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Expression of a constitutively activated plasma membrane H(+)-ATPase in Nicotiana tabacum BY-2 cells results in cell expansion.

Bibliographic reference Niczyj, Marta ; Champagne, Antoine ; Alam, Iftekhar ; Nader, Joseph ; Boutry, Marc. Expression of a constitutively activated plasma membrane H(+)-ATPase in Nicotiana tabacum BY-2 cells results in cell expansion.. In: Planta : an international journal of plant biology, Vol. 244, no. 5, p. 1109-1124 (2016)
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  1. Bibikova Tatiana N., Blancaflor Elison B., Gilroy Simon, Microtubules regulate tip growth and orientation in root hairs ofArabidopsis thaliana, 10.1046/j.1365-313x.1999.00415.x
  2. Caesar Katharina, Elgass Kirstin, Chen Zhonghua, Huppenberger Peter, Witthöft Janika, Schleifenbaum Frank, Blatt Michael R., Oecking Claudia, Harter Klaus, A fast brassinolide-regulated response pathway in the plasma membrane of Arabidopsis thaliana : A BL-regulated plasma membrane response pathway, 10.1111/j.1365-313x.2011.04510.x
  3. Campanoni P., Auxin-Dependent Cell Division and Cell Elongation. 1-Naphthaleneacetic Acid and 2,4-Dichlorophenoxyacetic Acid Activate Different Pathways, 10.1104/pp.104.053843
  4. Cosgrove Daniel J., Plant cell wall extensibility: connecting plant cell growth with cell wall structure, mechanics, and the action of wall-modifying enzymes, 10.1093/jxb/erv511
  5. de Pinto Maria Concetta, Paradiso Annalisa, Leonetti Paola, De Gara Laura, Hydrogen peroxide, nitric oxide and cytosolic ascorbate peroxidase at the crossroad between defence and cell death, 10.1111/j.1365-313x.2006.02919.x
  6. Duby Geoffrey, Boutry Marc, The plant plasma membrane proton pump ATPase: a highly regulated P-type ATPase with multiple physiological roles, 10.1007/s00424-008-0457-x
  7. Duby Geoffrey, Poreba Wojciech, Piotrowiak Dominik, Bobik Krzysztof, Derua Rita, Waelkens Etienne, Boutry Marc, Activation of Plant Plasma Membrane H+-ATPase by 14-3-3 Proteins Is Negatively Controlled by Two Phosphorylation Sites within the H+-ATPase C-terminal Region, 10.1074/jbc.m807311200
  8. Dumais Jacques, Modes of deformation of walled cells, 10.1093/jxb/ert268
  9. Engelsdorf Timo, Hamann Thorsten, An update on receptor-like kinase involvement in the maintenance of plant cell wall integrity, 10.1093/aob/mcu043
  10. Falhof Janus, Pedersen Jesper Torbøl, Fuglsang Anja Thoe, Palmgren Michael, Plasma Membrane H + -ATPase Regulation in the Center of Plant Physiology, 10.1016/j.molp.2015.11.002
  11. Foreman Julia, Demidchik Vadim, Bothwell John H. F., Mylona Panagiota, Miedema Henk, Torres Miguel Angel, Linstead Paul, Costa Silvia, Brownlee Colin, Jones Jonathan D. G., Davies Julia M., Dolan Liam, Reactive oxygen species produced by NADPH oxidase regulate plant cell growth, 10.1038/nature01485
  12. Fuglsang Anja T., Kristensen Astrid, Cuin Tracey A., Schulze Waltraud X., Persson Jörgen, Thuesen Kristina H., Ytting Cecilie K., Oehlenschlaeger Christian B., Mahmood Khalid, Sondergaard Teis E., Shabala Sergey, Palmgren Michael G., Receptor kinase-mediated control of primary active proton pumping at the plasma membrane, 10.1111/tpj.12680
