Using 2-deoxy-2-[18F]fluoro-D-glucose ([18F]FDG) to study carbon allocation in plants after herbivore attack
详细信息    查看全文
  • 作者:Stefan Meldau (1) (2) (3)
    Melkamu G Woldemariam (1) (4)
    Amol Fatangare (5)
    Ales Svatos (5)
    Ivan Galis (1) (6)

    1. Department of Molecular Ecology
    ; Max-Planck-Institute for Chemical Ecology ; Hans-Kn枚ll-Str.8 ; 07745 ; Jena ; Germany
    2. German Centre for integrative Biodiversity Research (iDiv)
    ; Deutscher Platz 5 ; 04107 ; Leipzig ; Germany
    3. Present address
    ; KWS SAAT AG ; Molecular Physiology ; R&D ; RD-ME-MP ; Grimsehlstrasse 31 ; D-37555 ; Einbeck ; Germany
    4. Present address
    ; Boyce Thompson Institute for Plant Research ; 533 Tower Road ; Ithaca ; 14853 ; NY ; USA
    5. Mass Spectrometry Research Group
    ; Max-Planck-Institute for Chemical Ecology ; Hans-Kn枚ll-Str.8 ; 07745 ; Jena ; Germany
    6. Present address
    ; Okayama University ; Institute of Plant Science and Resources ; Chuo 2-20-1 ; 710-0046 ; Kurashiki ; Japan
  • 关键词:2 ; deoxy ; 2 ; [18F]fluoro ; D ; glucose ([18F]FDG) ; Herbivory ; Jasmonate signalling ; Nicotiana attenuata ; Fatty acid ; amino acid conjugates
  • 刊名:BMC Research Notes
  • 出版年:2015
  • 出版时间:December 2015
  • 年:2015
  • 卷:8
  • 期:1
  • 全文大小:1,378 KB
  • 参考文献:1. Geyter, N, Gholami, A, Goormachtig, S, Goossens, A (2012) Transcriptional machineries in jasmonate-elicited plant secondary metabolism. Trends Plant Sci 17: pp. 349-359 plants.2012.03.001" target="_blank" title="It opens in new window">CrossRef
    2. Arnold, T, Appel, H, Patel, V, Stocum, E, Kavalier, A, Schultz, J (2004) Carbohydrate translocation determines the phenolic content of Populus foliage: a test of the sink-source model of plant defense. New Phytol 164: pp. 157-164 CrossRef
    3. Bolton, MD (2009) Primary metabolism and plant defense-fuel for the fire. Mol Plant Microbe In 22: pp. 487-497 CrossRef
    4. Broeckling, CD, Huhman, DV, Farag, MA, Smith, JT, May, GD, Mendes, P (2005) Metabolic profiling of Medicago truncatula cell cultures reveals the effects of biotic and abiotic elicitors on metabolism. J Exp Bot 56: pp. 323-336 CrossRef
    5. Hanik, N, Gomez, S, Best, M, Schueller, M, Orians, CM, Ferrieri, RA (2010) Partitioning of new carbon as C-11 in Nicotiana tabacum reveals insight into methyl jasmonate induced changes in metabolism. J Chem Ecol 36: pp. 1058-1067 CrossRef
    6. Hanik, N, Gomez, S, Schueller, M, Orians, CM, Ferrieri, RA (2010) Use of gaseous 13NH(3) administered to intact leaves of Nicotiana tabacum to study changes in nitrogen utilization during defence induction. Plant Cell Environ 33: pp. 2173-2179 CrossRef
    7. Schwachtje, J, Minchin, PE, Jahnke, S, Dongen, JT, Schittko, U, Baldwin, IT (2006) SNF1-related kinases allow plants to tolerate herbivory by allocating carbon to roots. Proc Natl Acad Sci U S A 103: pp. 12935-12940 CrossRef
    8. Baldwin, IT (1998) Jasmonate-induced responses are costly but benefit plants under attack in native populations. Proc Natl Acad Sci U S A 95: pp. 8113-8118 CrossRef
    9. Cipollini, D (2007) Consequences of the overproduction of methyl jasmonate on seed production, tolerance to defoliation and competitive effect and response of Arabidopsis thaliana. New Phytol 173: pp. 146-153 CrossRef
    10. Halitschke, R, Baldwin, IT (2003) Antisense LOX expression increases herbivore performance by decreasing defense responses and inhibiting growth-related transcriptional reorganization in Nicotiana attenuata. Plant J 36: pp. 794-807 CrossRef
    11. Meldau, S, Ullman-Zeunert, L, Govind, G, Bartram, S, Baldwin, IT (2012) MAPK-dependent JA and SA signalling in Nicotiana attenuata affects plant growth and fitness during competition with conspecifics. Bmc Plant Biology 12: pp. 213 CrossRef
