Cytoskeletal control of polar growth in plant cells

Current Opinion in Cell Biology

Volumn 10, Issue 1, 1998, Pages 117-122

  Kropf, Darryl L ^a   Bisgrove, Sherryl R ^a   Hable, Whitney E ^a  

^a UNIVERSITY OF UTAH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

F ACTIN;

CELL GROWTH; CELL WALL; CYTOSKELETON; FIBER; MICROTUBULE; PLANT CELL; PRIORITY JOURNAL; REVIEW;

EID: 0032006767     PISSN: 09550674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0955-0674(98)80094-X     Document Type: Article

References (67)

1. Green PB. Organogenesis - a biophysical view. Annu Rev Plant Physiol. 31:1980;51-82.
2. Sonobe S, Takahashi S. Association of microtubules with the plasma membrane of tobacco BY-2 cells in vitro. Plant Cell Physiol. 35:1994;451-460.
3. Williamson RE. Orientation of cortical microtubules in interphase plant cells. Int Rev Cytol. 129:1991;135-206.
4. Pear JR, Kawagoe Y, Schreckengost WE, Delmer DP, Stalker DM. Higher plants contain homologs of the bacterial cel A genes encoding the catalytic subunit of cellulose synthase. of special interest Proc Natl Acad SCi USA. 93:1996;12637-12642 Describes the cloning of the cDNA encoding the long sought after catalytic subunit cellulose synthase, a significant advance in plant cell biology.
5. Baskin TI, Wilson JE, Cork A, Williamson RE. Morphology and microtubule organization in Arabidopsis roots exposed to oryzalin or taxol. Plant Cell Physiol. 35:1994;935-942.
6. Cyr RJ. Microtubules in plant morphogenesis: role of the cortical array. Annu Rev Cell Biol. 10:1994;153-180.
7. Mizuta S, Watanabe S, Kimura S, Yoshida K. Possible involvement of membrane fluidity in helicoidal microfibrillar orientation in the coenocytic green alga, Boergesenia forbesii. Protoplasma. 180:1994;82-91.
8. Baskin TI, Bivens NJ. Stimulation of radial expansion in Arabidopsis roots by inhibitors of actomyosin and vesicle secretion but not by various inhibitors of metabolism. Planta. 197:1995;514-521.
9. Hush JM, Overall RL. Cortical microtubule reorientation in higher plants: dynamics and regulation. of special interest J Microsc. 181:1996;129-139 A comprehensive consideration of microtubule reorientation in higher plant cells in response to environmental signals.
10. Baskin TI, Wilson JE. Inhibitors of protein kinases and phosphatases alter root morphology and disorganize cortical microtubules. of special interest Plant Physiol. 113:1997;493-502 Demonstrates a role for phosphorylation/dephosphorylation in regulating the microtubule cytoskeleton and growth anisotropy.
11. McClinton RS, Sung ZR. Organization of cortical microtubules at the plasma membrane in Arabidopsis. Planta. 201:1997;252-260.
12. Stoppin V, Lambert AM, Vantard M. Plant microtubule-associated proteins (MAPs) affect microtubule nucleation and growth at plant nuclei and mammalian centrosomes. Eur J Cell Biol. 69:1996;11-23.
13. Shibaoka H. Plant hormone-induced changes in the orientation of cortical microtubules: alterations in the cross-linking between microtubules and the plasma membrane. Annu Rev Plant Physiol Plant Mol Biol. 45:1994;527-544.
14. Mayumi K, Shibaoka H. The cyclic reorientation of cortical microtubules on walls with a crossed polylamellate structure: effects of plant hormones and an inhibitor of protein kinases on the progression of the cycle. of outstanding interest Protoplasma. 195:1996;112-122 6-dimethylaminopurine, an inhibitor of protein kinases, causes microtubule reorientation from transverse to longitudinal, indicating that phosphorylation is important in this response.
