The roles of microtubules in tropisms

Plant Science

Volumn 175, Issue 6, 2008, Pages 747-755

  Bisgrove, Sherryl R ^a  

^a SIMON FRASER UNIVERSITY   (Canada)

Author keywords

Cell expansion; Cell wall; Cytoskeleton; Microtubule; Tropism

Indexed keywords

ANIMALIA;

EID: 54449090870     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2008.08.009     Document Type: Review

References (144)

1. Cassab G.I. Other tropisms and their relationship to gravitropism. In: Gilroy S., and Masson P.H. (Eds). Plant Tropisms (2008), Blackwell Publishing Ltd., Ames, Iowa 123-139
2. Braam J. In touch: plant responses to mechanical stimuli. New Phytol. 165 (2005) 373-389
3. Eapen D., Barroso M.L., Campos M.E., Ponce G., Corkidi G., Dubrovsky J.G., and Cassab G.I. A no hydrotropic response root mutant that responds positively to gravitropism in Arabidopsis. Plant Physiol. 131 (2003) 536-546
4. Kaneyasu T., Kobayashi A., Nakayama M., Fujii N., Takahashi H., and Miyazawa Y. Auxin response, but not its polar transport, plays a role in hydrotropism of Arabidopsis roots. J. Exp. Bot. (2007) 1143-1150
5. Kobayashi A., Takahashi A., Kakimoto Y., Miyazawa Y., Fujii N., Higashitani A., and Takahashi H. A gene essential for hydrotropism in roots. Proc. Natl. Acad. Sci. U.S.A. 104 (2007) 4724-4729
6. Ponce G., Rasgado F.A., and Cassab G.I. Roles of amyloplasts and water deficit in root tropisms. Plant Cell Environ. 31 (2008) 205-217
7. Haswell E.S., Peyronnet R., Barbier-Brygoo H., Meyerowitz E.M., and Frachisse J.-M. Two MscS homologs provide mechanosensitive channel activities in the Arabidopsis root. Curr. Biol. 18 (2008) 730-734
8. Kimbrough J.M., Salinas-Mondragon R., Boss W.F., Brown C.S., and Sederoff H.W. The fast and transient transcriptional network of gravity and mechanical stimulation in the Arabidopsis root apex. Plant Physiol. 136 (2004) 2790-2805
9. McCormack E., Velasquez L., Delk N.A., and Braam J. Touch-responsive behaviors and gene expression in plants. In: Frantisek Baluska S.M., and Dieter Volkmann (Eds). Communication in Plants (2006), Springer
10. Nakagawa Y., Katagiri T., Shinozaki K., Qi Z., Tatsumi H., Furuichi T., Kishigami A., Sokabe M., Kojima I., Sato S., Kato T., Tabata S., Iida K., Terashima A., Nakano M., Ikeda M., Yamanaka T., and Iida H. Arabidopsis plasma membrane protein crucial for Ca2+ influx and touch sensing in roots. Proc. Natl. Acad. Sci. U.S.A. 104 (2007) 3639-3644
11. Gilroy S. Plant tropisms. Curr. Biol. 18 (2008) R275-R277
12. Christie J.M. Phototropin blue-light receptors. Annu. Rev. Plant Biol. 58 (2007) 21-45
13. Esmon C.A., Pedmale U.V., and Liscum E. Plant tropisms: providing the power of movement to a sessile organism. Int. J. Dev. Biol. 49 (2005) 665-674
14. Harrison B.R., Morita M.T., Masson P.H., and Tasaka M. Signal transduction in gravitropism. In: Gilroy S., and Masson P.H. (Eds). Plant Tropisms (2008), Blackwell Publishing, Ames, Iowa 21-45
15. Kiss J.Z. Where's the water? Hydrotropism in plants. Proc. Natl. Acad. Sci. U.S.A. 104 (2007) 4247-4248
16. Monshausen G.B., Swanson S.J., and Gilroy S. Touch sensing and thigmotropism. In: Gilroy S., and Masson P.H. (Eds). Plant Tropisms (2008), Blackwell Publishing, Ames, Iowa 91-122
