User menu

Organization and function of the plant pleiotropic drug resistance ABC transporter family

Bibliographic reference Crouzet, Jérôme ; Trombik, Tomasz ; Fraysse, AS ; Boutry, Marc. Organization and function of the plant pleiotropic drug resistance ABC transporter family. In: FEBS Letters, Vol. 580, no. 4, p. 1123-1130 (2006)
Permanent URL
  1. Higgins Christopher F, ABC transporters: physiology, structure and mechanism – an overview, 10.1016/s0923-2508(01)01193-7
  2. Holland I.Barry, A. Blight Mark, ABC-ATPases, adaptable energy generators fuelling transmembrane movement of a variety of molecules in organisms from bacteria to humans, 10.1006/jmbi.1999.2993
  3. Decottignies Anabelle, Goffeau André, Complete inventory of the yeast ABC proteins, 10.1038/ng0297-137
  4. Bauer Bettina E, Wolfger Hubert, Kuchler Karl, Inventory and function of yeast ABC proteins: about sex, stress, pleiotropic drug and heavy metal resistance, 10.1016/s0005-2736(99)00160-1
  5. Rogers, J. Mol. Biotechnol., 3, 207 (2001)
  6. Piper P., The Pdr12 ABC transporter is required for the development of weak organic acid resistance in yeast, 10.1093/emboj/17.15.4257
  7. Sánchez-Fernández Rocı́o, Davies T. G. Emyr, Coleman Julian O. D., Rea Philip A., TheArabidopsis thalianaABC Protein Superfamily, a Complete Inventory, 10.1074/jbc.m103104200
  8. Martinoia Enrico, Klein Markus, Geisler Markus, Bovet Lucien, Forestier Cyrille, Kolukisaoglu Üner, Müller-Röber Bernd, Schulz Burkhard, Multifunctionality of plant ABC transporters – more than just detoxifiers, 10.1007/s004250100661
  9. van den Brûle Sybille, Smart Cheryl, The plant PDR family of ABC transporters, 10.1007/s00425-002-0889-z
  10. Jasinski M., The ATP-Binding Cassette Transporters: Structure, Function, and Gene Family Comparison between Rice and Arabidopsis, 10.1104/pp.102.014720
  11. Garcia Olivier, Bouige Philippe, Forestier Cyrille, Dassa Elie, Inventory and Comparative Analysis of Rice and Arabidopsis ATP-binding Cassette (ABC) Systems, 10.1016/j.jmb.2004.07.093
  12. Zimmermann P., GENEVESTIGATOR. Arabidopsis Microarray Database and Analysis Toolbox, 10.1104/pp.104.046367
  13. Sheps Jonathan A, Ralph Steven, Zhao Zhongying, Baillie David L, Ling Victor, 10.1186/gb-2004-5-3-r15
  14. Dassa Elie, Bouige Philippe, The ABC of ABCs: a phylogenetic and functional classification of ABC systems in living organisms, 10.1016/s0923-2508(01)01194-9
  15. Prasad Rajendra, Kapoor Khyati, Multidrug Resistance in Yeast Candida, International Review of Cytology (2004) ISBN:9780123646460 p.215-248, 10.1016/s0074-7696(04)42005-1
  16. Nakaune, Appl. Environ. Microb., 64, 3983 (1998)
  17. Urban M., An ATP-driven efflux pump is a novel pathogenicity factor in rice blast disease, 10.1093/emboj/18.3.512
  18. Fleiβner André, Sopalla Claudia, Weltring Klaus-Michael, An ATP-binding Cassette Multidrug-Resistance Transporter Is Necessary for Tolerance ofGibberella pulicaristo Phytoalexins and Virulence on Potato Tubers, 10.1094/mpmi.2002.15.2.102
  19. Schoonbeek H., Del Sorbo G., De Waard M. A., The ABC Transporter BcatrB Affects the Sensitivity ofBotrytis cinereato the Phytoalexin Resveratrol and the Fungicide Fenpiclonil, 10.1094/mpmi.2001.14.4.562
  20. Smart Cheryl C., Fleming Andrew J., Hormonal and Environmental Regulation of a Plant PDR5-like ABC Transporter, 10.1074/jbc.271.32.19351
  21. van den Brule Sybille, Muller Axel, Fleming Andrew J., Smart Cheryl C., The ABC transporter SpTUR2 confers resistance to the antifungal diterpene sclareol, 10.1046/j.1365-313x.2002.01321.x
  22. Moons Ann, Ospdr9, which encodes a PDR-type ABC transporter, is induced by heavy metals, hypoxic stress and redox perturbations in rice roots1, 10.1016/s0014-5793(03)01060-3
