth ceased and nuclear movement stopped. After the application of colchicine, MT structures disappeared, tip-growth was largely inhibited, and the nucleus moved towards the basal part of the cell. When both CB and colchicine were applied to the cell, no basipetal migration of cell nucleus was observed. These results suggest that the MT strands between the apex and the nucleus may have a role in the anchorage of the cell nucleus to the tip during tip-growth, and that the MF strands may be important for basipetal movement of the nucleus. When the nucleus was dislocated basipetally by centrifugation, cytoskeletal strands between the cell apex and the nucleus were still observed, and by acropetal movement the nucleus resumed its previous position. The acropetal movement of the nucleus was inhibited by the application of both CB and colchicine but not by CB alone nor by colchicine alone, indicating that both cytoskeletal elements are involved in the forward movement of cell nucleus.

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Abbreviations

CB:

cytochalasin B

DAPI4′:

6-diamino-2-phenylin-dole

DMSO:

dimethylsulfoxide

PIPES:

piperazine-N,N′-bis(2-ethane-sulfonic acid)

EGTA:

ethyleneglycol-bis-(β-aminoethyl-ether)-N,N,N′,N′-tetraacetic acid

MBS:

m-maleimidobenzoic acid N-hydroxysuccinimide ester

MF:

microfilament

MT:

microtubule

PMSF:

phenylmethylsulfonyl fluoride

PSM:

polyoxyethylene sorbitan monolaurate

Rh-Phal:

rhodamine-labeled phalloidin

References

  • Brawley SH, Robinson KR (1985) Cytochalasin treatment disrupts the endogenous currents associated with cell polarization in fucoid zygotes: studies of the role of F-actin in embryogenesis. J Cell Biol 100: 1173–1184

    PubMed  Google Scholar 

  • Conrad PA, Steucek GL, Hepler PK (1986) Bud formation inFunaria: organelle redistribution following cytokinin treatment. Protoplasma 131: 211–223

    Google Scholar 

  • Doonan JH (1991) The cytoskeleton and moss morphogenesis. In: Lloyd CW (ed) The cytoskeletal basis of plant growth and form. Academic Press, London, pp 289–301

    Google Scholar 

  • —, Jenkins GI, Cove DJ, Lloyd CW (1986) Microtubules connect the migrating nucleus to the prospective division site during side branch formation in the moss,Physcomitrella patens. Eur J Cell Biol 41: 157–164

    Google Scholar 

  • Franke WW, Herth W, Van Der Woude WJ, Morré DJ (1972) Tubular and filamentous structures in pollen tubes: possible involvement as guide elements in protoplasmic streaming and vectorial migration of secretory vesicles. Planta 105: 317–341

    Google Scholar 

  • Heath IB (1982) The effect of nocodazole on the growth and ultrastructure of the fungusSaprolegnia ferax: evidence against a simple mode of action. In: Cappuccinelli P, Morris NR (ed) Microtubules in microorganisms. Marcel Dekker, New York, pp 275–311

    Google Scholar 

  • Herr FB, Heath MC (1982) The effect of antimicrotubule agents on organelle positioning in the cowpea rust fungus,Uromyces phaseoli var.vignae. Exp Mycol 6: 15–24

    Google Scholar 

  • Heslop-Harrison J, Heslop-Harrison Y (1989) Conformation and movement of the vegetative nucleus of the angiosperm pollen tube: association with the actin cytoskeleton. J Cell Sci 93: 299–308

    Google Scholar 

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

    Google Scholar 

  • Kadota A, Furuya M (1977) Apical growth of protonemata inAdiantum capillus-veneris. I. Red far-red reversible effect on growth cessation in the dark. Dev Growth Differ 19: 357–365

    Google Scholar 

  • — —, Wada M (1989) Circular arrangement of cortical F-actin around the subapical region of a tip-growing fern protonemal cell. Plant Cell Physiol 30: 1183–1186

    Google Scholar 

  • — — (1992a) Reorganization of the cortical cytoskeleton in tip-growing fern protonemal cells during phytochrome-mediated phototropism and blue light-induced apical swelling. Protoplasma 166: 35–41

    Google Scholar 

  • — — (1992b) The circular arrangement of cortical microtubules around the subapex of tip-growing fern protonemata is sensitive to cytochalasin B. Plant Cell Physiol 33: 99–102

    Google Scholar 

  • Kagawa T, Kadota A, Wada M (1992) The junction between the plasma membrane and the cell wall in fern protonemal cells, as visualized after plasmolysis, and its dependence on arrays of cortical microtubules. Protoplasma 170: 186–190