15. cdc2/cyclin B to show that phosphorylation cascades are regulators of plant cytoskeletal arrays.
16. Palevitz BA. Potential significance of microtubule rearrangement, translocation and reutilization in plant cells. Lloyd CW. The Cytoskeletal Basis of Plant Growth and Form. 1991;45-55 Academic Press, Inc, London.
17. Cleary AL, Gunning BES, Wasteneys GO, Hepler PK. Microtubule and F-actin dynamics at the division site in living Tradescantia stamen hair cells. J Cell Sci. 103:1992;977-988.
18. Wasteneys GO, Gunning BES, Hepler PK. Microinjection of fluorescent brain tubulin reveals dynamic properties of cortical microtubules in living plant cells. Cell Motil Cytoskeleton. 24:1993;205-213.
19. Kropf DL, Williamson RE, Wasteneys GO. Microtubule orientation and dynamics in elongating characean internodal cells followed cytosolic acidification, induction of pH bands, or premature growth arrest. Protoplasma. 197:1997;188-198.
20. Wymer CL, Shaw PJ, Lloyd CW. Microinjection of fluorescent tubulin into plant cells provides a representative picture of the cortical microtubule array. Plant J. 12:1997;229-234.
21. Yuan M, Shaw PJ, Warn RM, Lloyd CW. Dynamic reorientation of cortical microtubules, from transverse to longitudinal, in living plant cells. Proc Nat Acad Sci USA. 91:1994;6050-6053.
22. Hush JM, Wadsworth P, Callaham DA, Hapler PK. Quantification of microtubule dynamics in living plant cells using fluorescence redistribution after photobleaching. J Cell Sci. 107:1994;775-784.
23. Lloyd CW, Shaw PJ, Warn RM, Yuan M. Gibberellic-acid-induced reorientation of cortical microtubules in living plant cells. J Microsc. 181:1996;140-144.
24. Liu B, Joshi HC, Wilson TJ, Silflow CD, Palevitz BA, Snustad DP. Gamma-tubulin in Arabidopsis:: gene sequence, immunoblot, and immunofluorescence studies. Plant Cell. 6:1994;303-314.
25. Kuss-Wymer CL, Cyr RJ. Tobacco protoplasts differentiate into elongate cells without net microtubule depolymerization. Protoplasma. 168:1992;64-72.
26. Wymer CL, Fisher DD, Moore RC, Cyr RJ. Elucidating the mechanism of cortical microtubule reorientation in plant cells. of outstanding interest Cell Motil Cytoskeleton. 35:1996;162-173 Microtubule reorientation in BY-2 cells occurs in the presence of taxol (a microtubule-stabilizing drug), suggesting the translocation of intact microtubules. Translocation does not require additional microtubule polymerization, but does require energy.
27. Moscatelli A, Del Casino C, Lozzi L, Cai G, Scali M, Tiezzi A, Cresti M. High molecular weight polypeptides related to dynein heavy chains in Nicotiana tabacum pollen tubes. J Cell Sci. 108:1995;1117-1125.
28. Asada T, Kuriyama R, Shibaoka H. TKRP125, a kinesin-related protein involved in the centrosome-independent organization of the cytokinetic apparatus in tobacco BY-2 cells. J Cell Sci. 110:1997;179-189.
29. Liu B, Cyr RJ, Palevitz BA. A kinesin-like protein, KatAp, in the cells of Arabidopsis and other plant cells. Plant Cell. 8:1996;119-132.
30. Steer MW, Steer JM. Pollen tube tip growth. New Phytol. 111:1989;323-358.
31. Miller D, de Ruijter N, Emons A. From signal to form: aspects of the cytoskeleton-plasma membrane-cell wall continuum in root hair tips. of special interest J Exp Bot. 1997; A comprehensive review of root hair growth, including the role of the cytoskeleton.
32. Li YQ, Zhang HQ, Pierson ES, Huang FY, Linskens HF, Hepler PK. Enforced growth-rate fluctuation causes pectin ring formation in the cell wall of Lilium longiflorum pollen tubes. Planta. 200:1996;41-49.
33. Emons AMC, Derksen J, Sassen MMA. Do microtubules orient plant cell wall microfibrils? Physiol Plant. 84:1992;486-493.
