Auxin effects on ion transport in Chara corallina

Journal of Plant Physiology

Volumn 193, Issue , 2016, Pages 37-44

  Zhang, Suyun ^a   de Boer, Albertus H ^c   van Duijn, Bert ^a,b  

^a LEIDEN UNIVERSITY   (Netherlands)

^b LEIDEN UNIVERSITY   (Netherlands)

^c VU UNIVERSITY AMSTERDAM   (Netherlands)

Author keywords

Chara corallina; H+ ATPase; IAA; Membrane potential; Potassium transport

Indexed keywords

INDOLEACETIC ACID DERIVATIVE; PHYTOHORMONE; POTASSIUM;

CELL MEMBRANE; CHARA; DRUG EFFECTS; ION TRANSPORT; MEMBRANE POTENTIAL; METABOLISM; PHYSIOLOGY; SIGNAL TRANSDUCTION;

CELL MEMBRANE; CHARA; INDOLEACETIC ACIDS; ION TRANSPORT; MEMBRANE POTENTIALS; PLANT GROWTH REGULATORS; POTASSIUM; SIGNAL TRANSDUCTION;

EID: 84961157836     PISSN: 01761617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jplph.2016.02.009     Document Type: Article

References (72)

1. Adamowski M., Friml J. PIN-dependent auxin transport: action, regulation, and evolution. Plant Cell 2015, 27:20-32.
2. Barbier-Brygoo H., Ephritikhine G., Klambt D., Ghislain M., Guern J. Functional evidence for an auxin receptor at the plasmalemma of tobacco mesophyll protoplasts. Proc. Natl. Acad. Sci. U. S. A. 1989, 86:891-895.
3. Baster P., Robert S., Kleine-Vehn J., Vanneste S., Kania U., Grunewald W., et al. SCF (TIR1/AFB)-auxin signalling regulates PIN vacuolar trafficking and auxin fluxes during root gravitropism. EMBO J. 2013, 32:260-274.
4. Beilby M.J. Salt tolerance at single cell level in giant-celled Characeae. Front. Plant Sci. 2015, 6:226. 10.3389/fpls.2015.00226.
5. Berecki G., Varga Z., Van Iren F., Van Duijn B. Anion channels in Chara corallina tonoplast membrane: calcium dependence and rectification. J. Membr. Biol. 1999, 172:159-168.
6. Berleth T., Krogan N.T., Scarpella E. Auxin signals-turning genes on and turning cells around. Curr. Opin. Plant Biol. 2004, 7:553-563.
7. + inward-rectifier evoked by auxin. Plant J. 1994, 5(1):55-68.
8. Boot K.J.M., Libbenga K.R., Hille S.C., Offringa R., Van Duijn B. Polar auxin transport: an early invention. J. Exp. Bot. 2012, 63(11):4213-4218. 10.1093/jxb/ers106.
9. Bulychev A.A., Van den Wijngaard P.W.J., De Boer A.H. Spatial coordination of chloroplast and plasma membrane activities in Chara cells and its disruption through inactivation of 14-3-3 proteins. Biochemistry (Mosc.) 2005, 70(1):55-61.
10. Christian M., Steffens B., Schenck D., Burmester S., Bottger M., Luthen H. How does auxin enhance cell elongation? Roles of auxin-binding proteins and potassium channels in growth control. Plant Biol. 2006, 8:346-352.
11. Claussen M., Luthen H., Blatt M., Bottger M. Axuin-induced growth and its linkage to potassium channels. Planta 1996, 201:227-234.
12. Cooke T.J., Poli D.B., Sztein A.E., Cohen J.D. Evolutionary patterns in auxin action. Plant Mol. Biol. 2002, 49:319-338.
13. De Smet I., Voß U., Lau S., Wilson M., Shao N., Timme R.E., et al. Unraveling the evolution of auxin signaling. Plant Physiol. 2011, 155:209-221.
14. Di D., Zhang C., Guo G. Involvement of secondary messengers and small organic molecules in auxin perception and signalling. Plant Cell Rep. 2015, 34:895-904.
15. Dibb-Fuller J.E., Morris D.A. Studies on the evolution of auxin carriers and phytotropin receptors: transmembrane auxin transport in unicellular and multicellular Chlorophyta. Planta 1992, 186:219-226.
16. Enders T.A., Strader L.C. Auxin activity: past, present, and future. Am. J. Bot. 2015, 102(2):180-196.
17. Ephritikhine G., Barbier-Brygoo H., Muller J.F., Guern J. Auxin effect on the transmembrane potential difference of wild-type and mutant tobacco protoplasts exhibiting a differential sensitivity to auxin. Plant physiol. 1987, 83:801-804.
18. Felle H., Bentrup F.W. Effect of light upon membrane potential, conductance and ion fluxes in Riccia fluitans. J. Membr. Biol. 1976, 27:153-170.