17. Mullen J.L., and Kiss J.Z. Phototropism and its relationship to gravitropism. In: Gilroy S., and Masson P.H. (Eds). Plant Tropisms (2008), Blackwell Publishing Ltd., Ames, Iowa 79-90
18. Valster A., and Blancaflor E.B. Mechanisms of gravity perception in higher plants. In: Gilroy S., and Masson P.H. (Eds). Plant Tropisms (2008), Blackwell Publishing, Ames, Iowa 3-19
19. Whippo C.W., and Hangarter R.P. Phototropism: bending towards enlightenment. Plant Cell 18 (2006) 1110-1119
20. Tokutomi S., Matsuoka D., and Zikihara K. Molecular structure and regulation of phototropin kinase by blue light. Biochim. Biophys. Acta 1784 (2008) 133-142
21. Kang B., Grancher N., KoyVmann V., Lardemer D., Burney S., and Ahmad M. Multiple interactions between cryptochrome and phototropin blue-light signalling pathways in Arabidopsis thaliana. Planta 227 (2008) 1091-1099
22. Inoue S., Kinoshita T., Matsumoto M., Nakayama K., Doi M., and Shimazaki K. Blue light-induced autophosphorylation of phototropin is a primary step for signaling. Proc. Natl. Acad. Sci. U.S.A. 105 (2008) 5626-5631
23. Morita M.T., and Tasaka M. Gravity sensing and signaling. Curr. Opin. Plant Biol. 7 (2004) 712-718
24. Wayne R., and Staves M.P. A down to earth model of gravisensing or Newton's Law of Gravitation from the apple's perspective. Physiol. Plant. 98 (1996) 917-921
25. Perrin R.M., Young L.-S., Murthy N., Harrison B.R., Wang Y.A.N., Will J.L., and Masson P.H. Gravity signal transduction in primary roots. Ann. Bot. 96 (2005) 737-743
26. Nick P. Microtubules as sensors for abiotic stimuli. In: Nick P. (Ed). Plant Microtubules (2008), Springer-Verlag, Berlin/Heidelberg 175-203
27. Takahashi N., Goto N., Okada K., and Takahashi H. Hydrotropism in abscisic acid, wavy, and gravitropic mutants of Arabidopsis thaliana. Planta 216 (2002) 203-211
28. Takahashi N., Yamazaki Y., Kobayashi A., Higashitani A., and Takahashi H. Hydrotropism interacts with gravitropism by degrading amyloplasts in seedling roots of Arabidopsis and radish. Plant Physiol. 132 (2003) 805-810
29. Eapen D., Barroso M.L., Ponce G., Campos M.E., and Cassab G.I. Hydrotropism: root growth responses to water. Trends Plant Sci. 10 (2005) 44-50
30. Muday G.K., and Rahman A. Auxin transport and the integration of gravitropic growth. In: Gilroy S., and Masson P.H. (Eds). Plant Tropisms (2008), Blackwell Publishing Ltd., Ames, Iowa 47-77
31. Yamamoto K.T. Happy end in sight after 70 years of controversy. Trends Plant Sci. 8 (2003) 359-360
32. Abas L., Benjamins R., Malenica N., Paciorek T., Wigniewska J., Moulinier-Anzola J.C., Sieberer T., Friml J., and Luschnig C. Intracellular trafficking and proteolysis of the Arabidopsis auxin-efflux facilitator PIN2 are involved in root gravitropism. Nat. Cell Biol. 8 (2006) 249-256
33. Esmon C.A., Tinsley A.G., Ljung K., Sandberg G., Hearne L.B., and Liscum E. A gradient of auxin and auxin-dependent transcription precedes tropic growth responses. Proc. Natl. Acad. Sci. U.S.A. 103 (2006) 236-241
34. Fuchs I., Philippar K., and Hedrich R. Ion channels meet auxin action. Plant Biol. 8 (2006) 353-359
35. Palme K., Dovzhenko A., and Ditengou F.A. Auxin transport and gravitational research: perspectives. Protoplasma 229 (2006) 175-181
36. Philosoph-Hadas S., Friedman H., Meir S., and Gerald L. Gravitropic bending and plant hormones. Vitam. Horm. 72 (2005) 31-78