34. Lancelle SA, Cresti M, Hepler PK. Ultrastructure of the cytoskeleton in freeze-substituted pollen tubes of Nicotiana alata. Protoplasma. 140:1987;141-150.
35. Cai G, Moscatelli A, Cresti M. Cytoskeletal organization and pollen tube growth. Trends Plant Sci. 2:1997;86-91.
36. Del Casino C, Li YQ, Moscatelli A, Scali M, Tiezzi A, Cresti M. Distribution of microtubules during the growth of tobacco pollen tubes. Biol Cell. 79:1993;125-132.
37. Heslop-Harrison J, Heslop-Harrison Y, Cresti M, Tiezzi A, Moscatelli A. Cytoskeletal elements, cell shaping and movement in the angiosperm pollen tube. J Cell Sci. 91:1988;49-60.
38. Allen V, Kropf DL. Nuclear rotation and lineage specification in Pelvetia embryos. Development. 115:1992;873-883.
39. Astrom H, Sorri O, Raudaskoski M. Role of microtubules in the movement of the vegatative nucleus and generative cell in tobacco pollen tubes. Sex Plant Reprod. 8:1995;61-69.
40. Joos U, van Aken J, Kristen U. Microtubules are involved in maintaining the cellular polarity in pollen tubes of Nicotiana sylvestris. Protoplasma. 179:1994;5-15.
41. Li Y, Moscatelli A, Cai G, Cresti M. Functional interactions among cytoskeleton, membranes, and cell wall in the pollen tube of flowering plants. of special interest Int Rev Cytol. 176:1997;133-199 A recent, detailed review of pollen tube growth.
42. Shimmen T, Yokota E. Physiological and biochemical aspects of cytoplasmic streaming. Int Rev Cytol. 155:1994;97-139.
43. Miller D, Scordilis S, Hepler P. Identification and localization of three classes of myosins in pollen tubes of Lilium longiflorum and Nicotiana alata. J Cell Sci. 108:1995;2549-2563.
44. Derksen J, Rutten T, Van Amstel T, De Win A, Doris F, Steer M. Regulation of pollen tube growth. Acta Bot Neerl. 44:1995;93-119.
45. Alfano F, Russel A, Gambardella R, Duckett J. The actin cytoskeleton of the liverwort Riccia fluitans: effects of cytochalasin B and aluminum ions on rhizoid tip growth. J Plant Physiol. 142:1993;569-574.
46. Alessa L, Oliveira L. Aluminum toxicity studies in Vaucheria longicaulis var. macounii II: effects on the F-actin array. of special interest J Plant Res. 1997; A dense meshwork of F-actin is present in the dome of live algal cells injected with fluorescent phalloidin.
47. Doris FP, Steer MW. Effects of fixatives and permeabilisation buffers on pollen tubes: implications for localisation of actin microfilaments using phallodin staining. of special interest Protoplasma. 195:1996;25-36 Provides a clear demonstration that the preservation of F-actin in chemically fixed cells varies depending on the specifics of the fixation protocol.
48. Miller DD, Lancelle SA, Hepler PK. Actin microfilaments do not form a dense meshwork in Lillum longiflorum pollen tube tips. of outstanding interest Protoplasma. 195:1996;123-132 The authors detect only sparse, individual actin filaments in the dome of freeze-substituted and rhodamine-phalloidin-microinjected pollen tubes, and question the presence of a dense meshwork.
49. Kagawa T, Kadota A, Wada M. 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. 170:1992;186-190.
50. Gupta GD, Heath IB. Actin disruption by latrunculin B causes turgor related changes in tip growth of Saprolegnia ferax hyphae. of special interest Fungal Gen Biol. 21:1997;64-75 Cytochalasins cause transient growth acceleration or deceleration in fungal hyphae under high or low turgor, respectively. This is interpreted to indicate that F-actin can restrain or drive tip elongation, depending on the conditions.
