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Emission of volatile organic compounds from petunia flowers is facilitated by an ABC transporter.

Bibliographic reference Adebesin, Funmilayo ; Widhalm, Joshua R ; Boachon, Benoît ; Lefèvre, François ; Pierman, Baptiste ; et. al. Emission of volatile organic compounds from petunia flowers is facilitated by an ABC transporter.. In: Science, Vol. 356, no.6345, p. 1386-1388 (2017)
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  1. PENUELAS J, Plant VOC emissions: making use of the unavoidable, 10.1016/j.tree.2004.06.002
  2. Glas Joris, Schimmel Bernardus, Alba Juan, Escobar-Bravo Rocío, Schuurink Robert, Kant Merijn, Plant Glandular Trichomes as Targets for Breeding or Engineering of Resistance to Herbivores, 10.3390/ijms131217077
  3. Cinege Gyöngyi, Louis Sandrine, Hänsch Robert, Schnitzler Jörg-Peter, Regulation of isoprene synthase promoter by environmental and internal factors, 10.1007/s11103-008-9441-2
  4. Niinemets Ülo, Loreto Francesco, Reichstein Markus, Physiological and physicochemical controls on foliar volatile organic compound emissions, 10.1016/j.tplants.2004.02.006
  5. Niinemets U., Stomatal Constraints May Affect Emission of Oxygenated Monoterpenoids from the Foliage of Pinus pinea, 10.1104/pp.009670
  6. Pichersky E., Biosynthesis of Plant Volatiles: Nature's Diversity and Ingenuity, 10.1126/science.1118510
  7. Borghi Monica, Fernie Alisdair R., Schiestl Florian P., Bouwmeester Harro J., The Sexual Advantage of Looking, Smelling, and Tasting Good: The Metabolic Network that Produces Signals for Pollinators, 10.1016/j.tplants.2016.12.009
  8. Schuman Meredith C., Valim Henrique A., Joo Youngsung, Temporal Dynamics of Plant Volatiles: Mechanistic Bases and Functional Consequences, Signaling and Communication in Plants (2016) ISBN:9783319334967 p.3-34, 10.1007/978-3-319-33498-1_1
  9. Widhalm Joshua R., Jaini Rohit, Morgan John A., Dudareva Natalia, Rethinking how volatiles are released from plant cells, 10.1016/j.tplants.2015.06.009
  10. Mendanha Sebastião Antonio, Alonso Antonio, Effects of terpenes on fluidity and lipid extraction in phospholipid membranes, 10.1016/j.bpc.2015.02.001
  11. McFarlane Heather E., Shin John J.H., Bird David A., Samuels A. Lacey, ArabidopsisABCG Transporters, Which Are Required for Export of Diverse Cuticular Lipids, Dimerize in Different Combinations, 10.1105/tpc.110.077974
  12. Dudareva Natalia, Negre Florence, Nagegowda Dinesh A., Orlova Irina, Plant Volatiles: Recent Advances and Future Perspectives, 10.1080/07352680600899973
  13. Crouzet Jérôme, Roland Julien, Peeters Emmanuel, Trombik Tomasz, Ducos Eric, Nader Joseph, Boutry Marc, NtPDR1, a plasma membrane ABC transporter from Nicotiana tabacum, is involved in diterpene transport, 10.1007/s11103-013-0053-0
  14. Widhalm Joshua R., Gutensohn Michael, Yoo Heejin, Adebesin Funmilayo, Qian Yichun, Guo Longyun, Jaini Rohit, Lynch Joseph H., McCoy Rachel M., Shreve Jacob T., Thimmapuram Jyothi, Rhodes David, Morgan John A., Dudareva Natalia, Identification of a plastidial phenylalanine exporter that influences flux distribution through the phenylalanine biosynthetic network, 10.1038/ncomms9142
  15. Verdonk Julian C, Ric de Vos C.H, Verhoeven Harrie A, Haring Michel A, van Tunen Arjen J, Schuurink Robert C, Regulation of floral scent production in petunia revealed by targeted metabolomics, 10.1016/s0031-9422(02)00707-0
