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Publikationen - Molekulare Signalverarbeitung

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Publikation

Ziegler, J.; Schmidt, S.; Strehmel, N.; Scheel, D.; Abel, S. Arabidopsis Transporter ABCG37/PDR9 contributes primarily highly oxygenated Coumarins to Root Exudation Sci Rep 7, 3704, (2017) DOI: 10.1038/s41598-017-03250-6

The chemical composition of root exudates strongly impacts the interactions of plants with microorganisms in the rhizosphere and the efficiency of nutrient acquisition. Exudation of metabolites is in part mediated by ATP-binding cassette (ABC) transporters. In order to assess the contribution of individual ABC transporters to root exudation, we performed an LC-MS based non-targeted metabolite profiling of semi-polar metabolites accumulating in root exudates of Arabidopsis thaliana plants and mutants deficient in the expression of ABCG36 (PDR8/PEN3), ABCG37 (PDR9) or both transporters. Comparison of the metabolite profiles indicated distinct roles for each ABC transporter in root exudation. Thymidine exudation could be attributed to ABCG36 function, whereas coumarin exudation was strongly reduced only in ABCG37 deficient plants. However, coumarin exudation was compromised in abcg37 mutants only with respect to certain metabolites of this substance class. The specificity of ABCG37 for individual coumarins was further verified by a targeted LC-MS based coumarin profiling method. The response to iron deficiency, which is known to strongly induce coumarin exudation, was also investigated. In either treatment, the distribution of individual coumarins between roots and exudates in the investigated genotypes suggested the involvement of ABCG37 in the exudation specifically of highly oxygenated rather than monohydroxylated coumarins.
Publikation

Wasternack, C. A plant's balance of growth and defense - revisited New Phytol 215, 1291-1294, (2017) DOI: 10.1111/nph.14720

This article is a Commentary on Major et al., 215: 1533–1547.
Publikation

Wasternack, C.; Song, S. Jasmonates: biosynthesis, metabolism, and signaling by proteins activating and repressing transciption J Exp Bot 68, 1303-1321, (2017) DOI: 10.1093/jxb/erw443

The lipid-derived phytohormone jasmonate (JA) regulates plant growth, development, secondary metabolism, defense against insect attack and pathogen infection, and tolerance to abiotic stresses such as wounding, UV light, salt, and drought. JA was first identified in 1962, and since the 1980s many studies have analyzed the physiological functions, biosynthesis, distribution, metabolism, perception, signaling, and crosstalk of JA, greatly expanding our knowledge of the hormone’s action. In response to fluctuating environmental cues and transient endogenous signals, the occurrence of multilayered organization of biosynthesis and inactivation of JA, and activation and repression of the COI1–JAZ-based perception and signaling contributes to the fine-tuning of JA responses. This review describes the JA biosynthetic enzymes in terms of gene families, enzymatic activity, location and regulation, substrate specificity and products, the metabolic pathways in converting JA to activate or inactivate compounds, JA signaling in perception, and the co-existence of signaling activators and repressors
Publikation

Liu, S.; Ziegler, J.; Zeier, J.; Birkenbihl, R. P.; Somssich, I. E. Botrytis cinerea B05.10 promotes disease development in Arabidopsis by suppressing WRKY33-mediated host immunity Plant Cell Environ 40, 2189-2206, (2017) DOI: 10.1111/pce.13022