51. Lin Y, Yang Z. Inhibition of pollen tube elongation by microinjected anti-Rop1Ps antibodies suggests a crucial role for rho-type GTPases in the control of tip growth. of outstanding interest Plant Cell. 9:1997;1647-1659 An antibody against a rho protein arrests growth but not cytoplasmic streaming when microinjected into pollen. As some rho proteins regulate F-actin, this may indicate separate regulatory pathways in the dome and farther back.
52. Kropf DL. Induction of polarity in fucoid zygotes. of special interest Plant Cell. 9:1997;1011-1020 A recent review of polarity establishment in tip-growing fucoid algae, emphasizing the fundamental role of F-actin.
53. Henry C, Jordan JR, Kropf DL. Localized membrane-wall adhesions in Pelvetia zygotes. of special interest Protoplasma. 190:1996;39-52 Physiological characterization of adhesions in the dome of tip-growing algal rhizoids, including the identification of cortical F-actin at the adhesion site.
54. Kaminskyj S, Heath I. Integrin and spectrin homologues, and cytoplasm-wall adhesion in tip growth. J Cell Sci. 108:1995;849-856.
55. Lord EM, Sanders LC. Roles for the extracellular matrix in plant development and pollination: a special case of cell movement in plants. Dev Biol. 153:1992;16-28.
56. Wagner V, Brian L, Quatrano R. Role of a vitronectin-like molecule in embryo adhesion of the brown alga Fucus. Proc Natl Acad Sci USA. 89:1992;3644-3648.
57. Wang C-S, Walling LL, Gu YO, Lord EM. Two classes of proteins and mRNAs in Lilium longiflorum L. identified by human vitronectin probes. Plant Physiol. 104:1994;711-717.
58. De Ruijter N, Emons A. Immunodetection of spectrin antigens in plant cells. Cell Biol Int. 17:1993;169-182.
59. Taylor L, Hepler P. Pollen germination and tube growth. of outstanding interest Annu Rev Plant Physiol Plant Molec Biol. 48:1997;461-491 A comprehensive review of pollen tube growth, including the role of the cytoskeleton.
60. 2+-induced fragmentation of actin filaments in pollen tubes. Protoplasma. 141:1987;177-179.
61. Staiger CJ, Gibbon BC, Kovar DR, Zonia LE. Profilin and actin-depolymerizing factor: modulators of actin organization in plants. of outstanding interest Trends Plant Sci. 2:1997;275-281 A short review of actin-binding proteins (profilin and actin-depolymerizing factor) in plant cells and their role in regulating F-actin structure and function.
62. Vidali L, Hepler PK. Characterization and localization of profilin in pollen grains and tubes of Lilium longiflorum. of special interest Cell Motil Cytoskeleton. 36:1997;323-338 Microinjection of fluorescent profilin indicates that profilin is distributed throughout the cytoplasmic volume and is not concentrated in the dome, at the plasma membrane or along actin cables.
63. Lopez I, Anthony RG, Maciver SK, Jiang CJ, Khan S, Weeds AG, Hussey PJ. Pollen specific expression of maize genes encoding actin deplymerizing factor-like proteins. Proc Natl Acad Sci USA. 93:1996;7415-7420.
64. Carpenter JL, Ploense SE, Snustad DP, Silflow CD. Preferential expression of an alpha-tubulin gene of Arabidopsis in pollen. Plant Cell. 4:1992;557-571.
65. Huang S, Yq A, McDowell JM, McKinney EC, Meagher RB. The Arabidopsis ACT11 actin gene is strongly expressed in tissues of the emerging inflorescence, pollen, and developing ovules. Plant Mol Biol. 33:1997;125-139.
66. Staiger CJ, Goodbody DC, Hussey PJ, Valenta R, Drobak BK, Lloyd CW. The profilin multigene family of maize: differential expression of three isoforms. Plant J. 4:1993;631-641.
67. McDowell JM, Huang S, McKinney EC, An YQ, Meagher RB. Structure and evolution of the actin gene family in Arabidopsis thaliana. Genetics. 142:1996;587-602.