  13. Germain Hugo, Gray-Mitsumune Madoka, Houde Josée, Benhamman Rachid, Sawasaki Tatsuya, Endo Yaeta, Matton Daniel P., The Solanum chacoense ovary receptor kinase 11 (ScORK11) undergoes tissue-dependent transcriptional, translational and post-translational regulation, 10.1016/j.plaphy.2013.05.036
  14. Gevaudant F., Duby G., von Stedingk E., Zhao R., Morsomme P., Boutry M., Expression of a Constitutively Activated Plasma Membrane H+-ATPase Alters Plant Development and Increases Salt Tolerance, 10.1104/pp.107.103762
  15. Grebe M., PLANT BIOLOGY: Enhanced: Growth by Auxin: When a Weed Needs Acid, 10.1126/science.1119735
  16. Hager Achim, Role of the plasma membrane H + -ATPase in auxin-induced elongation growth: historical and new aspects, 10.1007/s10265-003-0110-x
  17. Haruta M., Sabat G., Stecker K., Minkoff B. B., Sussman M. R., A Peptide Hormone and Its Receptor Protein Kinase Regulate Plant Cell Expansion, 10.1126/science.1244454
  18. Haruta Miyoshi, Gray William M, Sussman Michael R, Regulation of the plasma membrane proton pump (H + -ATPase) by phosphorylation, 10.1016/j.pbi.2015.09.005
  19. Hepler Peter K., The Cytoskeleton and Its Regulation by Calcium and Protons, 10.1104/pp.15.01506
  20. Höfte Herman, The Yin and Yang of Cell Wall Integrity Control: Brassinosteroid and FERONIA Signaling, 10.1093/pcp/pcu182
  21. Ito Hirokazu, Oshiro Tomoko, Fujita Yasuyuki, Kubota Sachiko, Naito Chikako, Ohtsuka Hokuto, Murakami Hiroshi, Aiba Hirofumi, Pma1, a P-type Proton ATPase, Is a Determinant of Chronological Life Span in Fission Yeast, 10.1074/jbc.m110.175562
  22. Jones K H, Senft J A, An improved method to determine cell viability by simultaneous staining with fluorescein diacetate-propidium iodide., 10.1177/33.1.2578146
  23. Kato Mariko, Aoyama Takashi, Maeshima Masayoshi, The Ca2+-binding protein PCaP2 located on the plasma membrane is involved in root hair development as a possible signal transducer, 10.1111/tpj.12155
  24. Kaur Gurpreet, Sharma Ashutosh, Guruprasad Kunchur, Pati Pratap Kumar, Versatile roles of plant NADPH oxidases and emerging concepts, 10.1016/j.biotechadv.2014.02.002
  25. Kurkdjian A, Guern J, Intracellular pH: Measurement and Importance in Cell Activity, 10.1146/annurev.pp.40.060189.001415
  26. KUTSCHERA U., The current status of the acid-growth hypothesis, 10.1111/j.1469-8137.1994.tb02951.x
  27. Kutschera; U., Acid Growth and Plant Development, 10.1126/science.311.5763.952b
  28. Ladwig Friederike, Dahlke Renate I., Stührwohldt Nils, Hartmann Jens, Harter Klaus, Sauter Margret, Phytosulfokine Regulates Growth in Arabidopsis through a Response Module at the Plasma Membrane That Includes CYCLIC NUCLEOTIDE-GATED CHANNEL17, H+-ATPase, and BAK1, 10.1105/tpc.15.00306
  29. LAEMMLI U. K., Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4, 10.1038/227680a0
  30. Larsson Christer, Widell Susanne, Kjellbom Per, [52] Preparation of high-purity plasma membranes, Methods in Enzymology (1987) ISBN:9780121820480 p.558-568, 10.1016/0076-6879(87)48054-3
  31. Li J., Wang X., Qin T., Zhang Y., Liu X., Sun J., Zhou Y., Zhu L., Zhang Z., Yuan M., Mao T., MDP25, A Novel Calcium Regulatory Protein, Mediates Hypocotyl Cell Elongation by Destabilizing Cortical Microtubules in Arabidopsis, 10.1105/tpc.111.092684
  32. Link Bruce M., Cosgrove Daniel J., Acid-Growth Response and α-Expansins in Suspension Cultures of Bright Yellow 2 Tobacco, 10.1104/pp.118.3.907