    12. Redman, AM, Cipollini, DF, Schultz, JC (2001) Fitness costs of jasmonic acid-induced defense in tomato, Lycopersicon esculentum. Oecologia 126: pp. 380-385 CrossRef
    13. Sturm, A, Chrispeels, MJ (1990) Cdna cloning of carrot extracellular beta-Fructosidase and its expression in response to wounding and bacterial-infection. Plant Cell 2: pp. 1107-1119
    14. Ohyama, A, Nishimura, S, Hirai, M (1998) Cloning of cDNA for a cell wall-bound acid invertase from tomato (Lycopersicon esculentum) and expression of soluble and cell wall-bound invertases in plants and wounded leaves of L. esculentum and L. peruvianum. Genes Genet Syst 73: pp. 149-157 CrossRef
    15. Arnold, TM, Schultz, JC (2002) Induced sink strength as a prerequisite for induced tannin biosynthesis in developing leaves of Populus. Oecologia 130: pp. 585-593 CrossRef
    16. Philippe, RN, Ralph, SG, Mansfield, SD, Bohlmann, J (2010) Transcriptome profiles of hybrid poplar (Populus trichocarpa x deltoides) reveal rapid changes in undamaged, systemic sink leaves after simulated feeding by forest tent caterpillar (Malacosoma disstria). New Phytol 188: pp. 787-802 CrossRef
    17. Zhang, L, Cohn, NS, Mitchell, JP (1996) Induction of a pea cell-wall invertase gene by wounding and its localized expression in phloem. Plant Physiol 112: pp. 1111-1117
    18. Babst, BA, Ferrieri, RA, Gray, DW, Lerdau, M, Schlyer, DJ, Schueller, M (2005) Jasmonic acid induces rapid changes in carbon transport and partitioning in Populus. New Phytol 167: pp. 63-72 CrossRef
    19. Gomez, S, Steinbrenner, AD, Osorio, S, Schueller, M, Ferrieri, RA, Fernie, AR (2012) From shoots to roots: transport and metabolic changes in tomato after simulated feeding by a specialist lepidopteran. Entomol Exp Appl 144: pp. 101-111 CrossRef
    20. Holland, JN, Cheng, WX, Crossley, DA (1996) Herbivore-induced changes in plant carbon allocation: Assessment of below-ground C fluxes using carbon-14. Oecologia 107: pp. 87-94 CrossRef
    21. Ferrieri, AP, Appel, H, Ferrieri, RA, Schultz, JC (2012) Novel application of 2-[F-18]fluoro-2-deoxy-D-glucose to study plant defenses. Nucl Med Biol 39: pp. 1152-1160 CrossRef
    22. Kallenbach, M, Alagna, F, Baldwin, IT, Bonaventure, G (2010) Nicotiana attenuata SIPK, WIPK, NPR1, and fatty acid-amino acid conjugates participate in the induction of jasmonic acid biosynthesis by affecting early enzymatic steps in the pathway. Plant Physiol 152: pp. 96-106 CrossRef
    23. Wu, JQ, Hettenhausen, C, Meldau, S, Baldwin, IT (2007) Herbivory rapidly activates MAPK signaling in attacked and unattacked leaf regions but not between leaves of Nicotiana attenuata. Plant Cell 19: pp. 1096-1122 CrossRef
    24. Wang, L, Halitschke, R, Kang, JH, Berg, A, Harnisch, F, Baldwin, IT (2007) Independently silencing two JAR family members impairs levels of trypsin proteinase inhibitors but not nicotine. Planta 226: pp. 159-167 CrossRef
    25. Paschold, A, Halitschke, R, Baldwin, IT (2007) Co(i)-ordinating defenses: NaCOI1 mediates herbivore- induced resistance in Nicotiana attenuata and reveals the role of herbivore movement in avoiding defenses. Plant J 51: pp. 79-91 CrossRef
    26. Woldemariam, MG, Dinh, ST, Oh, Y, Gaquerel, E, Baldwin, IT, Galis, I (2013) NaMYC2 transcription factor regulates a subset of plant defense responses in Nicotiana attenuata. BMC Plant Biol 13: pp. 73 CrossRef
    27. Babst, BA, Ferrieri, RA, Thorpe, MR, Orians, CM (2008) Lymantria dispar herbivory induces rapid changes in carbon transport and partitioning in Populus nigra. Entomol Exp Appl 128: pp. 117-125 CrossRef
    28. Bazot, S, Mikola, J, Nguyen, C, Robin, C (2005) Defoliation-induced changes in carbon allocation and root soluble carbon concentration in field-grown Lolium perenne plants: do they affect carbon availability, microbes and animal trophic groups in soil?. Funct Ecol 19: pp. 886-896 CrossRef
