Browsing by Subject "Schmalwand <Arabidopsis>"

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External nutrition stimuli induced proteome and phosphoproteome responses of maize root hairs and arabidopsis root microsomal fraction
(2021) Li, Zhi; Schulze, Waltraud
This work studied how the proteome from young maize root hair cells responds to different nutrition deprivation, and gives perspectives to the possible involvement of NRT1.1 and NRT2.1 in regulating root membrane phosphoproteome responses. This work also proposes a phospho-switch model that may explain how the NRT2.1 activity was regulated.
Funktionelle Charakterisierung der Subtilase At4g21630 aus Arabidopsis thaliana
(2012) Knappenberger, Mathias; Schaller, Andreas
The goal of this thesis was the molecular and functional characterization of the A. thaliana subtilase At4g21630.
Membrane transport and long-distance translocation of urea in Arabidopsis thaliana
(2011) Bohner, Anne; von Wirén, Nicolaus
Urea is a soil nitrogen (N) form available to plant roots and a secondary N metabolite liberated in plant cells by protein degradation, especially during senescence. Despite the fact that urea also represents the most widespread form in N fertilizers used in agricultural plant production, membrane transporters that might contribute to urea uptake in plant roots or urea retranslocation in senescent leaves have so far been characterized only in heterologous systems. The first part of the thesis investigated a role of the H+/urea cotransporter AtDUR3 in N nutrition of Arabidopsis thaliana plants. T-DNA insertion lines with a defective expression in AtDUR3 showed impaired growth on urea as a sole nitrogen source. In transgenic lines expressing an AtDUR3-promoter-GFP construct, promoter activity was upregulated under N deficiency and localized to the rhizodermis, including root hairs, as well as to the cortex in more basal root zones. The AtDUR3 protein accumulated in plasma membrane-enriched protein fractions, and AtDUR3 gene expression in N-deficient roots was repressed by ammonium and nitrate but induced after supply of urea. Higher urea accumulation in roots of wild-type plants relative to the T-DNA insertion lines confirmed that urea was the transported substrate of AtDUR3. Influx of 15N-labeled urea allowed the calculation of an affinity constant of 4 µM. These results indicated that AtDUR3 is the major transporter for high-affinity urea uptake in Arabidopsis roots and suggested that the high substrate affinity of AtDUR3 reflects an adaptation to the low urea levels usually found in unfertilized soils. A physiological function of urea and its transporters in leaves was investigated in the second part of the thesis. Currently it is unclear whether transport and metabolism of urea might limit the overall retranslocation of N during senescence. AtDUR3 transcript levels were only slightly de-repressed under N starvation, but strongly increased in senescent leaves. Urea concentrations in leaf samples of different plant and leaf age showed a strong increase after plants turned into generative growth. In parallel, mRNA as much as the protein abundance of AtDUR3 increased with leaf age. The analysis of leaf petiole exudates revealed that urea was indeed a translocated N form and urea-N represented approx. 13% of the total amino acid-N irrespective of the N status of the plant. Urea concentrations determined in apoplastic wash fluids supported a role of AtDUR3 in urea retrieval from the leaf apoplast, and transgenic AtDUR3-promoter-GUS lines indicated a localization of AtDUR3 promoter activity in the vasculature of old leaves. Thus, AtDUR3 might keep internal urea in the cytosol by urea retrieval from the apoplast, allowing urea to be transported to the vascular bundle, where it is either passively loaded to the phloem or converted into amino acids for long-distance N translocation. A strong daytime-dependent phenotype with shorter leaf petioles of an Arabidopsis line overexpressing AtDUR3 led to an in silico analysis of the AtDUR3 promoter sequence revealing that salicylic acid (SA) appears to induce AtDUR3 gene expression in senescent leaves. SA is well known for its involvement in the initiation of senescence. A strongly enhanced uptake capacity for 15N-labeled urea in N-sufficient Arabidopsis roots after SA pretreatment indicated that SA might be able to mimic N-deficiency conditions, paving the way to the possibility that SA builds a regulatory link between developmental and N deficiency-induced senescence.