37. Vieten A., Sauer M., Brewer P.B., and Friml J. Molecular and cellular aspects of auxin-transport-mediated development. Trends Plant Sci. 12 (2007) 160-168
38. Hager A. Role of the plasma membrane H+-ATPase in auxin-induced elongation growth: historical and new aspects. J. Plant Res. 116 (2003) 483-505
39. Grebe M. Growth by auxin: when a weed needs acid. Science 310 (2005) 60-61
40. Buer C.S., Sukumar P., and Muday G.K. Ethylene modulates flavonoid accumulation and gravitropic responses in roots of Arabidopsis. Plant Physiol. 140 (2006) 1384-1396
41. Blancaflor E.B. The cytoskeleton and gravitropism in higher plants. J. Plant Growth Reg. 21 (2002) 120-136
42. Ehrhardt D.W. Straighten up and fly right-microtubule dynamics and organization of non-centrosomal arrays in higher plants. Curr. Opin. Cell Biol. 20 (2008) 107-116
43. Hamada T. Microtubule-associated proteins in higher plants. J. Plant Res. 120 (2007) 79-98
44. Lucas J., and Shaw S.L. Cortical microtubule arrays in the Arabidopsis seedling. Curr. Opin. Plant Biol. 11 (2008) 94-98
45. Pastuglia M., and Bouchez D. Molecular encounters at microtubule ends in the plant cell cortex. Curr. Opin. Plant Biol. 10 (2007) 557-563
46. Sedbrook J.C., and Kaloriti D. Microtubules, MAPs and plant directional cell expansion. Trends Plant Sci. 13 (2008) 303-310
47. Ambrose J.C., Shoji T., Kotzer A.M., Pighin J.A., and Wasteneys G.O. The Arabidopsis CLASP gene encodes a microtubule-associated protein involved in cell expansion and division. Plant Cell 19 (2007) 2763-2775
48. Baskin T.I., Wilson J.E., Cork A., and Williamson R.E. Morphology and microtubule organization in Arabidopsis roots exposed to oryzalin or taxol. Plant Cell Physiol. 35 (1994) 935-942
49. McClinton R.S., and Sung R. Organization of cortical microtubules at the plasma membrane in Arabidopsis. Planta 201 (1997) 252-260
50. Sugimoto K., Himmelspach R., Williamson R.E., and Wasteneys G.O. Mutation or drug-dependent microtubule disruption causes radial swelling without altering parallel cellulose microfibril deposition in Arabidopsis root cells. Plant Cell 15 (2003) 1414-1429
51. Whittington A.T., Vugrek O., Wei K.J., Hasenbein N.G., Sugimoto K., Rashbrooke M.C., and Wasteneys G.O. MOR1 is essential for organizing cortical microtubules in plants. Nature 411 (2001) 610-613
52. Wasteneys G., and Fujita M. Establishing and maintaining axial growth: wall mechanical properties and the cytoskeleton. J. Plant Res. 119 (2006) 5-10
53. Wasteneys G.O., and Collings D.A. The cytoskeleton and co-ordination of directional expansion in a multicellular context. In: Verbelen J.-P., and Vissenberg K. (Eds). The Expanding Cell (2007), Springer-Verlag, Berlin/Heidelberg 217-248
54. Furutani I., Watanabe Y., Prieto R., Masukawa M., Suzuki K., Naoi K., Thitamadee S., Shikanai T., and Hashimoto T. The SPIRAL genes are required for directional control of cell elongation in Arabidopsis thaliana. Development 127 (2000) 4443-4453
55. Nakajima K., Furutani I., Tachimoto H., Matsubara H., and Hashimoto T. SPIRAL1 encodes a plant-specific microtubule-localized protein required for directional control of rapidly expanding Arabidopsis cells. Plant Cell 16 (2004) 1178-1190
