Removal of the fibrillar network surrounding Cichorium somatic embryos using cytoskeleton inhibitors: Analysis of proteic components

Plant Science

Volumn 150, Issue 1, 2000, Pages 103-114

  Chapman, Audrey ^a   Helleboid, Stéphane ^a   Blervacq, Anne Sophie ^a   Vasseur, Jacques ^a   Hilbert, Jean Louis ^a  

^a UNIV LILLE   (France)

Author keywords

Arabinogalactan proteins; Cichorium; Cytoskeleton; Extracellular matrix; Extracellular proteins; Somatic embryogenesis

Indexed keywords

ARABINOGALACTAN; COLCHICINE; CYTOCHALASIN B; GLYCOPROTEIN;

ARTICLE; CELL MEMBRANE; CHICORY; CYTOSKELETON; EMBRYO DEVELOPMENT; EXTRACELLULAR MATRIX; NONHUMAN; PROTEIN ANALYSIS; SIGNAL TRANSDUCTION; SOMATIC CELL;

EID: 0034645808     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-9452(99)00185-5     Document Type: Article

References (56)

1. Hay E.D. Collagen and embryonic development. Hay E.D. Cell Biology of Extracellular Matrix. 1981;379-409 Plenum Press, New York.
2. Ingber D. Integrin as mechanochemical transducers. Curr. Opin. Cell Biol. 3:1991;841-848.
3. Reuzeau C., Pont-Lezica R.F. Comparing plant and animal extracellular matrix-cytoskeleton connections - are they alike? Protoplasma. 186:1995;113-121.
4. Lamport D.T.A., Catt J.W. Glycoproteins and enzymes of the cell wall. Tanner W., Loewus F.A. Plant Carbohydrates Extracellular Carbohydrates. II: 1981;134-165 Springer-Verlag, New York.
5. Roberts K. Structures at the plant cell surface. Curr. Opin. Cell Biol. 2:1990;920-928.
6. Wyatt S.E., Carpita N.C. The plant cytoskeleton-cell wall continuum. Trends Cell Biol. 3:1993;413-417.
7. Schindler M., Meiners S., Cheresh D.A. RGD-dependent linkage between plant cell wall and plasma membrane: consequences for growth. J. Cell Biol. 108:1989;1955-1965.
8. Zhu J.K., Shi J., Singh U., Wyatt S.E., Bressan R.A., Hasegawa P.M., Carpita N.C. Enrichement of vitronectin and fibronectin-like proteins in NaCl-adapted plant cells and evidence for their involvement in plasma membrane-cell wall adhesion. Plant J. 3:1993;637-646.
9. Odani S., Takehico K., Ono T. Amino acid sequence of a soybean (Glycine max) seed protein having a poly(L-aspartic acid) structure. J. Biol. Chem. 262:1987;10502-10505.
10. Hocquette S., Pont-Lezica R. Involvement of vitronectin-like molecules in wall-to-membrane linkages in onion epidermis. Prakashi H. Past, Present and Future of Plant Biology. 1994;38-41 Washington University, St Louis.
11. Alberts B., Bray D., Lewis J., Raff M., Roberts K., Watson J.D. Molecular Biology of Cell. third ed. 1994;Garland Publishing, New York.
12. Serpe M.D., Nothnagel E.A. Effects of Yariv phenylglycosides on Rosa cell suspensions: evidence for the involvement of arabinogalactan-proteins in cell proliferation. Planta. 193:1994;542-550.
13. Egertsdotter U., von Arnold S. Importance of arabinogalactan proteins for the development of somatic embryos of Norway spruce (Picea abies). Physiol. Plant. 93:1995;334-345.
14. Thompson H.J.M., Knox J.P. Stage-specific responses of embryogenic carrot cell suspension, cultures to arabinogalactan protein-binding β-glycosyl Yariv reagent. Planta. 205:1998;32-38.
15. Pennell R.I., Roberts K. Sexual development in the pea is presaged by altered expression of arabinogalactan protein. Nature. 344:1990;547-549.
16. Dubois T., Guedira M., Dubois J., Vasseur J. Direct somatic embryogenesis in leaves of Cichorium. A histological and SEM study of early stages. Protoplasma. 162:1991;120-127.
