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Arabidopsis mutants for mediator head, middle, tail, and kinase modules reveal distinct roles in regulating the transcriptional response to salt stress
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics. Instituto de Ciencias de la Ingeniería, Universidad de O’Higgins, Av. Libertador Gral. Bernardo O'Higgins 611, O'Higgins, Rancagua, Chile.
Umeå University, Faculty of Medicine, Department of Medical Biochemistry and Biophysics.
Institute for Biochemistry and Biology, University of Potsdam, Potsdam 14469, Germany.
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2026 (English)In: Plant Stress, E-ISSN 2667-064X, Vol. 19, article id 101189Article in journal (Refereed) Published
Abstract [en]

Environmental changes trigger stress responses in living organisms. Although the underlying mechanisms are only partly understood, they involve intricate signaling pathways and transcription factors (TFs). Mediator is a conserved co-regulator complex required for transcriptional regulation of all eukaryotic protein-encoding genes. However, its function in abiotic stress responses is elusive. Here, we describe global gene expression changes induced by salt stress in Arabidopsis thaliana . To investigate the involvement of Mediator, we analyzed med9, med16, med18 , and cdk8 mutants, each representing one of the four Mediator modules. Our results demonstrate that promoters of differentially expressed genes (DEGs) for each mutant are enriched for binding sites of specific TFs. Phenotypic analyses further support the transcriptomic data: med16 and med18 , and to a lesser extent cdk8 , exhibit defects typical to mutations that affect abscisic acid and anthocyanin metabolism and we identify dysregulated signaling molecules, TFs, and target genes in these pathways. Our results reveal how signals from different stress response pathways are dependent on, and integrated by, Mediator subunits to coordinate a functional response to salt stress.

Place, publisher, year, edition, pages
Elsevier, 2026. Vol. 19, article id 101189
Keywords [en]
cdk8, med16, med18, med9, Mediator, RNAseq, Salt stress
National Category
Medical Biotechnology (Focus on Cell Biology, (incl. Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy) Genetics and Genomics Bioinformatics and Computational Biology
Identifiers
URN: urn:nbn:se:umu:diva-248207DOI: 10.1016/j.stress.2025.101189Scopus ID: 2-s2.0-105025704274OAI: oai:DiVA.org:umu-248207DiVA, id: diva2:2026973
Funder
Knut and Alice Wallenberg Foundation, 2015-0056Swedish Foundation for Strategic Research, SB16–0089Swedish Research Council, 2016-03943Swedish Research Council, 2016-04319Available from: 2026-01-12 Created: 2026-01-12 Last updated: 2026-01-12Bibliographically approved

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Karamat, FazeelatVergara, AlexanderBlomberg, JeanetteLehotai, NoraRentoft, MatildaStrand, ÅsaBjörklund, Stefan

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Karamat, FazeelatVergara, AlexanderBlomberg, JeanetteLehotai, NoraRentoft, MatildaStrand, ÅsaBjörklund, Stefan
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Department of Medical Biochemistry and BiophysicsDepartment of Molecular Biology (Faculty of Medicine)Department of Diagnostics and InterventionUmeå Plant Science Centre (UPSC)
Medical Biotechnology (Focus on Cell Biology, (incl. Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy)Genetics and GenomicsBioinformatics and Computational Biology

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