56. Sedbrook J.C., Ehrhardt D.W., Fisher S.E., Scheible W.-R., and Somerville C. The Arabidopsis SKU6/SPIRAL gene encodes a plus end-localized microtubule-interacting protein involved in directional cell expansion. Plant Cell 16 (2004) 1506-1520
57. Thitamadee S., Tuchihara K., and Hashimoto T. Microtubule basis for left-handed helical growth in Arabidopsis. Nature 417 (2002) 193-196
58. Ishida T., Kaneko Y., Iwano M., and Hashimoto T. Helical microtubule arrays in a collection of twisting tubulin mutants of Arabidopsis thaliana. Proc. Natl. Acad. Sci. U.S.A. 104 (2007) 8544-8549
59. Oliva M., and Dunand C. Waving and skewing: how gravity and the surface of growth media affect root development in Arabidopsis. New Phytol. 176 (2007) 37-43
60. Bannigan A., Wiedemeier A.M.D., Williamson R.E., Overall R.L., and Baskin T.I. Cortical microtubule arrays lose uniform alignment between cells and are oryzalin resistant in the Arabidopsis mutant, radially swollen 6. Plant Cell Physiol. 47 (2006) 949-958
61. Baskin T.I. Anisotropic expansion of the plant cell wall. Annu. Rev. Cell Dev. Biol. 21 (2005) 203-222
62. Cosgrove D.J. Growth of the plant cell wall. Nat. Rev. Mol. Cell Biol. 6 (2005) 850-861
63. Burgert I., and Fratzl P. Mechanics of the expanding cell wall. In: Verbelen J.-P., and Vissenberg K. (Eds). The Expanding Cell (2007), Springer-Verlag, Berlin/Heidelberg 191-215
64. Hematy K., and Hofte H. Cellulose and cell elongation. In: Verbelen J.-P., and Vissenberg K. (Eds). The Expanding Cell (2007), Springer-Verlag, Berlin/Heidelberg 33-56
65. Lerouxel O., Cavalier D.M., Liepman A.H., and Keegstra K. Biosynthesis of plant cell wall polysaccharides - a complex process. Curr. Opin. Plant Biol. 9 (2006) 621-630
66. Somerville C. Cellulose synthesis in higher plants. Annu. Rev. Cell Dev. Biol. 22 (2006) 53-78
67. Marga F., Grandbois M., Cosgrove D.J., and Baskin T.I. Cell wall extension results in the coordinate separation of parallel microfibrils: evidence from scanning electrons microscopy and atomic force microscopy. Plant J. 43 (2005) 181-190
68. McQueen-Mason S.J., Le N.T., and Brocklehurst D. Expansins. In: Verbelen J.-P., and Vissenberg K. (Eds). The Expanding Cell (2007), Springer-Verlag, Berlin/Heidelberg 117-138
69. Emons A.M.C., Hofte H., and Mulder B.M. Microtubules and cellulose microfibrils: how intimate is their relationship?. Trends Plant Sci. 12 (2007) 279-281
70. Lloyd C. Microtubules make tracks for cellulose. Science 312 (2006) 1482-1483
71. Alberts B., Bray D., Lewis J., Raff M., Roberts K., and Watson J.D. Molecular Biology of the Cell (1994), Garland Publishing Inc., New York
72. Paredez A.R., Somerville C.R., and Ehrhardt D.W. Visualization of cellulose synthase demonstrates functional association with microtubules. Science 312 (2006) 1491-1495
73. Paradez A., Wright A., and Ehrhardt D.W. Microtubule cortical array organization and plant cell morphogenesis. Curr. Opin. Plant Biol. 9 (2006) 571-578
74. Robert S., Bichet A., Grandjean O., Kierzkowski D., Satiat-Jeunemaitre B., Pelletier S., Hauser M.-T., Hofte H., and Vernhettes S. An Arabidopsis endo-1,4-β-d-glucanase involved in cellulose synthesis undergoes regulated intracellular cycling. Plant Cell 17 (2005) 3378-3389