17. Dubois T., Guedira M., Dubois J., Vasseur J. Direct somatic embryogenesis in roots of Cichorium: is callose an early marker? Ann. Bot. 65:1990;539-545.
18. Dubois T., Dubois J., Guedira M., Vasseur J. Embryogenèse somatique directe sur les styles de Cichorium: effets de la température et origine des embryoïdes. C.R. Acad. Sci. Paris. 307:1988;669-675.
19. Heller R. Recherches sur la nutrition minérale des tissus végétaux cultivés in vitro. Ann. Sci. Nat. Bot. Biol. Vég. 14:1953;1-223.
20. Morel G., Wetmore R.H. Fern callus tissue culture. Am. J. Bot. 38:1951;141-143.
21. Murashige T., Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol. Plant. 15:1962;473-497.
22. Maheswaran G., Williams E.G. Origin and development of somatic embryoids formed directly on immature embryos of Trifolium repens in vitro. Ann. Bot. 56:1985;619-630.
23. Helleboid S., Bauw G., Belingheri L., Vasseur J., Hilbert J.L. Extracellular β-1,3-glucanases are induced during early somatic embryogenesis in Cichorium. Planta. 205:1998;56-63.
24. Zivy M. Influence des ampholytes sur la révélation des protéines au nitrate d'argent. Galteau M.M., Siest G. Recent progresses in Two-Dimensional Electrophoresis. 1986;69 Presses Universitaires de Nancy, France.
25. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 227:1970;680-685.
26. Boyer C., Hilbert J.L., Vasseur J. Embryogenesis related protein synthesis and accumulation during early acquisition for somatic embryogenesis competence of Cichorium. Plant Sci. 93:1993;41-53.
27. Blum H., Beier H., Gross H.J. Improved silver staining of plant proteins, RNA and DNA in polyacrylamide gels. Electrophoresis. 8:1987;93-99.
28. Dubray G., Bezard G. A highly sensitive periodic acid-silver stain for 1,2-diol groups of glycoproteins and polysaccharides in polyacrylamide gels. Anal. Biochem. 119:1982;325-329.
29. Van Holst G.J., Clarke A.E. Quantification of arabinogalactan-protein in plant extracts by single radial gel diffusion. Anal. Biochem. 148:1985;446-450.
30. Yariv J., Rapport M.M., Graf L. The interaction of glycosides and saccharides with antibody to the corresponding phenylazo dyes. Biochem. J. 85:1962;383-388.
31. Knox J.P., Linstead P.J., Peart J., Cooper C., Roberts K. Developmentally regulated epitopes of cell surface arabinogalactan proteins and their relation to root tissue pattern formation. Plant J. 1:1991;317-326.
32. Smallwood M., Yates E.A., Willats W.G.T., Martin H., Knox J.P. Immunochemical comparison of membrane-associated and secreted arabinogalactan-proteins in rice and carrot. Planta. 198:1996;452-459.
33. Ohamura S., Kakiuchi M., Sano A., Kawajiri M. Loss of tubulin during cold treatment of cultured carrot cells. Physiol. Plant. 88:1993;93-98.
34. Venverloo C.J., Libbenga K.R. Regulation of the plane of cell division in vacuolated cells. I. The function of nuclear positioning and phragmosome formation. J. Plant Physiol. 131:1987;267-284.
35. Seagull R.W. The effects of microtubule and microfilament disrupting agents on cytoskeletal arrays and wall deposition in developing cotton fibers. Protoplasma. 159:1990;44-59.
36. Kobayashi H., Fukuda H., Shibaoka H. Interrelation between the spatial disposition of actin filaments and micotubules during the differentiation of tracheary elements in cultured Zinnia cells. Protoplasma. 143:1988;29-37.