    Google Scholar 

  • Kropf DL (1992) Role of the cytoskeleton in cellular morphogenesis of zygotes of fucoid algae. In: Menzel D (ed) The cytoskeleton of the algae. CRC Press, Boca Raton, pp 79–92

    Google Scholar 

  • —, Berge SK, Quatrano RS (1989) Actin localization duringFucus embryogenesis. Plant Cell 1: 191–200

    PubMed  Google Scholar 

  • Lloyd CW, Pearce KJ, Rawlins DJ, Ridge RW, Shaw PJ (1987) Endoplasmic microtubules connect the advancing nucleus to the tip of legume root hairs, but F-actin is involved in basipetal migration. Cell Motil Cytoskeleton 8: 27–36

    Google Scholar 

  • McKerracher LJ, Heath IB (1984) Microtubules around migrating nuclei in conventionally-fixed and freeze-substituted cells. Protoplasma 124: 162–172

    Google Scholar 

  • — — (1986) Fungal nuclear behaviour analysed by ultraviolet microbeam irradiation. Cell Motil Cytoskeleton 6: 35–47

    Google Scholar 

  • Mineyuki Y, Furuya M (1985) Involvement of microtubules on nuclear positioning during apical growth inAdiantum protonemata. Plant Cell Physiol 26: 627–634

    Google Scholar 

  • Murata T, Kadota A, Hogetsu T, Wada M (1987) Circular arrangement of cortical microtubules around the subapical part of a tip-growing fern protonema. Protoplasma 141: 135–138

    Google Scholar 

  • Nagai R (1993) Regulation of intracellular movements in plant cells by environmental stimuli. Int Rev Cytol 145: 251–310

    Google Scholar 

  • Oakley BR, Morris NR (1980) Nuclear movement is β-tubulin dependent inAspergillus nidulans. Cell 19: 255–262

    PubMed  Google Scholar 

  • Ridge RW (1992) A model of legume root hair growth andRhizobium infection. Symbiosis 14: 359–373

    Google Scholar 

  • Schmiedel G, Schnepf E (1979) Side branch formation and orientation in the caulonema of the moss,Funaria hygrometrica: experiments with inhibitors and with centrifugation. Protoplasma 101: 47–59

    Google Scholar 

  • Schnepf E (1986) Cellular polarity. Annu Rev Plant Physiol 37: 23–47

    Google Scholar 

  • Shimmen T (1992) The characean cytoskeleton: dissecting the streaming mechanism. In: Menzel D (ed) The cytoskeleton of the algae. CRC Press, Boca Raton, pp 297–314

    Google Scholar 

  • Tiwari SC, Polito VS (1988a) Spatial and temporal organization of actin during hydration, activation, and germination of pollen inPyrus communis L.: a population study. Protoplasma 147: 5–15

    Google Scholar 

  • — — (1988b) Organization of the cytoskeleton in pollen tubes ofPyrus communis: a study employing conventional and freeze substitution electron microscopy, immunofluorescence, and rhodamine-phalloidin. Protoplasma 147: 100–112

    Google Scholar 

  • Vogelmann TC, Bassel AR, Miller JH (1981) Effects of microtubule-inhibitors on nuclear migration and rhizoid differentiation in germinating fern spores (Onoclea sensibilis). Protoplasma 109: 295–316

    Google Scholar 

  • Wada M, O'Brien TP (1975) Observations on the structure of the protonemaAdiantum capillus-veneris L. undergoing cell division following white-light irradiation. Planta 126: 213–227

    Google Scholar 

  • —, Kadota A, Furuya M (1983) Intracellular localization and dichroic orientation of phytochrome in plasma membrane and/or ectoplasm of a centrifuged protonema of fernAdiantum capillusveneris L. Plant Cell Physiol 24: 1441–1447

    Google Scholar 

  • —, Mineyuki Y, Kadota A, Furuya M (1980) The changes of nuclear position and distribution of circumferentially aligned cortical microtubules during the progression of cell cycle inAdiantum protonemata. Bot Mag Tokyo 93: 237–245

    Google Scholar 

  • Williamson RE (1993) Organelle movements. Annu Rev Plant Physiol Plant Mol Biol 44: 181–202

    Google Scholar 

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Kadota, A., Wada, M. Cytoskeletal aspects of nuclear migration during tip-growth in the fernAdiantum protonemal cell. Protoplasma 188, 170–179 (1995). https://doi.org/10.1007/BF01280368

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