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Tufegdzic Vidakovic, A.

Publications and source records attributed to Tufegdzic Vidakovic, A..

3 recordsLinked to original sources

Post-transcriptional glucocorticoid receptor signalling synchronises circadian rhythms

Keeping cellular circadian clocks synchronised is critical for cellular and physiological health. Glucocorticoid (GC) hormones are the most potent systemic timing signal for cellular clocks, acting via the glucocorticoid receptor (GR), a transcription factor conventionally thought to synchronise cells by translocating into the nucleus and activating the transcription of clock genes. Our findings overturn this model: acute changes in GR translocation and nascent transcription are both dispensable for GC-resetting of the circadian clock. Instead, physiological GC pulses act post-transcriptionally to rapidly increase Period1 mRNA through enhanced RNA processing, not synthesis. This elevates PER1 protein production which, alone, is sufficient to reset the clock. Yet each pulse resets only a subset of cells, explaining why, in vivo, repeated daily hormonal cues are required for full re-entrainment after jet lag or shift work. We propose a new model for hormonal signalling to the circadian clock and identify RNA processing kinetics as a general regulatory lever for nuclear receptor signalling.

molecular biology↗

Hierarchical buffering of cellular RNA polymerase II pools maintains transcriptional homeostasis

RNA polymerase II (Pol II) abundance and transcriptional output are coordinated across diverse conditions to maintain mRNA homeostasis. To determine whether Pol II acts as a limiting factor for transcription, we combined acute perturbations with quantitative single-cell imaging and genome-wide profiling. We find that transcription remains stable across 70-180% of normal Pol II levels in human cells. This robustness emerges from hierarchical buffering mechanisms operating on distinct timescales. Within tens of minutes after monoallelic depletion of Pol II subunit POLR2A, cells maintain steady transcriptional output by drawing polymerases from a nucleoplasmic reserve pool. However, over hours, cellular Pol II holoenzyme levels also recover, driven by constitutive excess POLR2A subunit production rather than feedback sensing. Finally, strong depletion over days activates additional compensatory mechanisms. Together, these results reveal how temporal separation of buffering mechanisms provides robustness to perturbations of essential machinery, illuminating how cells maintain homeostatic control of essential complexes.

cell biology↗

Stalling of elongating Pol II triggers Ser7 phosphorylation in trans to drive transcription recovery

DNA is scattered with obstacles that stall RNA polymerase II (Pol II) and block the production of full-length transcripts. Two mechanisms are known to resolve stalled Pol II: transcription-coupled nucleotide excision repair (TC-NER) and the "last resort" Pol II ubiquitylation-degradation pathway. Here, we uncover a third, distinct mechanism that alerts incoming Pol II molecules to roadblocks ahead and primes them for efficient elongation. We show that transcription stalling triggers GSK3-mediated phosphorylation of Ser7 residues (Ser7P) on the Pol II C-terminal domain. Unexpectedly, this phosphorylation occurs in trans: obstacles in gene bodies induce Ser7P on Pol II complexes at gene beginnings. This modification enables processive transcription while restraining excessive Pol II degradation by the "last resort" pathway. Our findings reveal an adaptive system that preserves transcriptional homeostasis by coordinating polymerase behavior across the gene in response to elongation stress.

molecular biology↗