Treatments with Diquat Reveal the Relationship between Protein Phosphatases (PP2A) and Oxidative Stress during Mitosis in Arabidopsis thaliana Root Meristems.
Adrienn KelemenTamás GardaZoltán KónyaFerenc ErdődiLászló Ujlaky-NagyGabriella Petra JuhászCsongor FreytagMárta M-HamvasCsaba MáthéPublished in: Plants (Basel, Switzerland) (2024)
Reversible protein phosphorylation regulates various cellular mechanisms in eukaryotes by altering the conformation, activity, localization, and stability of substrate proteins. In Arabidopsis thaliana root meristems, histone post-translational modifications are crucial for proper cell division, and they are also involved in oxidative stress signaling. To investigate the link between reactive oxygen species (ROS) and mitosis, we treated various Arabidopsis genotypes, including wild-types and mutants showing dysfunctional PP2A, with the ROS-inducing herbicide diquat (DQ). Studying the c3c4 double catalytic subunit mutant and fass regulatory subunit mutants of PP2A provided insights into phosphorylation-dependent mitotic processes. DQ treatment reduced mitotic activity in all genotypes and caused early mitotic arrest in PP2A mutants, likely due to oxidative stress-induced damage to essential mitotic processes. DQ had a minimal effect on reversible histone H3 phosphorylation in wild-type plants but significantly decreased phospho-histone H3 levels in PP2A mutants. Following drug treatment, the phosphatase activity decreased only in the stronger phenotype mutant plants ( fass-5 and c3c4 ). Our findings demonstrate that (i) the studied PP2A loss-of-function mutants are more sensitive to increased intracellular ROS and (ii) DQ has indirect altering effects of mitotic activities and histone H3 phosphorylation. All these findings underscore the importance of PP2A in stress responses.
Keyphrases
- wild type
- reactive oxygen species
- arabidopsis thaliana
- cell cycle
- oxidative stress
- protein kinase
- dna damage
- cell death
- celiac disease
- transcription factor
- single cell
- ischemia reperfusion injury
- emergency department
- cell proliferation
- dna methylation
- stem cells
- mesenchymal stem cells
- bone marrow
- molecular dynamics simulations
- binding protein
- combination therapy
- replacement therapy
- crystal structure
- drug induced
- induced apoptosis