Transcription condensates are promoter hubs that enhance transcriptional bursts
Pandey, G.; Galeota-Sprung, J.; Budhathoki, A.; Medhanie, F. A.; Spille, J.-H.
Show abstract
Transcription of eukaryotic genes by RNA Polymerase II occurs in temporal bursts and spatial clusters. It is regulated by dozens of transcription factor and coactivator proteins and guided by epigenetic histone marks. Colocalization of transcription machinery in dense foci suggests that cooperative effects orchestrate the process. Factory or condensate models provide a framework for the spatial assembly of the transcription machinery at highly active chromatin loci. But conventional methods lack the resolution to determine how chromatin regulatory elements interact with spatial clusters of the transcription machinery, and whether chromatin structural features modulate functional output. Here, we use super-resolution microscopy to elucidate nanoscale organization of regulatory chromatin at Pol II clusters across scales. We find that Pol II clusters exist on a continuous spectrum of sizes and represent promoter chromatin hubs. We uncover a layered organization of regulatory chromatin, where Pol II clusters form at H3K27ac and H3K4me3-rich domains while H3K4me1 positions peripherally at the surface of large Pol II clusters. Perturbation experiments are consistent with a model in which cohesin loop extrusion forms the active chromatin scaffold underlying transcription assemblies while condensate-driven interactions play only a minor role in genome organization at these sites. Importantly, the number and size of transcriptional burst size increases with Pol II cluster size, revealing directly the cooperative benefits of transcription organization in promoter hubs and a functional consequence of local chromatin structure.
Matching journals
The top 3 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Extrusion fountains are hallmarks of chromosome organization emerging upon zygotic genome activation 98%
- Fine-mapping of nuclear compartments using ultra-deep Hi-C shows that active promoter and enhancer elements localize in the active A compartment even when adjacent sequences do not 97%
- YAP charge patterning mediates signal integration through transcriptional co-condensates 97%
Similar papers in this journal
Similar papers in this journal
- Chromatin arranges in chains of mesoscale domains with nanoscale functional topography independent of cohesin 96%
- Replication-dependent histone (Repli-Histo) labeling dissects the physical properties of euchromatin/heterochromatin in living human cells. 96%
- Clusters of lineage-specific genes are anchored by ZNF274 in repressive perinucleolar compartments 96%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.