Prediction of protein-protein complexes by combining size exclusion chromatography and mass spectrometric analysis
(2021) Gilbert, Max; Schulze, Waltraud
Two major objectives were pursued and met in this study. First, the goal was to add to the scientific toolbox a diligent method for uncovering PPi dynamics on a proteomic scale, with a focus on plant membranes. There are large-scale or high-throughput approaches, but they rely on genetically modified proteins or heterologous expression systems to describe PPi outside of their natural context. Similarly, those methods are incapable of describing the dynamics of protein interactions. In course of this study, a co-elution based approach was combined with modern mass spectrometric label free quantification in order to investigate PPi and interaction dynamics on a proteomic scale. A rigorous data processing pipeline was developed to not only address known fallacies of using co-elution based methods (such as for example random co elution), but also to access and utilize meta-information in form of protein abundance and protein network connectivity to draw conclusions not only on proteomic scale, but also for individual proteins. In total, 6.928 individual proteins extracted from Arabidopsis thaliana root membranes were detected under different nutritional conditions (full nutrition, nitrogen starvation and nitrogen resupply). The data processing pipeline described in this study was used to predict and discover connectivity information for at least 2.058 of these proteins. Each step in data processing was validated by comparison to database confirmed interactions to improve filtering criteria. Protein abundance was evaluated through a unique ranking system, allowing a seamless integration as network attributes for each condition. From the suggested interaction data, an interactome network of the various nutritional conditions was reconstructed. Using different network parameters from graph theory, protein significance and dynamic conditional changes were described. Second, this study applied the aforementioned approach to identify relevant proteins involved in nitrogen signaling in Arabidopsis thaliana root membranes. Through correlation analysis and network reconstruction, receptor kinase AT5G49770 was identified as a component of the nitrogen signaling network that collaborates with co-receptor QSK1, BAK1, the nitrogen transporter NRT2.1 and proton pump AHA2. In response to nitrogen deficiency, the network parameters of AT5G49770 reacted strongly and its involvement was demonstrated by a phenotypic similarity to knock-out lines of NRT2.1, NRT1.1 and AHA2 during a root growth assay of Arabidopsis seedlings. The interaction between QSK1 and BAK1 was further confirmed using FRET/FLIM microscopy and pulldown assays. These findings show that combining a co-elution based approach with a rigorous data processing pipeline and network analysis is suitable to study the protein interaction environment and signal response dynamics in plant root membranes. The modular experimental design allows for a simple adaptation to study different stimuli and the unbiased proteomic approach yields results for proteins regardless of the individual scientific focus. Meta-information such as protein abundance and network connectivity parameters can be used to prospect and identify important proteins involved in stress response dynamics. The author of this study is confident that the proteomic data produced can be utilized in further research and contributes to the understanding of nitrogen signaling in plant root membranes. Through integration of the data processing pipeline and adaptation to different scientific scenarios, valuable information beyond protein interaction is gained. Thus, this work makes an important contribution to the advancement of proteomic analysis and data interpretation methodology.
Regulation of ammonium transport in Arabidopsis thaliana
(2022) Ganz, Pascal; Ludewig, Uwe
The overarching question of this thesis deals with how plants ensure the selective uptake of ammonium while maintaining ion and pH homeostasis. A key component of this is ammonium transporters (AMTs) with high affinity towards their substrate, which are at the same time part of a multilayered protection system against uncontrolled ammonium influx. Conserved protein sequences inside the transporter were analyzed as well as the regulatory system based on post-translational modification of the transporter.