The large WRKY transcription factor family is mainly involved in regulating plant immune responses. Arabidopsis WRKY33 is a key transcriptional regulator of hormonal and metabolic processes towards Botrytis cinerea strain 2100 infection and is essential for resistance. In contrast to B. cinerea strain 2100, the strain B05.10 is virulent on wild-type (WT) Col-0 Arabidopsis plants highlighting the genetic diversity within this pathogen species. We analysed how early WRKY33-dependent responses are affected upon infection with strain B05.10 and found that most of these responses were strongly dampened during this interaction. Ectopic expression of WRKY33 resulted in complete resistance towards this strain indicating that virulence of B05.10, at least partly, depends on suppressing WRKY33 expression/protein accumulation. As a consequence, the expression levels of direct WRKY33 target genes, including those involved in the biosynthesis of camalexin, were also reduced upon infection. Concomitantly, elevated levels of the phytohormone abscisic acid (ABA) were observed. Molecular and genetic studies revealed that ABA negatively influences defence to B05.10 and effects jasmonic acid/ethylene (JA/ET) and salicylic acid (SA) levels. Susceptibility/resistance was determined by the antagonistic effect of ABA on JA, and this crosstalk required suppressing WRKY33 functions at early infection stages. This indicates that B. cinerea B05.10 promotes disease by suppressing WRKY33-mediated host defences.
Publikation

Wasternack, C. The Trojan horse coronatine: the COI1–JAZ2–MYC2,3,4–ANAC019,055,072 module in stomata dynamics upon bacterial infection. New Phytol 213, 972-975, (2017) DOI: 10.1111/nph.14417

Coronatine (COR) is a phytotoxin produced by a plasmid-encoded operon of genes in several strains of Pseudomonas syringae (Bender et al., 1999). It is a mimic of the defense-associated phytohormone jasmonic acid isoleucine and delivered by the phytopathogenic bacterium to gain access to host plants through stomatal entry and to repress a specific sector of plant immunity. In this issue of New Phytologist (pp. 1378–1392) Gimenez-Ibanez et al. reveal exciting insights into the transcriptional regulation of COR/jasmonic acid isoleucine-governed transcriptional networks modulating stomatal aperture during bacterial invasion.
Publikation

Sharma, V.K.; Monostori, T.; Hause, B.; Maucher, H.; Göbel, C.; Hornung, E.; Hänsch, R.; Bittner, F.; Wasternack, C.; Feussner, I.; Mendel, R.R.; Schulze, J. Genetic transformation of barley to modify expression of a 13-lipoxygenase Acta Biol. Szeged 49, 33-34 , (2005)

Immature scutella of barley were transformed with cDNA coding for a 13-li-poxygenase of barley (LOX-100) via particle bombardment. Regenerated plants were tested by PAT-assay, Western-analysis and PCR-screening. Immunocytochemical assay of T0 plants showed expression of the LOX cDNA both in the chloroplasts and in the cytosol, depending on the presence of the chloroplast signal peptide sequences in the cDNA. A few transgenic plants containing higher amounts of LOX-derived products have been found. These are the candidates for further analysis concerning pathogen resistance.
Publikation

Durgbanshi, A.; Arbona, V.; Pozo, O.; Miersch, O.; Sancho, J.V.; Gómez-Cadenas, A. Simultaneous determination of multiple phytohormones in plant extracts by liquid chromatography-electrospray tandem mass spectrometry J. Agric. Food Chem. 53, 8437-8442, (2005)

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Publikation

Gerhard, B.; Fischer, K.; Balkenhohl, T.J.; Pohnert, G.; Kühn, H.; Wasternack, C.; Feussner, I. Lipoxygenase-mediated metabolism of storage lipids in germinating sunflower cotyledons and b-oxidation of (9Z,11E,13S)-13-hydroxy-octadeca-9,11-dienoic acid by the cotyledonary glyoxysomes Planta 220, 919-930, (2005)

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Publikation

Denzano, A.M.; Vigliocco, A.; Miersch, O.; Abdala, G. Octadecanoid levels during stolon to tuber transition in potato. Potato Res. 107-115, (2005)

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Publikation

Meixner, C.; Ludwig-Müller, J.; Miersch, O.; Gresshoff, P.; Staehlin, C.; Vierheilig, H. Lack of mycorrhizal autoregulation and phytohormonal changes in the supernodulating soybean mutant nts1007 Planta 222, 709-715, (2005)

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