    29. Briske, DD, Boutton, TW, Wang, Z (1996) Contribution of flexible allocation priorities to herbivory tolerance in C-4 perennial grasses: An evaluation with C-13 labeling. Oecologia 105: pp. 151-159 CrossRef
    30. Dyer, MI, Acra, MA, Wang, GM, Coleman, DC, Freckman, DW, Mcnaughton, SJ (1991) Source-sink carbon relations in 2 Panicum coloratum ecotypes in response to herbivory. Ecology 72: pp. 1472-1483 CrossRef
    31. Gomez, S, Ferrieri, RA, Schueller, M, Orians, CM (2010) Methyl jasmonate elicits rapid changes in carbon and nitrogen dynamics in tomato. New Phytol 188: pp. 835-844 CrossRef
    32. Machado, RAR, Ferrieri, AP, Robert, CAM, Glauser, G, Kallenbach, M, Baldwin, IT (2013) Leaf-herbivore attack reduces carbon reserves and regrowth from the roots via jasmonate and auxin signaling. New Phytol 200: pp. 1234-1246 CrossRef
    33. Hummel, GM, Naumann, M, Schurr, U, Walter, A (2007) Root growth dynamics of Nicotiana attenuata seedlings are affected by simulated herbivore attack. Plant Cell Environ 30: pp. 1326-1336 CrossRef
    34. Hummel, GM, Schurr, U, Baldwin, IT, Walter, A (2009) Herbivore-induced jasmonic acid bursts in leaves of Nicotiana attenuata mediate short-term reductions in root growth. Plant Cell Environ 32: pp. 134-143 CrossRef
    35. Krugel, T, Lim, M, Gase, K, Halitschke, R, Baldwin, IT (2002) Agrobacterium-mediated transformation of Nicotiana attenuata, a model ecological expression system. Chemoecology 12: pp. 177-183 CrossRef
    36. Gromova, M, Roby, C (2010) Toward Arabidopsis thaliana hydrophilic metabolome: assessment of extraction methods and quantitative 1H NMR. Physiol Plantarum 140: pp. 111-127 CrossRef
    37. Hettenhausen, C, Baldwin, IT, Wu, J (2013) Nicotiana attenuata MPK4 suppresses a novel jasmonic acid (JA) signaling-independent defense pathway against the specialist insect Manduca sexta, but is not required for the resistance to the generalist Spodoptera littoralis. New Phytol 199: pp. 787-799 CrossRef
    38. Hattori, E, Uchida, H, Harada, N, Ohta, M, Tsukada, H, Hara, Y (2008) Incorporation and translocation of 2-deoxy-2-[F-18]fluoro-D-glucose in Sorghum bicolor (L.) Moench monitored using a planar positron imaging system. Planta 227: pp. 1181-1186 CrossRef
    39. Kaarstad, K, Bender, D, Bentzen, L, Munk, OL, Keiding, S (2002) Metabolic fate of F-18-FDG in mice bearing either SCCVII squamous cell carcinoma or C3H mammary carcinoma. J Nucl Med 43: pp. 940-947
    40. McSheehy, PMJ, Leach, MO, Judson, IR, Griffiths, JR (2000) Metabolites of 2 鈥?fluoro-2鈥?deoxy-D-glucose detected by F-19 magnetic resonance spectroscopy in vivo predict response of murine RIF-1 tumors to 5-fluorouracil. Cancer Res 60: pp. 2122-2127
    41. Southworth, R, Parry, CR, Parkes, HG, Medina, RA, Garlick, PB (2003) Tissue-specific differences in 2-fluoro-2-deoxyglucose metabolism beyond FDG-6-P: a (19)F NMR spectroscopy study in the rat. NMR Biomed 16: pp. 494-502 CrossRef
    42. Schmidt, L, Hummel, GM, Sch枚ttner, M, Schurr, U, Walter, A (2009) Jasmonic acid does not mediate root growth responses to wounding in Arabidopsis thaliana. Plant, Cell & Environment 33: pp. 104-16
    43. Diezel, C, Allmann, S, Baldwin, IT (2011) Mechanisms of optimal defense patterns in Nicotiana attenuata: flowering attenuates herbivory-elicited ethylene and jasmonate signaling. J Integr Plant Biol 53: pp. 971-983 CrossRef
    44. Ivanov, VB, Dubrovsky, JG (2013) Longitudinal zonation pattern in plant roots: conflicts and solutions. Trends Plant Sci 18: pp. 237-243 plants.2012.10.002" target="_blank" title="It opens in new window">CrossRef
    45. Pritchard, J, Tomos, AD, Farrar, JE, Minchin, PEH, Gould, N, Paul, MJ (2004) Turgor, solute import and growth in maize roots treated with galactose. Funct Plant Biol 31: pp. 1095-1103 CrossRef