  33. Luo Hong, Morsomme Pierre, Boutry Marc, The Two Major Types of Plant Plasma Membrane H+-ATPases Show Different Enzymatic Properties and Confer Differential pH Sensitivity of Yeast Growth, 10.1104/pp.119.2.627
  34. Mercx Sébastien, Tollet Jérémie, Magy Bertrand, Navarre Catherine, Boutry Marc, Gene Inactivation by CRISPR-Cas9 in Nicotiana tabacum BY-2 Suspension Cells, 10.3389/fpls.2016.00040
  35. Michelet B., Boutry M., The Plasma Membrane H+-ATPase (A Highly Regulated Enzyme with Multiple Physiological Functions), 10.1104/pp.108.1.1
  36. Moriau Luc, Michelet Baudouin, Bogaerts Pierre, Lambert Laurence, Michel Alain, Oufattole Mohammed, Boutry Marc, Expression analysis of two gene subfamilies encoding the plasma membrane H+-ATPase in Nicotiana plumbaginifolia reveals the major transport functions of this enzyme, 10.1046/j.1365-313x.1999.00495.x
  37. Morsomme P, De Kerchove D’exaerde A, De Meester S, Thines D, Goffeau A, Boutry M (1996) Single point mutations in various domains of a plant plasma membrane H+-ATPase expressed in Saccharomyces cerevisiae increase H+-pumping and permit yeast growth at low pH. EMBO J 15:5513–5526
  38. Morsomme Pierre, Dambly Stéphanie, Maudoux Olivier, Boutry Marc, Single Point Mutations Distributed in 10 Soluble and Membrane Regions of theNicotiana plumbaginifoliaPlasma Membrane PMA2 H+-ATPase Activate the Enzyme and Modify the Structure of the C-terminal Region, 10.1074/jbc.273.52.34837
  39. Nagata Toshiyuki, Nemoto Yasuyuki, Hasezawa Seiichiro, Tobacco BY-2 Cell Line as the “HeLa” Cell in the Cell Biology of Higher Plants, International Review of Cytology (1992) ISBN:9780123645326 p.1-30, 10.1016/s0074-7696(08)62452-3
  40. Naito Chikako, Ito Hirokazu, Oshiro Tomoko, Ohtsuka Hokuto, Murakami Hiroshi, Aiba Hirofumi, A newpma1mutation identified in a chronologically long-lived fission yeast mutant, 10.1016/j.fob.2014.09.006
  41. Navarre Catherine, Sallets Adrienne, Gauthy Emilie, Maîtrejean Marie, Magy Bertrand, Nader Joseph, Pety de Thozée Cédric, Crouzet Jérôme, Batoko Henri, Boutry Marc, Isolation of heat shock-induced Nicotiana tabacum transcription promoters and their potential as a tool for plant research and biotechnology, 10.1007/s11248-010-9459-5
  42. NESIUS KNEELAND K., FLETCHER JOHN S., Carbon Dioxide and pH Requirements of Non-Photosynthetic Tissue Culture Cells, 10.1111/j.1399-3054.1973.tb01186.x
  43. Palmgren Michael G, PLANTPLASMAMEMBRANEH+-ATPases: Powerhouses for Nutrient Uptake, 10.1146/annurev.arplant.52.1.817
  44. Piette Anne-Sophie, Derua Rita, Waelkens Etienne, Boutry Marc, Duby Geoffrey, A Phosphorylation in the C-terminal Auto-inhibitory Domain of the Plant Plasma Membrane H+-ATPase Activates the Enzyme with No Requirement for Regulatory 14-3-3 Proteins, 10.1074/jbc.m110.211953
  45. Pokotylo Igor, Kolesnikov Yaroslav, Kravets Volodymyr, Zachowski Alain, Ruelland Eric, Plant phosphoinositide-dependent phospholipases C: Variations around a canonical theme, 10.1016/j.biochi.2013.07.004
  46. Qin T., Liu X., Li J., Sun J., Song L., Mao T., Arabidopsis Microtubule-Destabilizing Protein 25 Functions in Pollen Tube Growth by Severing Actin Filaments, 10.1105/tpc.113.119768
  47. Rayle D L, Cleland R E, The Acid Growth Theory of auxin-induced cell elongation is alive and well., 10.1104/pp.99.4.1271