19. Felle H., Peters W., Palme K. The electrical response of maize to auxins. Biochim. Biophys. Acta 1991, 1064:199-204.
20. Feraru E., Vosolsobe S., Feraru M.I., Petrášek J., Kleine-Vehn J. Evolution and structural diversification of PILS putative auxin carriers in plants. Front. Plant Sci. 2012, 3:1-13.
21. Fisahn J., McConnaughey T., Lucas W.J. Oscillations in extracellular current: external pH and membrane potential and conductance in the alkaline bands of Nitella and Chara. J. Exp. Bot. 1989, 40(220):1185-1193.
22. Foissner I., Sommer A., Hoeftberger M. Photosynthesis-dependent formation of convoluted plasma membrane domains in Chara internodal cells is independent of chloroplast position. Protoplasma 2015, 252:1085-1096.
23. Fuchs I., Philippar K., Hedrich R. Ion channels meet auxin action. Plant Biol. 2006, 8:353-359.
24. Fujita T., Hasebe M. Convergences and divergences in polar auxin transport and shoot development in land plant evolution. Plant Signal. Behav. 2009, 4:313-315.
25. +-ATPase in auxin-induced elongation growth: historical and new aspects. J. Plant Res. 2003, 116:483-505.
26. +-ATPase. Planta 1991, 185:527-537.
27. +-ATPase activity. Planta 1996, 199:359-365.
28. Jones D.L., Shaff J.E., Kochian L.V. Role of calcium and other ions in directing root hair tip growth in Limnobium stoloniferum. Planta 1995, 197:672-680.
29. Katicheva L., Sukhov V., Akinchits E., Vodeneev V. Ionic nature of burn-induced variation potential in wheat leaves. Plant Cell Physiol. 2014, 55(8):1511-1519.
30. Kawamura G., Shimmen T., Tazawa M. Dependence of the membrane potential of Chara cells on external pH in the presence or absence of internal adenosinetriphosphate. Planta 1980, 149:213-218.
31. 2+-transport through plasma membrane as a test of auxin sensitivity. Plants 2014, 3:209-222.
32. Kramer E.M., Ackelsberg E.M. Auxin metabolism rates and implications for plant development. Front. Plant Sci. 2015, 6:150. 10.3389/fpls.2015.00150.
33. Lau S., Shao N., Bock R., Jürgens G., De Smet I. Auxin signaling in algal lineages: fact or myth. Trends Plant Sci. 2009, 14:182-188.
34. +-ATPase leads to glucose-dependent activation. J. Biol. Chem. 2007, 282:35471-35481.
35. Lee D.J., Park J.W., Lee H.W., Kim J. Genome-wide analysis of the auxin-responsive transcriptome downstream of iaa1 and its expression analysis reveal the diversity and complexity of auxin-regulated gene expression. J. Exp. Bot. 2009, 60(13):3935-3957.
36. Lew R.R. Electrogenic transport properties of growing Arabidopsis root hairs: the plasma membrane proton pump and potassium channels. Plant Physiol. 1991, 97(4):1527-1534.
37. 4+ efflux and GMPase activity. Plant Cell Environ. 2010, 33:1529-1542.
38. Morris D.A. Transmembrane auxin carrier systems-dynamic regulators of polar auxin transport. Plant Growth Regul. 2000, 32:161-172.
39. +-ATPase: structure, function and regulation. Biochim. Biophys. Acta 2000, 1465:1-16.
40. +-ATPase containing a penultimate threonine in the bryophyte. Plant Signal. Behav. 2012, 7(8):979-982.
41. +-ATPase in the liverwort Marchantia polymorpha. Plant Physiol. 2012, 159:826-834.
42. Osakabe Y., Arinaga N., Umezawa T., Katsura S., Nagamachi K., Tanaka H., et al. Osmotic stress responses and plant growth controlled by potassium transporters in Arabidopsis. Plant Cell 2013, 25:609-624.
43. +-channel genes expressed in seedlings of Arabidopsis thaliana. Plant J. 2004, 6:815-827.
44. Qin Y., Dong J. Focusing on the focus: what else beyond the master switches for polar cell growth. Mol. Plant 2015, 8:582-594.
45. Qiu Y.L., Palmer J.D. Phylogeny of early land plants: insight from genes and genomes. Trends Plant Sci. 1999, 4:26-30.
46. +-ATPase is involved in auxin-mediated cell elongation during wheat embryo development. Plant physiol. 2003, 131(3):1302-1312.
47. Saito K., Senda M. The effect of external pH on the membrane potential of Nitella and its linkage to metabolism. Plant Cell Physiol. 1973, 14:1045-1052.
