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Mutwil-Anderwald, D.

Publications and source records attributed to Mutwil-Anderwald, D..

3 recordsLinked to original sources

Parallel comparison reveals conservation and re-wiring of abiotic stress response networks across three plant species

Abiotic stresses trigger significant alterations in plant morphology, yield, and nutrient composition. To counter these stresses, plants have developed strategies involving gene expression adjustments, impacting their growth and development to ensure survival and reproduction. Although transcriptomic studies have extensively examined stress responses, our understanding of their conservation remains limited. We conducted a comprehensive study on the effects of 24 different environmental and nutrient conditions on the growth yield of three hydroponically grown leafy crops (cai xin, lettuce, and spinach). This research identified optimal conditions for maximizing yield and vitamin content and pinpointed conditions that induce abiotic stress. Our findings highlight the substantial impact of stress on various plant functions, with photosynthesis playing a pivotal role in vitamin content regulation. A detailed comparative analysis of gene expression across these crops revealed conserved gene sets potentially crucial for abiotic stress response. Furthermore, we introduced a novel method that merges regression and genomics to construct reliable gene regulatory networks for stress response. Despite significant conservation of these networks among the studied crops, their key transcription factors showed limited similarity to those in Arabidopsis thaliana, suggesting notable functional divergence. To give easy access to the data and comparative transcriptomic tools, we established StressPlantTools, an public online database (https://stress.sbs.ntu.edu.sg/), facilitating further research into stress-responsive genes.

plant biology↗

Genomic, transcriptomic, and metabolomic analysis of Traditional Chinese Medicine plant Oldenlandia corymbosa reveals the biosynthesis and mode of action of anti-cancer metabolites

Natural products from traditional medicinal plants are valuable candidates for clinical cancer therapy. Plants from the Oldenlandia-Hedyotis complex are popular ingredients of Traditional Chinese Medicine (TCM), however a major hurdle in the plant bioprospecting process of TCM plants is that the active metabolites, their biosynthetic pathways, and mode of action are often unknown. We show that Oldenlandia corymbosa extracts are active against breast cancer cell lines. To study the genes involved in the biosynthesis of active compounds in this medicinal plant, we assembled a high-quality genome. We show that the main active compound is ursolic acid and that abiotic stresses cause changes in anti-cancer activity, metabolite composition, and gene expression of plants. To reveal the mode of action of ursolic acid, we show that cancer cells undergo mitotic catastrophe, and we identify three high-confidence protein binding targets by Cellular Thermal Shift Assay (CETSA) and reverse docking.

plant biology↗

A G protein-coupled receptor-like module regulates Cellulose Synthase secretion from the endomembrane system in Arabidopsis

Cellulose synthesis is essential for plant morphology, water transport and defense, and provides raw material for biomaterials and fuels. Cellulose is produced at the plasma membrane by Cellulose Synthase (CESA) protein complexes (CSCs). CSCs are assembled in the endomembrane system and then trafficked from the Golgi apparatus and trans-Golgi Network (TGN) to the plasma membrane. Since CESA enzymes are only active in the plasma membrane, control of CSC secretion is a critical step in the regulation of cellulose synthesis. However, the regulatory framework for CSC secretion is not clarified. In this study, we identify members of a family of seven transmembrane domain-containing proteins (7TMs) as important for cellulose production during cell wall integrity stress. 7TM proteins are often associated with guanine nucleotide-binding protein (G) protein signalling and mutants in several of the canonical G protein complex components phenocopied the 7tm mutant plants. Unexpectedly, the 7TM proteins localized to the Golgi apparatus/TGN where they interacted with the G protein complex. Here, the 7TMs and G proteins regulated CESA trafficking, but did not affect general protein secretion. Furthermore, during cell wall stress, 7TMs localization was biased towards small CESA-containing vesicles, specifically associated with CSC trafficking. Our results thus outline how a G protein-coupled module regulates CESA trafficking and reveal that defects in this process lead to exacerbated responses upon exposure to cell wall integrity stress.

plant biology↗