75. Roudier F., Fernandez A.G., Fujita M., Himmelspach R., Borner G.H.H., Schindelman G., Song S., Baskin T.I., Dupree P., Wasteneys G.O., and Benfey P.N. COBRA, an Arabidopsis extracellular glycosyl-phosphatidyl inositol-anchored protein, specifically controls highly anisotropic expansion through its involvement in cellulose microfibril orientation. Plant Cell 17 (2005) 1749-1763
76. Blancaflor E.B., and Hasenstein K.H. Organization of cortical microtubules in graviresponding maize roots. Planta 191 (1993) 231-237
77. Nick P., Bergfeld R., Schafer E., and Schopfer P. Unilateral reorientation of microtubules at the outer epidermal wall during photo- and gravitropic curvature of maize coleoptiles and sunflower hypocotyls. Planta 181 (1990) 162-168
78. Blancaflor E.B., and Hasenstein K.H. Time course and auxin sensitivity of cortical microtubule reorientation in maize roots. Protoplasma 185 (1995) 72-82
79. Himmelspach R., Wymer C.L., Lloyd C.W., and Nick P. Gravity-induced reorientation of cortical microtubules observed in vivo. Plant J. 18 (1999) 449-453
80. Himmelspach R., and Nick P. Gravitropic microtubule reorientation can be uncoupled from growth. Planta 212 (2001) 184-189
81. Saiki M., Fujita H., Soga K., Wakabayashi K., Kamisaka S., Yamashita M., and Hoson T. Cellular basis for the automorphic curvature of rice coleoptiles on a three-dimensional clinostat: possible involvement of reorientation of cortical microtubules. J. Plant Res. 118 (2005) 199-205
82. Baluska F., Barlow P.W., and Volkmann D. Complete disintegration of the microtubular cytoskeleton precedes its auxin-mediated reconstruction in postmitotic maize root cells. Plant Cell Physiol. 37 (1996) 1013-1021
83. Fischer K., and Schopfer P. Interaction of auxin, light, and mechanical stress in orienting microtubules in relation to tropic curvature in the epidermis of maize coleoptiles. Protoplasma 196 (1997) 108-116
84. Hasenstein K.H., Blancaflor E.B., and Lee J.S. The microtubule cytoskeleton does not integrate auxin transport and gravitropism in maize roots. Physiol. Plant. 105 (1999) 729-738
85. Mayumi K., and 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. Protoplasma 195 (1996) 112-122
86. Nick P., Schafer E., and Furuya M. Auxin redistribution during first positive phototropism in corn coleoptiles: microtubule reorientation and the Cholodny-Went Theory. Plant Physiol. 99 (1992) 1302-1308
87. Vissenberg K., Quelo A.-H., Van Gestel K., Olyslaegers G., and Verbelen J.-P. From hormone signal, via the cytoskeleton, to cell growth in single cells of tobacco. Cell Biol. Int. 24 (2000) 343-349
88. Wiesler B., Wang Q.-Y., and Nick P. The stability of cortical microtubules depends on their orientation. Plant J. 32 (2002) 1023-1032
89. Baluska F., Hauskrecht M., Barlow P., and Sievers A. Gravitropism of the primary root of maize: a complex pattern of differential cellular growth in the cortex independent of the microtubular cytoskeleton. Planta 198 (1996) 310-318
90. Nick P., Schafer E., Hertel R., and Furuya M. On the putative role of microtubules in gravitropism of maize coleoptiles. Plant Cell Physiol. 32 (1991) 873-880
91. Zandomeni K., and Schopfer P. Mechanosensory microtubule reorientation in the epidermis of maize coleoptiles subjected to bending stress. Protoplasma 182 (1994) 96-101
92. Fischer K., and Schopfer P. Physical strain mediated microtubule reorientation in the epidermis of gravitropically or phototropically stimulated maize coleoptiles. Plant J. 15 (1998) 119-123
