| Literature DB >> 31421980 |
Diana A Stavreva1, David A Garcia2, Gregory Fettweis3, Prabhakar R Gudla3, George F Zaki4, Vikas Soni3, Andrew McGowan3, Geneva Williams3, Anh Huynh5, Murali Palangat3, R Louis Schiltz3, Thomas A Johnson3, Diego M Presman3, Matthew L Ferguson5, Gianluca Pegoraro3, Arpita Upadhyaya6, Gordon L Hager7.
Abstract
Genes are transcribed in a discontinuous pattern referred to as RNA bursting, but the mechanisms regulating this process are unclear. Although many physiological signals, including glucocorticoid hormones, are pulsatile, the effects of transient stimulation on bursting are unknown. Here we characterize RNA synthesis from single-copy glucocorticoid receptor (GR)-regulated transcription sites (TSs) under pulsed (ultradian) and constant hormone stimulation. In contrast to constant stimulation, pulsed stimulation induces restricted bursting centered around the hormonal pulse. Moreover, we demonstrate that transcription factor (TF) nuclear mobility determines burst duration, whereas its bound fraction determines burst frequency. Using 3D tracking of TSs, we directly correlate TF binding and RNA synthesis at a specific promoter. Finally, we uncover a striking co-bursting pattern between TSs located at proximal and distal positions in the nucleus. Together, our data reveal a dynamic interplay between TF mobility and RNA bursting that is responsive to stimuli strength, type, modality, and duration. Published by Elsevier Inc.Entities:
Keywords: 3D orbital tracking; RNA synthesis; bursting kinetics; circadian cycle; glucocorticoid receptor; high-throughput imaging; single cell; single molecule tracking; transcription dynamics; ultradian hormone stimulation
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Year: 2019 PMID: 31421980 PMCID: PMC6754282 DOI: 10.1016/j.molcel.2019.06.042
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970