  48. Roberts A. W., Haigler C. H., Cell Expansion and Tracheary Element Differentiation Are Regulated by Extracellular pH in Mesophyll Cultures of Zinnia elegans L, 10.1104/pp.105.2.699
  49. Rodrigues Rachel B., Sabat Gregorz, Minkoff Benjamin B., Burch Heather L., Nguyen Thao T., Sussman Michael R., Expression of a Translationally Fused TAP-Tagged Plasma Membrane Proton Pump inArabidopsis thaliana, 10.1021/bi401096m
  50. Sallets Adrienne, Beyaert Maxime, Boutry Marc, Champagne Antoine, Comparative Proteomics of Short and Tall Glandular Trichomes ofNicotiana tabacumReveals Differential Metabolic Activities, 10.1021/pr5002548
  51. Schopfer P., Determination of Auxin-Dependent pH Changes in Coleoptile Cell Walls by a Null-Point Method, 10.1104/pp.103.2.351
  52. Smith David L., Krikorian Abraham D., Low external pH prevents cell elongation but not multiplication of embryogenic carrot cells, 10.1111/j.1399-3054.1992.tb04696.x
  53. Smith P.K., Krohn R.I., Hermanson G.T., Mallia A.K., Gartner F.H., Provenzano M.D., Fujimoto E.K., Goeke N.M., Olson B.J., Klenk D.C., Measurement of protein using bicinchoninic acid, 10.1016/0003-2697(85)90442-7
  54. Spartz Angela K., Lee Sang H., Wenger Jonathan P., Gonzalez Nathalie, Itoh Hironori, Inzé Dirk, Peer Wendy A., Murphy Angus S., Overvoorde Paul J., Gray William M., The SAUR19 subfamily of SMALL AUXIN UP RNA genes promote cell expansion : SAUR fusion proteins promote cell expansion, 10.1111/j.1365-313x.2012.04946.x
  55. Spartz A. K., Ren H., Park M. Y., Grandt K. N., Lee S. H., Murphy A. S., Sussman M. R., Overvoorde P. J., Gray W. M., SAUR Inhibition of PP2C-D Phosphatases Activates Plasma Membrane H+-ATPases to Promote Cell Expansion in Arabidopsis, 10.1105/tpc.114.126037
  56. Takahashi K., Hayashi K.-i., Kinoshita T., Auxin Activates the Plasma Membrane H+-ATPase by Phosphorylation during Hypocotyl Elongation in Arabidopsis, 10.1104/pp.112.196428
  57. Tanimoto Eiichi, Regulation of Root Growth by Plant Hormones—Roles for Auxin and Gibberellin, 10.1080/07352680500196108
  58. Vacca R. A., Production of Reactive Oxygen Species, Alteration of Cytosolic Ascorbate Peroxidase, and Impairment of Mitochondrial Metabolism Are Early Events in Heat Shock-Induced Programmed Cell Death in Tobacco Bright-Yellow 2 Cells, 10.1104/pp.103.035956
  59. van der Fits Leslie, Deakin Edward A., Hoge J. Harry C., Memelink Johan, 10.1023/a:1006440221718
  60. Velasquez SM, Barbez E, Kleine-Vehn J, Estevez JM (2016) Auxin and cellular elongation. Plant Physiol 170:1206–1215
  61. Weerdenburg C, Seagull RW (1988) The effects of taxol and colchicine on microtubule and microfibril in elongating plant cells in culture. Can J Bot 66:1707–1716
  62. Wolf Sebastian, Hématy Kian, Höfte Herman, Growth Control and Cell Wall Signaling in Plants, 10.1146/annurev-arplant-042811-105449
  63. Xu Y. X., Liu Y., Chen S. T., Li X. Q., Xu L. G., Qi Y. H., Jiang D. A., Jin S. H., The B subfamily of plant ATP binding cassette transporters and their roles in auxin transport, 10.1007/s10535-014-0423-8
  64. Zhao R, Dielen V, Kinet JM, Boutry M (2000) Cosuppression of a plasma membrane H+-ATPase isoform impairs sucrose translocation, stomatal opening, plant growth, and male fertility. Plant Cell 12:535–546