93. Ikushima T., and Shimmen T. Mechano-sensitive orientation of cortical microtubules during gravitropism in azuki bean epicotyls. J. Plant Res. 118 (2005) 19-26
94. Zhang Z., Friedman H., Meir S., Rosenberger I., Halevy A.H., and Philosoph-Hadas S. Microtubule reorientation in shoots precedes bending during the gravitropic response of cut snapdragon spikes. J. Plant Physiol. 165 (2008) 289-296
95. Nick P., Furuya M., and Schafer E. Do microtubules control growth in tropism? Experiments with maize coleoptiles. Plant Cell Physiol. 32 (1991) 999-1006
96. 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
97. Sugimoto K., Williamson R.E., and Wasteneys G.O. New techniques enable comparative analysis of microtubule orientation, wall texture, and growth rate in intact roots of Arabidopsis. Plant Physiol. 124 (2000) 1493-1506
98. Rayle D.L., and Cleland R.E. The acid growth theory of auxin-induced cell elongation is alive and well. Plant Physiol. 99 (1992) 1271-1274
99. Blancaflor E.B., and Masson P.H. Plant gravitropism. Unraveling the ups and downs of a complex process. Plant Physiol. 133 (2003) 1677-1690
100. Christian M., Schenck D., Bottger M., Luthen H., and Steffens B. New insight into auxin perception, signal transduction, and transport. In: Esser U.L.K., Beyschlag W., and Murata J. (Eds). Progress in Botany (2006), Springer, Berlin/Heidelberg 219-247
101. Philippar K., Fuchs I., Luthen H., Hoth S., Bauer C.S., Haga K., Thiel G., Ljung K., Sandberg G., Bottger M., Becker D., and Hedrich R. Auxin-induced K+ channel expression represents an essential step in coleoptile growth and gravitropism. Proc. Natl. Acad. Sci. U.S.A. 96 (1999) 12186-12191
102. Teale W.D., Paponov I.A., and Palme K. Auxin in action: signalling, transport and the control of plant growth and development. Nat. Rev. Mol. Cell Biol. 7 (2006) 847-859
103. Zhang N., and Hasenstein K.H. Distribution of expansins in graviresponding maize roots. Plant Cell Physiol. 41 (2000) 1305-1312
104. Boutte Y., Vernhettes S., and Satiat-Jeunemaitre B. Involvement of the cytoskeleton in the secretory pathway and plasma membrane organisation of higher plant cells. Cell Biol. Int. 31 (2007) 649-654
105. Sardar H.S., Yang J., and Showalter A.M. Molecular interactions of arabinogalactan proteins with cortical microtubules and F-actin in bright yellow-2 tobacco cultured cells. Plant Physiol. 142 (2006) 1469-1479
106. Borner G.H.H., Sherrier D.J., Weimar T., Michaelson L.V., Hawkins N.D., MacAskill A., Napier J.A., Beale M.H., Lilley K.S., and Dupree P. Analysis of detergent-resistant membranes in Arabidopsis. Evidence for plasma membrane lipid rafts. Plant Physiol. 137 (2005) 104-116
107. Grennan A.K. Lipid rafts in plants. Plant Physiol. 143 (2007) 1083-1085
108. Seifert G.J., and Roberts K. The biology of arabinogalactan proteins. Annu. Rev. Plant Biol. 58 (2007) 137-161
109. Hullin-Matsuda F., and Kobayashi T. Monitoring the distribution and dynamics of signaling microdomains in living cells with lipid-specific probes. Cell. Mol. Life Sci. 64 (2007) 2492-2504
110. Sengupta P., Baird B., and Holowka D. Lipid rafts, fluid/fluid phase separation, and their relevance to plasma membrane structure and function. Sem. Cell Dev. Biol. 18 (2007) 583-590
