Dinesh, D. C.; Calderón Villalobos, L. I. A.; Abel, S. Structural Biology of Nuclear Auxin Action Trends Plant Sci. 21, 302-316, (2016) DOI: 10.1016/j.tplants.2015.10.019
Auxin coordinates plant development largely via hierarchical control of gene expression. During the past decades, the study of early auxin genes paired with the power of Arabidopsis genetics have unraveled key nuclear components and molecular interactions that perceive the hormone and activate primary response genes. Recent research in the realm of structural biology allowed unprecedented insight into: (i) the recognition of auxin-responsive DNA elements by auxin transcription factors; (ii) the inactivation of those auxin response factors by early auxin-inducible repressors; and (iii) the activation of target genes by auxin-triggered repressor degradation. The biophysical studies reviewed here provide an impetus for elucidating the molecular determinants of the intricate interactions between core components of the nuclear auxin response module.
Wasternack, C.; Strnad, M. Jasmonate signaling in plant stress responses and development – active and inactive compounds New Biotechnology 33 B, 604-613, (2016) DOI: 10.1016/j.nbt.2015.11.001
Jasmonates (JAs) are lipid-derived signals mediating plant responses to biotic and abiotic stresses and in plant development. Following the elucidation of each step in their biosynthesis and the important components of perception and signaling, several activators, repressors and co-repressors have been identified which contribute to fine-tuning the regulation of JA-induced gene expression. Many of the metabolic reactions in which JA participates, such as conjugation with amino acids, glucosylation, hydroxylation, carboxylation, sulfation and methylation, lead to numerous compounds with different biological activities. These metabolites may be highly active, partially active in specific processes or inactive. Hydroxylation, carboxylation and sulfation inactivate JA signaling. The precursor of JA biosynthesis, 12-oxo-phytodienoic acid (OPDA), has been identified as a JA-independent signaling compound. An increasing number of OPDA-specific processes is being identified. To conclude, the numerous JA compounds and their different modes of action allow plants to respond specifically and flexibly to alterations in the environment.
Floková, K.; Feussner, K.; Herrfurth, C.; Miersch, O.; Mik, V.; Tarkowská, D.; Strnad, M.; Feussner, I.; Wasternack, C.; Novák, O. A previously undescribed jasmonate compound in flowering Arabidopsis thaliana – The identification of cis-(+)-OPDA-Ile. Phytochemistry 122, 230-237, (2016) DOI: 10.1016/j.phytochem.2015.11.012
Jasmonates (JAs) are plant hormones that integrate external stress stimuli with physiological responses. (+)-7-iso-JA-L-Ile is the natural JA ligand of COI1, a component of a known JA receptor. The upstream JA biosynthetic precursor cis-(+)-12-oxo-phytodienoic acid (cis-(+)-OPDA) has been reported to act independently of COI1 as an essential signal in several stress-induced and developmental processes. Wound-induced increases in the endogenous levels of JA/JA-Ile are accompanied by two to tenfold increases in the concentration of OPDA, but its means of perception and metabolism are unknown. To screen for putative OPDA metabolites, vegetative tissues of flowering Arabidopsis thaliana were extracted with 25% aqueous methanol (v/v), purified by single-step reversed-phase polymer-based solid-phase extraction, and analyzed by high throughput mass spectrometry. This enabled the detection and quantitation of a low abundant OPDA analog of the biologically active (+)-7-iso-JA-L-Ile in plant tissue samples. Levels of the newly identified compound and the related phytohormones JA, JA-Ile and cis-(+)-OPDA were monitored in wounded leaves of flowering Arabidopsis lines (Col-0 and Ws) and compared to the levels observed in Arabidopsis mutants deficient in the biosynthesis of JA (dde2-2, opr3) and JA-Ile (jar1). The observed cis-(+)-OPDA-Ile levels varied widely, raising questions concerning its role in Arabidopsis stress responses.
Ziegler, J.; Schmidt, S.; Chutia, R.; Müller, J.; Böttcher, C.; Strehmel, N.; Scheel, D.; Abel, S. Non-targeted profiling of semi-polar metabolites
in Arabidopsis root exudates uncovers a role for coumarin secretion and
lignification during the local response to phosphate limitation J Exp Bot 67, 1421-1432, (2016) DOI: 10.1093/jxb/erv539
Plants have evolved two major strategies to cope with phosphate (Pi) limitation. The systemic response, mainly comprising increased Pi uptake and metabolic adjustments for more efficient Pi use, and the local response, enabling plants to explore Pi-rich soil patches by reorganization of the root system architecture. Unlike previous reports, this study focused on root exudation controlled by the local response to Pi deficiency. To approach this, a hydroponic system separating the local and systemic responses was developed. Arabidopsis thaliana genotypes exhibiting distinct sensitivities to Pi deficiency could be clearly distinguished by their root exudate composition as determined by non-targeted reversed-phase ultraperformance liquid chromatography electrospray ionization quadrupole-time-of-flight mass spectrometry metabolite profiling. Compared with wild-type plants or insensitive low phosphate root 1 and 2 (lpr1 lpr2) double mutant plants, the hypersensitive phosphate deficiency response 2 (pdr2) mutant exhibited a reduced number of differential features in root exudates after Pi starvation, suggesting the involvement of PDR2-encoded P5-type ATPase in root exudation. Identification and analysis of coumarins revealed common and antagonistic regulatory pathways between Pi and Fe deficiency-induced coumarin secretion. The accumulation of oligolignols in root exudates after Pi deficiency was inversely correlated with Pi starvation-induced lignification at the root tips. The strongest oligolignol accumulation in root exudates was observed for the insensitive lpr1 lpr2 double mutant, which was accompanied by the absence of Pi deficiency-induced lignin deposition, suggesting a role of LPR ferroxidases in lignin polymerization during Pi starvation.