  16. Van Moerkercke A., Galvan-Ampudia C. S., Verdonk J. C., Haring M. A., Schuurink R. C., Regulators of floral fragrance production and their target genes in petunia are not exclusively active in the epidermal cells of petals, 10.1093/jxb/ers034
  17. Verdonk J. C., ODORANT1 Regulates Fragrance Biosynthesis in Petunia Flowers, 10.1105/tpc.104.028837
  18. Cseke L., Dudareva N., Pichersky E., Structure and Evolution of Linalool Synthase, 10.1093/oxfordjournals.molbev.a025876
  19. 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
  20. Kang Joohyun, Park Jiyoung, Choi Hyunju, Burla Bo, Kretzschmar Tobias, Lee Youngsook, Martinoia Enrico, Plant ABC Transporters, 10.1199/tab.0153
  21. Rolny Nadia, Costa Lorenza, Carrión Cristian, Guiamet Juan José, Is the electrolyte leakage assay an unequivocal test of membrane deterioration during leaf senescence?, 10.1016/j.plaphy.2011.06.010
  22. Krasnow M., Matthews M., Shackel K., Evidence for substantial maintenance of membrane integrity and cell viability in normally developing grape (Vitis vinifera L.) berries throughout development, 10.1093/jxb/erm372
  23. Pichersky Eran, Gershenzon Jonathan, The formation and function of plant volatiles: perfumes for pollinator attraction and defense, 10.1016/s1369-5266(02)00251-0
  24. Fernandez-Pozo Noe, Rosli Hernan G., Martin Gregory B., Mueller Lukas A., The SGN VIGS Tool: User-Friendly Software to Design Virus-Induced Gene Silencing (VIGS) Constructs for Functional Genomics, 10.1016/j.molp.2014.11.024
  25. Bombarely Aureliano, Moser Michel, Amrad Avichai, Bao Manzhu, Bapaume Laure, Barry Cornelius S., Bliek Mattijs, Boersma Maaike R., Borghi Lorenzo, Bruggmann Rémy, Bucher Marcel, D'Agostino Nunzio, Davies Kevin, Druege Uwe, Dudareva Natalia, Egea-Cortines Marcos, Delledonne Massimo, Fernandez-Pozo Noe, Franken Philipp, Grandont Laurie, Heslop-Harrison J. S., Hintzsche Jennifer, Johns Mitrick, Koes Ronald, Lv Xiaodan, Lyons Eric, Malla Diwa, Martinoia Enrico, Mattson Neil S., Morel Patrice, Mueller Lukas A., Muhlemann Joëlle, Nouri Eva, Passeri Valentina, Pezzotti Mario, Qi Qinzhou, Reinhardt Didier, Rich Melanie, Richert-Pöggeler Katja R., Robbins Tim P., Schatz Michael C., Schranz M. Eric, Schuurink Robert C., Schwarzacher Trude, Spelt Kees, Tang Haibao, Urbanus Susan L., Vandenbussche Michiel, Vijverberg Kitty, Villarino Gonzalo H., Warner Ryan M., Weiss Julia, Yue Zhen, Zethof Jan, Quattrocchio Francesca, Sims Thomas L., Kuhlemeier Cris, Insight into the evolution of the Solanaceae from the parental genomes of Petunia hybrida, 10.1038/nplants.2016.74
  26. Parrish Susan, Fleenor Jamie, Xu SiQun, Mello Craig, Fire Andrew, Functional Anatomy of a dsRNA Trigger, 10.1016/s1097-2765(00)00106-4
  27. Segal, Genetics, 165, 387 (2003)
  28. Gleave Andrew P., A versatile binary vector system with a T-DNA organisational structure conducive to efficient integration of cloned DNA into the plant genome, 10.1007/bf00028910
  29. A Simple and General Method for Transferring Genes into Plants, 10.1126/science.227.4691.1229
  30. Klempien A., Kaminaga Y., Qualley A., Nagegowda D. A., Widhalm J. R., Orlova I., Shasany A. K., Taguchi G., Kish C. M., Cooper B. R., D'Auria J. C., Rhodes D., Pichersky E., Dudareva N., Contribution of CoA Ligases to Benzenoid Biosynthesis in Petunia Flowers, 10.1105/tpc.112.097519
  31. Dudareva N., Developmental Regulation of Methyl Benzoate Biosynthesis and Emission in Snapdragon Flowers, 10.1105/tpc.12.6.949