111. Lefebvre B., Furt F., Hartmann M.-A., Michaelson L.V., Carde J.-P., Sargueil-Boiron F., Rossignol M., Napier J.A., Cullimore J., Bessoule J.-J., and Mongrand S. Characterization of lipid rafts from Medicago truncatula root plasma membranes: a proteomic study reveals the presence of a raft-associated redox system. Plant Physiol. 144 (2007) 402-418
112. Sardar H.S., and Showalter A.M. A cellular networking model involving interactions among glycosyl-phosphatidylinositol (GPI)-anchored plasma membrane arabidoglactan proteins (AGPs), microtubules and F-actin in tobacco BY-2 Cells. Plant Signal. Behav. 2 (2007) 8-9
113. Akhmanova A., and Steinmetz M.O. Tracking the ends: a dynamic protein network controls the fate of microtubule tips. Nat. Rev. Mol. Cell Biol. 9 (2008) 309-322
114. Lansbergen G., and Akhmanova A. Microtubule plus end: a hub of cellular activities. Traffic 7 (2006) 499-507
115. Bisgrove S.R., Hable W.E., and Kropf D.L. +TIPs and microtubule regulation. The beginning of the plus end in plants. Plant Physiol. 136 (2004) 3855-3863
116. Bisgrove S.R., Lee Y.-R.J., Liu B., Peters N.T., and Kropf D.L. The microtubule plus-end binding protein EB1 functions in root responses to touch and gravity signals in Arabidopsis. Plant Cell 20 (2008) 396-410
117. Chan J., Calder G.M., Doonan J.H., and Lloyd C.W. EB1 reveals mobile microtubule nucleation sites in Arabidopsis. Nat. Cell Biol. 5 (2003) 967-971
118. Dixit R., Chang E., and Cyr R. Establishment of polarity during organization of the acentrosomal plant cortical microtubule array. Mol. Biol. Cell 17 (2006) 1298-1305
119. Mathur J., Mathur N., Kernebeck B., Srinivas B.P., and Hulskamp M. A novel localization pattern for an EB1-like protein links microtubule dynamics to endomembrane organization. Curr. Biol. 13 (2003) 1991-1997
120. Van Damme D., Van Poucke K., Boutant E., Ritzenthaler C., Inze D., and Geelen D. In vivo dynamics and differential microtubule-binding activities of MAP65 proteins. Plant Physiol. 136 (2004) 3956-3967
121. Mimori-Kiyosue Y., and Tsukita S. Search-and-Capture" of microtubules through plus-end-binding proteins (+TIPs). J. Biochem. 134 (2003) 321-326
122. Barth A.I.M., Siemers K.A., and Nelson W.J. Dissecting interactions between EB1, microtubules and APC in cortical clusters at the plasma membrane. J. Cell Sci. 115 (2002) 1583-1590
123. Grigoriev I., Gouveia S.M., van der Vaart B., Demmers J., Smyth J.T., Honnappa S., Splinter D., Steinmetz M.O., Putney Jr. J.W., Hoogenraad C.C., and Akhmanova A. STIM1 is a MT-plus-end-tracking protein involved in remodeling of the ER. Curr. Biol. 18 (2008) 177-182
124. Gu C., Zhou W., Puthenveedu M.A., Xu M., Jan Y.N., and Jan L.Y. The microtubule plus-end tracking protein EB1 is required for Kv1 voltage-gated K+ channel axonal targeting. Neuron 52 (2006) 803-816
125. Honnappa S., Okhrimenko O., Jaussi R., Jawhari H., Jelesarov I., Winkler F.K., and Steinmetz M.O. Key interaction modes of dynamic +TIP networks. Mol. Cell 23 (2006) 663-671
126. Rogers S.L., Wiedemann U., Hacker U., Turck C., and Vale R.D. Drosophila RhoGEF2 associates with microtubule plus ends in an EB1-dependent manner. Curr. Biol 14 (2004) 1827-1833
