Feeling green: mechanosensing in plants

Trends in Cell Biology

Volumn 19, Issue 5, 2009, Pages 228-235

  Monshausen, Gabriele B ^a   Gilroy, Simon ^a  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ESCHERICHIA COLI; FORCE; IMPEDANCE; MECHANORECEPTOR; MORPHOGENESIS; MUTANT; PLANT DEVELOPMENT; PLANT GROWTH; PLANT ROOT; PRIORITY JOURNAL; REVIEW; SACCHAROMYCES CEREVISIAE; SENSOR; SESSILE SPECIES; SIGNAL TRANSDUCTION; SOIL; WIND;

CALCIUM; ION CHANNELS; MECHANORECEPTORS; MECHANOTRANSDUCTION, CELLULAR; MEMBRANE PROTEINS; MORPHOGENESIS; PLANTS; PROTEIN KINASES; STRESS, MECHANICAL;

ESCHERICHIA COLI; SACCHAROMYCES CEREVISIAE;

EID: 65149086156     PISSN: 09628924     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tcb.2009.02.005     Document Type: Review

References (70)

1. Darwin C., and Darwin F. The Power of Movement in Plants (1880), William Clowes and Sons
2. Braam J. In touch: plant responses to mechanical stimuli. New Phytol. 165 (2005) 373-389
3. Monshausen G.B., et al. Touch Sensing and Thigmotropism (2008), Blackwell
4. Green P. Expansin and morphology: a role for biophysics. Trends Plant Sci. 2 (1997) 365-366
5. Selker J.M., et al. Biophysical mechanisms for morphogenetic progressions at the shoot apex. Dev. Biol. 153 (1992) 29-43
6. Pien S., et al. Local expression of expansin induces the entire process of leaf development and modifies leaf shape. Proc. Natl. Acad. Sci. U. S. A. 98 (2001) 11812-11817
7. Casimiro I., et al. Dissecting Arabidopsis lateral root development. Trends Plant Sci. 8 (2003) 165-171
8. De Smet I., et al. Auxin-dependent regulation of lateral root positioning in the basal meristem of Arabidopsis. Development 134 (2007) 681-690
9. De Smet I., et al. Lateral root initiation or the birth of a new meristem. Plant Mol. Biol. 60 (2006) 871-887
10. Malamy J.E. Intrinsic and environmental response pathways that regulate root system architecture. Plant Cell Environ. 28 (2005) 67-77
11. Malamy J.E., and Ryan K.S. Environmental regulation of lateral root initiation in Arabidopsis. Plant Physiol. 127 (2001) 899-909
12. O'Brien E.E., et al. Roots in space: a spatially explicit model for below-ground competition in plants. Proc. Biol. Sci. 274 (2007) 929-934
13. Noll F. Uber den bestimmenden Einfluss von Wurzelkrummengen auf Entstehung und Anordnung der Seitcnwurzeln. Landtwirtschaftliche Jahrbuchecr 29 (1900) 361-426
14. Lucas M., et al. Auxin fluxes in the root apex co-regulate gravitropism and lateral root initiation. J. Exp. Bot. 59 (2008) 55-66
15. 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 47-78
16. Ditengou F.A., et al. Mechanical induction of lateral root initiation in Arabidopsis thaliana. Proc. Natl. Acad. Sci. U. S. A. 105 (2008) 18818-18823
17. Laskowski M., et al. Root system architecture from coupling cell shape to auxin transport. PLoS Biol. 6 (2008) e307
18. Massa G.D., and Gilroy S. Touch modulates gravity sensing to regulate the growth of primary roots of Arabidopsis thaliana. Plant J. 33 (2003) 435-445
19. Plieth C., and Trewavas A.J. Reorientation of seedlings in the earth's gravitational field induces cytosolic calcium transients. Plant Physiol. 129 (2002) 786-796
20. Toyota M., et al. Cytoplasmic calcium increases in response to changes in the gravity vector in hypocotyls and petioles of Arabidopsis seedlings. Plant Physiol. 146 (2008) 505-514
21. Gus-Mayer S., et al. Local mechanical stimulation induces components of the pathogen defense response in parsley. Proc. Natl. Acad. Sci. U. S. A. 95 (1998) 8398-8403