  32. Orlova I., Marshall-Colon A., Schnepp J., Wood B., Varbanova M., Fridman E., Blakeslee J. J., Peer W. A., Murphy A. S., Rhodes D., Pichersky E., Dudareva N., Reduction of Benzenoid Synthesis in Petunia Flowers Reveals Multiple Pathways to Benzoic Acid and Enhancement in Auxin Transport, 10.1105/tpc.106.046227
  33. Yanagisawa Makoto, Desyatova Anastasia S., Belteton Samuel A., Mallery Eileen L., Turner Joseph A., Szymanski Daniel B., Patterning mechanisms of cytoskeletal and cell wall systems during leaf trichome morphogenesis, 10.1038/nplants.2015.14
  34. Loreto Francesco, Schnitzler Jörg-Peter, Abiotic stresses and induced BVOCs, 10.1016/j.tplants.2009.12.006
  35. Boatright J., Understanding in Vivo Benzenoid Metabolism in Petunia Petal Tissue, 10.1104/pp.104.045468
  36. Goderis Inge J.W.M., De Bolle Miguel F.C., François Isabelle E.J.A., Wouters Piet F.J., Broekaert Willem F., Cammue Bruno P.A., 10.1023/a:1016052416053
  37. De Muynck Benoit, Navarre Catherine, Nizet Yannick, Stadlmann Johannes, Boutry Marc, Different subcellular localization and glycosylation for a functional antibody expressed in Nicotiana tabacum plants and suspension cells, 10.1007/s11248-008-9240-1
  38. 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
  39. 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, 10.1007/s00425-016-2571-x
  40. Jasinski M., A Plant Plasma Membrane ATP Binding Cassette-Type Transporter Is Involved in Antifungal Terpenoid Secretion, 10.1105/tpc.13.5.1095
  41. 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
  42. Toussaint Frédéric, Pierman Baptiste, Bertin Aurélie, Lévy Daniel, Boutry Marc, Purification and biochemical characterization of NpABCG5/NpPDR5, a plant pleiotropic drug resistance transporter expressed in Nicotiana tabacum BY-2 suspension cells , 10.1042/bcj20170108
  43. Yoo Heejin, Widhalm Joshua R., Qian Yichun, Maeda Hiroshi, Cooper Bruce R., Jannasch Amber S., Gonda Itay, Lewinsohn Efraim, Rhodes David, Dudareva Natalia, An alternative pathway contributes to phenylalanine biosynthesis in plants via a cytosolic tyrosine:phenylpyruvate aminotransferase, 10.1038/ncomms3833
  44. Wetzstein, J. Am. Soc. Hortic. Sci., 136, 83 (2011)
  45. Zhao D. F., Buchholz A., Tillmann R., Kleist E., Wu C., Rubach F., Kiendler-Scharr A., Rudich Y., Wildt J., Mentel Th. F., Environmental conditions regulate the impact of plants on cloud formation, 10.1038/ncomms14067
  46. Tamura Koichiro, Stecher Glen, Peterson Daniel, Filipski Alan, Kumar Sudhir, MEGA6: Molecular Evolutionary Genetics Analysis Version 6.0, 10.1093/molbev/mst197
  47. Misztal P.K., Hewitt C.N., Wildt J., Blande J.D., Eller A.S.D., Fares S., Gentner D.R., Gilman J.B., Graus M., Greenberg J., Guenther A.B., Hansel A., Harley P., Huang M., Jardine K., Karl T., Kaser L., Keutsch F.N., Kiendler-Scharr A., Kleist E., Lerner B.M., Li T., Mak J., Nölscher A.C., Schnitzhofer R., Sinha V., Thornton B., Warneke C., Wegener F., Werner C., Williams J., Worton D.R., Yassaa N., Goldstein A.H., Atmospheric benzenoid emissions from plants rival those from fossil fuels, 10.1038/srep12064
  48. Kolosova N., Cellular and Subcellular Localization of S-Adenosyl-L-Methionine:Benzoic Acid Carboxyl Methyltransferase, the Enzyme Responsible for Biosynthesis of the Volatile Ester Methylbenzoate in Snapdragon Flowers, 10.1104/pp.126.3.956
  49. Scalliet G., Role of Petal-Specific Orcinol O-Methyltransferases in the Evolution of Rose Scent, 10.1104/pp.105.070961
  50. Chen F., Characterization of a Root-Specific Arabidopsis Terpene Synthase Responsible for the Formation of the Volatile Monoterpene 1,8-Cineole, 10.1104/pp.104.044388