Bücher und Buchkapitel
Jasmonic acid and other fatty-acid-derived compounds called oxylipins are signals in stress responses and development of plants. The receptor complex, signal transduction components as well as repressors and activators in jasmonate-induced gene expression have been elucidated. Different regulatory levels and cross-talk with other hormones are responsible for the multiplicity of plant responses to environmental and developmental cues.
Wasternack, C.; Hause, B. OPDA-Ile – a new JA-Ile-independent signal? Plant Signal Behav 11, e125364600, (2016) DOI: 10.1080/15592324.2016.1253646
AbstractExpression takes place for most of the jasmonic acid (JA)-induced genes in a COI1- dependent manner via perception of its conjugate JA-Ile in the SCFCOI1-JAZ co-receptor complex. There are, however, numerous genes and processes, which are preferentially induced COI1-independently by the precursor of JA, 12-oxo-phytodienoic acid (OPDA). After recent identification of the Ile-conjugate of OPDA, OPDA-Ile, biological activity of this compound could be unequivocally proven in terms of gene expression. Any interference of OPDA, JA, or JA-Ile in OPDA-Ile-induced gene expression could be excluded by using different genetic background. The data suggest individual signaling properties of OPDA-Ile. Future studies for analysis of an SCFCOI1-JAZ co-receptor-independent route of signaling are proposed.
Hoehenwarter, W.; Mönchgesang, S.; Neumann, S.; Majovsky, P.; Abel, S.; Müller, J. Comparative expression profiling reveals a role of the root apoplast in local phosphate response BMC Plant Biol 16 , 106, (2016) DOI: 10.1186/s12870-016-0790-8
BackgroundPlant adaptation to limited phosphate availability
comprises a wide range of responses to conserve and remobilize internal
phosphate sources and to enhance phosphate acquisition. Vigorous
restructuring of root system architecture provides a developmental
strategy for topsoil exploration and phosphate scavenging. Changes in
external phosphate availability are locally sensed at root tips and
adjust root growth by modulating cell expansion and cell division. The
functionally interacting Arabidopsis genes, LOW PHOSPHATE RESPONSE 1 and
2 (LPR1/LPR2) and PHOSPHATE DEFICIENCY RESPONSE 2 (PDR2), are key
components of root phosphate sensing. We recently demonstrated that the
LOW PHOSPHATE RESPONSE 1 - PHOSPHATE DEFICIENCY RESPONSE 2 (LPR1-PDR2)
module mediates apoplastic deposition of ferric iron (Fe3+) in the
growing root tip during phosphate limitation. Iron deposition coincides
with sites of reactive oxygen species generation and triggers cell wall
thickening and callose accumulation, which interfere with cell-to-cell
communication and inhibit root growth.ResultsWe took advantage of
the opposite phosphate-conditional root phenotype of the phosphate
deficiency response 2 mutant (hypersensitive) and low phosphate response
1 and 2 double mutant (insensitive) to investigate the phosphate
dependent regulation of gene and protein expression in roots using
genome-wide transcriptome and proteome analysis. We observed an
overrepresentation of genes and proteins that are involved in the
regulation of iron homeostasis, cell wall remodeling and reactive oxygen
species formation, and we highlight a number of candidate genes with a
potential function in root adaptation to limited phosphate availability.
Our experiments reveal that FERRIC REDUCTASE DEFECTIVE 3 mediated,
apoplastic iron redistribution, but not intracellular iron uptake and
iron storage, triggers phosphate-dependent root growth modulation. We
further highlight expressional changes of several cell wall-modifying
enzymes and provide evidence for adjustment of the pectin network at
sites of iron accumulation in the root.ConclusionOur study
reveals new aspects of the elaborate interplay between phosphate
starvation responses and changes in iron homeostasis. The results
emphasize the importance of apoplastic iron redistribution to mediate
phosphate-dependent root growth adjustment and suggest an important role
for citrate in phosphate-dependent apoplastic iron transport. We
further demonstrate that root growth modulation correlates with an
altered expression of cell wall modifying enzymes and changes in the
pectin network of the phosphate-deprived root tip, supporting the
hypothesis that pectins are involved in iron binding and/or phosphate