48. Schmolzer P.M., Hoftberger M., Foissner I. Plasma membrane domains participate in pH banding of Chara internodal cells. Plant Cell Physiol. 2011, 52(8):1274-1288.
49. 2+ ion fluxes around the elongation region of corn roots and effects of external pH. Plant Physiol. 1997, 133:111-118.
50. Shimmen T. Studies on mechano-perception in Characeae: decrease in electrical membrane resistance in receptor potentials. Plant Cell Physiol. 1997, 38(11):1298-1301.
51. + concentrations in internodal cells of Chara corallina. J. Plant Res. 2001, 114:59-66.
52. 2+. J. Membr. Biol. 1977, 37:167-192.
53. Shimmen T., Wakabayashi A. Involvement of membrane potential in alkaline band formation by intermodal cells of Chara corallina. Plant Cell Physiol. 2008, 49(10):1614-1620.
54. Shimmen T., Kikuyama M., Tazawa M. Demonstration of two stable potential states of plasmalemma of Chara without tonoplast. J. Membr. Biol. 1976, 30:249-270.
55. Shimmen T., Mimura T., Kikuyama M., Tazawa M. Characean cells as a tool for studying electrophysiological characteristics of plant cells. Cell Struct. Funct. 1994, 19:263-278.
56. Sun J., Qi L., Li Y., Zhai Q., Li C. PIF4 and PIF5 transcription factors link blue light and auxin to regulate the phototropic response in Arabidopsis. Plant Cell 2013, 25:2102-2114.
57. +-ATPase by phosphorylation during hypocotyl elongation in Arabidopsis. Plant Physiol. 2012, 159:632-641.
58. Tarakhovskaya E.R., Maslov Y.I., Shishova M.F. Phytohormones in algae. Russ. J. Plant Physiol 2007, 54:163-170.
59. Tatematsu K., Kumagai S., Muto H., Sato A., Watahiki M., Harper R.M., et al. MASSUGU2 encodes Aux/IAA19, an auxin-regulated protein that functions together with the transcriptional activator NPH4/ARF7 to regulate differential growth responses of hypocotyl and formation of lateral roots in Arabidopsis thaliana. Plant Cell 2004, 16:379-393.
60. Tazawa M., Shimmen T. How characean cells have contributed to the progress of plant membrane biophysics. Aust. J. Plant Physiol. 2001, 28:523-539.
61. + pump activity in the plasma membrane of internally perfused Chara corallina. Plant Cell Physiol. 2001, 42(5):531-537.
62. Timme R.E., Bachvaroff T.R., Delwiche C.F. Broad phylogenomic sampling and the sister lineage of land plants. PLoS One 2012, 7(1):e29696. 10.1371/journal.pone.0029696.
63. Van Duijn B., Heimovaara-Dijkstra S. Intracellular microelectrode membrane potential measurements in tobacco cell-suspension protoplasts and barley aleurone protoplasts: interpretation and artifacts. Biochim. Biophys. Acta 1994, 1193:77-84.
64. Van Overbeek J. Auxin in marine algae. Plant Physiol. 1940, 15:291-299.
65. Vernoux T., Besnard F., Traas J. Auxin at the shoot apical meristem. Cold Spring Harb. Perspect. Biol. 2010, 2:a001487.
66. Viaene T., Delwiche C.F., Rensing S.A., Friml J. Origin and evolution of PIN auxin transporters in the green lineage. Trends Plant Sci. 2013, 18:5-10.
67. Viaene T., Landberg K., Thelander M., Medvecka E., Pederson E., Feraru E., et al. Directional auxin transport mechanisms in early diverging land plants. Curr. Biol. 2014, 24(23):2786-2791. 10.1016/j.cub.2014.09.056.
68. +-ATPase by lysophospholipids depends on the autoinhibitory N- and C-terminal domains. J. Biol. Chem. 2015, 290(26):16281-16291.
69. Wodniok S., Brinkmann H., Glockner G., Heidel A.J., Philippe H., Melkonian M., Becker B. Origin of land plants: do conjugating green algae hold the key?. BMC Evol. Biol. 2011, 11:e104.
70. Wright, R.C., Nemhauser, J.L., New tangles in the auxin signaling web. F1000Prime Rep 2015; 7: 19. 10.12703/P7-19.
71. Xu W., Jia L., Shi W., Liang J., Zhou F., Li Q., Zhang J. Abscisic acid accumulation modulates auxin transport in the root tip to enhance proton secretion for maintaining root growth under moderate water stress. New Phytol. 2012, 197:139-150. 10.1111/nph.12004.
72. Zhang S., van Duijn B. Cellular auxin transport in algae. Plants 2014, 3:58-69.