22. Yahraus T., et al. Evidence for a mechanically induced oxidative burst. Plant Physiol. 109 (1995) 1259-1266
23. Gao H., et al. RGD-dependent mechanotransduction of suspension cultured Taxus cell in response to shear stress. Biotechnol. Prog. 23 (2007) 673-679
24. Feijo J.A., et al. Growing pollen tubes possess a constitutive alkaline band in the clear zone and a growth-dependent acidic tip. J. Cell Biol. 144 (1999) 483-496
25. 2+ lag growth pulses of Lilium longiflorum pollen tubes. J. Cell Sci. 112 (1999) 1497-1509
26. Monshausen G.B., et al. Oscillations in extracellular pH and reactive oxygen species modulate tip growth of Arabidopsis root hairs. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 20996-21001
27. 2+ during pollen tube growth. Dev. Biol. 222 (2000) 84-98
28. 2+ follow oscillating increases in growth in root hairs of Arabidopsis. Plant Physiol. 147 (2008) 1690-1698
29. 2. Plant Physiol. 115 (1997) 87-92
30. Cannon M.C., et al. Self-assembly of the plant cell wall requires an extensin scaffold. Proc. Natl. Acad. Sci. U. S. A. 105 (2008) 2226-2231
31. Christensen A.P., and Corey D.P. TRP channels in mechanosensation: direct or indirect activation? Nat. Rev. Neurosci. 8 (2007) 510-521
32. Folgering J.H., et al. Molecular basis of the mammalian pressure-sensitive ion channels: focus on vascular mechanotransduction. Prog. Biophys. Mol. Biol. 97 (2008) 180-195
33. Bianchi L. Mechanotransduction: touch and feel at the molecular level as modeled in Caenorhabditis elegans. Mol. Neurobiol. 36 (2007) 254-271
34. Corry B., and Martinac B. Bacterial mechanosensitive channels: experiment and theory. Biochim. Biophys. Acta 1778 (2008) 1859-1870
35. Haswell E.S., and Meyerowitz E.M. MscS-like proteins control plastid size and shape in Arabidopsis thaliana. Curr. Biol. 16 (2006) 1-11
36. Haswell E.S., et al. Two MscS homologs provide mechanosensitive channel activities in the Arabidopsis root. Curr. Biol. 18 (2008) 730-734
37. 2+ influx and touch sensing in roots. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 3639-3644
38. Braam J., and Davis R.W. Rain-, wind-, and touch-induced expression of calmodulin and calmodulin-related genes in Arabidopsis. Cell 60 (1990) 357-364
39. Smith M.L., et al. Force-induced unfolding of fibronectin in the extracellular matrix of living cells. PLoS Biol. 5 (2007) e268
40. Vogel V. Mechanotransduction involving multimodular proteins: converting force into biochemical signals. Annu. Rev. Biophys. Biomol. Struct. 35 (2006) 459-488
41. Ingber D.E. Cellular mechanotransduction: putting all the pieces together again. FASEB J. 20 (2006) 811-827
42. Schindler M., et al. RGD-dependent linkage between plant cell wall and plasma membrane: consequences for growth. J. Cell Biol. 108 (1989) 1955-1965
43. Staves M., and Wayne R. The touch-induced action-potential in Chara - inquiry into the ionic basis and the mechanoreceptor. Aust. J. Plant Physiol. 20 (1993) 471-488
44. Katembe W.J., et al. Immunolocalization of integrin-like proteins in Arabidopsis and Chara. Physiol. Plant. 99 (1997) 7-14
45. Swatzell L.J., et al. Integrin-like proteins are localized to plasma membrane fractions, not plastids, in Arabidopsis. Plant Cell Physiol. 40 (1999) 173-183
46. Canut H., et al. High affinity RGD-binding sites at the plasma membrane of Arabidopsis thaliana links the cell wall. Plant J. 16 (1998) 63-71
