Arabidopsis Col0 5 week-old plants: effect of DCMU on high-light treated plants
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ABSTRACT: Transcriptional profiling of fully developed leaves of Arabidopsis Col0 plants treated with 50 µM DCMU in high light stress.The aim of the experiment was to determine the specific effect of uncoupling electron transport from Photosystem II (by treatment of leaves with DCMU) under high light conditions compared with the effect of high light treatment alone.
Project description:Transcriptional profiling of fully developed leaves of Arabidopsis Col0 after 30 min of high-light stress (1000 umol*m-2*s-1). Goal was to find early transcriptional responses to immediate high-light stress, before acclimation responses appear.
Project description:Transcriptional profiling of fully developed leaves of Arabidopsis Col0 plants heat-stressed for 25 min at 27.7 degrees Celsius. Goal was to isolate and study the influence of temperature and vpd change in the 30 min high light-stress experiments, since the Isolight rises leaf temperature to 27.5C and increases the vpd from 5 min of exposure.
Project description:Purpose: Overexpression of VDE, ZEP and PsbS (VPZ) in plants confers enhanced dynamics of non-photochemical quenching of NPQ under FL light. VPZ overexpression in tobacco has been reported to increase plant biomass under fluctuating light. However, our work demonstrates that such strategy had no advantageous effect when asssayed in Arabidopsis thaliana. To investigate whether this observation is due to impairements in signaling pathways due to the expression of VPZ in Arabidopsis thaliana, transcriptome profiles of VPZ plants exposed to fluctuating light or high light were conducted. Methods: mRNA-Seq libraries were prepared from 21-d-old Col0 plants and VPZ lines #2 and #4 cultivated under standard control conditions and then exposed to fluctuating light or high light for 6h and 30 h. Standard Illumina protocols were used for mRNA-Seq sequencing. Triplicates for 3 independent plants were used. Adaptor sequences were removed with Trimmomatic and resulting reads mapped to the Arabidopsis genome (Araport11) with Tophat 2.1.1. Normalised counts reads were quantified with featureCounts to provide processed data files and differential expression analysis were conducted with the DEseq2 pipeline. Results: mRNA-Seq libraries contained app. 9 milion reads each. Transcript analysis for differential gene expression was conducted according to the Tophat/featureCounts/DESeq2 pipeline. To declare significant differences, a cut-off for absolute log2(FC) ≥ 1 compared to the initial timepoint (0h) and FDR ≤ 0.05 was applied. Significant transcripts exclusively found for Col0 and both VPZ lines in each time-point were considered for subsequent analysis. Accordingly, 528 and 415 transcripts (6h and 30h) were found for Col0, and 326 and 896 (6h and 30h) for the VPZ under control conditions. For FL, 490 and 591 transcripts qualified as specific (6h and 30h) for Col0 and 938 and 401 (6h and 30h) for VPZ. Strikingly, the amount of transcripts raised to 2847 and 2902 DEGs (6h and 30h) for Col0, whereas only 546 and 304 (6h and 30h) were detected for VPZ under HL. transcripts). Conclusions: the overexpression of VPZ in Arabidopsis leads to particular transcriptome response under fluctuating light related to changes in photosynthesis and response to abscisic acid, among all. However, Col0 displayed wider transcriptome responses than VPZ after exposure to high light .
Project description:gnp07_regeneome_embryogenesis - embryogenesis col0 - Identify genes involved in somatic embryogenesis - compare embryogenic areas of a callus with undifferenciate area in the same callus
Project description:To analyze the impact of photosynthetic redox signals, light sources with spectral qualities that preferentially excite either Photosystem I (PSI light) or Photosystem II (PSII light) were used. The light sources have been described in (Fey et al., 2005). Strong reduction and oxidation signals were induced by light shifts from PSI to PSII light (PSI-II) and the reverse light shift (PSII-I), respectivly. The acclimation responses were monitored at 0.5, 2, 8, and 48h after a light shift. Samples taken prior to changing the light quality (0h) served as control. Keywords: photosynthesis, redox regulation, light acclimation, retrograde signalling, long term response
Project description:Transcriptome profiling (RNA-seq) of local and systemic tissue of Arabidopsis Col plants exposed to a local treatment of high light, heat stress and a combination of high light and heat stress on the same leafs or in different leaves
Project description:Transcriptomic analysis by RNAseq of Col leaves subjected to high light, heat stress and the combination of high light and heat stress
Project description:Series of 6 repetitions of hybridization of treatment (PSI_DCMU) and control (PSI) each. Comparison of plants grown under PSI-specific light and treated with the electron transport inhibitor DCMU versus plants grown under PSI-specific light without DCMU treatment. T. Pfannschmidt, unpublished Keywords: repeat sample