127. Shaw R.M., Fay A.J., Puthenveedu M.A., von Zastrow M., Jan Y.-N., and Jan L.Y. Microtubule plus-end-tracking proteins target gap junctions directly from the cell interior to adherens junctions. Cell 128 (2007) 547-560
128. Sun L., Gao J., Dong X., Liu M., Li D., Shi X., Dong J.-T., Lu X., Liu C., and Zhou J. EB1 promotes Aurora-B kinase activity through blocking its inactivation by protein phosphatase 2A. Proc. Natl. Acad. Sci. U.S.A. 105 (2008) 7153-7158
129. Vaughan K.T. TIP maker and TIP marker; EB1 as a master controller of microtubule plus ends. J. Cell Biol. 171 (2005) 197-200
130. Wen Y., Eng C.H., Schmoranzer J., Cabrera-Poch N., Morris E.J.S., Chen M., Wallar B.J., Alberts A.S., and Gundersen G.G. EB1 and APC bind to mDia to stabilize microtubules downstream of Rho and promote cell migration. Nat. Cell Biol. 6 (2004) 820-830
131. Wu X.S., Tsan G.L., and Hammer III J.A. Melanophilin and myosin Va track the microtubule plus end on EB1. J. Cell Biol. 171 (2005) 201-207
132. Dhonukshe P., Mathur J., Hulskamp M., and Gadella T.J. Microtubule plus-ends reveal essential links between intracellular polarization and localized modulation of endocytosis during division-plane establishment in plant cells. BMC Biol. 3 (2005) 11-25
133. Robatzek S., Chinchilla D., and Boller T. Ligand-induced endocytosis of the pattern recognition receptor FLS2 in Arabidopsis. Genes Dev. 20 (2006) 537-542
134. Gifford M.L., Robertson F.C., Soares D.C., and Ingram G.C. Arabidopsis CRINKLY4 function, internalization, and turnover are dependent on the extracellular crinkly repeat domain. Plant Cell 17 (2005) 1154-1166
135. Russinova E., Borst J.-W., Kwaaitaal M., Cano-Delgado A., Yin Y., Chory J., and de Vries S.C. Heterodimerization and endocytosis of Arabidopsis brassinosteroid receptors BRI1 and AtSERK3 (BAK1). Plant Cell 16 (2004) 3216-3229
136. Sutter J.-U., Sieben C., Hartel A., Eisenach C., Thiel G., and Blatt M.R. Abscisic acid triggers the endocytosis of the Arabidopsis KAT1 K+ channel and its recycling to the plasma membrane. Curr. Biol. 17 (2007) 1396-1402
137. Baluska F., and Hasenstein K.H. Root cytoskeleton: its role in perception of and response to gravity. Planta 203 (1997) S69-S78
138. Nick P., Godbole R., and Wang Q.Y. Probing rice gravitropism with cytoskeletal drugs and cytoskeletal mutants. Biol. Bull. 192 (1997) 141-143
139. Gutjahr C., and Nick P. Acrylamide inhibits gravitropism and affects microtubules in rice coleoptiles. Protoplasma 227 (2006) 211-222
140. Tavernarakis N., and Driscoll M. Molecular modeling of mechanotransduction in the nematode Caenorhabditis elegans. Annu. Rev. Physiol. 59 (1997) 659-689
141. Cueva J.G., Mulholland A., and Goodman M.B. Nanoscale organization of the MEC-4 DEG/ENaC sensory mechanotransduction channel in Caenorhabditis elegans touch receptor neurons. J. Neurosci. 27 (2007) 14089-14098
142. Ernstrom G.G., and Chalfie M. Genetics of sensory mechanotransduction. Annu. Rev. Genet. 36 (2002) 411-453
143. Ding J.P., and Pickard B.G. Mechanosensory calcium-selective cation channels in epidermal cells 3 (1993) 83-110
144. Granger C.L., and Cyr R.J. Spatiotemporal relationships between growth and microtubule orientation as revealed in living root cells of Arabidopsis thaliana transformed with green-fluorescent-protein gene construct GFP-MBD. Protoplasma 216 (2001) 201-214