47. Mellersh D.G., and Heath M.C. Plasma membrane-cell wall adhesion is required for expression of plant defense responses during fungal penetration. Plant Cell 13 (2001) 413-424
48. Lynch T.M., and Lintilhac P.M. Mechanical signals in plant development: a new method for single cell studies. Dev. Biol. 181 (1997) 246-256
49. Zhou J., et al. Responses of Chrysanthemum cells to mechanical stimulation require intact microtubules and plasma membrane-cell wall adhesion. J. Plant Growth Regul. 26 (2007) 55-68
50. Gouget A., et al. Lectin receptor kinases participate in protein-protein interactions to mediate plasma membrane-cell wall adhesions in Arabidopsis. Plant Physiol. 140 (2006) 81-90
51. Anderson C.M., et al. WAKs: cell wall-associated kinases linking the cytoplasm to the extracellular matrix. Plant Mol. Biol. 47 (2001) 197-206
52. Kohorn B.D., et al. Wall-associated kinase 1 (WAK1) is crosslinked in endomembranes, and transport to the cell surface requires correct cell-wall synthesis. J. Cell Sci. 119 (2006) 2282-2290
53. Humphrey T.V., et al. Sentinels at the wall: cell wall receptors and sensors. New Phytol. 176 (2007) 7-21
54. Decreux A., and Messiaen J. Wall-associated kinase WAK1 interacts with cell wall pectins in a calcium-induced conformation. Plant Cell Physiol. 46 (2005) 268-278
55. Kohorn B.D., et al. An Arabidopsis cell wall-associated kinase required for inveratse activity and cell growth. Plant J. 46 (2006) 307-316
56. Cosgrove D.J. Growth of the plant cell wall. Nat. Rev. Mol. Cell Biol. 6 (2005) 850-861
57. Hutzler F., et al. Protein N-glycosylation determines functionality of the Saccharomyces cerevisiae cell wall integrity sensor Mid2p. Mol. Microbiol. 68 (2008) 1438-1449
58. Piao H.L., et al. NPFXD-mediated endocytosis is required for polarity and function of a yeast cell wall stress sensor. Mol. Biol. Cell 18 (2007) 57-65
59. Hématy K., and Höfte H. Novel receptor kinases involved in growth regulation. Curr. Opin. Plant Biol. 11 (2008) 321-328
60. Hématy K., et al. A receptor-like kinase mediates the response of Arabidopsis cells to the inhibition of cellulose synthesis. Curr. Biol. 17 (2007) 922-931
61. Urao T., et al. A transmembrane hybrid-type histidine kinase in Arabidopsis functions as an osmosensor. Plant Cell 11 (1999) 1743-1754
62. Wohlbach D.J., et al. Analysis of the Arabidopsis histidine kinase ATHK1 reveals a connection between vegetative osmotic stress sensing and seed maturation. Plant Cell 20 (2008) 1101-1117
63. Reiser V., et al. Yeast osmosensor Sln1 and plant cytokinin receptor Cre1 respond to changes in turgor pressure. J. Cell Biol. 161 (2003) 1035-1040
64. Morris E.R., and Walker J.C. Receptor-like protein kinases: the keys to response. Curr. Opin. Plant Biol. 6 (2003) 339-342
65. Knight M.R., et al. Transgenic plant aequorin reports the effects of touch and cold-shock and elicitors on cytoplasmic calcium. Nature 352 (1991) 524-526
66. Knight M.R., et al. Wind-induced plant motion immediately increases cytosolic calcium. Proc. Natl. Acad. Sci. U. S. A. 89 (1992) 4967-4971
67. Pierson E.S., et al. Tip-localized calcium entry fluctuates during pollen tube growth. Dev. Biol. 174 (1996) 160-173
68. Takeda S., et al. Local positive feedback regulation determines cell shape in root hair cells. Science 319 (2008) 1241-1244
69. Wang W., et al. The structure of an open form of an E. coli mechanosensitive channel at 3.45 A resolution. Science 321 (2008) 1179-1183
70. Wang Y., et al. MMDB: annotating protein sequences with Entrez's 3D-structure database. Nucleic Acids Res. 35 (2007) D298-D300