    46. Kim, SG, Yon, F, Gaquerel, E, Gulati, J, Baldwin, IT (2011) Tissue specific diurnal rhythms of metabolites and their regulation during herbivore attack in a native tobacco, Nicotiana attenuata. PLoS One 6: pp. e26214 CrossRef
    47. Erb, M, Meldau, S, Howe, GA (2012) Role of phytohormones in insect-specific plant reactions. Trends Plant Sci 17: pp. 250-259 plants.2012.01.003" target="_blank" title="It opens in new window">CrossRef
    48. McSteen, P, Leyser, O (2005) Shoot branching. Annu Rev Plant Biol 56: pp. 353-374 plant.56.032604.144122" target="_blank" title="It opens in new window">CrossRef
    49. Booker, J, Chatfield, S, Leyser, O (2003) Auxin acts in xylem-associated or medullary cells to mediate apical dominance. Plant Cell 15: pp. 495-507 CrossRef
    50. Hillman, JR, Math, VB, Medlow, GC (1977) Apical dominance and levels of indole acetic-acid in Phaseolus lateral buds. Planta 134: pp. 191-193 CrossRef
    51. Morris, DA (1977) Transport of exogenous auxin in 2-branched dwarf Pea-seedlings (Pisum-sativum-L) - Some implications for polarity and apical dominance. Planta 136: pp. 91-96 CrossRef
    52. Bangerth, F (1994) Response of cytokinin concentration in the xylem exudate of Bean (Phaseolus-vulgaris L) plants to decapitation and auxin treatment, and relationship to apical dominance. Planta 194: pp. 439-442 CrossRef
    53. Eklof, S, Astot, C, Blackwell, J, Moritz, T, Olsson, O, Sandberg, G (1997) Auxin-cytokinin interactions in wild-type and transgenic tobacco. Plant Cell Physiol 38: pp. 225-235 fordjournals.pcp.a029157" target="_blank" title="It opens in new window">CrossRef
    54. Nordstrom, A, Tarkowski, P, Tarkowska, D, Norbaek, R, Astot, C, Dolezal, K (2004) Auxin regulation of cytokinin biosynthesis in Arabidopsis thaliana: A factor of potential importance for auxin-cytokinin-regulated development. Proc Natl Acad Sci U S A 101: pp. 8039-8044 CrossRef
    55. Argueso, CT, Ferreira, FJ, Kieber, JJ (2009) Environmental perception avenues: the interaction of cytokinin and environmental response pathways. Plant Cell Environ 32: pp. 1147-1160 CrossRef
    56. Dello Loio, R, Linhares, FS, Sabatini, S (2008) Emerging role of cytokinin as a regulator of cellular differentiation. Curr Opin Plant Biol 11: pp. 23-27 CrossRef
    57. Werner, T, Motyka, V, Laucou, V, Smets, R, Onckelen, H, Schmulling, T (2003) Cytokinin-deficient transgenic Arabidopsis plants show multiple developmental alterations indicating opposite functions of cytokinins in the regulation of shoot and root meristem activity. Plant Cell 15: pp. 2532-2550 CrossRef
  • 刊物主题:Biomedicine general; Medicine/Public Health, general; Life Sciences, general;
  • 出版者:BioMed Central
  • ISSN:1756-0500
文摘
Background Although leaf herbivory-induced changes in allocation of recently assimilated carbon between the shoot and below-ground tissues have been described in several species, it is still unclear which part of the root system is affected by resource allocation changes and which signalling pathways are involved. We investigated carbon partitioning in root tissues following wounding and simulated leaf herbivory in young Nicotiana attenuata plants. Results Using 2-deoxy-2-[18F]fluoro-D-glucose ([18F]FDG), which was incorporated into disaccharides in planta, we found that simulated herbivory reduced carbon partitioning specifically to the root tips in wild type plants. In jasmonate (JA) signalling-deficient COI1 plants, the wound-induced allocation of [18F]FDG to the roots was decreased, while more [18F]FDG was transported to young leaves, demonstrating an important role of the JA pathway in regulating the wound-induced carbon partitioning between shoots and roots. Conclusions Our data highlight the use of [18F]FDG to study stress-induced carbon allocation responses in plants and indicate an important role of the JA pathway in regulating wound-induced shoot to root signalling.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700