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Ryabova, L.

Publications and source records attributed to Ryabova, L..

2 recordsLinked to original sources

TOR kinase controls shoot development by translational regulation of cytokinin catabolic enzymes

Plants continuously adjust their developmental program including organ initiation and growth in accordance with endogenous and environmental signals. This plasticity requires that a diversity of signaling pathways acts in concert to modulate stem cell activity. We have shown previously that the TOR kinase network integrates metabolic- and light signals and controls expression of WUSCHEL, a transcriptional master regulator of stem cells in the shoot apical meristem. However, the mechanism linking TOR activity with the WUSCHEL promoter remained unresolved. Here we demonstrate that TOR regulates the accumulation of trans-zeatin, the cytokinin species mainly responsible for shoot development. Importantly, we identify translational repression of RNAs encoding cytokinin degrading CYTOKININ OXIDASES/DEHYDROGENASE enzymes by TOR as an underlying mechanism. Employing this system, plants can quickly adjust stem cell activity and developmental programs in response to changes in their environment.

plant biology↗

TOR represses stress responses through global regulation of H3K27 trimethylation in plants

Target of Rapamycin (TOR) functions as a central sensory hub to link a wide range of external stimuli to gene expression. However, the mechanisms underlying stimulus-specific transcriptional reprogramming by TOR remains elusive. Our in silico analysis in Arabidopsis demonstrates that TOR-repressed genes are associated with either bistable or silent chromatin states. Both states regulated by TOR signaling pathway are associated with high level of H3K27me3 deposited by CURLY LEAF (CLF) in specific context with LIKE HETEROCHROMATIN PROTEIN1 (LHP1). Combinations of epigenetic modifications H3K4me3 and H3K27me3 implicate bistable feature which alternates between on and off state allowing rapid transcriptional changes upon external stimuli. Chromatin remodeler SWI2/SNF2 ATPase BRAHMA (BRM) activates TOR-repressed genes only at bistable chromatin domains to rapidly induce biotic stress responses. Here we demonstrated both in silico and in vivo that TOR represses transcriptional stress responses through global maintenance of H3K27me3.

plant biology↗