37. Dubois T., Dubois J., Guedira M., Diop A., Vasseur J. SEM characterization of an extracellular matrix around somatic proembryos in roots of Cichorium. Ann. Bot. 70:1992;119-124.
38. Woessner JF. The extracellular matrix. FASEB J 1993;735-736.
39. Basile D.V., Kushner B.K., Basile M.R. A new method for separating and comparing arabinogalactan proteins for the chemosystematics of the Hepaticae. Bryologist. 92:1989;164-169.
40. Samaj J., Bobak M., Blehova A., Kristin J., Auxtova-Samajova O. Developmental SEM observations on an extracellular matrix in embryogenic calli of Drosera rotundifolia and Zea mays. Protoplasma. 186:1995;45-49.
41. Jasik J., Salajova T., Salaj J. Developmental anatomy and ultrastructure of early somatic embryos in European blake pine (Pinus nigra Arn.). Protoplasma. 185:1995;205-211.
42. McCann M.C., Wells B., Roberts K. Direct visualization of cross-links in the primary plant cell wall. J. Cell Sci. 96:1990;323-334.
43. Kachar B., Parakkal M., Fex J. Structural basis for mechanical transduction in the frog vestibular sensory apparatus. I. The otholic membrane. Hearing Res. 45:1990;179-190.
44. Mazars C., Thion L., Thuleau P., Graziana A., Knight M.R., Moreau M., Ranjeva R. Organization of cytoskeleton controls the changes in cytosolic calcium of cold-shocked Nicotiana plumbaginifolia protoplasts. Cell Calcium. 22:1997;413-420.
45. Weedenburg C., Seagull R.W. The effects of taxol and colchicine on microtubule arrays in elongating plant cells in culture. Can. J. Bot. 66:1987;1707-1716.
46. Salitz A., Schmitz K. Influence of microfilament and inhibitors applied by immersion and microinjection on circulation streaming in the staminal hairs of Tradescantia blossfeldiana. Protoplasma. 153:1989;37-45.
47. Robatche-Claive A.S., Couillerot J.P., Dubois J., Dubois T., Vasseur J. Embryogenèse somatique directe dans les feuilles du Cichorium hybride '474': synchronisation de l'induction. C. R. Acad. Sci. Paris. 314:1992;371-377.
48. Ruoslahti E., Pierschbacher M.D. New perspectives in cell adhesion: RGD and integrin. Science. 238:1987;491-497.
49. Basile D.V., Basile M.R. The role and control of the place-dependent suppression of cell division in plant morphogenesis and phylogeny. Memoirs Torrey Bot. Club. 25:1993;63-83.
50. Schopfer P. Cytochemical identification of arabinogalactan protein in the outer epidermal wall of maize coleoptiles. Planta. 183:1990;139-142.
51. Zhu J.K., Bressan R.A., Hasegawa P.M. Loss of arabinogalactan-proteins from the plasma membrane of NaCl-adapted tobacco cells. Planta. 190:1993;221-226.
52. Kreuger M., van Holst G.J. Arabinogalactan-proteins are essentiel in somatic embryogenesis of Daucus carota L. Planta. 189:1993;243-248.
53. Kreuger M., van Holst G.J. Arabinogalactan-protein epitopes in somatic embryogenesis of Daucus carota L. Planta. 197:1995;135-141.
54. Anderson R.L., Clarke A.E., Jermyn M.A., Knox R.B., Stone B.A. A carbohydrate-binding arabinogalactan protein from liquid suspension culture of endosperm from Lolium multiflorum. Aust. J. Plant Physiol. 4:1977;143-158.
55. Hori H., Takeuchi Y., Fujui T. Structure of an arabinogalactan of extracellular hydroxyproline-rich glycoprotein in suspension-culture tobacco cells. Phytochemistry. 19:1980;2755-2756.
56. Roy S., Jauh G.Y., Helper P.K., Lord E.M. Effects of Yariv phenylglycoside on cell wall assembly in the lily pollen tube. Planta. 204:1998;450-458.