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Plants sense the presence of potentially competing nearby individuals as a reduction in the red to far-red ratio of the incoming light. In anticipation of eventual shading, a set of plant responses known as the shade avoidance syndrome (SAS) is initiated soon after detection of this signal by the phytochrome photoreceptors. Here we analyze the function of PHYTOCHROME RAPIDLY REGULATED1 (PAR1) and PAR2, two Arabidopsis thaliana genes rapidly upregulated after simulated shade perception. These genes encode two closely related atypical basic helix-loop-helix proteins with no previously assigned function in plant development. Using reverse genetic approaches, we show that PAR1 and PAR2 act in the nucleus to broadly control plant development, acting as negative regulators of a variety of SAS responses, including seedling elongation and photosynthetic pigment accumulation. Molecularly, PAR1 and PAR2 act as direct transcriptional repressors of two auxin-responsive genes, SMALL AUXIN UPREGULATED15 (SAUR15) and SAUR68. Additional results support that PAR1 and PAR2 function in integrating shade and hormone transcriptional networks, rapidly connecting phytochrome-sensed light changes with auxin responsiveness.
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http://dx.doi.org/10.1038/sj.emboj.7601890 | DOI Listing |
Front Oncol
July 2025
Department of Pharmacology, University Medicine Greifswald, Greifswald, Germany.
Background: Glioblastoma (GBM) remains the most aggressive and common malignant brain tumor in adults, often accompanied by venous thromboembolism due to hypercoagulability. Protease-activated receptors (PAR1-4) are thought to influence GBM progression, which in this study led to examine their expression in both tissue from GBM patients and in a GBM cell model.
Methods: Using quantitative PCR and immunoblot analyses, we investigated the expression of PAR1-4 in human GBM samples compared to non-malignant brain and evaluated its role in patient survival.
Front Oncol
July 2025
Pharmacology and Toxicology, University Medicine Oldenburg, Carl von Ossietzky Universität Oldenburg, Oldenburg, Germany.
Colon cancer is among the most common cancer types worldwide. Signaling pathways that control cell proliferation and migration play a crucial role in its progression. The G-protein-coupled protease-activated receptors (PARs) are associated mediators in this process.
View Article and Find Full Text PDFInflammopharmacology
July 2025
Faculty of Pharmaceutical Sciences, University of Central Punjab (UCP), Lahore, 54000, Pakistan.
Rheumatoid arthritis (RA) is an autoimmune condition that involves inflammation of the joints, cartilage destruction, and progressive bone loss. RA is a disabling disease that may result in poor quality of life and permanent physical disability. Current interventions like NSAIDs, DMARDs, and biologics are more symptom-relieving and disease-preventing.
View Article and Find Full Text PDFMol Syndromol
May 2025
Center for Reproductive Medicine, Yokohama City University Medical Center, Yokohama, Japan.
Introduction: Turner syndrome is a complicated gonadal insufficiency, infertility, and endocrine disease caused by the partial to complete loss of one X chromosome. Women with Turner syndrome have been reported to show altered effector T-cell subgroups; however, the relationship between T-cell subgroups and chromosome type remains unknown.
Methods: In this study, we investigated immune abnormalities and karyotypes of Turner syndrome.
Am J Physiol Lung Cell Mol Physiol
July 2025
Department of Cardiovascular Medicine, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.
Activated factor X (FXa) induces inflammatory response and cell proliferation in various cell types via activation of proteinase-activated receptor-1 (PAR) and/or PAR. We thus aimed to investigate the impact of FXa on the development of pulmonary arterial hypertension (PAH) and the mechanisms involved. The effects of edoxaban, a selective FXa inhibitor, on hemodynamic, right ventricular (RV) hypertrophy, and vascular remodeling were evaluated in a monocrotaline (MCT)-exposed pulmonary hypertension (PH) rat model.
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