  23. Lee M., AtPDR12 Contributes to Lead Resistance in Arabidopsis, 10.1104/pp.104.058107
  24. Jasinski M., A Plant Plasma Membrane ATP Binding Cassette-Type Transporter Is Involved in Antifungal Terpenoid Secretion, 10.1105/tpc.13.5.1095
  25. Campbell E. J., Pathogen-Responsive Expression of a Putative ATP-Binding Cassette Transporter Gene Conferring Resistance to the Diterpenoid Sclareol Is Regulated by Multiple Defense Signaling Pathways in Arabidopsis, 10.1104/pp.103.024182
  26. Stukkens Y., NpPDR1, a Pleiotropic Drug Resistance-Type ATP-Binding Cassette Transporter from Nicotiana plumbaginifolia, Plays a Major Role in Plant Pathogen Defense, 10.1104/pp.105.062372
  27. Grec S��bastien, Vanham Delphine, De Ribaucourt Jeoffrey Christyn, Purnelle B��n��dicte, Boutry Marc, Identification of regulatory sequence elements within the transcription promoter region of NpABC1, a gene encoding a plant ABC transporter induced by diterpenes : Diterpene activation of a transcription promoter, 10.1046/j.1365-313x.2003.01792.x
  28. Sasabe Michiko, Toyoda Kazuhiro, Shiraishi Tomonori, Inagaki Yoshishige, Ichinose Yuki, cDNA cloning and characterization of tobacco ABC transporter:NtPDR1is a novel elicitor-responsive gene1, 10.1016/s0014-5793(02)02697-2
  29. Nee Sean, More than meets the eye, 10.1038/429804a
  30. Seo S., A Diterpene as an Endogenous Signal for the Activation of Defense Responses to Infection with Tobacco mosaic virus and Wounding in Tobacco, 10.1105/tpc.010231
  31. Dudareva Natalia, Pichersky Eran, Biochemical and Molecular Genetic Aspects of Floral Scents, 10.1104/pp.122.3.627
  32. Akiyama Kohki, Matsuzaki Ken-ichi, Hayashi Hideo, Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi, 10.1038/nature03608
  33. Ducos Eric, Fraysse Å Staffan, Boutry Marc, NtPDR3, an iron-deficiency inducible ABC transporter inNicotiana tabacum, 10.1016/j.febslet.2005.11.014
  34. Kobayashi Takanori, Nakayama Yuko, Itai Reiko Nakanishi, Nakanishi Hiromi, Yoshihara Toshihiro, Mori Satoshi, Nishizawa Naoko K., Identification of novelcis-acting elements, IDE1 and IDE2, of the barleyIDS2gene promoter conferring iron-deficiency-inducible, root-specific expression in heterogeneous tobacco plants, 10.1046/j.1365-313x.2003.01920.x
  35. Colangelo E. P., The Essential Basic Helix-Loop-Helix Protein FIT1 Is Required for the Iron Deficiency Response, 10.1105/tpc.104.024315
  36. Romheld Volker, Different strategies for iron acquisition in higher plants, 10.1111/j.1399-3054.1987.tb06137.x
  37. Cardinale Francesca, Meskiene Irute, Ouaked Fatma, Hirt Heribert, Convergence and Divergence of Stress-Induced Mitogen-Activated Protein Kinase Signaling Pathways at the Level of Two Distinct Mitogen-Activated Protein Kinase Kinases, 10.1105/tpc.010256
  38. Curie Catherine, Briat Jean-François, IRONTRANSPORT ANDSIGNALING INPLANTS, 10.1146/annurev.arplant.54.031902.135018
  39. Klein Markus, Geisler Markus, Suh Su Jeoung, Kolukisaoglu H. Üner, Azevedo Louis, Plaza Sonia, Curtis Mark D., Richter Andreas, Weder Barbara, Schulz Burkhard, Martinoia Enrico, Disruption ofAtMRP4, a guard cell plasma membrane ABCC-type ABC transporter, leads to deregulation of stomatal opening and increased drought susceptibility, 10.1111/j.1365-313x.2004.02125.x
  40. Baxter I., Genomic Comparison of P-Type ATPase Ion Pumps in Arabidopsis and Rice, 10.1104/pp.103.021923
  41. Thompson Julie D., Higgins Desmond G., Gibson Toby J., CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice, 10.1093/nar/22.22.4673
  42. Felsenstein Joseph, Confidence Limits on Phylogenies: An Approach Using the Bootstrap, 10.2307/2408678