Transcriptional and proteomic responses towards early nitrogen depletion in Arabidopsis thaliana
(2016) Menz, Jochen; Ludewig, Uwe
Plant roots acquire nitrogen predominantly as ammonium and nitrate, which besides serving as nutrients, also have signaling roles. Re-addition of nitrate to starved plants rapidly and di-rectly transcriptionally re-programs the metabolism and induces root architectural changes, but the earliest responses to nitrogen deprivation are unknown. In this thesis, the early transcriptional response of developed roots to nitrate or ammonium deprivation were analyzed in two Arabidopsis ecotypes contrasting in their nitrogen use efficiency: the inefficient genotype Col-0 and the efficient Tsu-0. The rapid transcriptional repression of known nitrate-induced genes proceeded the tissue NO3- concentration drop, with the transcription factor genes LBD37/38 and HRS1/HHO1 among those with earliest significant change. Some transcripts were stabilized by nitrate, but similar rapid transcriptional repression occurred in loss-of-function mutants of the nitrate response factor NLP7. In contrast, an early transcriptional response to ammonium deprivation was almost completely absent. In Col-0, the analysis was extended with the proteome and phospho-proteome resulting in a rapid and transient perturbation of the proteome induced by ammonium deprivation and a differential phosphorylation pattern in proteins involved in adjusting the pH and cation homeostasis, plasma membrane H+, NH4+, K+ and water fluxes. Fewer differential phosphorylation patterns in transporters, kinases and other proteins occurred with nitrate deprivation. The deprivation responses are not just opposite to the resupply responses, identify NO3--deprivation induced mRNA decay and signaling candidates potentially reporting the external nitrate status to the cell. Transcrip-tome comparison revealed only few N-nutrition related genes between both ecotypes contributing the increased NUE of Tsu-0, which probably relies on higher biomass accumulation. Besides, Tsu-0 confirmed the transcriptional depletion response of Col-0.
Transporters mediating ammonium uptake in plants and their regulation by the abiotic stress signaling pathway
(2023) Porras Murillo, Romano; Ludewig, Uwe
Nitrogen nutrition refers to the uptake, assimilation, and utilization of ammonium, nitrate, and organic nitrogen sources. Ammonium is energetically a more cost-effective nitrogen source than nitrate but can be toxic for plants, and its use by plants is regulated at different levels. Ammonium transporters (AMTs) take up ammonium and are localized primarily in plant roots, working as trimers in the plasma membrane. Under high external ammonium concentrations, phosphorylation in AMTs C-termini shuts down transport to avoid toxicity. This phosphorylation is performed by CIPK23, a kinase shown to be inhibited by Clade A PP2Cs. This study aimed to characterize AMTs from wheat and analyze their transcriptional response to ammonium. Another aim was to determine the role of clade A PP2Cs and PYR/PYL receptor proteins for abscisic acid in ammonium nutrition. Chapter I describes the physiological responses of winter wheat to different nitrogen sources and ammonium concentrations. The plants mainly used root morphological responses to adapt to differences in the nitrogen source. High external concentrations of ammonium reduced plant growth, while these conditions induced the expression of TaAMT1;1 and TaAMT1;2. In Chapter II, we studied the capacity of TaAMT2s to transport ammonium and their transcriptional responsiveness to ammonium nutrition. From the six TaAMT2s, only TaAMT2;1 could transport ammonium in a yeast complementation line. Besides, its expression in roots is lower under ammonium than under nitrate. The expression pattern among the remaining TaAMT2s (TaAMT2;2-TaAMT2;6) is similar, with higher expression under ammonium, in both roots and leaves, compared to nitrate. Chapter III focused on the role of the PP2C phosphatase ABI1 (ABA-insensitive 1) in ammonium nutrition and the effect of external ammonium concentrations on ABA concentrations. Ammonium increased ABA concentrations in roots by activating ABA-GE, meaning ammonium toxicity could be sensed as abiotic stress through ABA. Without ammonium, ABI1 dephosphorylates AMTs and inhibits CIPK23; with ammonium, ABA-PYR/PYL complex-mediated inhibition of ABI1 releases CIPK23 to phosphorylate AMTs and avoids ammonium toxicity. Finally, in Chapter IV, we studied the role of AIP1 and its ammonium-dependent regulator, PYL8, in nitrogen nutrition. We described the function of AIP1, which was redundant to ABI1 in AMT regulation. Based on ammonium-dependent root architecture changes, and higher auxin accumulation in pyl8-1 root tips compared to the wild type, we suggest that PYL8 is involved in root-phenotype modulation in an ammonium-dependent manner.